Skip to main content

REVIEW article

Front. Pharmacol., 14 July 2021
Sec. Inflammation Pharmacology

Natural Anti-Inflammatory Compounds as Drug Candidates for Inflammatory Bowel Disease

  • 1School of Pharmaceutical Sciences Xiamen University, Xiamen, China
  • 2Institute of Gastrointestinal Oncology, Medical College of Xiamen University, Xiamen, China
  • 3Department of Gastrointestinal Surgery, Zhongshan Hospital of Xiamen University, Xiamen, China

Inflammatory bowel disease (IBD) represents chronic recurrent intestinal inflammation resulting from various factors. Crohn’s disease (CD) and ulcerative colitis (UC) have been identified as the two major types of IBD. Currently, most of the drugs for IBD used commonly in the clinic have adverse reactions, and only a few drugs present long-lasting treatment effects. Moreover, issues of drug resistance and disease recurrence are frequent and difficult to resolve. Together, these issues cause difficulties in treating patients with IBD. Therefore, the development of novel therapeutic agents for the prevention and treatment of IBD is of significance. In this context, research on natural compounds exhibiting anti-inflammatory activity could be a novel approach to developing effective therapeutic strategies for IBD. Phytochemicals such as astragalus polysaccharide (APS), quercetin, limonin, ginsenoside Rd, luteolin, kaempferol, and icariin are reported to be effective in IBD treatment. In brief, natural compounds with anti-inflammatory activities are considered important candidate drugs for IBD treatment. The present review discusses the potential of certain natural compounds and their synthetic derivatives in the prevention and treatment of IBD.

Introduction

Inflammatory bowel disease (IBD) is a complex condition with unknown etiology and a tendency of recurrence throughout life. It is a concerning public health issue that is becoming increasingly critical. IBD may be classified into two major pathological subtypes: Crohn’s disease (CD) and ulcerative colitis (UC). UC is a non-specific chronic inflammatory disorder of the rectum and colon, limited mainly to the large intestinal mucosa and submucosa. CD is a chronic inflammatory granuloma, which frequently occurs in the adjacent colon and terminal ileum, although it may affect the whole digestive tract, with a segmental distribution. The etiology of IBD is unclear so far, although the disorder exhibits genetic susceptibility, and its occurrence and development have been associated with immune disorders, environmental factors, and mucosal dysfunction (Park and Jeen, 2019; Larabi et al., 2020; Lee and Chang, 2021). Recent studies have suggested that IBD might be connected with the loss of gut microbial immunological tolerance (Nunes et al., 2018). IBD has become a global disease because of the increasing incidence rate caused by the continuous progress of global industrialization, urbanization, and improving diagnosis (Ng et al., 2017; GBD 2017 Inflammatory Bowel Disease Collaborators, 2020). According to statistics, Europe reports the highest annual incidence rates for CD and UC, 12.7/100,000 and 24.3/100,000 individuals each year, respectively (Molodecky et al., 2012; Mak et al., 2020). Previous studies have shown that the incidence of IBD in Western developed countries tends to be stable (Kotze et al., 2020). Although the incidence of IBD is gradually increasing in Latin America and Asia, the overall prevalence of IBD remains lower compared to the Western world (Kotze et al., 2020).

Currently, the clinical treatment for IBD is mainly based on drugs and surgery, although drug treatment is often accompanied by adverse reactions, which limits the drug usage, and its effect cannot be guaranteed (Rosen et al., 2015; Verstockt et al., 2018). For example, treatment with anti-TNF-α agents increases the risk of opportunistic infection and malignant tumor (Kennedy et al., 2019). Tofacitinib might cause severe infection and increase the risk of malignant tumor (Danese et al., 2018). Surgical treatment also has the risk of complications such as pelvic infection, massive hemorrhage, and intestinal perforation, and it is limited by the age of the patients and physical status (Bhakta et al., 2016). Therefore, it is imperative to develop novel treatment approaches for IBDs. In this context, certain natural compounds and their synthetic derivatives represent a potential research direction and have been adopted in several current research works to unravel their potential in preventing and treating IBD and identify novel candidate drugs for IBD. This paper aims to discuss the present situation of IBD and the natural compounds with the potential to treat IBD.

Hallmarks of Inflammatory Bowel Disease

Epidemic Distribution of Inflammatory Bowel Disease in China

According to the existing epidemiological studies conducted in China, Guangdong Province (southern China) has the highest IBD incidence of 1.97–3.44/million individuals each year. In comparison, the Sichuan (Chengdu in southwest China) and Shanxi (Xi’an in northern China) have the lowest IBD incidence of 0.54/million individuals each year (Cui and Yuan, 2018). These data indicate that in China, the incidence of UC and CD is higher in the south compared to the north. Approximately 25% of the IBD patients are aged below 18, and the disease is often more severe in adolescents than in adults. Although China, despite being the most populous developing country in the world, has managed to maintain relatively low prevalence and incidence rates of IBD compared to most of the western nations, an overall upward trend has been observed, with the incidence of IBD rising sharply in recent years (Jiang et al., 2006; Yang et al., 2014a). To date, a national population epidemiological study covering all parts of China is non-existent, and there could be a significantly higher number of IBD patients in China than expected/reported, even higher than the numbers in the western nations (Huang and Aw, 2020). Therefore, vigilance is a must. The current situation of IBD in China is just the tip of the iceberg. Besides China, the prevalence and incidence rates of IBD have demonstrated an upward trend worldwide, indicating that IBD is gradually becoming a global health concern (Kaplan, 2015). According to reports, 80% of the CD patients require intestinal surgery, while over 10% of them require permanent colostomy (Cosnes et al., 2011), which is a great burden on the patients as well as on the whole society (Park et al., 2020).

Pathogenesis of Inflammatory Bowel Disease

The etiology of IBD is complex and not completely understood, and could be related to the interaction with the environment, heredity, infection, immunity, and intestinal microorganisms as showed in Figure 1 (Kim et al., 2019). The relevant literature reports multifactorial findings. A detailed understanding of the pathogenesis is necessary for developing an appropriate treatment plan and resolving the limitations and shortcomings of the existing treatment model. The current research on IBD is focused on helper T cells (Th) as previous studies have confirmed that CD is an inflammation condition dominated by Th-1, which produce a large amount of IFN-g and TNF after induction by IL-12, and UC is associated with the Th-2 cells, in which there is a higher production of IL-4, IL-5, and IL-13 while the level of IFN-g is normal (Alfen et al., 2018; Barnig et al., 2019; Bauché et al., 2020; Tindemans et al., 2020). Chronic mucosal inflammation mediated by Th1 or Th2 cells leads to the loss of intestinal wall integrity. It prevents the epithelial barrier regeneration, allowing the intestinal contents, including microorganisms and dietary antigens, to easily infiltrate into the intestine and activate the lamina propria-based immune response, which then leads to IBD. In addition to the classical Th1 and Th2 cell reactions, Th17 cells are reported to have strong correlations with the inflammatory reactions in IBD (Kim et al., 2011; Cătană et al., 2015; Salem et al., 2019). Genetic studies have revealed a certain relationship between the genetic susceptibility of CD and the expression of Th17 cytokines (Patel and Kuchroo, 2015). Th17 cells contribute to the secretion of IL-17 and promote the occurrence of allergic reactions and autoimmunity. Interleukin (IL)-23 is capable of inducing Th17 cells to produce cytokines through the congenital lymphocytes (ILCs) (Cella et al., 2009; Buonocore et al., 2010). IL-17 may induce the production of pro-inflammatory chemokines and cytokines, thereby attracting monocytes and neutrophils at the site of inflammation which promotes the occurrence of inflammatory reactions (Mantovani et al., 2011; Lee et al., 2013; Flannigan et al., 2017; Nadeem et al., 2020). Inhibition of Th17 cells may inhibit the occurrence of inflammation and decelerate the development of colitis. Dendritic cells (DCs) may induce the initial T cells to differentiate into Th1 cells by secreting IL-12, and also produce a large amount of interferon (IFN)-γ to mediate the intestinal mucosal inflammation. The incidence of IBD is closely related to susceptibility genes, such as the IL-23R gene (cWurdinger et al., 2012). Previous studies have revealed that the mechanism underlying IBD pathogenesis involves IL-23R variants. Typically, IBD cases exhibit markedly increased serum IL-23 expression than healthy subjects, which is also positively correlated with UC severity (Neurath, 2019). Since the IL-23 axis is a commonly observed inflammatory pathway in chronic enteritis, blocking the transmission of information through the IL-23/Th17 axis could reduce the development of inflammation (Geremia et al., 2014; Zwicky et al., 2020). In addition, the IL-23R variants are linked with certain extraintestinal diseases associated with IBD, such as psoriasis and ankylosing spondylitis (Brant et al., 2017). Modern treatment of IBD mainly relies on drugs capable of inhibiting these inflammations (Mumolo et al., 2018). Other susceptibility genes related to IBD are NOD2, the autophagy-related genes ATG16L1 and IRGM, IL12B, JAK2, STAT3, CARD15, among others (Lees et al., 2011; Bunte and Beikler, 2019). In addition, Toll-like receptors are strongly associated with the pathogenic mechanism of IBD. Toll-like receptor (TLR) is a pattern recognition receptor that recognizes pathogen-related molecular patterns (PAMPs). Upon activation, TLR is dimerized and then induces a downstream signal cascade reaction to mediate IκB phosphorylation. Consequently, various inflammatory cytokines are produced, leading to the activation of the NF-κB immune signal pathway for excessive immune stimulation. In addition, these cytokines promote Th1/Th2 cell growth and differentiation and modulate dendritic cells (DC) maturation (Chen et al., 2016; Satoh and Akira, 2016; Shi et al., 2019). NOD2, a susceptibility gene, negatively regulates the TLRs and inhibits the overactivation of the NF-κB immune signal pathway. In certain NOD2 variants, this negative regulation might be absent, and the NF-κB immune signal pathway may be abnormally activated, thereby inducing massive Th-1 response and several inflammatory pathways (Schirbel et al., 2019). NOD2 variants may also decrease the ability of the intestinal wall to respond to LPS, which could be related to inflammatory bowel disease (Bonen et al., 2003; Strober et al., 2014). Besides the NF-κB immune signal pathway, the JAK/STAT and the TGF-β1/SMADs signal pathways are involved in the pathogenic mechanism of IBD (Cordes et al., 2020; de Ceuninck van Capelle et al., 2020). In addition, genome-wide association studies have, for the first time, indicated that the pathogenesis of CD might be associated with autophagy (Rioux et al., 2007). Autophagy is a process of cell degradation and recycling, which also contributes to removing intracellular microbes, and is regulated via the lysosomes. Impaired autophagy has been observed in the cells of a series of IBD patients, and several CD-related genetic loci are involved in autophagy homeostasis (Rioux et al., 2007). In 2008, a study evaluated the abnormal miRNA levels in the intestines of UC patients (Wu et al., 2008). Further studies confirmed a possible involvement of miRNAs in IBD via CD68 and NOS2, and also intestinal autophagy through the modulation of the autophagic genes associated with IBD, including ATG16L1, NOD2, and IRGM. It is reported that miRNAs participate in autophagy by regulating the responses of unfolded proteins to the autophagy and IBD-related endoplasmic reticulum (ER) stress, which is achieved via the modulation of the mTOR and NF-κB signal pathways, which allows them to influence pro-/anti-inflammatory effects and inflammatory factors (Sohn et al., 2012; Krissansen et al., 2015; Boros and Nagy, 2019; Arab et al., 2021). The pathways such as NOD2 and autophagy pathways may lead to functional damage in Paneth cells, dendritic cells, macrophages, and absorbent IECs, increasing the risk of developing IBD.

FIGURE 1
www.frontiersin.org

FIGURE 1. The etiology of IBD.

Therapeutic Targets and Drug-Use Strategy for Inflammatory Bowel Disease

Various therapeutic targets have been approved for IBD. Several attempts have been made to create the next generation of small molecules to be used as specific targets for IBD therapy. For example, in a previous, it was demonstrated, for the first time, that the changes occurring in TGF-β1 in UC and CD are different (Del Zotto et al., 2003). A balanced intestinal immune dynamic relies on the regulation of TGF-β by specific intestinal microorganisms, and abnormal transforming growth factor-β signal has been reported in some instances of IBD, which suggests that TGF-β1 could be used as a therapeutic target in IBD therapy (Ihara et al., 2017). However, several novel methods that could successfully block TNF in RA were ineffective in treating CD (Friedrich et al., 2019), suggesting the possible involvement of additional mechanisms besides simply neutralizing soluble TNF (Levin et al., 2016). In order to develop effective IBD therapies, it is imperative to identify novel potential drug targets and re-examine the existing targets for IBD. The current therapeutic targets for IBD are shown in Table 1.

TABLE 1
www.frontiersin.org

TABLE 1. Therapeutic targets of IBD.

In the past decades, extensive research has been conducted to decipher the pathogenesis of IBD, with good results in terms of treatment outcomes. The existing drug treatments for IBD are designed for suppressing massive inflammation and assisting in repairing the digestive tract lining, thereby improving the quality of life of patients with IBD (Wils et al., 2016). The frequently used clinical agents include corticosteroids, aminosalicylates, immunosuppressants, biotherapy agents [different antitumor necrosis factor (TNF) compounds], selective intestinal integrin antagonists, TNF inhibitors, and IL-12/IL-23 inhibitors approved by the Food and Drug Administration (FDA) (Baumgart and Sandborn, 2007). However, these therapeutic agents have certain limitations regarding efficacy, side effects, and administration routes, and their cost is also considerably high. Moreover, long-term usage of drugs or treatments that affect the immune system directly may enhance cancer genesis and progression (Axelrad et al., 2012). If the drug therapy is unsuccessful or the case is complex, surgical intervention is necessary.

European and American guidelines recommend some aminosalicylic acid drugs, such as mesalamine, olsalazine, balsalazide and sulfasalazine, for the induction and maintenance of remission of UC in mild and moderate activity (Harbord et al., 2017). The main adverse reactions are pancreatitis, cardiotoxicity, hepatorenal toxicity and sexual dysfunction (Wang et al., 2016). Corticosteroids (prednisone, hydrocortisone, budesonide, prednisolone, dexamethasone) are mainly used in moderate and severe IBD, especially in acute attacks. Corticosteroids play a decisive role in immunosuppression effects while it also causes severe adverse reactions, such as osteoporosis, mood changes, sleep disorders, which increased the mortality (Berends et al., 2019; Damião et al., 2019). Traditional small molecular immunosuppressive drugs, including azathioprine, 6-mercaptopurine, and methotrexate, inhibit inflammation and inhibit immune response and increase the risk of infection (Broekman et al., 2017; Liu et al., 2017). Currently, the treatment of new biologics for IBD are emerging, including antitumor necrosis factor, anti-adhesion molecule agents, anti-IL-12/IL-23 agents, Janus kinase (JAK) inhibitors. Some novel agents are still under development, becoming the primary option in IBD pharmacological therapies (Chudy-Onwugaje et al., 2019). Tumor necrosis factor inhibitors, among the most commonly used therapeutic drugs, including Remicade (infliximab) and AVX-47091, may improve the clinical scores and mucosal healing in several patients while prolonging the non-recurrence period (Dubé et al., 2015; Andersen et al., 2017). However, patients treated with anti-TNF-α agents will increase the risk of adverse events such as pulmonary tuberculosis and non-melanoma skin cancer (Lichtenstein et al., 2012; Silva et al., 2012; Terdiman et al., 2013). At the same time, tofacitinib and mongersen (GED-0301) are the inhibitors of the Smad7 and JAK signaling pathways (Argollo et al., 2017). The commonly used JAK inhibitors are tofacitinib and filgotinib, in which FDA and EMA have approved tofacitinib to treat moderate and severe UC patients, but there is a black box warning of severe infection and increased risk of malignant tumor in the drug instruction (Olivera et al., 2017). Ustekinumab, aprimod mesylate, risankizumab, brazikumab, mirikizumab are IL-12/IL-23 inhibitors. For instance, aprimod mesylate suppresses the transcription of IL-12/IL-23. In addition, the anti-IL-12ABT-874/J695 monoclonal antibodies may be adopted for targeting the p40 units between IL-12 and IL-23, while SCH-900222 may be used for targeting the p19 subunit specific to IL-23 (Sands et al., 2010). Ustekinumab, an antibody against IL-21 and IL-21, also decreases IL-17 production in the lymphocytes of lamina propria, which inhibits both Th17 and Th1 cells (Fina et al., 2008; Sandborn et al., 2012). In ustekinumab clinical trials, the most common adverse reactions included nasopharyngitis, upper respiratory tract infection, and cough (Davies et al., 2019). Some drugs target the components of the transport pathway, such as MadCAM-1 targeting the adhesion molecules, and anti-α4β7, natalizumab, vedolizumab, and etrolizumab targeting anti-integrin (Moens et al., 2019; Allner et al., 2020). At present, various studies have proved that vedolizumab has good safety in the treatment of IBD, but the high price increases the burden on the patients (Yu et al., 2018a).

It is essential to develop novel therapeutic drugs for IBD. According to recent studies, an increasing number of IBD cases are being reported each day, and in particular, the number of confirmed cases in pediatrics has increased sharply. Moreover, long-term UC and CD are expected to lead to an elevated incidence of intestinal cancer (Bopanna et al., 2017). Parenteral manifestations of IBD are also common, involving the skin, joints, eyes, and kidneys (Bernstein et al., 2001). In addition, there is a higher incidence of other chronic immunological disorders, including primary sclerosing cholangitis, psoriasis, and ankylosing spondylitis (Bernstein et al., 2005). If appropriate measures are not implemented in the next few years, the burden on families and society will increase immensely.

In comparison to western medicine, natural compounds provide the advantages of high efficacy, less adverse reactions, and good tolerance and have, therefore, become the focus of IBD drug research (Khan et al., 2019). In view of the urgent requirement for an effective IBD treatment, the development of novel therapeutics is of significance, and identifying and analyzing the natural compounds exhibiting anti-inflammatory activity may be the appropriate research direction. It would be beneficial to derive lessons from previous research and then focus on developing novel treatments to accelerate the translation of basic research results to clinical application.

Anti-Inflammatory Natural Compounds as Promising Candidates for Inflammatory Bowel Disease Treatment

Despite the incredible progress of modern medicine, there remain significant obstacles in the path of curing inflammatory bowel disease, which is one of the challenging health concerns for humans worldwide. Novel treatment options for IBD are continuously explored, and novel drugs are being discovered. However, chemically synthesized drugs are always accompanied by adverse reactions. Furthermore, their routes of administration are limited, and their effect cannot be guaranteed. Therefore, in searching for novel pharmacologically active substances that could be used for treating IBD, natural ingredients from various sources, such as plants, animals, and microorganisms, are receiving great attention nowadays. Studies have demonstrated that natural products, including natural medicines, their extracts, and their metabolites, can effectively treat IBD. The section ahead describes these natural products, such as flavonoids, terpenoids, polysaccharides, and alkaloids.

Flavonoids

Naringenin (4',5,7-trihydroxyflavanone flavonoid) is the aglycon of naringin which is abundant in grapefruit (Zaidun et al., 2018; Den Hartogh and Tsiani, 2019). In recent studies, naringenin has demonstrated potential effects in different experimental models of IBD (Pinho-Ribeiro et al., 2016; Zeng et al., 2018). A study reported that naringeninis insoluble in water and soluble in organic solvents as alcohol (Zobeiri et al., 2018). A study demonstrated that naringenin could significantly improve the extent of intestinal edema in a dextran sodium sulfate (DSS)-induced colitis mouse model (Alam et al., 2014). Dou and colleagues reported that naringenin could protect against the DSS-caused colitis in a mouse model. Administration of naringenin before modeling markedly mitigated colitis while promoting monocyte chemotaxis and the colonic secretion of pro-inflammatory factors, such as intercellular adhesion molecule-1 (ICAM-1) and inducible NO synthase (iNOS) (Dou et al., 2013). In addition, the mRNA expressions of IL-6, MCP-1, TNF-α, and cyclooxygenase-2 (Cox2) were decreased. Moreover, the in vitro NF-κB reporter assays conducted in naringenin-treated human colonic HT-29 cells revealed that the expression of NF-κB luciferase mediated by TNF-α was significantly suppressed. The above findings are consistent with the results of studies conducted in vitro. Naringenin was also demonstrated to protect against colitis in two diverse experimental models. It was reported that naringenin could reduce the expression of PGE2, macrophage inflammatory protein (MIP-2), NO, IL-1b, IL-6, and IL-17A interferon (INF)-c by elevating the colonic mucosal content (Al-Rejaie et al., 2013).

