Haifeng Zhou1†
Junyi Li
Faxi Wang
Heng Fan
Desheng Hu- 1Department of Integrated Traditional Chinese and Western Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
- 2The Center for Biomedical Research, Key Laboratory of Organ Transplantation, Ministry of Education, NHC Key Laboratory of Organ Transplantation, Chinese Academy of Medical Sciences, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
Aloperine, a quinolizidine-type alkaloid, was first isolated from the seeds and leaves of herbal plant, Sophora alopecuroides L. Empirically, Sophora alopecuroides L. is appreciated for its anti-dysentry effect, a property that is commonly observed in other Sophora Genus phytomedicines. Following the rationale of reductionism, subsequent biochemical analyses attribute such anti-dysentry effect to the bactericidal activity of aloperine. From then on, the multiple roles of aloperine are gradually revealed. Accumulating evidence suggests that aloperine possesses multiple pharmacological activities and holds a promising potential in clinical conditions including skin hyper-sensitivity, tumor and inflammatory disorders etc.; however, the current knowledge on aloperine is interspersed and needs to be summarized. To facilitate further investigation, herein, we conclude the key pharmacological functions of aloperine, and most importantly, the underlying cellular and molecular mechanisms are clarified in detail to explain the functional mode of aloperine.
Introduction
Many herbal plants have been proved to offer medical benefits and widely applied in clinical practice for thousands of years (Xu et al., 2013). Despite of the observed therapeutic effect, the miscellaneous components and obscure drug targets hinder their further utilization. Dosage and safety issues are of huge concerns; in addition, unknown pharmaceutical properties may exist. Along with the development of modern medical science, researchers are paying more attention to traditional herbal medicine, which helps to elucidate the underlying pharmacological function and accelerate the process of new drug discovery.
The genus of Sophora (family Fabaceae) contains approximately 70 species, most of which are distributed in tropical and temperate zones serving as pesticides and/or nectariferous plants (Aly et al., 2019). Apart from these, several Sophora species including Sophora flavescens Ait (Ku shen) and Sophora subprostrata (Sang zhi huai) etc. were used as traditional herbal in Eastern Asian countries (He et al., 2015; Aly et al., 2019). According to the theory of traditional Chinese medicine (TCM), these natural products display various activities in “clearing heat”, “dispelling dampness”, “relieving pain and swelling” and “sedation and detoxification”. From the viewpoints of modern medicine, “heat evil” in TCM is generally caused by exogenous virus or bacterial infection or endogenous functional over-activity, and “dampness evil” is often linked to inflammation-related responses or inflammatory exudation (Ren et al., 2017). Furthermore, the so-called “dampness and heat” in TCM is actually a very broad concept that is associated with many basic pathophysiological processes. Therefore, Sophora genus could provide valuable resources for screening of active ingredients.
Among the Sophora genus, Sophora alopecuroides L. (also known as Ku dou zi or Ku gan cao) mainly distributes in Western and Central Asia (Figure 1A), which is 1-m tall perennial herb with excellent capacity to withstand drought and alkali (Gao et al., 2011; Yugang and Hao, 2013). Based on the distinct feature of leaflets, Sophora alopecuroides L. can be divided into two major subspecies: one is Sophora alopecuroides var. alopecuroides (original variant) with appressed villous leaflets; another is Sophora alopecuroides var. tomentosa with densely patulous-tomentose ones. Strikingly, regardless of the subdivisions, almost all parts of the plant, including root, leaves and seeds, have been taken as medicinal herbs. Traditionally, Sophora alopecuroides L. was used effectively in the treatment of various clinical disorders, such as dysentery, eczema, recurrent dermatitis, furuncle, cancer and infectious diseases etc. (Gao et al., 2011; Wang et al., 2020). Chemical analysis revealed that Sophora alopecuroides L. contains many bioactive substances, including alkaloids, flavonoids, steroids and polysaccharides (Pu et al., 1987; Wu et al., 2018; Li Y. et al., 2020). Among these compounds, alkaloids are believed to make predominant contributions to the therapeutic effect of the herbal and thus have been extensively studied.
FIGURE 1. (A) Image of sophora alopecuroids L.(B) 2D chemical structure of aloperine (synthesized from piperidine-2-ethanol). C16-C17 double bond and N12 are important structural motifs that are commonly modified to improve the activities of aloperine.