Catechins are a kind of polyphenols whose chemical structure have a flavonoid parent nucleus structure, occurring in certain foods and medicinal plants, such as tea, legumes, Rubiaceae, Abarema cochliocarpos, Camellia sinensis, teas, Mouriri pusa Garden, buckwheat, grapes, cocoa beans, litchis, and apples (Fathima and Rao, 2016a; Martínez Leal et al., 2018; Cardoso et al., 2020). Catechins mainly include catechin, epicatechin (EC), epicatechin gallate (ECG), (2)-epigallocatechin-3-gallate (EGC) and its stereoisomer gallocatechin (GC), EGCG, and stereoisomer gallocatechin gallate (GCG). Recently, the role of catechins in the prevention and treatment of colitis has been gradually explored. As discovered by Xue et al., EGCG relieved the colitis induced by DSS in the experimental rats. EGCG administered orally at 50 mg/kg BW efficiently reduces colonic mucosal injury and suppresses inflammatory response, consistent with previous findings (Mascia et al., 2010; Sergent et al., 2010; Oz et al., 2013). In addition, EGCG (40 mg/kg BW) also improved the Th1/Th2 balance and diminished the expression levels of TLR4/MyD88/NF-κB pathway-Related proteins (Bing et al., 2017). Increasing studies indicated that the catechins can alter the intestinal flora. Bin and colleagues reported that catechin could inhibit Bacteroidetes and Firmicutes’ growth while down-regulated the rate of Bacteroidetes to Firmicutes (Xue et al., 2016). Catechin also has a selective preference for the virulence of bacteria. Fathima A and workers used catechin to treat gram-positive bacteria (B. subtilis) and gram-negative bacteria (E. coli). They observed that catechin could be more toxic toward gram-positive bacteria (Fathima and Rao, 2016b). Through the continuous deepening of the research on catechins, researchers found that the concentrations of catechins play an essential role when they are applied to intestinal inflammation. Du and colleagues discovered that the low concentrations of EGCG (20 mg/kg/d) tended to have a better effect on DSS-induced colitis compared to high concentrations of EGCG (50 mg/kg/d). EGCG administered orally at 20 mg/kg/d has higher body weight and lower DAI scores (Du et al., 2019). Bitzer et al. also found that when they administered orally at 3.2 mg/ml EGCG containing drinking water, which equates to 480 mg/kg/d (assuming mice drink 15 ml/100 g body weight of water per day), to feed DSS-induced CF-1 mice, the bodyweight loss induced by DSS was significantly accelerated (Bitzer et al., 2016). These findings were consistent with previous findings. To be specific, Mihye Kim and colleagues demonstrated that higher doses of green tea polyphenols could aggravate DSS-induced colitis (Kim et al., 2010). The same results reported by Guan et al. that EGCG (0.1–0.5%), which equates to 150–750 mg/kg/d, exacerbated bleeding and body weight loss (Guan et al., 2012). A clinical trial observed that treat with EGCG is a benefit to UC patients. Twenty UC Patients were treated by 400 mg of EGCG twice daily, after 56 days, the UC disease activity index score of these Patients was reduced. Moreover, EGCG treatment resulted in only minor side effects (Dryden et al., 2013). Therefore, the dose of catechol is the key to its treatment and prevention of colitis, but there are not many clinical reports on the dose suitable for humans, and further studies are needed.

Hesperetin (5,7,3ʹ-trihydroxy-4ʹ-methoxyflavanone) is a natural flavanone glycoside, abundant in citrus fruits, including lemons, limes, mandarins, and oranges (Liu et al., 2016; Shirzad et al., 2017; González-Alfonso et al., 2018). Hesperetin represents various pharmacological characters, including anti-inflammatory, anti-oxidative, anti-tumor potentials (Parhiz et al., 2015; Alu'datt et al., 2017; Chen et al., 2019a; Li et al., 2020a). It is reported to alleviate colitis via blocking the intestinal epithelial necroptosis in the DSS-induced experimental mice model (Zhang et al., 2020). Mayada G and workers reported that hesperetin (50 and 100 mg/kg, p.o.) could improve TNBS-induced colitis symptoms in the experimental rat model, including body weight changes and macroscopic colon damage. In addition, hesperetin also significantly decreased the protein expression of p-JAK2 and p-STAT3 while significantly increased the protein expression of SOCS3 (Elhennawy et al., 2021). As discovered by Fatin et al., hesperetin administered at 100 mg/kg, p.o orally, protected against TNBS-induced colitis in the experimental rat model. It could significantly reduce the levels of MPO, MDA, and pro-inflammatory (Polat et al., 2018). The outcomes were consistent with the results of He et al. (2019a). Hesperetin, as the aglycon of hespeprtin, also possesses an anti-inflammatory character (Guazelli et al., 2021). Clinical data regarding the treatment of colitis have not been accurately studied, but researchers used orange juice, which contains abundant hesperetin, to evaluate its effect on the healthy. A report suggested that the plasma concentration of flavonoids is relatively high after taking orange juice. Then, people who regularly consume orange juice maybe have considerable health effects (Erlund et al., 2001).

Genistein (4′, 5, 7-trihydroxyisoflavone) is a plant-derived isoflavone, which is well-known. The sources of genistein are soy-based foods, such as soy cheese, soy drinks, soy milk, and soy-based beverages (Ganai and Farooqi, 2015; Sahin et al., 2019). A study observed that mature soybeans constituted 5.6–276 mg/100 g of genistein (Sefrina et al., 2020). Some plants and foods have also been demonstrated to contain genistein, cauliflower, clover sprouts, barley meal, broccoli, sunflower, caraway, and clover seed (Spagnuolo et al., 2015). An increasing number of reports suggested Genistein possesses favorable pharmacological properties in IBD. Zhang and colleagues added 600 mg genistein/kg diet in the daily diet to feed DSS-induced colitis BALB/C mice for 7 days. They found that colonic inflammatory, inflammation, and gut dysfunction could be relieved by feeding with genistein (Zhang et al., 2017a). Abron and workers also demonstrated that genistein could relieve the colitis induced by DSS in the experimental mice. Genistein could promote the conversion of M1 macrophage to M2 and reduced the inflammatory cytokine levels, such as IL-6, TNFα, MCP-1, and IL-1β. Notably, The above study indicated that in a pilot experiment, they found that the 10 mg/kg body weight dose of genistein used in this study was more efficacious in reducing colitis progression than were other tested doses at 5, 20,40, or100 mg/kg (Abron et al., 2018). However, Yu et al. suggest that when genistein is used at doses 5, 15, 45 mg/kg BW to feed DSS-induced colitis BALB/C mice for ten days, the genistein at 45 mg/kg BW should be given priority consideration (Chen et al., 2019b). No clinical studies have been found to have evaluated the appropriate dosage and drug administration time of genistein to benefit colitis patients. However, 16.7 mg genistein given to postmenopausal women with associated vasomotor symptoms was found to be a safe dosage without any adverse effects (Schneider et al., 2019). Thus, the specific dose and drug administration time of genistein to reduce colitis must be further confirmed.

Anthocyanin is a kind of water-soluble natural pigments widely found in plants and foods, such as grape seeds, red grapes, saskatoon berries, Lycium ruthenicum, Murray, blueberries, blackberries, purple sweet potatoes, and purple cabbage. It is colored aglycones obtained from the hydrolysis of anthocyanins (Jaakola, 2013; Sui et al., 2016; Silva et al., 2017). Some Anthocyanins can be absorbed from the stomach and the intestines; the others can reach the large intestine in significant amounts (Fang, 2014). A growing body of evidence confirms that regular intake of anthocyanins could benefit human health (Chun et al., 2007; Del Rio et al., 2010; Sharma et al., 2017b). Anthocyanins could modulate the gut microbiota in improving various diseases (Thumann et al., 2019; Tian et al., 2019; Khan et al., 2020). A report suggested that anthocyanins from the fruits of Lycium ruthenicum Murray to feed mice at 200 mg/kg/d for days 7 days could reverse the decreases in the relative abundances of Porphyromonadaceae, Rikenellaceae, and Prevotellaceae induced by DSS (Peng et al., 2019). In a report by Wu et al., anthocyanins, extracted from blueberry, were administered orally at 10, 20 and 40 mg/kg BW and showed positive effect on TNBS-induced experimental mice (Wu et al., 2011). Anthocyanin extracted from black rice and bilberries showed almost identical efficacy in relieving colitis (Piberger et al., 2011; Zhao et al., 2018). The difference is that the anthocyanins from different sources are not unique in the dose of administration in the experiment colitis mice. In clinical study, a 50 mg/subject anthocyanin dose was given to healthy volunteers and had no side effects (Nomi et al., 2019).

Farrerol is a 2,3-dihydroflavonoid extracted from rhododendron. Farrerol is reported to exhibit various biological effects, such as anti-inflammation, antibiosis, and antioxidation (Lai et al., 2016; Wang et al., 2019a). Xin Ran et al. reported that farrerol could protect against 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis in a mouse model. Administration of farrerol could significantly improve the body weight (BW) changes, damage to the intestinal epithelial barrier, colon length, and clinical scores, while the generation of inflammatory factors was evidently decreased (Azuma et al., 2013). Farrerol is also reported to protect the LPS-treated RAW264.7 cells. Studies have demonstrated that farrerol significantly reduces the production of inflammatory factors, including TNF-α, IL-6, and IL-1β, by suppressing the phosphorylation of NF-κB, p65, AKT, JNK1/2, and ERK1/2 (Ran et al., 2018).

Lcariin (also known as icariin) is the main active ingredient of epimedium. It is an 8-prenylflavonoid glycoside compound and can be extracted from the dried stems and leaves of Epimedium sagittatum, Epimedium pubescens, Epimedium wushanense, Epimedium koreanum, etc. (Ma et al., 2011; Wang et al., 2018a; He et al., 2020). Tao and colleagues observed that icariin, as the main active ingredient of the Epimedium family, protected against DSS-induced enteritis in mice. Moreover, orally administered icariin remarkably mitigates colitis-related pathological alterations and postpones disease progression. In addition, Oral icariin may inhibit p-STAT1, p-STAT3, and p-p65 expressions and pro-inflammatory factor generation in colonic tissues. Furthermore, icariin is also suggested to suppress T lymphocyte activation and growth in a dose-dependent manner, while suppressing the production of pro-inflammatory factors by activated T cells. Icariin is also reported to suppress the phosphorylation of STAT1 (Th1 transcription factor TF) and STAT3 (Th17 TF) in CD4+ T cells (Ci et al., 2012).

Quercetin is a frequently used natural flavonoid compound, generally existing in glycosylated forms, such as rutoside (3-rhamnosy-glucosyl quercetin) and quercitrin (3-rhamnosylquercetin) (Tao et al., 2013). Quercetin is reported to alter the intestinal host–microbial relationship through the recovery of the pro-inflammatory, anti-inflammatory, and bactericidal activities of intestinal macrophages, which leads to improvement in colitis (Nogata et al., 2006). Comalada M and colleagues observed that quercetin protected against DSS-induced colitis in the experimental rat model. Quercetin is released when gut microbiota cleave glycosides, which mediate its activity (Caddeo et al., 2014). In vitro experiments have revealed that quercetin reduces the bone marrow-derived macrophages’ inflammatory response. Moreover, both in vivo or in vitro studies have revealed that quercetin inhibits cytokine production and induces NOS through the suppression of the NF-κB signaling pathway while does not affect c-Jun N-terminal kinase (Ju et al., 2018). Dodda et al. verified that 50/100 mg/kg quercetin decreased the TNBS-caused morphological, clinical, and biochemical alterations in rats (Comalada et al., 2005). Another study demonstrated that quercetin could reduce colon damage, regulate MPO activity and MDA levels, and significantly increase the glutathione (GSH) content in a TNBS-induced mouse colitis model (Dodda et al., 2014a). Camuesco D reported that quercetin (1 mg/kg/day) could assist in restoring the inflamed mucosa. In addition, quercetin treatment could improve the DSS-induced colon injury in rats, which was associated with the downregulation of the colonic NOS activity and improved intestinal oxidative stress mediated by the reduction in the iNOS protein expression (Dodda et al., 2014b). Ulcerative colitis organoids are a reliable experimental system with supporting evidence for the positive effect on colitis after administrating quercetin (Dicarlo et al., 2019). In 2010, quercetin supplements were added to the U.S. Food and Drug Administration’s generally recognized safe (GRAS) list as a supplemental ingredient that can be added to foods and beverages up to 500 mg per serving (Food and Drug Administration, 2019).

Myricetin and kaempferol are natural flavonol compounds that exist mainly in the form of aglycones in plants. Myricetin is a natural polyhydroxy flavonoid compound extracted from the bark, plant seeds and leaves of Myrica rubra (Jones et al., 2011; Imran et al., 2019a; Wang et al., 2019b). The pharmacological activities of these two flavonols, such as antitumor, anti-inflammation, antibiosis, and antioxidation, have been studied extensively (Camuesco et al., 2004). Park et al. reported that kaempferol supplementation in diet mitigated the DSS-induced colitis through a decrease in the biochemical and clinical inflammatory factors, such as IL-6, IL-1b, COX-2, TNF-a, and iNOS, and reduction in the MPO, PGE2, and NO levels in colonic mucosa (Semwal et al., 2016). In addition, kaempferol is reported to upregulate the expression of the trefoil factor family 3 (TFF3) gene, indicating that it exerts a protective effect on the function of goblet cells (Park et al., 2012). The use of 80 mg/kg myricetin was reported to remarkably improve acute UC and upregulate the expressions of TGF-β and IL-10. Myricetin could also evidently elevate the levels of regulatory T cells (Qu et al., 2020).

Apigenin is a flavonoid present naturally in several vegetables and fruits, particularly citrus fruits, with grapefruit being particularly rich in its content (Nabavi et al., 2018; Yu et al., 2020). Apigenin possesses excellent antioxidation and anti-inflammation activities and has been recently demonstrated to provide relief in inflammatory bowel disease. Hoensch and colleagues reported that flavonoids could induce protective cytokines and enzymes, resulting in enhanced anti-inflammation through the upregulation of the arylates of hydrocarbon (AH) receptors (Hoensch and Weigmann, 2018). Marquez-Flores et al. demonstrated that apigenin protected against colitis induced by DSS in mice. Moreover, apigenin reduces COX-2, MMP-3, iNOS, TNF-a, and IL-1b expressions by suppressing the inflammasome pathway (Márquez-Flores et al., 2016).

Luteolin (3',4',5,7-tetrahydroxyflavone) is a common flavonoid that is isolated from celery, honeysuckle, garden bitter melon stems, and other plants across the world (Lin et al., 2008; Aziz et al., 2018; Imran et al., 2019b). Among all flavonoids, luteolin is the one that exerts a significant effect against IBD, as confirmed in various experimental models of IBD. For instance, as reported by Nunes et al., luteolin treatment modulated intracellular inflammatory signaling in HT-29 colonic epithelial cells by suppressing the JAK/STAT pathway (Nunes et al., 2017). Furthermore, this effect was enhanced by administering luteolin in the DDS-mediated colitis mice, probably through the activation of the Nrf2 signaling pathway (Li et al., 2016). According to Nishitani and his colleagues, who conducted both in vivo and in vitro experiments, luteolin mitigated colitis (Nishitani et al., 2013). An in vivo experiment revealed that luteolin protected against colitis in IL-10-deficient (IL-10−/−) mice (Karrasch et al., 2007). A recent study suggested that luteolin could affect the intestinal flora, especially the proportion of Lactobacillus and Prevotella-9 (Li et al., 2021). A brief illustration of the different flavonoid phytochemicals is presented in Figure 2.

FIGURE 2
www.frontiersin.org

FIGURE 2. Chemical structures of flavonoid phytochemicals: (A) Naringenin (B) Catechins (C) Hesperetin (D) Genistein (E) Anthocyanin (F) Farrerol (G) Lcariin (H) Quercetin (I) Myricetin (J) Kaempferol (K) Apigenin (L) Luteolin.

Terpenoids

Ginsenoside is the major component of ginseng. It exhibits immunomodulation and anti-inflammation against IBD and results in an increase in BW and reduction in the colon weight and DAI (Wang et al., 2018b). Notably, the ginseng fruit extract (GB) can suppress the activation of colonic neutrophils, infiltrative T cells, macrophages, and DCs in rats with DSS-mediated colitis. In addition, GB enhances the CD103+CD11c+DCs migration in the colonic tissues of colitis mice while promoting Foxp3+Treg cell differentiation and growth (Zhang et al., 2016a). Fermented red ginseng is reported to inhibit macrophage activity, modulate Th1/Treg cell differentiation, and reduce TNBS-induced colitis (Kim et al., 2018). TGF-β signaling is recognized as a vital anti-inflammatory signal transduction pathway. In vivo experimental studies suggest that ginsenosides enhance intestinal mucosal epithelial cell proliferation and modulate the immunocyte differentiation as well as inflammatory factor production, thereby efficiently mitigating the IBD symptoms (Yang et al., 2020). Yang reported that ginsenoside Rd could alleviate the TNBS-induced UC symptoms in animals by enhancing the oxidation resistance of injured colons and suppressing neutrophil infiltration (Yang et al., 2012a). On the other hand, ginsenoside Rd is reported to decompose the NLRP3 inflammasome via the AMPK ULK1-p62 axis by means of autophagy and reduce the IL-1β production through the suppression of macrophages, which eventually treats acute colitis in mice (Liu et al., 2018). Ginsenoside Rd is also reported to protect against TNBS-mediated recurrent colitis, possibly through the modulation of p38 and JNK activation, decreasing the expression of the pro-inflammatory factors (IL-1β, IL-6, and TNF-α), and suppressing leukocyte aggregation (Yang et al., 2012b). Ginsenoside Rg1 (20 (S)-protopanaxatriol) metabolite could inhibit the effect of a combination of LPS and TLR4 on macrophage membrane, recover the balance between Th17 cells and Tregs, and mitigate the inflammatory disorders, including colitis (Lee et al., 2015). It is reported that ginsenoside Rg1 inhibits the production of pro-inflammatory cytokines (TNF-α and IL-1β) by increasing the NLRP2 expression, thereby mitigating the inflammatory reactions in the mice with DSS-mediated colitis. Lee and colleagues used ginsenoside Re to treat mice with TNBS-mediated colitis and reported that ginsenoside Re prevented LPS from binding to TLR4 present on the macrophage membrane, thereby efficiently treating inflammation in the blood-brain barrier (BBB) (Lee et al., 2012). Ginsenoside Rh2 may provide significant relief in the IBD symptoms by activating the activation of the TGF-β signaling pathway and increasing the phosphorylation of the decapentaplegic (Smad) signals from the downstream microblasts. In addition, it may suppress the activation of the pro-inflammatory signal transduction pathways, such as the MAPK and NF-κB signaling pathways (Ye et al., 2014). Tian M and workers observed that ginsenoside RK3 remarkably relieved the colitis mediated by DSS by suppressing the production of pro-inflammatory factors IL-6, IL-1β and TNF-α (Tian et al., 2020). Ginsenoside Rb1 administrated by gavaging reduced the expression of pro-inflammatory factors IL-1β, IL-6, and TNF-α, while elevating the expression of the anti-inflammatory factor IL-10 (Joh et al., 2011). According to Li, Ginsenoside metabolite compound K mitigated the histopathological outcomes caused due to DSS-mediated colitis in mice, decreased the MPO activity, declined the generation of pro-inflammatory factors IL-6, IL-1β, and TNF-α, and elevated IL-10 expression in the peripheral blood and colonic tissue (Li et al., 2014). Further investigation demonstrated that Ginsenoside metabolite compound K inhibited the production of pro-inflammatory factors within the LPS-activated macrophages through the suppression of the NF-κB signal transduction pathway (Yang et al., 2015).

Limonin is a secondary metabolite with high biological activity in plants. It is present mainly in the fruits of Rutaceae plants, such as navel oranges, citruses, oranges, and grapefruits (Zhang et al., 2015; Wang et al., 2018c; Fan et al., 2019). The content in the core (seed) of the fruit is higher, while the content in the peel is low. Studies have demonstrated that limonin significantly reduces the disease activity index (DAI) of IBD, intestinal injury, and pro-inflammatory factor expression. Moreover, limonin remarkably suppresses the production of pro-inflammatory factors in the normal colonic epithelial cells cultured in vitro. Furthermore, limonin is suggested to improve UC prognosis by down-regulating p-STAT3/miR-214 (Liu et al., 2019).

Glycyrrhizic acid is one of the active components extracted from roots and rhizomes of Glycyrrhiza uralensis Fisch., Glycyrrhiza inflata Bat. and Glycyrrhiza glabra L. Glycyrrhizic (He et al., 2019b; Chrzanowski et al., 2021). Liu and workers reported that catechin at 50 mg/kg BW was used to feed TNBS-induced experiment colitis mice and it significantly attenuated pathological changes in the colon. In addition, glycyrrhizic acid (100 mg/ml) reduced the IL-6 production and elevated interleukin-10 production in LPS-challenged macrophages (Liu et al., 2011). The other report suggests that dipotassium glycyrrhizate , a salt of the glycoconjugated triterpene glycyrrhizin, could relieve intestinal inflammation and modify gut mucosal healing. Dipotassium glycyrrhizate could down-regulate the expression levels of gut mucosal healing genes in the acute colitis mice model (Stronati et al., 2019). The solution with glycyrrhizic as the main component has been commercialized. Glycyrrhizin preparation was launched by Minophagen Pharmaceutical (Tokyo, Japan), which has been demonstrated to relieve colitis and decrease the expression levels of pro-inflammatory cytokines and chemokines, including IL-1β IL-6, TNF-α, Cinc-2 (Kudo et al., 2011). Although glycyrrhizic is widely recognized, it still has some limitations. Some researchers observed that glycyrrhizin maybe has side effects, including asthenia and muscle cramps (De Putter and Donck, 2014). A brief illustration of the different terpenoid phytochemicals is presented in Figure 3.

FIGURE 3
www.frontiersin.org

FIGURE 3. Chemical structures of terpenoid phytochemicals: (A) Ginsenoside (B) Ginsenoside Rd (C) Ginsenoside Rg1 (D) Ginsenoside Re (E) Ginsenoside Rh2 (F) Ginsenoside RK3 (G) Ginsenoside metabolite compound K (H) Limonin (I) Glycyrrhizin acid.

Polysaccharides

Astragalus polysaccharide is extracted from Astragalus membranaceus and exhibits various clinical effects (Jin et al., 2014; Auyeung et al., 2016; Zhang et al., 2019). Studies have demonstrated that astragalus polysaccharide (APS) relieves the induction of trinitrobenzene sulfonic acid (TNBS) in colitis rat models. Furthermore, this mitigation effect could be related to the regulation of TNF-α, IL-1β, and NFATc4 expressions (Yang et al., 2014b). Gao and colleagues reported that astragalus polysaccharides promoted the expression of GATA-3 and T-bet, adjusted the GATA-3/T-bet ratio, and exhibited a colonic protective effect in experimental colitis (Gao et al., 2016). Another study demonstrated that the APS treatment could significantly increase BW and improve the DAI and colitis history in a DSS-induced colitis mouse model. Moreover, APS also reduces the NF-ĸВ DNA phosphorylation and downregulates IL-6, IL-17, IL-1β, and TNF-α (Lv et al., 2017). A report demonstrated that APS alone or combined with matrine could alleviate colitis in experimental rats (Yan et al., 2020).

Laminarin, a PLS obtained from seaweed, is constituted of the β-(1,3)-linked glucans containing β-(1,6)-linked side chains of lengths and with different distributions (Florez et al., 2017). Rattigan R analyzed the role of chitosan or laminarin supplementation in the diet in the colonic health of DSS-exposed pigs and reported that relative to the baseline DSS group, the kelp DSS group exhibited decreased relative abundances of Escherichia coli/Shigella and an increased molar ratio of acetic acid. In addition, kelp was observed to suppress the proliferation of the pathogenic bacteria and increase the content of volatile fatty acids in the colon of the colitis pig model (Rattigan et al., 2020). Rioux L. E., Turgeon S., and Beaulieu M. characterized the polysaccharides extracted from brown seaweeds (Rioux et al., 2010). A brief illustration of the different polysaccharide phytochemicals is presented in Figure 4.

FIGURE 4
www.frontiersin.org

FIGURE 4. Chemical structures of polysaccharides phytochemicals: (A) Astragalus polysaccharide (B) Laminarin.

Alkaloids

Oxymatrine is a derivative of matrine n-oxide that is present naturally in Sophora flavescens (Xia et al., 2011; Cao and He, 2020). The research on oxymatrine and matrine suggests that oxymatrine at a dose of 63 mg/kg mouse BW remarkably mitigates the colonic damage in the mice with TNBS-mediated colitis, probably through the regulation of the imbalance of Th1/Th2 cytokines. Moreover, the reduction in the colonic IL-2 expression is associated with the increase in the IL-10 levels. Such benefit is associated with the inhibition of p65 NF-kB and b2-adrenergic receptor (b2AR) b-arrestin-2 subunit in the colon and spleen (Wen et al., 2014). Guzman and colleagues studied mice with DSS-mediated colitis and reported that oxymatrine (10 mg/kg BW; i.p.) could block NF-kB's nuclear translocation and activity induced by LPS, thereby improving the overall process of intestinal inflammation, which is unrelated to IkBa degradation/phosphorylation (Guzman et al., 2013). Chen Q and colleagues also observed that oxymatrine (dose: 25, 50, and 100 mg/kg mouse BW; i.p.) could inhibit colonic Th1 and Th17 cell responses via the PI3K/AKT pathway (Chen et al., 2017). Chen F, along with colleagues, constructed a colitis model by administrating a mixture of TNBS and ethanol, followed by oxymatrine [oxymatrine group (20 mg/kg)] seven days after modeling. Consequently, the rats in the oxymatrine group exhibited markedly increased BW, and the length of the colon was also increased significantly. The pathological damage caused to the colonic mucosa had improved markedly. Meanwhile, ICAM-1 and IL-2 expressions had remarkably decreased, in addition to a significant increase in numbers of IL-10, CD11c+, CD103+, and E-cadherin+ cells. Therefore, it was inferred that oxymatrine could increase the number of CD11c+, CD103+, and E-cadherin+ cells by regulating IL-10, IL-2, and ICAM-1, and could also reduce colon inflammation in the experimental rats (Chen et al., 2019c). Certain studies reported that the LD50 value of oxymatrine administered via the intraperitoneal route in male and female mice was 347.44 and 429.15 mg/kg, respectively (Danese, 2012).

Aloperine is a tricyclic quinoline alkaloid isolated from Sophora vulgaris (Qiu et al., 2020; Wang et al., 2020). As discovered by Fu et al., aloperine protected against the colitis induced by DSS in the experimental mice; to be specific, aloperine administered orally at 40 mg/kg BW efficiently enhanced the DSS-mediated colitis severity, reduced the T cell ratio, and upregulated the Foxp3 levels in mesenteric lymph nodes and spleen. In addition, aloperine (40 mg/kg BW) also inhibits the colonic p-PI3K p85, p-mTOR, and p-Akt expressions in colitis mice while upregulating the protein phosphatase 2A (PP2A) expression. In vitro studies have demonstrated that aloperine (0.5 and 1 mM) inhibits the apoptosis of mouse naïve and Jurkat T-cells by suppressing the PI3K/Akt/mTOR signal transduction pathway, although the PP2A inhibitor LB-100 could reverse this beneficial effect. These results suggest that aloperine modulates the colitis-induced inflammatory response by suppressing the PI3K/Akt/mTOR signal transduction pathway via pp2a (Fu et al., 2017; Shi et al., 2018).

N-methylcytisine is another tricyclic quinoline alkaloid extracted from Sophora alopecuroides and honeysuckle (Laburnum anagyroides) seeds (Zhang et al., 2016b; Li et al., 2020b). Its oral administration at the doses of 4 and 16 mg/kg BW markedly mitigated colitis in mice. Moreover, N-methylcytisine could dramatically mitigate the pathological changes and clinical symptoms in DSS-induced colitis mice, which were associated with suppressing colonic pro-inflammatory factors via activating NF-kB by restraining the phosphorylation of IKK and IkB (Jiao et al., 2018).

Berberine is a popular alkaloid extracted mostly from Phellodendron and Coptis (James et al., 2011; Zhu et al., 2020). Zhang et al. discovered that oral administration of 100 mg/kg BW of berberine remarkably mitigated the DSS-induced weight loss, shortening of the colon and colon damage. Moreover, berberine promoted intestinal barrier function, anti-inflammatory factor production, and anti-oxidative stress responses, possibly via the STAT3 signaling pathway (Zhang et al., 2017b). In comparison to the model group, berberine could inhibit the expression of IL-1, IL-1β, IL-6, IL-12, TNF-α, TGF-β, and interferon-γ, while upregulating the IL-4 and iL-10 expressions. Moreover, berberine treatment could effectively increase the SIgA level and downregulate MDA and MPO levels. The anti-inflammatory mechanism of berberine hydrochloride is probably associated with suppressing the IL-6/STAT3/NF-κB signal transduction pathway (Zhu et al., 2019). Zhao and colleagues discovered that berberine exerted an effect on the intestinal barrier function of the DSS-mediated colitis mice; besides, berberine at a dose of 100 mg/kg BW markedly suppressed the alterations in the serum expression of zonula occluden-1 (fluorescein isothiocyanate-dextran) and inhibited the expression of epithelial cadherin in colonic tissues (Zhao et al., 2017). Cui, along with colleagues, discovered that berberine at a dose of 40 mg/kg BW (p.o.) decreased gut microbial diversity and interfered with the relative abundances of Bacteroides, Desulfovibrio, and Eubacterium. Berberine treatment in mouse stool transplantation could relieve UC and regulate the balance of Treg/Th17 (Cui et al., 2018). Wang and colleagues reported that berberine markedly enhanced the pathological phenotype of DSS-mediated colitis rats, destruction of the intestinal barrier, and inflammation of the colon. In addition, microbiota analysis based on 16S rDNA revealed that berberine could alleviate intestinal disorders in rats. Berberine is also reported to mitigate DSS-mediated colitis in rats by regulating intestinal microbe-related tryptophan metabolites for activating AhR, thereby greatly improving the impaired intestinal barrier function (Jing et al., 2021). The clinic research observed that berberine administrated at 900 mg/day for 3 months could significantly decrease the Geboes grade of colonic tissue in colitis patients as well as has almost any side effect (Xu et al., 2020).

Berberrubine is a natural isoquinoline alkaloid and a major berberine metabolite in vivo (Spinozzi et al., 2014). Berberine and berberrubine have been detected in Rhizoma Coptidis. The mice receiving berberrubine at the dose of 10/20 mg/kg BW (orders) exhibited markedly alleviated DSS-mediated colitis through a decrease in the DAI and infiltration of the inflammatory cells and the suppression of cytokine generation (IL-4, IL-6, TNF-a, and IFN-g) and the MPO activity. Moreover, it could also upregulate the levels of mRNA adhesion and tight junction (TJ) proteins, including zonula occludens-1/-2, occluding, and claudin-1, while reducing the expression of these proteins reduced the Bax/Bcl-2 ratio. Such benefit is comparable to the use of berberine at a dose of 50 mg/kg mouse BW (p.o.), which suggests the obvious better effect of berberrubine against colitis compared to berberine (Yu et al., 2018b). Yan F, along with colleagues, observed that Berberrubine could suppress the generation of pro-inflammatory factors within the epithelial cells and colonic macrophages in mice while inhibiting apoptosis in colonic macrophages. Berberine also reduces the activation of signaling pathways induced by the pro-inflammatory cytokines MAPK and NF-κB in the macrophages and epithelial cells of the mouse colon treated by the demand side (Yan et al., 2012).

Caffeine is a typical naturally occurring xanthine alkaloid. As discovered by Lee et al., exposure to caffeine prevents colitis through a decrease in the expression of chitinase 3-like 1 in the intestinal epithelial cells (IECs). The in vitro studies by these authors suggest that caffeine treatment at the doses of 2.5 and 5 mM markedly reduces the mRNA levels of chitinase 3-like 1 in the IEC strain, thereby reducing bacterial invasion in a dose-dependent manner. In addition, compared to the control group mice, the caffeine-treated colitis mice produced fewer pro-inflammatory cytokines, and fewer bacteria entered the other organs (Lee et al., 2014).

Theophylline is an alkaloid extracted from tea, which is similar to caffeine in structure and pharmacology (Senchina et al., 2014; Singleton et al., 2019; Zhou et al., 2019). According to a report by Ghassemi and colleagues, theophylline treatment at the doses of 20 and 50 mg/kg mouse BW (i.p.) decreased acetic colitis severity through a decrease in the cytokine levels (IL-6, IL-1b, and TNF-a) and MPO activity in the colon (Ghasemi-Pirbaluti et al., 2017).

Pentoxifylline is a xanthine derivative (Annamaraju and Baradhi, 2020). Reyhan and colleagues conducted experiments on rats with ischemic colitis and observed that pentoxifylline administered orally at the dose of 50 mg/kg BW markedly decreased the MDA levels and the ischemic area in the colon (Reyhan et al., 2014). Similarly, Karatay and colleagues reported that pentoxifylline administration at the dose of 100 mg/kg BW affected the TNBS-mediated colitis in rats. According to their results, intrarectal and intraperitoneal administration of pentoxifylline markedly mitigated colonic damage by reducing the MDA levels, as well as the levels of TGF-b1 MPO, MMP-1, and MMP-3 levels, thereby recovering the SOD activity. As indicated by these results, pentoxifylline inhibits colitis partially through the suppression of metalloproteinase activity and oxidative stress. It is noteworthy that caffeine and theophylline also exert toxic effects. The suggested lethal dose of caffeine in the bloodstream is 80–100 mg/ml, which is reached by consuming approximately 10 g or higher of caffeine (Karatay et al., 2017).

Palmatine is present in Phellodendron chinense, coptis, corydalis, and other plants (Ryuk et al., 2012; Li et al., 2017; Hao et al., 2020). Zhang X. and colleagues reported that the use of palmatine at the doses of 50 and 100 mg/kg mouse BW (p.o.) during DSS-induced mouse experiments improved the integrity of the mucosa and inhibited epithelial cell apoptosis. In addition, palmatine treatment increased the relative abundances of Firmicutes and Bacteroidetes, which then reduced the bacterial quantity, thereby effectively promoting the recovery of colitis (Zhang et al., 2018). Furthermore, Cyclosporin A is reported to remarkably suppress the efficacy of palmatine in treating DSS mice, which suggested that the anti-colitis effect of palmatine was strongly associated with mitochondrial autophagy (Mai et al., 2019). A brief illustration of the different alkaloid phytochemicals is presented in Figure 5.

FIGURE 5
www.frontiersin.org

FIGURE 5. Chemical structures of alkaloid phytochemicals: (A) Oxymatrine (B) Aloperine (C) N-methylcytisine (D) Berberine (E) Berberrubine (F) Caffeine (G) Theophylline (H) Pentoxifylline (I) Palmatine.

Conclusion

As the pervasiveness of inflammatory bowel disorder across the world is increasing and the available clinical drugs against IBD present side effects and limitations, novel treatments are required. The existing studies explain the pathogenesis of IBD in terms of etiology and pathology. However, there is strong evidence that natural products play vital roles in preventing and treating IBD. In comparison to conventional drugs as alternative treatments, natural products are in high demand as they are safe and effective in treating IBD. A review of the literature revealed that natural components have demonstrated favorable results in various in vivo and in vitro IBD studies and could be used to treat and avert the progression of IBD. The present report lists and describes the targets reported in the existing research. Moreover, it also reviews the anti-inflammation effects of various natural compounds and their underlying mechanisms in the prevention and treatment of IBD. Natural compounds have positive effects on production of inflammatory cytokines and could protect or relieve colitis. Therefore, natural anti-inflammatory compounds are the first choice when we are developing drugs to treat colitis. In addition, most of the experimental studies have been performed on mice model and the identical compound was used in different dosages to demonstrate its anti-inflammatory activity. However, there is still no clear clinical study to illustrate the optimal dose for colitis patients. Although natural anti-inflammatory compounds have great potential to be developed for treatment of IBD, we need more data to support their safety, dosage and metabolism.

Author Contributions

LD and SC designed the “ideas”; GL helped LD and SC to deal with the information efficiently; LD and SC wrote the manuscript; GL, LL, YL, and DW revised the manuscript. All authors agree to be accountable for the content of the work.

Funding

This work was supported by a grant from The National Natural Science Foundation of China (No. 81870388); Special Project for Marine Economic Development of Xiamen City (No. 17GYY001NF01).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

Abron, J. D., Singh, N. P., Price, R. L., Nagarkatti, M., Nagarkatti, P. S., and Singh, U. P. (2018). Genistein Induces Macrophage Polarization and Systemic Cytokine to Ameliorate Experimental Colitis. PLoS One 13 (7), e0199631. doi:10.1371/journal.pone.0199631

PubMed Abstract | CrossRef Full Text | Google Scholar

Al-Rejaie, S. S., Abuohashish, H. M., Al-Enazi, M. M., Al-Assaf, A. H., Parmar, M. Y., and Ahmed, M. M. (2013). Protective Effect of Naringenin on Acetic Acid-Induced Ulcerative Colitis in Rats. World J. Gastroenterol. 19 (34), 5633–5644. doi:10.3748/wjg.v19.i34.5633

PubMed Abstract | CrossRef Full Text | Google Scholar

Alam, M. A., Subhan, N., Rahman, M. M., Uddin, S. J., Reza, H. M., and Sarker, S. D. (2014). Effect of Citrus Flavonoids, Naringin and Naringenin, on Metabolic Syndrome and Their Mechanisms of Action. Adv. Nutr. 5 (4), 404–417. doi:10.3945/an.113.005603

PubMed Abstract | CrossRef Full Text | Google Scholar

Alfen, J. S., Larghi, P., Facciotti, F., Gagliani, N., Bosotti, R., Paroni, M., et al. (2018). Intestinal IFN-γ-Producing Type 1 Regulatory T Cells Coexpress CCR5 and Programmed Cell Death Protein 1 and Downregulate IL-10 in the Inflamed Guts of Patients with Inflammatory Bowel Disease. J. Allergy Clin. Immunol. 142 (5), 1537–1547. doi:10.1016/j.jaci.2017.12.984

PubMed Abstract | CrossRef Full Text | Google Scholar

Allner, C., Melde, M., Becker, E., Fuchs, F., Mühl, L., Klenske, E., et al. (2020). Baseline Levels of Dynamic CD4+ T Cell Adhesion to MAdCAM-1 Correlate with Clinical Response to Vedolizumab Treatment in Ulcerative Colitis: a Cohort Study. BMC Gastroenterol. 20 (1), 103. doi:10.1186/s12876-020-01253-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Allocca, M., Gilardi, D., Fiorino, G., Furfaro, F., Argollo, M., Peyrin-Biroulet, L., et al. (2018). PF-00547659 for the Treatment of Crohn’s Disease and Ulcerative Colitis. Exp. Opin. Investig. Drugs 27 (7), 623–629. doi:10.1080/13543784.2018.1494722

CrossRef Full Text | Google Scholar

Allocca, M., Jovani, M., Fiorino, G., Schreiber, S., and Danese, S. (2013). Anti-IL-6 Treatment for Inflammatory Bowel Diseases: Next Cytokine, Next Target. Curr. Drug Targets 14 (12), 1508–1521. doi:10.2174/13894501113146660224

PubMed Abstract | CrossRef Full Text | Google Scholar

Alu'datt, M. H., Rababah, T., Alhamad, M. N., Al-Mahasneh, M. A., Ereifej, K., Al-Karaki, G., et al. (2017). Profiles of Free and Bound Phenolics Extracted from Citrus Fruits and Their Roles in Biological Systems: Content, and Antioxidant, Anti-diabetic and Anti-Hypertensive Properties. Food Funct. 8 (9), 3187–3197. doi:10.1039/c7fo00212b

PubMed Abstract | CrossRef Full Text | Google Scholar

Andersen, V., Holmskov, U., Sørensen, S., Jawhara, M., Andersen, K., Bygum, A., et al. (2017). A Proposal for a Study on Treatment Selection and Lifestyle Recommendations in Chronic Inflammatory Diseases: A Danish Multidisciplinary Collaboration on Prognostic Factors and Personalised Medicine. Nutrients 9 (5), 499. doi:10.3390/nu9050499

PubMed Abstract | CrossRef Full Text | Google Scholar

Annamaraju, P., and Baradhi, K. M. P. (2020). StatPearls [Internet]. Treasure Island, FL: StatPearls Publishing.