Aloperine was firstly discovered in 1935 as a natural alkaloid extracted from the seeds and leaves of Sophora alopecuroides L. Later on, it was also identified in other medical plants, such as Sophorae flavescentis and Leptorhabdos parviflora Benth. Purified aloperine is a white to yellowish crystalline powder with a molecular weight of 232.4, which can be stably stored at 4°C avoiding moisture and sunlight. It is soluble in organic solvents, such as ethanol and dimethyl formamide, but hard to dissolve in aqueous buffers. The identified absolute stereochemical structure and configuration of aloperine is of crucial importance for understanding the engaged biological processes and synthesis of aloperine based derivatives (Figure 1B) (Brosius and Overman, 1997; Brosius et al., 1997; Passarella et al., 2002; Yamauchi and Omi, 2005). Recently, a growing body of evidence from both basic science and clinical trials has demonstrated the pharmacological effects of aloperine. This review aims to summarize the current knowledge of aloperine mediated pharmaceutical activities with a focus on the mechanistic explanations, and hopefully, to also provide valuable insights for its clinical application.
Antitumor Effect of Aloperine
In recent years, small natural compounds derived from herbal plants have drawn considerable attention due to their potential chemotherapeutic capacity and bio-safety (Cianciosi et al., 2018; Paier et al., 2018). Accumulative data demonstrated that aloperine itself and the modified derivatives display powerful antitumor effect on various cancer types both in vivo and in vitro. The ability of aloperine to target on multiple pathways makes it to be an extremely potent anticancer agent (Table 1).
TABLE 1. The effects and mechanisms of aloperine.
Aloperine Impedes Tumor Survival
Research conducted by Jiang’s group tested the in vitro anticancer activities of six different kinds of quinolizidine alkaloids derived from Sophora flavescensa, including sophoridine, aloperine, sophocarpine, matrine, oxymatrine and cytisine. They found aloperine exerts the most potent cytotoxic activity on leukemia cell lines HL-60, U937 and K562, oesophageal cancer EC109 cells, lung cancer cells, glioma cells, ovarian cancer cells and the hepatocellular carcinoma HepG2 cell line (Wang et al., 2015; Liu et al., 2019; Xu et al., 2019; Muhammad et al., 2020; Qiu et al., 2020b). The mechanism inferred that occurrence of apoptosis (fragmentation of DNA, cleavage of PARP and decreased protein level of Bcl-2) and formation of acidic vacuole, a marker of autophagy. These results suggested that apoptotic and autophagic pathways are critically engaged (Lin et al., 2011).
Specifically, the antitumor activity of aloperine on prostate LNCaP, PC3 and DU145 cancer cell lines was investigated in vitro and in vivo. Aloperine inhibits PI3K/Akt and Ras/Erk signaling pathway, thus inducing the expression of pro-apoptotic gene caspase-3, decreasing the ratio of Bcl-2/Bax and upregulating the level of tumor suppressor p53 and p21 (Ling et al., 2018). Song’s group pointed out that aloperine significantly inhibits the viability of bladder cancer cells via suppressing hypoxia induced activation of mTOR/p70S6K/4E-BP1 pathway (Lv W. et al., 2020). Besides, Liu et al. illustrated that aloperine induces apoptosis and G2/M cell cycle arrest in hepatocellular carcinoma cell lines Hep3B and Huh7 in vitro, and suppresses tumor development in the zebrafish xenograft model in vivo (Liu et al., 2019). Similar mechanisms were confirmed on other cancer types. For instance, aloperine treatment inhibits proliferation and induces apoptosis of human breast cancer line via blocking Ras/Erk signaling (Tian et al., 2018); as well as for thyroid cancer cell lines, multiple myeloma cell lines and osteoscarcoma MG-63 and U2OS cell lines, inactivation of PI3K/Akt pathway is predominantly involved (Wang et al., 2015; Chen et al., 2018; Lee et al., 2018). Moreover, aloperine administration produced potent effects against HCT116 colon cancer cell line in a dose and time dependent manner, indicating a promising chemotherapeutic potential in human colon cancer (Zhang et al., 2014).
Tumor progression is a multi-factorial process, which involves interaction between tumor cells and immune cells in the intricate tumor microenvironment (Wu and Dai, 2017; Altorki et al., 2019). An alternative strategy for cancer treatment is to unleash immune inhibitory signals and re-energize the cytotoxicity of tumor-killing NK and CD8+ T cells. SA-49, a novel aloperine derivative, decreases the expression of PD-L1 on non-small cell lung cancer cells through promoting the translocation of PD-L1 for lysosomal degradation and subsequently enhancing the cytotoxicity of co-cultured T and NK cells. In Lewis tumor xenograft model, the tumor-killing effect of SA-49 was further testified (Zhang et al., 2019). These data unveiled a unique anti-tumor function of aloperine, which is distinct from that of other herbal compounds and conventional immune check-point inhibitors.