Arab, H. H., Al-Shorbagy, M. Y., and Saad, M. A. (2021). Activation of Autophagy and Suppression of Apoptosis by Dapagliflozin Attenuates Experimental Inflammatory Bowel Disease in Rats: Targeting AMPK/mTOR, HMGB1/RAGE and Nrf2/HO-1 Pathways. Chem. Biol. Interact. 335, 109368. doi:10.1016/j.cbi.2021.109368

PubMed Abstract | CrossRef Full Text | Google Scholar

Argollo, M., Fiorino, G., Hindryckx, P., Peyrin-Biroulet, L., and Danese, S. (2017). Novel Therapeutic Targets for Inflammatory Bowel Disease. J. Autoimmun. 85, 103–116. doi:10.1016/j.jaut.2017.07.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Auyeung, K. K., Han, Q.-B., and Ko, J. K. (2016). Astragalus Membranaceus: A Review of its Protection against Inflammation and Gastrointestinal Cancers. Am. J. Chin. Med. 44 (1), 1–22. doi:10.1142/S0192415X16500014

PubMed Abstract | CrossRef Full Text | Google Scholar

Axelrad, J. E., Fowler, S. A., Friedman, S., Ananthakrishnan, A. N., and Yajnik, V. (2012). Effects of Cancer Treatment on Inflammatory Bowel Disease Remission and Reactivation. Clin. Gastroenterol. Hepatol. 10 (9), 1021–1027. doi:10.1016/j.cgh.2012.06.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Aziz, N., Kim, M.-Y., and Cho, J. Y. (2018). Anti-inflammatory Effects of Luteolin: A Review of In Vitro, In Vivo, and In Silico Studies. J. Ethnopharmacol. 225, 342–358. doi:10.1016/j.jep.2018.05.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Azuma, T., Shigeshiro, M., Kodama, M., Tanabe, S., and Suzuki, T. (2013). Supplemental Naringenin Prevents Intestinal Barrier Defects and Inflammation in Colitic Mice. J. Nutr. 143 (6), 827–834. doi:10.3945/jn.113.174508

PubMed Abstract | CrossRef Full Text | Google Scholar

Balasubramanian, I., and Gao, N. (2017). From Sensing to Shaping Microbiota: Insights into the Role of NOD2 in Intestinal Homeostasis and Progression of Crohn's Disease. Am. J. Physiol. Gastrointestinal Liver Physiol. 313 (1), G7–G13. doi:10.1152/ajpgi.00330.2016

CrossRef Full Text | Google Scholar

Barnig, C., Bezema, T., Calder, P. C., Charloux, A., Frossard, N., Garssen, J., et al. (2019). Activation of Resolution Pathways to Prevent and Fight Chronic Inflammation: Lessons From Asthma and Inflammatory Bowel Disease. Front. Immunol. 10, 1699. doi:10.3389/fimmu.2019.01699

PubMed Abstract | CrossRef Full Text | Google Scholar

Bauché, D., Joyce-Shaikh, B., Fong, J., Villarino, A. V., Ku, K. S., Jain, R., et al. (2020). IL-23 and IL-2 Activation of STAT5 is Required for Optimal IL-22 Production in ILC3s during Colitis. Sci. Immunol. 5 (46), eaav1080. doi:10.1126/sciimmunol.aav1080

PubMed Abstract | CrossRef Full Text | Google Scholar

Baumgart, D. C., and Sandborn, W. J. (2007). Inflammatory Bowel Disease: Clinical Aspects and Established and Evolving Therapies. Lancet 369 (9573), 1641–1657. doi:10.1016/s0140-6736(07)60751-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Becker, C., Watson, A. J., and Neurath, M. F. (2013). Complex Roles of Caspases in the Pathogenesis of Inflammatory Bowel Disease. Gastroenterology 144 (2), 283–293. doi:10.1053/j.gastro.2012.11.035

PubMed Abstract | CrossRef Full Text | Google Scholar

Berends, S. E., Strik, A. S., Löwenberg, M., D’Haens, G. R., and Mathôt, R. A. A. (2019). Clinical Pharmacokinetic and Pharmacodynamic Considerations in the Treatment of Ulcerative Colitis. Clin. Pharmacokinet. 58 (1), 15–37. doi:10.1007/s40262-018-0676-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Bernstein, C. N., Blanchard, J. F., Rawsthorne, P., and Yu, N. (2001). The Prevalence of Extraintestinal Diseases in Inflammatory Bowel Disease: a Population-Based Study. Am. J. Gastroenterol. 96 (4), 1116–1122. doi:10.1111/j.1572-0241.2001.03756.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Bernstein, C. N., Wajda, A., and Blanchard, J. F. (2005). The Clustering of Other Chronic Inflammatory Diseases in Inflammatory Bowel Disease: a Population-Based Study. Gastroenterology 129 (3), 827–836. doi:10.1053/j.gastro.2005.06.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Bertani, L., Caviglia, G. P., Antonioli, L., Pellicano, R., Fagoonee, S., Astegiano, M., et al. (2020). Serum Interleukin-6 and -8 as Predictors of Response to Vedolizumab in Inflammatory Bowel Diseases. J. Clin. Med. 9 (5), 1323. doi:10.3390/jcm9051323

PubMed Abstract | CrossRef Full Text | Google Scholar

Bhakta, A., Tafen, M., Glotzer, O., Ata, A., Chismark, A. D., Valerian, B. T., et al. (2016). Increased Incidence of Surgical Site Infection in IBD Patients. Dis. Colon Rectum 59 (4), 316–322. doi:10.1097/DCR.0000000000000550

PubMed Abstract | CrossRef Full Text | Google Scholar

Binder, M.-T., Becker, E., Wiendl, M., Schleier, L., Fuchs, F., Leppkes, M., et al. (2018). Similar Inhibition of Dynamic Adhesion of Lymphocytes From IBD Patients to MAdCAM-1 by Vedolizumab and Etrolizumab-s. Inflamm. Bowel Dis. 24 (6), 1237–1250. doi:10.1093/ibd/izy077

PubMed Abstract | CrossRef Full Text | Google Scholar

Bing, X., Xuelei, L., Wanwei, D., Linlang, L., and Keyan, C. (2017). EGCG Maintains Th1/Th2 Balance and Mitigates Ulcerative Colitis Induced by Dextran Sulfate Sodium through TLR4/MyD88/NF-κB Signaling Pathway in Rats. Can. J. Gastroenterol. Hepatol. 2017, 1–9. doi:10.1155/2017/3057268

PubMed Abstract | CrossRef Full Text | Google Scholar

Bitzer, Z. T., Elias, R. J., Vijay-Kumar, M., and Lambert, J. D. (2016). (-)-Epigallocatechin-3-Gallate Decreases Colonic Inflammation and Permeability in a Mouse Model of Colitis, but Reduces Macronutrient Digestion and Exacerbates Weight Loss. Mol. Nutr. Food Res. 60, 2267–2274. doi:10.1002/mnfr.201501042

PubMed Abstract | CrossRef Full Text | Google Scholar

Bonen, D. K., Ogura, Y., Nicolae, D. L., Inohara, N., Saab, L., Tanabe, T., et al. (2003). Crohn’s Disease-Associated NOD2 Variants Share a Signaling Defect in Response to Lipopolysaccharide and Peptidoglycan. Gastroenterology 124 (1), 140–146. doi:10.1053/gast.2003.50019

PubMed Abstract | CrossRef Full Text | Google Scholar

Bopanna, S., Ananthakrishnan, A. N., Kedia, S., Yajnik, V., and Ahuja, V. (2017). Risk of Colorectal Cancer in Asian Patients with Ulcerative Colitis: a Systematic Review and Meta-Analysis. Lancet Gastroenterol. Hepatol. 2 (4), 269–276. doi:10.1016/s2468-1253(17)30004-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Boros, É., and Nagy, I. (2019). The Role of MicroRNAs upon Epithelial-to-Mesenchymal Transition in Inflammatory Bowel Disease. Cells 8 (11), 1461. doi:10.3390/cells8111461

PubMed Abstract | CrossRef Full Text | Google Scholar

Brant, S. R., Okou, D. T., Simpson, C. L., Cutler, D. J., Haritunians, T., Bradfield, J. P., et al. (2017). Genome-Wide Association Study Identifies African-specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease. Gastroenterology 152 (1), 206–217. doi:10.1053/j.gastro.2016.09.032

PubMed Abstract | CrossRef Full Text | Google Scholar

Broekman, M. M. T. J., Coenen, M. J. H., van Marrewijk, C. J., Wanten, G. J. A., Wong, D. R., Verbeek, A. L. M., et al. (2017). More Dose-dependent Side Effects with Mercaptopurine over Azathioprine in IBD Treatment Due to Relatively Higher Dosing. Inflamm. Bowel Dis. 23 (10), 1873–1881. doi:10.1097/MIB.0000000000001163

PubMed Abstract | CrossRef Full Text | Google Scholar

Bunte, K., and Beikler, T. (2019). Th17 Cells and the IL-23/IL-17 Axis in the Pathogenesis of Periodontitis and Immune-Mediated Inflammatory Diseases. Int. J. Mol. Sci. 20 (14), 3394. doi:10.3390/ijms20143394

PubMed Abstract | CrossRef Full Text | Google Scholar

Buonocore, S., Ahern, P. P., Uhlig, H. H., Ivanov, I. I., Littman, D. R., Maloy, K. J., et al. (2010). Innate Lymphoid Cells Drive Interleukin-23-dependent Innate Intestinal Pathology. Nature 464 (7293), 1371–1375. doi:10.1038/nature08949

PubMed Abstract | CrossRef Full Text | Google Scholar

Caddeo, C., Nácher, A., Díez-Sales, O., Merino-Sanjuán, M., Fadda, A. M., and Manconi, M. (2014). Chitosan-xanthan Gum Microparticle-Based Oral Tablet for Colon-Targeted and Sustained Delivery of Quercetin. J. Microencapsul. 31 (7), 694–699. doi:10.3109/02652048.2014.913726

PubMed Abstract | CrossRef Full Text | Google Scholar

Camuesco, D., Comalada, M., Rodríguez-Cabezas, M. E., Nieto, A., Lorente, M. D., Concha, A., et al. (2004). The Intestinal Anti-inflammatory Effect of Quercitrin is Associated with an Inhibition in iNOS Expression. Br. J. Pharmacol. 143 (7), 908–918. doi:10.1038/sj.bjp.0705941

PubMed Abstract | CrossRef Full Text | Google Scholar

Cao, W., Kayama, H., Chen, M. L., Delmas, A., Sun, A., Kim, S. Y., et al. (2017). The Xenobiotic Transporter Mdr1 Enforces T Cell Homeostasis in the Presence of Intestinal Bile Acids. Immunity 47 (6), 1182–1196. doi:10.1016/j.immuni.2017.11.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Cao, X., and He, Q. (2020). Anti-Tumor Activities of Bioactive Phytochemicals in Sophora Flavescens for Breast Cancer. Cmar Vol. 12, 1457–1467. doi:10.2147/CMAR.S243127

PubMed Abstract | CrossRef Full Text | Google Scholar

Cardoso, R. R., Neto, R. O., Dos Santos D'Almeida, C. T., do Nascimento, T. P., Pressete, C. G., Azevedo, L., et al. (2020). Kombuchas from Green and Black Teas Have Different Phenolic Profile, Which Impacts Their Antioxidant Capacities, Antibacterial and Antiproliferative Activities. Food Res. Int. 128, 108782. doi:10.1016/j.foodres.2019.108782

PubMed Abstract | CrossRef Full Text | Google Scholar

Castro-Dopico, T., Dennison, T. W., Ferdinand, J. R., Mathews, R. J., Fleming, A., Clift, D., et al. (2019). Anti-Commensal IgG Drives Intestinal Inflammation and Type 17 Immunity in Ulcerative Colitis. Immunity 50 (4), 1099–1114. doi:10.1016/j.immuni.2019.02.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Cella, M., Fuchs, A., Vermi, W., Facchetti, F., Otero, K., Lennerz, J. K. M., et al. (2009). A Human Natural Killer Cell Subset Provides an Innate Source of IL-22 for Mucosal Immunity. Nature 457 (7230), 722–725. doi:10.1038/nature07537

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, F., Yin, Y., Liu, Y., Liu, X., Liu, F., Zhang, X., et al. (2019). [Oxymatrine Alleviates the Inflammatory Damage and its Mechanism in Rats with TNBS-Induced Colitis]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi 35 (1), 1–5.

PubMed Abstract | Google Scholar

Chen, J.-Q., Szodoray, P., and Zeher, M. (2016). Toll-Like Receptor Pathways in Autoimmune Diseases. Clinic Rev. Allergy Immunol. 50 (1), 1–17. doi:10.1007/s12016-015-8473-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, Q., Duan, X., Fan, H., Xu, M., Tang, Q., Zhang, L., et al. (2017). Oxymatrine Protects against DSS-Induced Colitis via Inhibiting the PI3K/AKT Signaling Pathway. Int. Immunopharmacol. 53, 149–157. doi:10.1016/j.intimp.2017.10.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, X., Wei, W., Li, Y., Huang, J., and Ci, X. (2019). Hesperetin Relieves Cisplatin-Induced Acute Kidney Injury by Mitigating Oxidative Stress, Inflammation and Apoptosis. Chem. Biol. Interact. 308, 269–278. doi:10.1016/j.cbi.2019.05.040

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, Y., Le, T. H., Du, Q., Zhao, Z., Liu, Y., Zou, J., et al. (2019). Genistein Protects against DSS-Induced Colitis by Inhibiting NLRP3 Inflammasome via TGR5-cAMP Signaling. Int. Immunopharmacol. 71, 144–154. doi:10.1016/j.intimp.2019.01.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Chrzanowski, J., Chrzanowska, A., and Graboń, W. (2021). Glycyrrhizin: An Old Weapon against a Novel Coronavirus. Phytotherapy Res. 35 (2), 629–636. doi:10.1002/ptr.6852

CrossRef Full Text | Google Scholar

Chudy-Onwugaje, K. O., Christian, K. E., Farraye, F. A., and Cross, R. K. (2019). A State-Of-The-Art Review of New and Emerging Therapies for the Treatment of IBD. Inflamm. Bowel Dis. 25 (5), 820–830. doi:10.1093/ibd/izy327

PubMed Abstract | CrossRef Full Text | Google Scholar

Chun, O. K., Chung, S. J., and Song, W. O. (2007). Estimated Dietary Flavonoid Intake and Major Food Sources of U.S. Adults. J. Nutr. 137 (5), 1244–1252. doi:10.1093/jn/137.5.1244

PubMed Abstract | CrossRef Full Text | Google Scholar

Ci, X., Chu, X., Wei, M., Yang, X., Cai, Q., and Deng, X. (2012). Different Effects of Farrerol on an OVA-Induced Allergic Asthma and LPS-Induced Acute Lung Injury. PLoS One 7 (4), e34634. doi:10.1371/journal.pone.0034634

PubMed Abstract | CrossRef Full Text | Google Scholar

Comalada, M., Camuesco, D., Sierra, S., Ballester, I., Xaus, J., Gálvez, J., et al. (2005). In Vivoquercitrin Anti-inflammatory Effect Involves Release of Quercetin, Which Inhibits Inflammation Through Down-Regulation of the NF-κB Pathway. Eur. J. Immunol. 35 (2), 584–592. doi:10.1002/eji.200425778

PubMed Abstract | CrossRef Full Text | Google Scholar

Cordes, F., Foell, D., Ding, J. N., Varga, G., and Bettenworth, D. (2020). Differential Regulation of JAK/STAT-signaling in Patients with Ulcerative Colitis and Crohn’s Disease. World J. Gastroenterol. 26 (28), 4055–4075. doi:10.3748/wjg.v26.i28.4055

PubMed Abstract | CrossRef Full Text | Google Scholar

Cosnes, J., Gower–Rousseau, C., Seksik, P., and Cortot, A. (2011). Epidemiology and Natural History of Inflammatory Bowel Diseases. Gastroenterology 140 (6), 1785–1794. doi:10.1053/j.gastro.2011.01.055

PubMed Abstract | CrossRef Full Text | Google Scholar

Croxford, A. L., Kulig, P., and Becher, B. (2014). IL-12-and IL-23 in Health and Disease. Cytokine Growth Factor. Rev. 25 (4), 415–421. doi:10.1016/j.cytogfr.2014.07.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Cui, G., and Yuan, A. (2018). A Systematic Review of Epidemiology and Risk Factors Associated With Chinese Inflammatory Bowel Disease. Front. Med. 5, 183. doi:10.3389/fmed.2018.00183

PubMed Abstract | CrossRef Full Text | Google Scholar

Cui, H., Cai, Y., Wang, L., Jia, B., Li, J., Zhao, S., et al. (2018). Berberine Regulates Treg/Th17 Balance to Treat Ulcerative Colitis through Modulating the Gut Microbiota in the Colon. Front. Pharmacol. 9, 571. doi:10.3389/fphar.2018.00571

PubMed Abstract | CrossRef Full Text | Google Scholar

cWurdinger, T., Bouma, G., and Kraal, G. (2012). Cutting Edge: a Variant of the IL-23R Gene Associated with Inflammatory Bowel Disease Induces Loss of microRNA Regulation and Enhanced Protein Production. J. Immunol. 188 (4), 1573–1577. doi:10.4049/jimmunol.1101494

PubMed Abstract | CrossRef Full Text | Google Scholar

Cătană, C. S., Berindan Neagoe, I., Cozma, V., Magdaş, C., Tăbăran, F., and Dumitraşcu, D. L. (2015). Contribution of the IL-17/IL-23 Axis to the Pathogenesis of Inflammatory Bowel Disease. World J. Gastroenterol. 21 (19), 5823–5830. doi:10.3748/wjg.v21.i19.5823

PubMed Abstract | CrossRef Full Text | Google Scholar

Damião, A. O. M. C., Azevedo, M. F. C. d., Carlos, A. d. S., Wada, M. Y., Silva, T. V. M., and Feitosa, F. d. C. (2019). Conventional Therapy for Moderate to Severe Inflammatory Bowel Disease: A Systematic Literature Review. World J. Gastroenterol. 25 (9), 1142–1157. doi:10.3748/wjg.v25.i9.1142

PubMed Abstract | CrossRef Full Text | Google Scholar

Danese, S., Furfaro, F., and Vetrano, S. (2018). Targeting S1P in Inflammatory Bowel Disease: New Avenues for Modulating Intestinal Leukocyte Migration. J. Crohns Colitis 12 (Suppl. l_2), S678–S686. doi:10.1093/ecco-jcc/jjx107

PubMed Abstract | CrossRef Full Text | Google Scholar

Danese, S. (2012). New Therapies for Inflammatory Bowel Disease: from the Bench to the Bedside. Gut 61 (6), 918–932. doi:10.1136/gutjnl-2011-300904

PubMed Abstract | CrossRef Full Text | Google Scholar

Danese, S., Vermeire, S., Hellstern, P., Panaccione, R., Rogler, G., Fraser, G., et al. (2019). Randomised Trial and Open-Label Extension Study of an Anti-Interleukin-6 Antibody in Crohn’s Disease (ANDANTE I and II). Gut 68 (1), 40–48. doi:10.1136/gutjnl-2017-314562

PubMed Abstract | CrossRef Full Text | Google Scholar

Davies, S. C., Nguyen, T. M., Parker, C. E., MacDonald, J. K., Jairath, V., and Khanna, R. (2019). Anti-IL-12/23p40 Antibodies for Maintenance of Remission in Crohn's Disease. Cochrane Database Syst. Rev. 12 (12), CD012804. doi:10.1002/14651858.CD012804.pub2

PubMed Abstract | CrossRef Full Text | Google Scholar

de Ceuninck van Capelle, C., Spit, M., and Ten Dijke, P. (2020). Current Perspectives on Inhibitory SMAD7 in Health and Disease. Crit. Rev. Biochem. Mol. Biol. 55 (6), 691–715. doi:10.1080/10409238.2020.1828260

PubMed Abstract | CrossRef Full Text | Google Scholar

De Putter, R., and Donck, J. (2014). Low-dose Liquorice Ingestion Resulting in Severe Hypokalaemic Paraparesis, Rhabdomyolysis and Nephrogenic Diabetes Insipidus. Clin. Kidney J. 7, 73–75. doi:10.1093/ckj/sft159

PubMed Abstract | CrossRef Full Text | Google Scholar

Del Rio, D., Borges, G., and Crozier, A. (2010). Berry Flavonoids and Phenolics: Bioavailability and Evidence of Protective Effects. Br. J. Nutr. 104 (Suppl. 3), S67–S90. doi:10.1017/S0007114510003958

PubMed Abstract | CrossRef Full Text | Google Scholar

Del Zotto, B., Mumolo, G., Pronio, A. M., Montesani, C., Tersigni, R., and Boirivant, M. (2003). TGF-β 1 Production in Inflammatory Bowel Disease: Differing Production Patterns in Crohn’s Disease and Ulcerative Colitis. Clin. Exp. Immunol. 134 (1), 120–126. doi:10.1046/j.1365-2249.2003.02250.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Den Hartogh, D. J., and Tsiani, E. (2019). Antidiabetic Properties of Naringenin: A Citrus Fruit Polyphenol. Biomolecules 9 (3), 99. doi:10.3390/biom9030099

CrossRef Full Text | Google Scholar

Dicarlo, M., Teti, G., Verna, G., Liso, M., Cavalcanti, E., Sila, A., et al. (2019). Quercetin Exposure Suppresses the Inflammatory Pathway in Intestinal Organoids from Winnie Mice. Int. J. Mol. Sci. 20 (22), 5771. doi:10.3390/ijms20225771

PubMed Abstract | CrossRef Full Text | Google Scholar

Dodda, D., Chhajed, R., Mishra, J., and Padhy, M. (2014). Targeting Oxidative Stress Attenuates Trinitrobenzene Sulphonic Acid Induced Inflammatory Bowel Disease Like Symptoms in Rats: Role of Quercetin. Indian J. Pharmacol. 46 (3), 286–291. doi:10.4103/0253-7613.132160

PubMed Abstract | CrossRef Full Text | Google Scholar

Dodda, D., Chhajed, R., and Mishra, J. (2014). Protective Effect of Quercetin against Acetic Acid Induced Inflammatory Bowel Disease (IBD) Like Symptoms in Rats: Possible Morphological and Biochemical Alterations. Pharmacol. Rep. 66 (1), 169–173. doi:10.1016/j.pharep.2013.08.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Dostert, C., Grusdat, M., Letellier, E., and Brenner, D. (2019). The TNF Family of Ligands and Receptors: Communication Modules in the Immune System and beyond. Physiol. Rev. 99 (1), 115–160. doi:10.1152/physrev.00045.2017

PubMed Abstract | CrossRef Full Text | Google Scholar

Dou, W., Zhang, J., Sun, A., Zhang, E., Ding, L., Mukherjee, S., et al. (2013). Protective Effect of Naringenin against Experimental Colitis via Suppression of Toll-like Receptor 4/NF-κB Signalling. Br. J. Nutr. 110 (4), 599–608. doi:10.1017/S0007114512005594

PubMed Abstract | CrossRef Full Text | Google Scholar

Dryden, G. W., Lam, A., Beatty, K., Qazzaz, H. H., and McClain, C. J. (2013). A Pilot Study to Evaluate the Safety and Efficacy of an Oral Dose of (−)-Epigallocatechin-3-Gallate-Rich Polyphenon E in Patients With Mild to Moderate Ulcerative Colitis. Inflamm. Bowel Dis. 19 (9), 1–12. doi:10.1097/MIB.0b013e31828f5198

PubMed Abstract | CrossRef Full Text | Google Scholar

Du, Y., Ding, H., Vanarsa, K., Soomro, S., Baig, S., Hicks, J., et al. (2019). Low Dose Epigallocatechin Gallate Alleviates Experimental Colitis by Subduing Inflammatory Cells and Cytokines, and Improving Intestinal Permeability. Nutrients 11 (8), 1743. doi:10.3390/nu11081743

PubMed Abstract | CrossRef Full Text | Google Scholar

Dubé, P. E., Punit, S., and Polk, D. B. (2015). Redeeming an Old Foe: Protective as Well as Pathophysiological Roles for Tumor Necrosis Factor in Inflammatory Bowel Disease. Am. J. Physiol. Gastrointest. Liver Physiol. 308 (3), G161–G170. doi:10.1152/ajpgi.00142.2014

PubMed Abstract | CrossRef Full Text | Google Scholar

Elhennawy, M. G., Abdelaleem, E. A., Zaki, A. A., and Mohamed, W. R. (2021). Cinnamaldehyde and Hesperetin Attenuate TNBS-Induced Ulcerative Colitis in Rats Through Modulation of the JAk2/STAT3/SOCS3 Pathway. J. Biochem. Mol. Toxicol. 35 (5), e22730. doi:10.1002/jbt.22730

PubMed Abstract | CrossRef Full Text | Google Scholar

Erlund, I., Meririnne, E., Alfthan, G., and Aro, A. (2001). Plasma Kinetics and Urinary Excretion of the Flavanones Naringenin and Hesperetin in Humans after Ingestion of orange Juice and Grapefruit Juice. J. Nutr. 131 (2), 235–241. doi:10.1093/jn/131.2.235

PubMed Abstract | CrossRef Full Text | Google Scholar

Fan, S., Zhang, C., Luo, T., Wang, J., Tang, Y., Chen, Z., et al. (2019). Limonin: A Review of Its Pharmacology, Toxicity, and Pharmacokinetics. Molecules 24 (20), 3679. doi:10.3390/molecules24203679

PubMed Abstract | CrossRef Full Text | Google Scholar

Fang, J. (2014). Bioavailability of Anthocyanins. Drug Metab. Rev. 46 (4), 508–520. doi:10.3109/03602532.2014.978080

PubMed Abstract | CrossRef Full Text | Google Scholar

Fathima, A., and Rao, J. R. (2016). Selective Toxicity of Catechin-A Natural Flavonoid towards Bacteria. Appl. Microbiol. Biotechnol. 100 (14), 6395–6402. doi:10.1007/s00253-016-7492-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Fathima, A., and Rao, J. R. (2016). Selective Toxicity of Catechin—A Natural Flavonoid toward Bacteria. Appl. Microbiol. Biotechnol. 100, 1–8. doi:10.1007/s00253-016-7492-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Feagan, B. G., Sandborn, W. J., D'Haens, G., Panés, J., Kaser, A., Ferrante, M., et al. (2017). Induction Therapy with the Selective Interleukin-23 Inhibitor Risankizumab in Patients with Moderate-to-Severe Crohn's Disease: a Randomised, Double-Blind, Placebo-Controlled Phase 2 Study. Lancet 389 (10080), 1699–1709. doi:10.1016/s0140-6736(17)30570-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Feagan, B. G., Sandborn, W. J., Gasink, C., Jacobstein, D., Lang, Y., Friedman, J. R., et al. (2016). Ustekinumab as Induction and Maintenance Therapy for Crohn's Disease. N. Engl. J. Med. 375 (20), 1946–1960. doi:10.1056/NEJMoa1602773

PubMed Abstract | CrossRef Full Text | Google Scholar

Fina, D., Sarra, M., Fantini, M. C., Rizzo, A., Caruso, R., Caprioli, F., et al. (2008). Regulation of Gut Inflammation and Th17 Cell Response by Interleukin-21. Gastroenterology 134 (4), 1038–1048. doi:10.1053/j.gastro.2008.01.041

PubMed Abstract | CrossRef Full Text | Google Scholar

Flannigan, K. L., Ngo, V. L., Geem, D., Harusato, A., Hirota, S. A., Parkos, C. A., et al. (2017). IL-17A-mediated Neutrophil Recruitment Limits Expansion of Segmented Filamentous Bacteria. Mucosal Immunol. 10 (3), 673–684. doi:10.1038/mi.2016.80

PubMed Abstract | CrossRef Full Text | Google Scholar

Florez, N., Gonzalez-Munoz, M., Ribeiro, D., Fernandes, E., Dominguez, H., and Freitas, M. (2017). Algae Polysaccharides’ Chemical Characterization and Their Role in the Inflammatory Process. Curr. Med. Chem. 24 (2), 149–175. doi:10.2174/0929867323666161028160416

PubMed Abstract | CrossRef Full Text | Google Scholar

Food and Drug Administration (2019). GRAS Notice Inventory-Agency Response Letter GRAS Notice No GRN 000341. Available at: https://wayback.archiveit.org/7993/20171031012354/https://www.fda.gov/Food/IngredientsPackagingLabeling/GRAS/NoticeInventory/ucm235935.htm (Accessed on April 1, 2019).

Google Scholar

Friedrich, M., Pohin, M., and Powrie, F. (2019). Cytokine Networks in the Pathophysiology of Inflammatory Bowel Disease. Immunity 50 (4), 992–1006. doi:10.1016/j.immuni.2019.03.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Fu, X., Sun, F., Wang, F., Zhang, J., Zheng, B., Zhong, J., et al. (2017). Aloperine Protects Mice against DSS-Induced Colitis by PP2A-Mediated PI3K/Akt/mTOR Signaling Suppression. Mediators Inflamm. 2017, 1–14. doi:10.1155/2017/5706152

PubMed Abstract | CrossRef Full Text | Google Scholar

Ganai, A. A., and Farooqi, H. (2015). Bioactivity of Genistein: A Review of In Vitro and In Vivo Studies. Biomed. Pharmacother. 76, 30–38. doi:10.1016/j.biopha.2015.10.026

PubMed Abstract | CrossRef Full Text | Google Scholar

Gao, Y.-j., Zhu, F., Qian, J.-m., and Dai, J.-y. (2016). Therapeutic and Immunoregulatory Effect of GATA-Binding Protein-3/T-Box Expressed in T-Cells Ratio of Astragalus Polysaccharides on 2,4,6-trinitrobenzene Sulfonic Acid-Induced Colitis in Rats. Chin. J. Integr. Med. 22 (12), 918–924. doi:10.1007/s11655-015-2151-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Garo, L. P., Ajay, A. K., Fujiwara, M., Beynon, V., Kuhn, C., Gabriely, G., et al. (2019). Smad7 Controls Immunoregulatory PDL2/1-PD1 Signaling in Intestinal Inflammation and Autoimmunity. Cell Rep. 28 (13), 3353–3366. doi:10.1016/j.celrep.2019.07.065

PubMed Abstract | CrossRef Full Text | Google Scholar

GBD 2017 Inflammatory Bowel Disease Collaborators (2020). The Global, Regional, and National burden of Inflammatory Bowel Disease in 195 Countries and Territories, 1990–2017: A Systematic Analysis for the Global Burden of Disease Study 2017. Lancet Gastroenterol. Hepatol. 5 (1), 17–30. doi:10.1016/S2468-1253(19)30333-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Geremia, A., Biancheri, P., Allan, P., Corazza, G. R., and Di Sabatino, A. (2014). Innate and Adaptive Immunity in Inflammatory Bowel Disease. Autoimmun. Rev. 13 (1), 3–10. doi:10.1016/j.autrev.2013.06.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Ghasemi-Pirbaluti, M., Motaghi, E., Najafi, A., and Hosseini, M. J. (2017). The Effect of Theophylline on Acetic Acid Induced Ulcerative Colitis in Rats. Biomed. Pharmacother. 90, 153–159. doi:10.1016/j.biopha.2017.03.038

PubMed Abstract | CrossRef Full Text | Google Scholar

Girardin, M., Dionne, S., Goyette, P., Rioux, J., Bitton, A., Elimrani, I., et al. (2012). Expression and Functional Analysis of Intestinal Organic cation/L-Carnitine Transporter (OCTN) in Crohn’s Disease. J. Crohn’s Colitis 6 (2), 189–197. doi:10.1016/j.crohns.2011.08.003

PubMed Abstract | CrossRef Full Text | Google Scholar

González-Alfonso, J., Míguez, N., Padilla, J., Leemans, L., Poveda, A., Jiménez-Barbero, J., et al. (2018). Optimization of Regioselective α-Glucosylation of Hesperetin Catalyzed by Cyclodextrin Glucanotransferase. Molecules 23 (11), 2885. doi:10.3390/molecules23112885

CrossRef Full Text | Google Scholar

Greving, C. N. A., and Towne, J. E. (2019). A Role for IL-12 in IBD After All?. Immunity 51 (2), 209–211. doi:10.1016/j.immuni.2019.07.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Guan, F., Liu, A. B., Li, G., Yang, Z., Sun, Y., Yang, C. S., et al. (2012). Deleterious Effects of High Concentrations of (-)-Epigallocatechin-3-Gallate and Atorvastatin in Mice with Colon Inflammation. Nutr. Cancer 64, 847–855. doi:10.1080/01635581.2012.695424

PubMed Abstract | CrossRef Full Text | Google Scholar

Guazelli, C. F. S., Fattori, V., Ferraz, C. R., Borghi, S. M., Casagrande, R., Baracat, M. M., et al. (2021). Antioxidant and Anti-inflammatory Effects of Hesperidin Methyl Chalcone in Experimental Ulcerative Colitis. Chem. Biol. Interact. 333, 109315. doi:10.1016/j.cbi.2020.109315

PubMed Abstract | CrossRef Full Text | Google Scholar

Guzman, J. R., Koo, J. S., Goldsmith, J. R., Mühlbauer, M., Narula, A., and Jobin, C. (2013). Oxymatrine Prevents NF-κB Nuclear Translocation and Ameliorates Acute Intestinal Inflammation. Sci. Rep. 3, 1629. doi:10.1038/srep01629

PubMed Abstract | CrossRef Full Text | Google Scholar

Hao, Y., Huo, J., Wang, T., Sun, G., and Wang, W. (2020). Chemical Profiling of Coptis Rootlet and Screening of its Bioactive Compounds in Inhibiting Staphylococcus aureus by UPLC-Q-TOF/MS. J. Pharm. Biomed. Anal. 180, 113089. doi:10.1016/j.jpba.2019.113089

PubMed Abstract | CrossRef Full Text | Google Scholar

Harbord, M., Eliakim, R., Bettenworth, D., Karmiris, K., Katsanos, K., Kopylov, U., et al. (2017)Third European Evidence-Based Consensus on Diagnosis and Management of Ulcerative Colitis. Part 2: Current Management. J. Crohns Colitis 11 (7), 769–784. doi:10.1093/ecco-jcc/jjx009

PubMed Abstract | CrossRef Full Text | Google Scholar

He, C., Wang, Z., and Shi, J. (2020). Pharmacological Effects of Icariin. Adv. Pharmacol. 87, 179–203. doi:10.1016/bs.apha.2019.10.004

PubMed Abstract | CrossRef Full Text | Google Scholar

He, H., Wei, D., Liu, H., Zhu, C., Lu, Y., Ke, Z., et al. (2019). Glycyrrhizin Protects Against Sodium Iodate-Induced RPE and Retinal Injury Though Activation of AKT and Nrf2/HO-1 Pathway. J. Cel Mol Med 23 (5), 3495–3504. doi:10.1111/jcmm.14246

PubMed Abstract | CrossRef Full Text | Google Scholar

He, W., Liu, M., Li, Y., Yu, H., Wang, D., Chen, Q., et al. (2019). Flavonoids from Citrus Aurantium Ameliorate TNBS-Induced Ulcerative Colitis through Protecting Colonic Mucus Layer Integrity. Eur. J. Pharmacol. 857, 172456. doi:10.1016/j.ejphar.2019.172456

PubMed Abstract | CrossRef Full Text | Google Scholar

Ho, G.-T., Aird, R. E., Liu, B., Boyapati, R. K., Kennedy, N. A., Dorward, D. A., et al. (2018). MDR1 Deficiency Impairs Mitochondrial Homeostasis and Promotes Intestinal Inflammation. Mucosal Immunol. 11 (1), 120–130. doi:10.1038/mi.2017.31

PubMed Abstract | CrossRef Full Text | Google Scholar

Hoensch, H. P., and Weigmann, B. (2018). Regulation of the Intestinal Immune System by Flavonoids and its Utility in Chronic Inflammatory Bowel Disease. World J. Gastroenterol. 24 (8), 877–881. doi:10.3748/wjg.v24.i8.877

PubMed Abstract | CrossRef Full Text | Google Scholar

Huang, J. G., and Aw, M. M. (2020). Pediatric Inflammatory Bowel Disease in Asia: Epidemiology and Natural History. Pediatr. Neonatal. 61 (3), 263–271. doi:10.1016/j.pedneo.2019.12.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Hueber, W., Sands, B. E., Lewitzky, S., Vandemeulebroecke, M., Reinisch, W., Higgins, P. D. R., et al. (2012). Secukinumab, a Human Anti-IL-17A Monoclonal Antibody, for Moderate to Severe Crohn’s Disease: Unexpected Results of a Randomised, Double-Blind Placebo-Controlled Trial. Gut 61 (12), 1693–1700. doi:10.1136/gutjnl-2011-301668

PubMed Abstract | CrossRef Full Text | Google Scholar

Ihara, S., Hirata, Y., and Koike, K. (2017). TGF-β in Inflammatory Bowel Disease: a Key Regulator of Immune Cells, Epithelium, and the Intestinal Microbiota. J. Gastroenterol. 52 (7), 777–787. doi:10.1007/s00535-017-1350-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Imran, M., Rauf, A., Abu-Izneid, T., Nadeem, M., Shariati, M. A., Khan, I. A., et al. (2019). Luteolin, a Flavonoid, as an Anticancer Agent: A Review. Biomed. Pharmacother. 112, 108612. doi:10.1016/j.biopha.2019.108612

PubMed Abstract | CrossRef Full Text | Google Scholar

Imran, M., Salehi, B., Sharifi-Rad, J., Aslam Gondal, T., Saeed, F., Imran, A., et al. (2019). Kaempferol: A Key Emphasis to its Anticancer Potential. Molecules 24 (12), 2277. doi:10.3390/molecules24122277

PubMed Abstract | CrossRef Full Text | Google Scholar

Jaakola, L. (2013). New Insights into the Regulation of Anthocyanin Biosynthesis in Fruits. Trends Plant Sci. 18 (9), 477–483. doi:10.1016/j.tplants.2013.06.003

PubMed Abstract | CrossRef Full Text | Google Scholar

James, M. A., Fu, H., Liu, Y., Chen, D.-R., and You, M. (2011). Dietary Administration of Berberine or Phellodendron Amurense Extract Inhibits Cell Cycle Progression and Lung Tumorigenesis. Mol. Carcinog. 50 (1), 1–7. doi:10.1002/mc.20690

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiang, L., Xia, B., Li, J., Ye, M., Yan, W., Deng, C., et al. (2006). Retrospective Survey of 452 Patients with Inflammatory Bowel Disease in Wuhan City, central China. Inflamm. Bowel Dis. 12 (3), 212–217. doi:10.1097/01.MIB.0000201098.26450.ae

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiao, Y.-F., Lu, M., Zhao, Y.-P., Liu, N., Niu, Y.-T., Niu, Y., et al. (2018). N-methylcytisine Ameliorates Dextran-Sulfate-Sodium-Induced Colitis in Mice by Inhibiting the Inflammatory Response. Molecules 23 (3), 510. doi:10.3390/molecules23030510

PubMed Abstract | CrossRef Full Text | Google Scholar

Jin, M., Zhao, K., Huang, Q., and Shang, P. (2014). Structural Features and Biological Activities of the Polysaccharides from Astragalus Membranaceus. Int. J. Biol. Macromol. 64, 257–266. doi:10.1016/j.ijbiomac.2013.12.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Jing, W., Dong, S., Luo, X., Liu, J., Wei, B., Du, W., et al. (2021). Berberine Improves Colitis by Triggering AhR Activation by Microbial Tryptophan Catabolites. Pharmacol. Res. 164, 105358. doi:10.1016/j.phrs.2020.105358

PubMed Abstract | CrossRef Full Text | Google Scholar

Joh, E.-H., Lee, I.-A., Jung, I.-H., and Kim, D.-H. (2011). Ginsenoside Rb1 and its Metabolite Compound K Inhibit IRAK-1 Activation-The Key Step of Inflammation. Biochem. Pharmacol. 82 (3), 278–286. doi:10.1016/j.bcp.2011.05.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Jones, J. R., Lebar, M. D., Jinwal, U. K., Abisambra, J. F., Koren, J., Blair, L., et al. (2011). The Diarylheptanoid (+)-aR,11S-Myricanol and Two Flavones from Bayberry (Myrica cerifera) Destabilize the Microtubule-Associated Protein Tau. J. Nat. Prod. 74 (1), 38–44. doi:10.1021/np100572z

PubMed Abstract | CrossRef Full Text | Google Scholar

Ju, S., Ge, Y., Li, P., Tian, X., Wang, H., Zheng, X., et al. (2018). Dietary Quercetin Ameliorates Experimental Colitis in Mouse by Remodeling the Function of Colonic Macrophages via a Heme Oxygenase-1-dependent Pathway. Cell Cycle 17 (1), 53–63. doi:10.1080/15384101.2017.1387701

PubMed Abstract | CrossRef Full Text | Google Scholar

Kaplan, G. G. (2015). The Global burden of IBD: from 2015 to 2025. Nat. Rev. Gastroenterol. Hepatol. 12 (12), 720–727. doi:10.1038/nrgastro.2015.150

PubMed Abstract | CrossRef Full Text | Google Scholar

Karatay, E., Gül Utku, Ö., Erdal, H., Arhan, M., Önal, İ. K., İbi̇ş, M., et al. (2017). Pentoxifylline Attenuates Mucosal Damage in an Experimental Model of Rat Colitis by Modulating Tissue Biomarkers of Inflammation, Oxidative Stress, and Fibrosis. Turk J. Med. Sci. 47 (1), 348–356. doi:10.3906/sag-1508-98