Aloperine Inhibits Tumor Metastasis
Aloperine executes antitumor effect through direct killing and also the inhibition of tumor migration and metastasis. The metastatic process, which is mediated by matrix metalloproteinases (MMPs), plays a vital role in the development of various cancers and is positively linked to the poor prognosis of cancer patients (Wan et al., 2013; Li K. et al., 2020). Thus, interference of tumor metastasis is crucial to tumor therapy, especially for the malignant subtypes. Gao and Tian’s group found that aloperine treatment remarkably suppresses the invasive capability of osteosarcoma and breast cancer cells through down-regulating the expression level of MMP-2/9 (Chen et al., 2018; Tian et al., 2018). Nonetheless, the research on metastasis part is relatively inadequate compared to that of survival field; thus, more future studies are needed to clarify the metastasis-inhibition function of aloperine.
In conclusion, aloperine, when used alone or in combination with other chemotherapeutic drugs, is effective in fighting against various cancers, including hepatoma, colon cancer, prostate cancer, breast cancer, thyroid cancer, osteosarcoma and leukemia. This wide range of anti-tumor effect is mainly accomplished through apoptosis induction, cell cycle arrest, growth inhibition and suppression of migration, which hinder the survivability and metastasis of tumor cells. Although the definite interacting molecules and more detailed mechanisms remain to be determined, undoubtedly, aloperine and its derivatives could act as promising candidates in cancer treatment.
Anti-Microbial Effect of Aloperine and Its Derivatives
Sophora alopecuroides L. has been traditionally used as an antimicrobial agent, the function of which can be largely attributed to the broad-spectrum antibacterial and antiviral activities of aloperine (Shi et al., 2003). As a quinolizidine alkaloid extracted from Sophora alopecuroides L., aloperine possesses significant nematocidal and insecticidal activities via binding to the nicotinic acetylcholine receptor (Liu et al., 2008). Ho et al. firstly revealed the potent activity of aloperine against P. gingivalis invasion and the effect on its outer membrane vesicles formation (Ho et al., 2016). The mechanisms are related to the regulation of microtube arrangement and expression of fimA, a major form of fimbriae that is necessary for P. gingivalis’ attachment to oral surface and co-adhesion with other oral bacteria (Figure 2A).
FIGURE 2. Anti-microbial effect of aloperine. (A) Aloperine blocks the entry of P. gingivalis and its outer membrane vesicles (OMVs) into oral keratinocytes through inducing unique microtubule arrangement of host cells and inhibiting expression of firmA of P. gingivalis. (B) Aloperine hinders the stage of viral entry via various mechanisms. On the one hand, aloperine could directly disrupt protein mediated cell-cell fusion. On the other hand, aloperine targets certain proteins in host cells to prevent infection, such as cysteine cathepsin B.
Peng’s group demonstrated that, through inhibition of endocytosis, aloperine effectively prevents the propagation of hepatitis virus C (HCV) in Huh7.5 cell line and primary human hepatocytes without showing cytotoxicity (Lv X. et al., 2020). Zhang et al. took aloperine as a leading structure to design the compound 7f, a derivative displaying good oral pharmacokinetics and safety profile while exhibiting the potential potency with low EC50 value (micro-molar level). Compound 7f is effective in fighting against both wild type and direct-acting antiviral agents-resistant HCV variants via targeting on viral entry stage (Zhang et al., 2018b). Similarly, Chen’s group identified aloperine as a novel anti-HIV agent. At the same time, they optimized the structure of aloperine to acquire “compound 19” that possesses markedly improved anti-HIV activity. Mechanistic study revealed that “compound 19” prevents the virus from fusing with the host cell membrane rather than inhibiting the binding of HIV-1 to its receptors (Dang et al., 2017). Interestingly, their group also got a series of analogues of aloperine that have improved anti-Influenza A Virus (IAV) activity through targeting nucleoprotein of IAV with a different mechanism of action from that of oseltamivir, a first-line anti-IAV drug (Table 2) (Dang et al., 2014). In addition, Zhang et al. introduced a N12 dichlorobenzyl group to aloperine to obtain a new drug named “compound 2e”, which exhibits the most potent anti-ebola virus and anti-marburg virus effect both in vitro and in vivo. Compound 2e could block the late stage of viral entry, mainly through inhibiting cysteine cathepsin B activity of host components (Figure 2B) (Zhang et al., 2018a).