PubMed Abstract | CrossRef Full Text | Google Scholar

Karmele, E. P., Pasricha, T. S., Pasricha, T. S., Ramalingam, T. R., Thompson, R. W., Gieseck, R. L., et al. (2019). Anti-IL-13Rα2 Therapy Promotes Recovery in a Murine Model of Inflammatory Bowel Disease. Mucosal Immunol. 12 (5), 1174–1186. doi:10.1038/s41385-019-0189-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Karrasch, T., Kim, J.-S., Jang, B. I., and Jobin, C. (2007). The Flavonoid Luteolin Worsens Chemical-Induced Colitis in NF-κBEGFP Transgenic Mice through Blockade of NF-κB-Dependent Protective Molecules. PLoS One 2 (7), e596. doi:10.1371/journal.pone.0000596

PubMed Abstract | CrossRef Full Text | Google Scholar

Kennedy, N. A., Heap, G. A., Green, H. D., Hamilton, B., Bewshea, C., Walker, G. J., et al. (2019). Predictors of Anti-TNF Treatment Failure in Anti-TNF-naive Patients with Active Luminal Crohn’s Disease: A Prospective, Multicentre, Cohort Study. Lancet Gastroenterol. Hepatol. 4 (5), 341–353. doi:10.1016/S2468-1253(19)30012-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Khan, I., Ullah, N., Zha, L., Bai, Y., Khan, A., Zhao, T., et al. (2019). Alteration of Gut Microbiota in Inflammatory Bowel Disease (IBD): Cause or Consequence? IBD Treatment Targeting the Gut Microbiome. Pathogens 8 (3), 126. doi:10.3390/pathogens8030126

PubMed Abstract | CrossRef Full Text | Google Scholar

Khan, M. S., Ikram, M., Park, J. S., Park, T. J., and Kim, M. O. (2020). Gut Microbiota, its Role in Induction of Alzheimer’s Disease Pathology, and Possible Therapeutic Interventions: Special Focus on Anthocyanins. Cells 9 (4), 853. doi:10.3390/cells9040853

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, J.-K., Kim, J.-Y., Jang, S.-E., Choi, M.-S., Jang, H.-M., Yoo, H.-H., et al. (2018). Fermented Red Ginseng Alleviates Cyclophosphamide-Induced Immunosuppression and 2,4,6-Trinitrobenzenesulfonic Acid-Induced Colitis in Mice by Regulating Macrophage Activation and T Cell Differentiation. Am. J. Chin. Med. 46 (8), 1879–1897. doi:10.1142/S0192415X18500945

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, M., Murakami, A., Miyamoto, S., Tanaka, T., and Ohigashi, H. (2010). The Modifying Effects of green tea Polyphenols on Acute Colitis and Inflammation-Associated colon Carcinogenesis in Male ICR Mice. Biofactors 36 (1), 43–51. doi:10.1002/biof.69

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, M., Gu, B., Madison, M. C., Song, H. W., Norwood, K., Hill, A. A., et al. (2019). Cigarette Smoke Induces Intestinal Inflammation via a Th17 Cell-Neutrophil Axis. Front. Immunol. 10, 75. doi:10.3389/fimmu.2019.00075

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, S. W., Kim, E. S., Moon, C. M., Park, J. J., Kim, T. I., Kim, W. H., et al. (2011). Genetic Polymorphisms of IL-23R and IL-17A and Novel Insights into Their Associations with Inflammatory Bowel Disease. Gut 60 (11), 1527–1536. doi:10.1136/gut.2011.238477

PubMed Abstract | CrossRef Full Text | Google Scholar

Koeninger, L., Armbruster, N. S., Brinch, K. S., Kjaerulf, S., Andersen, B., Langnau, C., et al. (2020). Human β-Defensin 2 Mediated Immune Modulation as Treatment for Experimental Colitis. Front. Immunol. 11, 93. doi:10.3389/fimmu.2020.00093

PubMed Abstract | CrossRef Full Text | Google Scholar

Kordjazy, N., Haj-Mirzaian, A., Haj-Mirzaian, A., Rohani, M. M., Gelfand, E. W., Rezaei, N., et al. (2018). Role of Toll-Like Receptors in Inflammatory Bowel Disease. Pharmacol. Res. 129, 204–215. doi:10.1016/j.phrs.2017.11.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Kotlarz, D., Marquardt, B., Barøy, T., Lee, W. S., Konnikova, L., Hollizeck, S., et al. (2018). Human TGF-Β1 Deficiency Causes Severe Inflammatory Bowel Disease and Encephalopathy. Nat. Genet. 50 (3), 344–348. doi:10.1038/s41588-018-0063-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Kotze, P. G., Underwood, F. E., Damião, A. O. M. C., Ferraz, J. G. P., Saad-Hossne, R., Toro, M., et al. (2020). Progression of Inflammatory Bowel Diseases throughout Latin America and the Caribbean: A Systematic Review. Clin. Gastroenterol. Hepatol. 18 (2), 304–312. doi:10.1016/j.cgh.2019.06.030

PubMed Abstract | CrossRef Full Text | Google Scholar

Krissansen, G. W., Yang, Y., McQueen, F. M., Leung, E., Peek, D., Chan, Y. C., et al. (2015). Overexpression of miR-595 and miR-1246 in the Sera of Patients with Active Forms of Inflammatory Bowel Disease. Inflamm. Bowel Dis. 21 (3), 520–530. doi:10.1097/MIB.0000000000000285

PubMed Abstract | CrossRef Full Text | Google Scholar

Kudo, T., Okamura, S., Zhang, Y., Masuo, T., and Mori, M. (2011). Topical Application of Glycyrrhizin Preparation Ameliorates Experimentally Induced Colitis in Rats. World J. Gastroenterol. 17 (17), 2223–2228. doi:10.3748/wjg.v17.i17.2223

PubMed Abstract | CrossRef Full Text | Google Scholar

Lai, Y., Zeng, H., He, M., Qian, H., Wu, Z., Luo, Z., et al. (2016). 6,8-Di-C-methyl-flavonoids with Neuroprotective Activities from Rhododendron Fortunei. Fitoterapia 112, 237–243. doi:10.1016/j.fitote.2016.06.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Langer, V., Vivi, E., Regensburger, D., Winkler, T. H., Waldner, M. J., Rath, T., et al. (2019). IFN-γ Drives Inflammatory Bowel Disease Pathogenesis through VE-Cadherin-Directed Vascular Barrier Disruption. J. Clin. Invest. 129 (11), 4691–4707. doi:10.1172/JCI124884

PubMed Abstract | CrossRef Full Text | Google Scholar

Larabi, A., Barnich, N., and Nguyen, H. T. T. (2020). New Insights into the Interplay between Autophagy, Gut Microbiota and Inflammatory Responses in IBD. Autophagy 16 (1), 38–51. doi:10.1080/15548627.2019.1635384

PubMed Abstract | CrossRef Full Text | Google Scholar

Lee, H. T., Kim, M., Kim, J. Y., Brown, K. M., Ham, A., D’Agati, V. D., et al. (2013). Critical Role of interleukin-17A in Murine Intestinal Ischemia-Reperfusion Injury. Am. J. Physiol. Gastrointest. Liver Physiol. 304 (1), G12–G25. doi:10.1152/ajpgi.00201.2012

PubMed Abstract | CrossRef Full Text | Google Scholar

Lee, I.-A., Hyam, S. R., Jang, S.-E., Han, M. J., and Kim, D.-H. (2012). Ginsenoside Re Ameliorates Inflammation by Inhibiting the Binding of Lipopolysaccharide to TLR4 on Macrophages. J. Agric. Food Chem. 60 (38), 9595–9602. doi:10.1021/jf301372g

PubMed Abstract | CrossRef Full Text | Google Scholar

Lee, I.-A., Low, D., Kamba, A., Llado, V., and Mizoguchi, E. (2014). Oral Caffeine Administration Ameliorates Acute Colitis by Suppressing Chitinase 3-Like 1 Expression in Intestinal Epithelial Cells. J. Gastroenterol. 49 (8), 1206–1216. doi:10.1007/s00535-013-0865-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Lee, M., and Chang, E. B. (2021). Inflammatory Bowel Diseases (IBD) and the Microbiome-Searching the Crime Scene for Clues. Gastroenterology 160 (2), 524–537. doi:10.1053/j.gastro.2020.09.056

PubMed Abstract | CrossRef Full Text | Google Scholar

Lee, S.-Y., Jeong, J.-J., Eun, S.-H., and Kim, D.-H. (2015). Anti-inflammatory Effects of Ginsenoside Rg1 and its Metabolites Ginsenoside Rh1 and 20(S)-protopanaxatriol in Mice with TNBS-Induced Colitis. Eur. J. Pharmacol. 762, 333–343. doi:10.1016/j.ejphar.2015.06.011

PubMed Abstract | CrossRef Full Text | Google Scholar

Lees, C. W., Barrett, J. C., Parkes, M., and Satsangi, J. (2011). New IBD Genetics: Common Pathways with Other Diseases. Gut 60 (12), 1739–1753. doi:10.1136/gut.2009.199679

PubMed Abstract | CrossRef Full Text | Google Scholar

Levin, A. D., Wildenberg, M. E., and van den Brink, G. R. (2016). Mechanism of Action of Anti-TNF Therapy in Inflammatory Bowel Disease. J. Crohns Colitis 10 (8), 989–997. doi:10.1093/ecco-jcc/jjw053

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, B., Du, P., Du, Y., Zhao, D., Cai, Y., Yang, Q., et al. (2021). Luteolin Alleviates Inflammation and Modulates Gut Microbiota in Ulcerative Colitis Rats. Life Sci. 269, 119008. doi:10.1016/j.lfs.2020.119008

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, J.-C., Zhang, Z.-J., Liu, D., Jiang, M.-Y., Li, R.-T., and Li, H.-M. (2020). Quinolizidine Alkaloids from the Roots of Sophora Flavescens. Nat. Product Res. 1–8. doi:10.1080/14786419.2020.1817011

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, J., Zhong, W., Wang, W., Hu, S., Yuan, J., Zhang, B., et al. (2014). Ginsenoside Metabolite Compound K Promotes Recovery of Dextran Sulfate Sodium-Induced Colitis and Inhibits Inflammatory Responses by Suppressing NF-Κb Activation. PLoS One 9 (2), e87810. doi:10.1371/journal.pone.0087810

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, Q., Guan, H., Wang, X., He, Y., Sun, H., Tan, W., et al. (2017). Fingerprint-efficacy Study of the Quaternary Alkaloids in Corydalis Yanhusuo. J. Ethnopharmacol. 207, 108–117. doi:10.1016/j.jep.2017.06.036

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, Q., Miao, Z., Wang, R., Yang, J., and Zhang, D. (2020). Hesperetin Induces Apoptosis in Human Glioblastoma Cells via p38 MAPK Activation. Nutr. Cancer 72 (3), 538–545. doi:10.1080/01635581.2019.1638424

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, Y., Shen, L., and Luo, H. (2016). Luteolin Ameliorates Dextran Sulfate Sodium-Induced Colitis in Mice Possibly through Activation of the Nrf2 Signaling Pathway. Int. Immunopharmacol. 40, 24–31. doi:10.1016/j.intimp.2016.08.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Lichtenstein, G. R., Rutgeerts, P., Sandborn, W. J., Sands, B. E., Diamond, R. H., Blank, M., et al. (2012). A Pooled Analysis of Infections, Malignancy, and Mortality in Infliximab- and Immunomodulator-Treated Adult Patients With Inflammatory Bowel Disease. Am. J. Gastroenterol. 107 (7), 1051–1063. doi:10.1038/ajg.2012.89

PubMed Abstract | CrossRef Full Text | Google Scholar

Lin, Y., Shi, R., Wang, X., and Shen, H.-M. (2008). Luteolin, a Flavonoid with Potential for Cancer Prevention and Therapy. Ccdt 8 (7), 634–646. doi:10.2174/156800908786241050

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, C., Wang, J., Yang, Y., Liu, X., Zhu, Y., Zou, J., et al. (2018). Ginsenoside Rd Ameliorates Colitis by Inducing P62-Driven Mitophagy-Mediated NLRP3 Inflammasome Inactivation in Mice. Biochem. Pharmacol. 155, 366–379. doi:10.1016/j.bcp.2018.07.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, D., Wu, J., Xie, H., Liu, M., Takau, I., Zhang, H., et al. (2016). Inhibitory Effect of Hesperetin and Naringenin on Human UDP-Glucuronosyltransferase Enzymes: Implications for Herb-Drug Interactions. Biol. Pharm. Bull. 39 (12), 2052–2059. doi:10.1248/bpb.b16-00581

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, F., Ma, R., Riordan, S. M., Grimm, M. C., Liu, L., Wang, Y., et al. (2017). Azathioprine, Mercaptopurine, and 5-Aminosalicylic Acid Affect the Growth of IBD-Associated Campylobacter Species and Other Enteric Microbes. Front. Microbiol. 8, 527. doi:10.3389/fmicb.2017.00527

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, S., Zhang, S., Lv, X., Lu, J., Ren, C., Zeng, Z., et al. (2019). Limonin Ameliorates Ulcerative Colitis by Regulating STAT3/miR-214 Signaling Pathway. Int. Immunopharmacol. 75, 105768. doi:10.1016/j.intimp.2019.105768

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, Y., Xiang, J., Liu, M., Wang, S., Lee, R. J., and Ding, H. (2011). Protective Effects of Glycyrrhizic Acid by Rectal Treatment on a TNBS-Induced Rat Colitis Model. J. Pharm. Pharmacol. 63 (3), 439–446. doi:10.1111/j.2042-7158.2010.01185.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Lv, J., Zhang, Y., Tian, Z., Liu, F., Shi, Y., Liu, Y., et al. (2017). Astragalus Polysaccharides Protect against Dextran Sulfate Sodium-Induced Colitis by Inhibiting NF-Κв Activation. Int. J. Biol. Macromol. 98, 723–729. doi:10.1016/j.ijbiomac.2017.02.024

PubMed Abstract | CrossRef Full Text | Google Scholar

Ma, H., He, X., Yang, Y., Li, M., Hao, D., and Jia, Z. (2011). The Genus Epimedium: An Ethnopharmacological and Phytochemical Review. J. Ethnopharmacology 134 (3), 519–541. doi:10.1016/j.jep.2011.01.001

CrossRef Full Text | Google Scholar

Mai, C.-T., Wu, M.-M., Wang, C.-L., Su, Z.-R., Cheng, Y.-Y., and Zhang, X.-J. (2019). Palmatine Attenuated Dextran Sulfate Sodium (DSS)-induced Colitis via Promoting Mitophagy-Mediated NLRP3 Inflammasome Inactivation. Mol. Immunol. 105, 76–85. doi:10.1016/j.molimm.2018.10.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Mak, W. Y., Zhao, M., Ng, S. C., and Burisch, J. (2020). The Epidemiology of Inflammatory Bowel Disease: East Meets West. J. Gastroenterol. Hepatol. 35(3), 380–389. doi:10.1111/jgh.14872

PubMed Abstract | CrossRef Full Text | Google Scholar

Mantovani, A., Cassatella, M. A., Costantini, C., and Jaillon, S. (2011). Neutrophils in the Activation and Regulation of Innate and Adaptive Immunity. Nat. Rev. Immunol. 11 (8), 519–531. doi:10.1038/nri3024

PubMed Abstract | CrossRef Full Text | Google Scholar

Márquez-Flores, Y. K., Villegas, I., Cárdeno, A., Rosillo, M. Á., and Alarcón-de-la-Lastra, C. (2016). Apigenin Supplementation Protects the Development of Dextran Sulfate Sodium-Induced Murine Experimental Colitis by Inhibiting Canonical and Non-Canonical Inflammasome Signaling Pathways. J. Nutr. Biochem. 30, 143–152. doi:10.1016/j.jnutbio.2015.12.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Martínez Leal, J., Valenzuela Suárez, L., Jayabalan, R., Huerta Oros, J., and Escalante-Aburto, A. (2018). A Review on Health Benefits of Kombucha Nutritional Compounds and Metabolites. CyTA-Journal of Food 16 (1), 390–399. doi:10.1080/19476337.2017.1410499

CrossRef Full Text | Google Scholar

Mascia, C., Maina, M., Chiarpotto, E., Leonarduzzi, G., Poli, G., and Biasi, F. (2010). Proinflammatory Effect of Cholesterol and its Oxidation Products on CaCo-2 Human Enterocyte-Like Cells: Effective Protection by Epigallocatechin-3-Gallate. Free Radic. Biol. Med. 49, 2049–2057. doi:10.1016/j.freeradbiomed.2010.09.033

PubMed Abstract | CrossRef Full Text | Google Scholar

Moens, A., van Hoeve, K., Humblet, E., Rahier, J.-F., Bossuyt, P., Dewit, S., et al. (2019). Outcome of Pregnancies in Female Patients with Inflammatory Bowel Diseases Treated with Vedolizumab. J. Crohns Colitis 13 (1), 12–18. doi:10.1093/ecco-jcc/jjy142

PubMed Abstract | CrossRef Full Text | Google Scholar

Molodecky, N. A., Soon, I. S., Rabi, D. M., Ghali, W. A., Ferris, M., Chernoff, G., et al. (2012). Increasing Incidence and Prevalence of the Inflammatory Bowel Diseases with Time, Based on Systematic Review. Gastroenterology 142 (1), 46–54. doi:10.1053/j.gastro.2011.10.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Moschen, A. R., Tilg, H., and Raine, T. (2019). IL-12, IL-23 and IL-17 in IBD: Immunobiology and Therapeutic Targeting. Nat. Rev. Gastroenterol. Hepatol. 16 (3), 185–196. doi:10.1038/s41575-018-0084-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Mumolo, M. G., Bertani, L., Ceccarelli, L., Laino, G., Fluri, G. D., Albano, E., et al. (2018). From Bench to Bedside: Fecal Calprotectin in Inflammatory Bowel Diseases Clinical Setting. World J. Gastroenterol. 24 (33), 3681–3694. doi:10.3748/wjg.v24.i33.3681

PubMed Abstract | CrossRef Full Text | Google Scholar

Nabavi, S. F., Khan, H., D'onofrio, G., Šamec, D., Shirooie, S., Dehpour, A. R., et al. (2018). Apigenin as Neuroprotective Agent: Of Mice and Men. Pharmacol. Res. 128, 359–365. doi:10.1016/j.phrs.2017.10.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Nadeem, M. S., Kumar, V., Al-Abbasi, F. A., Kamal, M. A., and Anwar, F. (2020). Risk of Colorectal Cancer in Inflammatory Bowel Diseases. Semin. Cancer Biol. 64, 51–60. doi:10.1016/j.semcancer.2019.05.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Neumann, C., Scheffold, A., and Rutz, S. (2019). Functions and Regulation of T Cell-Derived Interleukin-10. Semin. Immunol. 44, 101344. doi:10.1016/j.smim.2019.101344

PubMed Abstract | CrossRef Full Text | Google Scholar

Neurath, M. F. (2019). IL-23 in Inflammatory Bowel Diseases and colon Cancer. Cytokine Growth Factor Rev. 45, 1–8. doi:10.1016/j.cytogfr.2018.12.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Ng, S. C., Shi, H. Y., Hamidi, N., Underwood, F. E., Tang, W., Benchimol, E. I., et al. (2017). Worldwide Incidence and Prevalence of Inflammatory Bowel Disease in the 21st century: a Systematic Review of Population-Based Studies. Lancet 390 (10114), 2769–2778. doi:10.1016/s0140-6736(17)32448-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Nishitani, Y., Yamamoto, K., Yoshida, M., Azuma, T., Kanazawa, K., Hashimoto, T., et al. (2013). Intestinal Anti-inflammatory Activity of Luteolin: Role of the Aglycone in NF-Κb Inactivation in Macrophages Co-cultured with Intestinal Epithelial Cells. Biofactors 39 (5), 522–533. doi:10.1002/biof.1091

PubMed Abstract | CrossRef Full Text | Google Scholar

Nogata, Y., Sakamoto, K., Shiratsuchi, H., Ishii, T., Yano, M., and Ohta, H. (2006). Flavonoid Composition of Fruit Tissues of Citrus Species. Biosci. Biotechnol. Biochem. 70 (1), 178–192. doi:10.1271/bbb.70.178

PubMed Abstract | CrossRef Full Text | Google Scholar

Nomi, Y., Iwasaki-Kurashige, K., and Matsumoto, H. (2019). Therapeutic Effects of Anthocyanins for Vision and Eye Health. Molecules 24 (18), 3311. doi:10.3390/molecules24183311

PubMed Abstract | CrossRef Full Text | Google Scholar

Nunes, C., Almeida, L., Barbosa, R. M., and Laranjinha, J. (2017). Luteolin Suppresses the JAK/STAT Pathway in a Cellular Model of Intestinal Inflammation. Food Funct. 8 (1), 387–396. doi:10.1039/c6fo01529h

PubMed Abstract | CrossRef Full Text | Google Scholar

Nunes, S., Danesi, F., Del Rio, D., and Silva, P. (2018). Resveratrol and Inflammatory Bowel Disease: The Evidence So Far. Nutr. Res. Rev. 31 (1), 85–97. doi:10.1017/S095442241700021X

PubMed Abstract | CrossRef Full Text | Google Scholar

Olivera, P., Danese, S., and Peyrin-Biroulet, L. (2017). JAK Inhibition in Inflammatory Bowel Disease. Expert Rev. Clin. Immunol. 13 (7), 693–703. doi:10.1080/1744666X.2017.1291342

PubMed Abstract | CrossRef Full Text | Google Scholar

Oz, H. S., Chen, T., and de Villiers, W. J. S. (2013). Green Tea Polyphenols and Sulfasalazine Have Parallel Anti-inflammatory Properties in Colitis Models. Front. Immunol. 4, 132. doi:10.3389/fimmu.2013.00132

PubMed Abstract | CrossRef Full Text | Google Scholar

Parhiz, H., Roohbakhsh, A., Soltani, F., Rezaee, R., and Iranshahi, M. (2015). Antioxidant and Anti-inflammatory Properties of the Citrus Flavonoids Hesperidin and Hesperetin: an Updated Review of Their Molecular Mechanisms and Experimental Models. Phytother. Res. 29 (3), 323–331. doi:10.1002/ptr.5256

PubMed Abstract | CrossRef Full Text | Google Scholar

Park, K. T., Ehrlich, O. G., Allen, J. I., Meadows, P., Szigethy, E. M., Henrichsen, K., et al. (2020). The Cost of Inflammatory Bowel Disease: An Initiative From the Crohn’s & Colitis Foundation. Inflamm. Bowel Dis. 26(1), 1–10. doi:10.1093/ibd/izz104

PubMed Abstract | CrossRef Full Text | Google Scholar

Park, M.-Y., Ji, G. E., and Sung, M.-K. (2012). Dietary Kaempferol Suppresses Inflammation of Dextran Sulfate Sodium-Induced Colitis in Mice. Dig. Dis. Sci. 57 (2), 355–363. doi:10.1007/s10620-011-1883-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Park, S. C., and Jeen, Y. T. (2019). Genetic Studies of Inflammatory Bowel Disease-Focusing on Asian Patients. Cells 8 (5), 404. doi:10.3390/cells8050404

PubMed Abstract | CrossRef Full Text | Google Scholar

Patel, D. D., and Kuchroo, V. K. (2015). Th17 Cell Pathway in Human Immunity: Lessons from Genetics and Therapeutic Interventions. Immunity 43 (6), 1040–1051. doi:10.1016/j.immuni.2015.12.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Peng, Y., Yan, Y., Wan, P., Chen, D., Ding, Y., Ran, L., et al. (2019). Gut Microbiota Modulation and Anti-inflammatory Properties of Anthocyanins from the Fruits of Lycium Ruthenicum Murray in Dextran Sodium Sulfate-Induced Colitis in Mice. Free Radic. Biol. Med. 136, 96–108. doi:10.1016/j.freeradbiomed.2019.04.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Peyrin-Biroulet, L., Christopher, R., Behan, D., and Lassen, C. (2017). Modulation of Sphingosine-1-Phosphate in Inflammatory Bowel Disease. Autoimmun. Rev. 16 (5), 495–503. doi:10.1016/j.autrev.2017.03.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Piberger, H., Oehme, A., Hofmann, C., Dreiseitel, A., Sand, P. G., Obermeier, F., et al. (2011). Bilberries and Their Anthocyanins Ameliorate Experimental Colitis. Mol. Nutr. Food Res. 55 (11), 1724–1729. doi:10.1002/mnfr.201100380

PubMed Abstract | CrossRef Full Text | Google Scholar

Pinho-Ribeiro, F. A., Zarpelon, A. C., Fattori, V., Manchope, M. F., Mizokami, S. S., Casagrande, R., et al. (2016). Naringenin Reduces Inflammatory Pain in Mice. Neuropharmacology 105, 508–519. doi:10.1016/j.neuropharm.2016.02.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Polat, F. R., Karaboga, I., Polat, M. S., Erboga, Z., Yilmaz, A., and Güzel, S. (2018). Effect of Hesperetin on Inflammatory and Oxidative Status in Trinitrobenzene Sulfonic Acid-Induced Experimental Colitis Model. Cell Mol. Biol. 64 (11), 58–65. doi:10.14715/cmb/2018.64.11.11

CrossRef Full Text | Google Scholar

Qiu, M., Liu, J., Feng, P., Su, Y., Guo, R., Shi, F., et al. (2020). Cytochrome P450s Regulates Aloperine-Induced Pathological Changes in Mouse Liver and Kidney. Res. Vet. Sci. 132, 97–100. doi:10.1016/j.rvsc.2020.06.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Qu, X., Li, Q., Song, Y., Xue, A., Liu, Y., Qi, D., et al. (2020). Potential of Myricetin to Restore the Immune Balance in Dextran Sulfate Sodium-Induced Acute Murine Ulcerative Colitis. J. Pharm. Pharmacol. 72 (1), 92–100. doi:10.1111/jphp.13197

PubMed Abstract | CrossRef Full Text | Google Scholar

Ran, X., Li, Y., Chen, G., Fu, S., He, D., Huang, B., et al. (2018). Farrerol Ameliorates TNBS-Induced Colonic Inflammation by Inhibiting ERK1/2, JNK1/2, and NF-κB Signaling Pathway. Ijms 19 (7), 2037. doi:10.3390/ijms19072037

PubMed Abstract | CrossRef Full Text | Google Scholar

Rattigan, R., O’Doherty, J. V., Vigors, S., Ryan, M. T., Sebastiano, R. S., Callanan, J. J., et al. (2020). The Effects of the Marine-Derived Polysaccharides Laminarin and Chitosan on Aspects of Colonic Health in Pigs Challenged with Dextran Sodium Sulphate. Mar. Drugs 18 (5), 262. doi:10.3390/md18050262

PubMed Abstract | CrossRef Full Text | Google Scholar

Reyhan, E., Irkorucu, O., Surmelioglu, A., Ozkara, S., Deger, K. C., Aziret, M., et al. (2014). Efficacy of Pentoxifylline and Tadalafil in Rat Model of Ischemic Colitis. J. Invest. Surg. 27 (6), 349–353. doi:10.3109/08941939.2014.971204

PubMed Abstract | CrossRef Full Text | Google Scholar

Rioux, J. D., Xavier, R. J., Taylor, K. D., Silverberg, M. S., Goyette, P., Huett, A., et al. (2007). Genome-wide Association Study Identifies New Susceptibility Loci for Crohn Disease and Implicates Autophagy in Disease Pathogenesis. Nat. Genet. 39 (5), 596–604. doi:10.1038/ng2032

PubMed Abstract | CrossRef Full Text | Google Scholar

Rioux, L.-E., Turgeon, S. L., and Beaulieu, M. (2010). Structural Characterization of Laminaran and Galactofucan Extracted from the Brown Seaweed Saccharina Longicruris. Phytochemistry 71 (13), 1586–1595. doi:10.1016/j.phytochem.2010.05.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Rosen, M. J., Dhawan, A., and Saeed, S. A. (2015). Inflammatory Bowel Disease in Children and Adolescents. JAMA Pediatr. 169 (11), 1053–1060. doi:10.1001/jamapediatrics.2015.1982

PubMed Abstract | CrossRef Full Text | Google Scholar

Ryuk, J. A., Zheng, M. S., Lee, M. Y., Seo, C. S., Li, Y., Lee, S. H., et al. (2012). Discrimination of Phellodendron Amurense and P. Chinense Based on DNA Analysis and the Simultaneous Analysis of Alkaloids. Arch. Pharm. Res. 35 (6), 1045–1054. doi:10.1007/s12272-012-0612-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Sahin, I., Bilir, B., Ali, S., Sahin, K., and Kucuk, O. (2019). Soy Isoflavones in Integrative Oncology: Increased Efficacy and Decreased Toxicity of Cancer Therapy. Integr. Cancer Ther. 18, 1534735419835310. doi:10.1177/1534735419835310

PubMed Abstract | CrossRef Full Text | Google Scholar

Salas, A., Hernandez-Rocha, C., Duijvestein, M., Faubion, W., McGovern, D., Vermeire, S., et al. (2020). JAK-STAT Pathway Targeting for the Treatment of Inflammatory Bowel Disease. Nat. Rev. Gastroenterol. Hepatol. 17 (6), 323–337. doi:10.1038/s41575-020-0273-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Salem, M., El Azreq, M.-A., Pelletier, J., Robaye, B., Aoudjit, F., and Sévigny, J. (2019). Exacerbated Intestinal Inflammation in P2Y6 Deficient Mice Is Associated with Th17 Activation. Biochim. Biophys. Acta 1865 (10), 2595–2605. doi:10.1016/j.bbadis.2019.06.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Sandborn, W. J., Gasink, C., Gao, L.-L., Blank, M. A., Johanns, J., Guzzo, C., et al. CERTIFI Study Group (2012). Ustekinumab Induction and Maintenance Therapy in Refractory Crohn's Disease. N. Engl. J. Med. 367 (16), 1519–1528. doi:10.1056/NEJMoa1203572

PubMed Abstract | CrossRef Full Text | Google Scholar

Sands, B. E., Jacobson, E. W., Sylwestrowicz, T., Younes, Z., Dryden, G., Fedorak, R., et al. (2010). Randomized, Double-Blind, Placebo-Controlled Trial of the Oral Interleukin-12/23 Inhibitor Apilimod Mesylate for Treatment of Active Crohnʼs Disease. Inflamm. Bowel Dis. 16 (7), 1209–1218. doi:10.1002/ibd.21159

PubMed Abstract | CrossRef Full Text | Google Scholar

Sarra, M., Pallone, F., Macdonald, T. T., and Monteleone, G. (2010). IL-23/IL-17 axis in IBD. Inflamm. Bowel Dis. 16 (10), 1808–1813. doi:10.1002/ibd.21248

PubMed Abstract | CrossRef Full Text | Google Scholar

Satoh, T., and Akira, S. (2016). Toll-Like Receptor Signaling and its Inducible Proteins. Microbiol. Spectr. 4 (6), 1–7. doi:10.1128/microbiolspec.mchd-0040-2016

PubMed Abstract | CrossRef Full Text | Google Scholar

Schirbel, A., Rebert, N., Sadler, T., West, G., Rieder, F., Wagener, C., et al. (2019). Mutual Regulation of TLR/NLR and CEACAM1 in the Intestinal Microvasculature: Implications for IBD Pathogenesis and Therapy. Inflamm. Bowel Dis. 25 (2), 294–305. doi:10.1093/ibd/izy316

PubMed Abstract | CrossRef Full Text | Google Scholar

Schneider, L. S., Hernandez, G., Zhao, L., Franke, A. A., Chen, Y.-L., Pawluczyk, S., et al. (2019). Safety and Feasibility of Estrogen Receptor-β Targeted phytoSERM Formulation for Menopausal Symptoms: Phase 1b/2a Randomized Clinical Trial. Menopause 26 (8), 874–884. doi:10.1097/GME.0000000000001325

PubMed Abstract | CrossRef Full Text | Google Scholar

Sefrina, L. R., Briawan, D., Sinaga, T., and Permaesih, D. (2020). Flavonoid Database Based on Indonesian Foods. J. Nutr. Sci. Vitaminol. 66, S251–S255. doi:10.3177/jnsv.66.S251

PubMed Abstract | CrossRef Full Text | Google Scholar

Semwal, D., Semwal, R., Combrinck, S., and Viljoen, A. (2016). Myricetin: A Dietary Molecule with Diverse Biological Activities. Nutrients 8 (2), 90. doi:10.3390/nu8020090

PubMed Abstract | CrossRef Full Text | Google Scholar

Senchina, D. S., Hallam, J. E., Kohut, M. L., Nguyen, N. A., and Perera, M. A. (2014). Alkaloids and Athlete Immune Function: Caffeine, Theophylline, Gingerol, Ephedrine, and Their Congeners. Exerc. Immunol. Rev. 20, 68–93.

PubMed Abstract | Google Scholar

Sergent, T., Piront, N., Meurice, J., Toussaint, O., and Schneider, Y.-J. (2010). Anti-inflammatory Effects of Dietary Phenolic Compounds in an In Vitro Model of Inflamed Human Intestinal Epithelium. Chem. Biol. Interact. 188 (3), 659–667. doi:10.1016/j.cbi.2010.08.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Sharma, P., McClees, S., and Afaq, F. (2017). Pomegranate for Prevention and Treatment of Cancer: An Update. Molecules 22 (1), 177. doi:10.3390/molecules22010177

PubMed Abstract | CrossRef Full Text | Google Scholar

Sharma, R., Sharma, R., Khaket, T. P., Dutta, C., Chakraborty, B., and Mukherjee, T. K. (2017). Breast Cancer Metastasis: Putative Therapeutic Role of Vascular Cell Adhesion Molecule-1. Cell Oncol. 40 (3), 199–208. doi:10.1007/s13402-017-0324-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Shi, H.-J., Song, H.-B., Wang, L., Xiao, S.-X., Bo, K.-P., and Ma, W. (2018). The Synergy of Diammonium Glycyrrhizinate Remarkably Reduces the Toxicity of Oxymatrine in ICR Mice. Biomed. Pharmacother. 97, 19–25. doi:10.1016/j.biopha.2017.09.039

PubMed Abstract | CrossRef Full Text | Google Scholar

Shi, Y.-J., Hu, S.-J., Zhao, Q.-Q., Liu, X.-S., Liu, C., and Wang, H. (2019). Toll-like Receptor 4 (TLR4) Deficiency Aggravates Dextran Sulfate Sodium (DSS)-induced Intestinal Injury by Down-Regulating IL6, CCL2 and CSF3. Ann. Transl. Med. 7 (23), 713. doi:10.21037/atm.2019.12.28

PubMed Abstract | CrossRef Full Text | Google Scholar

Shirzad, M., Heidarian, E., Beshkar, P., and Gholami-Arjenaki, M. (2017). Biological Effects of Hesperetin on Interleukin-6/Phosphorylated Signal Transducer and Activator of Transcription 3 Pathway Signaling in Prostate Cancer PC3 Cells. Pharmacognosy Res. 9 (2), 188–194. doi:10.4103/0974-8490.204655

PubMed Abstract | CrossRef Full Text | Google Scholar

Shouval, D. S., Biswas, A., Kang, Y. H., Griffith, A. E., Konnikova, L., Mascanfroni, I. D., et al. (2016). Interleukin 1β Mediates Intestinal Inflammation in Mice and Patients With Interleukin 10 Receptor Deficiency. Gastroenterology 151 (6), 1100–1104. doi:10.1053/j.gastro.2016.08.055

PubMed Abstract | CrossRef Full Text | Google Scholar

Silva, P. S. A., Nguyen, D. D., Sauk, J., Korzenik, J., Yajnik, V., and Ananthakrishnan, A. N. (2012). Long-term Outcome of a Third Anti-TNF Monoclonal Antibody after the Failure of Two Prior Anti-TNFs in Inflammatory Bowel Disease. Aliment. Pharmacol. Ther. 36 (5), 459–466. doi:10.1111/j.1365–2036.2012.05214.x10.1111/j.1365-2036.2012.05214.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Silva, S., Costa, E. M., Calhau, C., Morais, R. M., and Pintado, M. E. (2017). Anthocyanin Extraction from Plant Tissues: A Review. Crit. Rev. Food Sci. Nutr. 57 (14), 3072–3083. doi:10.1080/10408398.2015.1087963

PubMed Abstract | CrossRef Full Text | Google Scholar

Singleton, E. L., Le, N., and Ness, G. L. (2019). Theophylline and Caffeine as Alternatives during an Aminophylline Shortage. Ann. Pharmacother. 53 (3), 316–320. doi:10.1177/1060028018806624

PubMed Abstract | CrossRef Full Text | Google Scholar

Sohn, J. J., Schetter, A. J., Yfantis, H. G., Ridnour, L. A., Horikawa, I., Khan, M. A., et al. (2012). Macrophages, Nitric Oxide and microRNAs Are Associated with DNA Damage Response Pathway and Senescence in Inflammatory Bowel Disease. PLoS One 7 (9), e44156. doi:10.1371/journal.pone.0044156

PubMed Abstract | CrossRef Full Text | Google Scholar

Spagnuolo, C., Russo, G. L., Orhan, I. E., Habtemariam, S., Daglia, M., Sureda, A., et al. (2015). Genistein and Cancer: Current Status, Challenges, and Future Directions. Adv. Nutr. 6 (4), 408–419. doi:10.3945/an.114.008052

PubMed Abstract | CrossRef Full Text | Google Scholar

Spinozzi, S., Colliva, C., Camborata, C., Roberti, M., Ianni, C., Neri, F., et al. (2014). Berberine and its Metabolites: Relationship between Physicochemical Properties and Plasma Levels after Administration to Human Subjects. J. Nat. Prod. 77 (4), 766–772. doi:10.1021/np400607k

PubMed Abstract | CrossRef Full Text | Google Scholar

Strober, W., Asano, N., Fuss, I., Kitani, A., and Watanabe, T. (2014). Cellular and Molecular Mechanisms Underlying NOD2 Risk-Associated Polymorphisms in Crohn's Disease. Immunol. Rev. 260 (1), 249–260. doi:10.1111/imr.12193

PubMed Abstract | CrossRef Full Text | Google Scholar

Stronati, L., Palone, F., Negroni, A., Colantoni, E., Mancuso, A. B., Cucchiara, S., et al. (2019). Dipotassium Glycyrrhizate Improves Intestinal Mucosal Healing by Modulating Extracellular Matrix Remodeling Genes and Restoring Epithelial Barrier Functions. Front. Immunol. 10, 939. doi:10.3389/fimmu.2019.00939

PubMed Abstract | CrossRef Full Text | Google Scholar

Sui, X., Zhang, Y., and Zhou, W. (2016). Bread Fortified with Anthocyanin-Rich Extract from Black rice as Nutraceutical Sources: Its Quality Attributes and In Vitro Digestibility. Food Chem. 196, 910–916. doi:10.1016/j.foodchem.2015.09.113

PubMed Abstract | CrossRef Full Text | Google Scholar

Tao, F., Qian, C., Guo, W., Luo, Q., Xu, Q., and Sun, Y. (2013). Inhibition of Th1/Th17 Responses via Suppression of STAT1 and STAT3 Activation Contributes to the Amelioration of Murine Experimental Colitis by a Natural Flavonoid Glucoside Icariin. Biochem. Pharmacol. 85 (6), 798–807. doi:10.1016/j.bcp.2012.12.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Terdiman, J. P., Gruss, C. B., Heidelbaugh, J. J., Sultan, S., and Falck–Ytter, Y. T. (2013). American Gastroenterological Association Institute Guideline on the Use of Thiopurines, Methotrexate, and Anti-TNF-α Biologic Drugs for the Induction and Maintenance of Remission in Inflammatory Crohn’s Disease. Gastroenterology 145 (6), 1459–1463. doi:10.1053/j.gastro.2013.10.047

PubMed Abstract | CrossRef Full Text | Google Scholar

Thumann, T. A., Pferschy-Wenzig, E.-M., Moissl-Eichinger, C., and Bauer, R. (2019). The Role of Gut Microbiota for the Activity of Medicinal Plants Traditionally Used in the European Union for Gastrointestinal Disorders. J. Ethnopharmacol. 245, 112153. doi:10.1016/j.jep.2019.112153

PubMed Abstract | CrossRef Full Text | Google Scholar

Tian, L., Tan, Y., Chen, G., Wang, G., Sun, J., Ou, S., et al. (2019). Metabolism of Anthocyanins and Consequent Effects on the Gut Microbiota. Crit. Rev. Food Sci. Nutr. 59 (6), 982–991. doi:10.1080/10408398.2018.1533517

PubMed Abstract | CrossRef Full Text | Google Scholar

Tian, M., Ma, P., Zhang, Y., Mi, Y., and Fan, D. (2020). Ginsenoside Rk3 Alleviated DSS-Induced Ulcerative Colitis by Protecting colon Barrier and Inhibiting NLRP3 Inflammasome Pathway. Int. Immunopharmacol. 85, 106645. doi:10.1016/j.intimp.2020.106645

PubMed Abstract | CrossRef Full Text | Google Scholar

Tindemans, I., Joosse, M. E., and Samsom, J. N. (2020). Dissecting the Heterogeneity in T-Cell Mediated Inflammation in IBD. Cells 9 (1), 110. doi:10.3390/cells9010110

PubMed Abstract | CrossRef Full Text | Google Scholar

Verstockt, B., Ferrante, M., Vermeire, S., and Van Assche, G. (2018). New Treatment Options for Inflammatory Bowel Diseases. J. Gastroenterol. 53 (5), 585–590. doi:10.1007/s00535-018-1449-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Verstockt, S., Verstockt, B., and Vermeire, S. (2019). Oncostatin M as a New Diagnostic, Prognostic and Therapeutic Target in Inflammatory Bowel Disease (IBD). Expert Opin. Ther. Targets 23 (11), 943–954. doi:10.1080/14728222.2019.1677608

PubMed Abstract | CrossRef Full Text | Google Scholar

Vetuschi, A., Pompili, S., Gaudio, E., Latella, G., and Sferra, R. (2018). PPAR-γ with its Anti-inflammatory and Anti-Fibrotic Action Could Be an Effective Therapeutic Target in IBD. Eur. Rev. Med. Pharmacol. Sci. 22 (24), 8839–8848. doi:10.26355/eurrev_201812_16652

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, C.-Z., Yao, H., Zhang, C.-F., Chen, L., Wan, J.-Y., Huang, W.-H., et al. (2018). American Ginseng Microbial Metabolites Attenuate DSS-Induced Colitis and Abdominal Pain. Int. Immunopharmacol. 64, 246–251. doi:10.1016/j.intimp.2018.09.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, L., Wei, W., Xiao, Q., Yang, H., and Ci, X. (2019). Farrerol Ameliorates APAP-Induced Hepatotoxicity via Activation of Nrf2 and Autophagy. Int. J. Biol. Sci. 15 (4), 788–799. doi:10.7150/ijbs.30677

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, L., Wu, H., Yang, F., and Dong, W. (2019). The Protective Effects of Myricetin against Cardiovascular Disease. J. Nutr. Sci. Vitaminol 65 (6), 470–476. doi:10.3177/jnsv.65.470

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, R., Deng, X., Gao, Q., Wu, X., Han, L., Gao, X., et al. (2020). Sophora Alopecuroides L.: An Ethnopharmacological, Phytochemical, and Pharmacological Review. J. Ethnopharmacol. 248, 112172. doi:10.1016/j.jep.2019.112172

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, S.-C., Yang, Y., Liu, J., Jiang, A.-D., Chu, Z.-X., Chen, S.-Y., et al. (2018). Discovery of Novel Limonin Derivatives as Potent Anti-Inflammatory and Analgesic Agents. Chin. J. Nat. Med. 16 (3), 231–240. doi:10.1016/s1875-5364(18)30052-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Y., Parker, C. E., Bhanji, T., Feagan, B. G., and MacDonald, J. K. (2016). Oral 5-Aminosalicylic Acid for Induction of Remission in Ulcerative Colitis. Cochrane Database Syst. Rev. 4 (4), CD000543. doi:10.1002/14651858.CD000543.pub4

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Z., Wang, D., Yang, D., Zhen, W., Zhang, J., and Peng, S. (2018). The Effect of Icariin on Bone Metabolism and its Potential Clinical Application. Osteoporos. Int. 29 (3), 535–544. doi:10.1007/s00198-017-4255-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Wen, J.-B., Zhu, F.-Q., Chen, W.-G., Jiang, L.-P., Chen, J., Hu, Z.-P., et al. (2014). Oxymatrine Improves Intestinal Epithelial Barrier Function Involving NF-κB-Mediated Signaling Pathway in CCl4-Induced Cirrhotic Rats. PLoS One 9 (8), e106082. doi:10.1371/journal.pone.0106082

PubMed Abstract | CrossRef Full Text | Google Scholar

Williams, M. A., O’Callaghan, A., and Corr, S. C. (2019). IL-33 and IL-18 in Inflammatory Bowel Disease Etiology and Microbial Interactions. Front. Immunol. 10, 1091. doi:10.3389/fimmu.2019.01091

PubMed Abstract | CrossRef Full Text | Google Scholar

Wils, P., Bouhnik, Y., Michetti, P., Flourie, B., Brixi, H., Bourrier, A., et al. (2016). Subcutaneous Ustekinumab Provides Clinical Benefit for Two-Thirds of Patients with Crohn’s Disease Refractory to Anti-Tumor Necrosis Factor Agents. Clin. Gastroenterol. Hepatol. 14 (2), 242–250. doi:10.1016/j.cgh.2015.09.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Withers, D. R., Hepworth, M. R., Wang, X., Mackley, E. C., Halford, E. E., Dutton, E. E., et al. (2016). Transient Inhibition of ROR-γt Therapeutically Limits Intestinal Inflammation by Reducing TH17 Cells and Preserving Group 3 Innate Lymphoid Cells. Nat. Med. 22 (3), 319–323. doi:10.1038/nm.4046

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, F., Zikusoka, M., Trindade, A., Dassopoulos, T., Harris, M. L., Bayless, T. M., et al. (2008). MicroRNAs Are Differentially Expressed in Ulcerative Colitis and Alter Expression of Macrophage Inflammatory Peptide-2α. Gastroenterology 135 (5), 1624–1635. doi:10.1053/j.gastro.2008.07.068

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, L.-H., Xu, Z.-L., Dong, D., He, S.-A., and Yu, H. (2011). Protective Effect of Anthocyanins Extract from Blueberry on TNBS-Induced IBD Model of Mice. Evid. Based Complement. Alternat. Med. 2011, 1–8. doi:10.1093/ecam/neq040

PubMed Abstract | CrossRef Full Text | Google Scholar

Xia, E.-Q., Cui, B., Xu, X.-R., Song, Y., Ai, X.-X., and Li, H.-B. (2011). Microwave-Assisted Extraction of Oxymatrine from Sophora flavescens. Molecules 16 (9), 7391–7400. doi:10.3390/molecules16097391

PubMed Abstract | CrossRef Full Text | Google Scholar

Xie, A., Robles, R. J., Mukherjee, S., Zhang, H., Feldbrügge, L., Csizmadia, E., et al. (2018). HIF-1α-induced Xenobiotic Transporters Promote Th17 Responses in Crohn’s Disease. J. Autoimmun. 94, 122–133. doi:10.1016/j.jaut.2018.07.022

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, L., Zhang, Y., Xue, X., Liu, J., Li, Z.-S., Yang, G.-Y., et al. (2020). A Phase I Trial of Berberine in Chinese with Ulcerative Colitis. Cancer Prev. Res. 13 (1), 117–126. doi:10.1158/1940-6207.capr-19-0258

PubMed Abstract | CrossRef Full Text | Google Scholar

Xue, B., Xie, J., Huang, J., Chen, L., Gao, L., Ou, S., et al. (2016). Plant Polyphenols Alter a Pathway of Energy Metabolism by Inhibiting Fecal Bacteroidetes and Firmicutes In Vitro. Food Funct. 7 (3), 1501–1507. doi:10.1039/c5fo01438g

PubMed Abstract | CrossRef Full Text | Google Scholar

Yan, F., Wang, L., Shi, Y., Cao, H., Liu, L., Washington, M. K., et al. (2012). Berberine Promotes Recovery of Colitis and Inhibits Inflammatory Responses in Colonic Macrophages and Epithelial Cells in DSS-Treated Mice. Am. J. Physiol. Gastrointest. Liver Physiol. 302 (5), G504–G514. doi:10.1152/ajpgi.00312.2011

PubMed Abstract | CrossRef Full Text | Google Scholar

Yan, X., Lu, Q.-G., Zeng, L., Li, X.-H., Liu, Y., Du, X.-F., et al. (2020). Synergistic Protection of Astragalus Polysaccharides and Matrine Against Ulcerative Colitis and Associated Lung Injury in Rats. World J. Gastroenterol. 26 (1), 55–69. doi:10.3748/wjg.v26.i1.55

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, H., Li, Y., Wu, W., Sun, Q., Zhang, Y., Zhao, W., et al. (2014). The Incidence of Inflammatory Bowel Disease in Northern China: a Prospective Population-Based Study. PLoS One 9 (7), e101296. doi:10.1371/journal.pone.0101296

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, M., Lin, H.-B., Gong, S., Chen, P.-Y., Geng, L.-L., Zeng, Y.-M., et al. (2014). Effect of Astragalus Polysaccharides on Expression of TNF-α, IL-1β and NFATc4 in a Rat Model of Experimental Colitis. Cytokine 70 (2), 81–86. doi:10.1016/j.cyto.2014.07.250

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, N., Liang, G., Lin, J., Zhang, S., Lin, Q., Ji, X., et al. (2020). Ginsenoside Rd Therapy Improves Histological and Functional Recovery in a Rat Model of Inflammatory Bowel Disease. Phytother. Res. 34 (11), 3019–3028. doi:10.1002/ptr.6734

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, X.-D., Yang, Y.-Y., Ouyang, D.-S., and Yang, G.-P. (2015). A Review of Biotransformation and Pharmacology of Ginsenoside Compound K. Fitoterapia 100, 208–220. doi:10.1016/j.fitote.2014.11.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, X.-L., Guo, T.-K., Wang, Y.-H., Gao, M.-T., Qin, H., and Wu, Y.-J. (2012). Therapeutic Effect of Ginsenoside Rd in Rats with TNBS-Induced Recurrent Ulcerative Colitis. Arch. Pharm. Res. 35 (7), 1231–1239. doi:10.1007/s12272-012-0714-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, X.-L., Guo, T.-K., Wang, Y.-H., Huang, Y.-H., Liu, X., Wang, X.-X., et al. (2012). Ginsenoside Rd Attenuates the Inflammatory Response via Modulating P38 and JNK Signaling Pathways in Rats with TNBS-Induced Relapsing Colitis. Int. Immunopharmacol. 12 (2), 408–414. doi:10.1016/j.intimp.2011.12.014

PubMed Abstract | CrossRef Full Text | Google Scholar

Ye, H., Wu, Q., Zhu, Y., Guo, C., and Zheng, X. (2014). Ginsenoside Rh2 Alleviates Dextran Sulfate Sodium-Induced Colitis via Augmenting TGFβ Signaling. Mol. Biol. Rep. 41 (8), 5485–5490. doi:10.1007/s11033-014-3422-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Yi, Q., Wang, J., Song, Y., Guo, Z., Lei, S., Yang, X., et al. (2019). Ascl2 Facilitates IL-10 Production in Th17 Cells to Restrain Their Pathogenicity in Inflammatory Bowel Disease. Biochem. Biophys. Res. Commun. 510 (3), 435–441. doi:10.1016/j.bbrc.2019.01.123

PubMed Abstract | CrossRef Full Text | Google Scholar

Yu, H., MacIsaac, D., Wong, J. J., Sellers, Z. M., Wren, A. A., Bensen, R., et al. (2018). Market Share and Costs of Biologic Therapies for Inflammatory Bowel Disease in the USA. Aliment. Pharmacol. Ther. 47 (3), 364–370. doi:10.1111/apt.14430

PubMed Abstract | CrossRef Full Text | Google Scholar

Yu, T., Xiong, Y., Luu, S., You, X., Li, B., Xia, J., et al. (2020). The Shared KEGG Pathways between Icariin-Targeted Genes and Osteoporosis. Aging 12 (9), 8191–8201. doi:10.18632/aging.103133

PubMed Abstract | CrossRef Full Text | Google Scholar

Yu, X.-T., Xu, Y.-F., Huang, Y.-F., Qu, C., Xu, L.-Q., Su, Z.-R., et al. (2018). Berberrubine Attenuates Mucosal Lesions and Inflammation in Dextran Sodium Sulfate-Induced Colitis in Mice. PLoS One 13 (3), e0194069. doi:10.1371/journal.pone.0194069

PubMed Abstract | CrossRef Full Text | Google Scholar

Zaidun, N. H., Thent, Z. C., and Latiff, A. A. (2018). Combating Oxidative Stress Disorders with Citrus Flavonoid: Naringenin. Life Sci. 208, 111–122. doi:10.1016/j.lfs.2018.07.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Zeng, W., Jin, L., Zhang, F., Zhang, C., and Liang, W. (2018). Naringenin as a Potential Immunomodulator in Therapeutics. Pharmacol. Res. 135, 122–126. doi:10.1016/j.phrs.2018.08.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, A., Wang, H., Sun, H., Zhang, Y., An, N., Yan, G., et al. (2015). Metabolomics Strategy Reveals Therapeutical Assessment of Limonin on Nonbacterial Prostatitis. Food Funct. 6 (11), 3540–3549. doi:10.1039/c5fo00489f

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, H. Q., Zhu, Z. H., Qian, D. W., Weng, Z. B., Guo, S., Duan, J. A., et al. (2016). [Analysis and Evaluation of Alkaloids and Flavonoids in Flower of Sophora Flavescens from Shanxi Province]. Zhongguo Zhong Yao Za Zhi 41 (24), 4621–4627. doi:10.4268/cjcmm20162422

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, J., Lei, H., Hu, X., and Dong, W. (2020). Hesperetin Ameliorates DSS-Induced Colitis by Maintaining the Epithelial Barrier via Blocking RIPK3/MLKL Necroptosis Signaling. Eur. J. Pharmacol. 873, 172992. doi:10.1016/j.ejphar.2020.172992

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, L.-C., Wang, Y., Tong, L.-C., Sun, S., Liu, W.-Y., Zhang, S., et al. (2017). Berberine Alleviates Dextran Sodium Sulfate-Induced Colitis by Improving Intestinal Barrier Function and Reducing Inflammation and Oxidative Stress. Exp. Ther. Med. 13 (6), 3374–3382. doi:10.3892/etm.2017.4402

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, R., Xu, J., Zhao, J., and Chen, Y. (2017). Genistein Improves Inflammatory Response and Colonic Function through NF-κB Signal in DSS-Induced Colonic Injury. Oncotarget 8 (37), 61385–61392. doi:10.18632/oncotarget.18219

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, W., Xu, L., Cho, S.-Y., Min, K.-J., Oda, T., Zhang, L., et al. (2016). Ginseng Berry Extract Attenuates Dextran Sodium Sulfate-Induced Acute and Chronic Colitis. Nutrients 8 (4), 199. doi:10.3390/nu8040199

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, X.-J., Yuan, Z.-W., Qu, C., Yu, X.-T., Huang, T., Chen, P. V., et al. (2018). Palmatine Ameliorated Murine Colitis by Suppressing Tryptophan Metabolism and Regulating Gut Microbiota. Pharmacol. Res. 137, 34–46. doi:10.1016/j.phrs.2018.09.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, Z., Zhang, L., and Xu, H. (2019). Effect of Astragalus Polysaccharide in Treatment of Diabetes Mellitus: a Narrative Review. J. Tradit Chin. Med. 39 (1), 133–138.

PubMed Abstract | Google Scholar

Zhao, L., Xiao, H.-t., Mu, H.-x., Huang, T., Lin, Z.-s., Zhong, L., et al. (2017). Magnolol, a Natural Polyphenol, Attenuates Dextran Sulfate Sodium-Induced Colitis in Mice. Molecules 22 (7), 1218. doi:10.3390/molecules22071218

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhao, L., Zhang, Y., Liu, G., Hao, S., Wang, C., and Wang, Y. (2018). Black rice Anthocyanin-Rich Extract and Rosmarinic Acid, Alone and in Combination, Protect against DSS-Induced Colitis in Mice. Food Funct. 9 (5), 2796–2808. doi:10.1039/c7fo01490b

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhou, B., Ma, C., Ren, X., Xia, T., Li, X., and Wu, Y. (2019). Production of Theophylline via Aerobic Fermentation of Pu-Erh tea Using Tea-Derived Fungi. BMC Microbiol. 19 (1), 261. doi:10.1186/s12866-019-1640-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, L., Gu, P., and Shen, H. (2019). Protective Effects of Berberine Hydrochloride on DSS-Induced Ulcerative Colitis in Rats. Int. Immunopharmacology 68, 242–251. doi:10.1016/j.intimp.2018.12.036

CrossRef Full Text | Google Scholar

Zhu, Z., Xueying, L., Chunlin, L., Wen, X., Rongrong, Z., Jing, H., et al. (2020). Effect of Berberine on LPS-Induced Expression of NF-Κb/MAPK Signalling Pathway and Related Inflammatory Cytokines in Porcine Intestinal Epithelial Cells. Innate Immun. 26 (7), 627–634. doi:10.1177/1753425920930074

PubMed Abstract | CrossRef Full Text | Google Scholar

Zobeiri, M., Belwal, T., Parvizi, F., Naseri, R., Farzaei, M. H., Nabavi, S. F., et al. (2018). Naringenin and its Nano-Formulations for Fatty Liver: Cellular Modes of Action and Clinical Perspective. Curr. Pharm. Biotechnol. 19 (3), 196–205. doi:10.2174/1389201019666180514170122

PubMed Abstract | CrossRef Full Text | Google Scholar

Zwicky, P., Unger, S., and Becher, B. (2020). Targeting Interleukin-17 in Chronic Inflammatory Disease: A Clinical Perspective. J. Exp. Med. 217 (1), e20191123. doi:10.1084/jem.20191123

PubMed Abstract | CrossRef Full Text | Google Scholar

Glossary

IBD inflammatory bowel disease

CD Crohn’s disease

UC ulcerative colitis

APS astragalus polysaccharide

Th helper T cells

TNF-α Tumor Necrosis Factor alpha

TGF transforming growth factor

IFN-γ interferon γ

IL Interleukin

ILCs innate lymphoid cells

DCs Dendritic cells

TLR toll like receptor

PAMPs pathogen-related molecular patterns

NF-κB nuclear factor kappa-B

LPS lipopolysaccharide

JAK Janus kinase

STAT signal transducer and activator of transcription

NOS2 nitric oxide synthase 2

ATG16L1 Autophagy related like 1

IRGM Immunity-related GTPase family M protein

ER endoplasmic reticulum

mTOR mammalian target of rapamycin

IECs intestinal epithelial cells

FDA Food and Drug Administration

EMA European Medicines Agency

MAdCAM-1 mucosal addressing cell adhesion molecule-1

DSS dextran sodium sulfate

ICAM-1 intercellular cell adhesion molecule-1

iNOS inducible NO synthase

Cox2 cyclooxygenase-2

MCP-1 Monocyte chemoattractant protein-1

PEG2 prostaglandin E2

MIP-2 macrophage inflammatory protein

OSM Oncostatin M

VCAM-1 vascular cell adhesion molecule-1

RORs related orphan receptor

MDR1 multi-drug resistance gene

CBAs conjugated bile acids

PPAR-γ peroxisome proliferators-activated receptors-γ

Ascl2 achaete-scute family BHLH transcription factor 2

OCTN Recombinant Organic Cation/Ergothioneine Transporter

HIF-1 hypoxia inducible factor-1

S1P sphingosine-1-phosphate

EC epicatechin

ECG epicatechin gallate

EGC (2)-epigallocatechin-3-gallate

DAI disease activity index

SOCS3 Suppressor of cytokine signaling 3

TNBS 2,4,6-trinitrobenzene sulfonic acid

MPO Myeloperoxidase

MDA malondialdehyde

BW body weight

Keywords: inflammatory bowel disease, inflammatory, natural anti-inflammatory compounds, drugs, ulcerative colitis (uc), Crohn’s disease (CD)

Citation: Duan L, Cheng S, Li L, Liu Y, Wang D and Liu G (2021) Natural Anti-Inflammatory Compounds as Drug Candidates for Inflammatory Bowel Disease. Front. Pharmacol. 12:684486. doi: 10.3389/fphar.2021.684486

Received: 23 March 2021; Accepted: 02 July 2021;
Published: 14 July 2021.

Edited by:

Daniel Merk, Goethe University Frankfurt, Germany

Reviewed by:

Sheng Wang, Fifth People’s Hospital of Suzhou, China
Ouliana Ziouzenkova, The Ohio State University, United States
Anna Negroni, National Agency for New Technologies Energy and Sustainable Economic Development, United Kingdom

Copyright © 2021 Duan, Cheng, Li, Liu, Wang and Liu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Guoyan Liu, bGl1Z3VveWFuQHhtdS5lZHUuY24=

These authors have contributed equally to this work and share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.