TABLE 2. Improved activities of midified aloperine derivatives.
In brief, aloperine not only represents a novel antibacterial and antivirus agent, but also provides a privileged scaffold which can be further optimized by introduction of different chemical modifications.
Cardiovascular Protection Effect of Aloperine
Cardiovascular disease (CVD) increasingly becomes a public health issue that ranks 1 of the leading causes of death (Roth et al., 2017; Zhao et al., 2019). The prevalence of CVD and its comorbidities poses a huge challenge for modern medicine, thus, there is an urgent need to develop novel effective therapeutic and prophylactic agents (Joseph et al., 2017). Many TCMs, like Danshen, Sanqi and Chuanxiong etc., are commonly used in CVD treatment (Li et al., 2012; Liu and Huang, 2016; Wang et al., 2017). Here, we emphasize the protective effects of aloperine on various CVD complications, which may provide useful hints for future drug screening work.
Anti-Atherosclerosis Effect of Aloperine
Atherosclerosis (AS) is a common CVD characterized by arterial inflammation and stenosis (Herrington et al., 2016). The pathogenesis of AS involves multiple factors, such as hyperlipidemia, endothelial cells damage, foam cell formation as well as excessive proliferation and migration of vascular smooth muscle cells (VSMCs) (Zimmer et al., 2015). Several studies demonstrated that Compound Kudouzi could lower blood lipid level in high fat diet induced rat AS model (Wang and Chen, 2006; Liu and Chen, 2014; Wang et al., 2020). Moreover, a recent study reported that aloperine administration provides protection from oxidized LDL induced injuries and inhibits the adhesion of U937 monocytes to HUVECs via reducing the expression of IL-6, MCP-1, VCAM-1 and E-selectin (Li Y. et al., 2020). Decreased oxidative stress may also contribute to the beneficial effect of aloperine. However, the related evidence is still insufficient and more in vivo studies remain to be carried out to elucidate whether these activities are authentically reliable.
Anti-Hypertension Effect of Aloperine
Hypertension, frequently accompanied by dyslipidemia and hyperglycemia, is so far the most important trigger of CVD (Van Kleef and Spiering, 2017). Commonly used antihypertensive drugs include ACE inhibitors, alpha blockers, calcium channel blockers, diuretics and vasodilators with distinct modes of action (Laurent, 2017). The hypotensive effect of natural herbs has gained increasing attention due to their unique advantages, such as the multi-target efficacy, safety as well as low cost (Tabassum and Ahmad, 2011).
The Vasodilation Effect of Aloperine
Generally, vasodilation agents are the first-line drugs in hypertension treatment. For example, as a calcium channel blocker, amlodipine reduces intracellular calcium concentration and leads to arterial smooth muscle relaxation (Little and Cheng, 1994). However, few antihypertensive drugs that target on potassium ion channels have been reported.
For the first time, Zhou’s group demonstrated that aloperine shows a vasodilation effect in rat thoracic aortic rings via an unknown mechanism (Yang et al., 2018). To make a step forward, Abbott et al. revealed that aloperine is a potassium voltage-gated channel subfamily Q member (KCNQ)-dependent vasorelaxant that isoform selectively activates potassium voltage-gated channel subfamily Q member (KCNQ5) by binding to the “foot” of the potassium channel voltage sensor (Manville et al., 2019). Although several extracts from Sophora flavescens confer vasodilatory effect, including aloperine, matrine, and oxymatrine, Abbott suggested that aloperine is the specific KCNQ5 activator through directly binding to KCNQ5 R212 site. These studies not only identified aloperine as a potential agent in hypertension treatment, but also provide examples for the understanding of TCM theory from a perspective of modern medicine.
Aloperine Inhibits Vascular Remodeling
Chronic high blood pressure induces vascular and cardiac remodeling, which then push CVD into an irreversible stage. Abnormal proliferation, migration and apoptosis resistance of VSMCs play important roles in vascular remodeling (Harvey et al., 2016; Brown et al., 2018). Besides, under external stimuli, activated NF-κB and NOX activity subsequently accelerate the disease progression (Montezano et al., 2015).
Wu et al. reported that intragastric administration of aloperine exerts protective effect on pulmonary hypertension (PAH) induced by monocrotaline, which was characterized by decreased collagen deposition and improved PAAT and PAD parameters (Wu et al., 2017a). On the one hand, aloperine significantly suppresses the proliferation of pulmonary arterial VSMCs that act as driving force in the initiation and development of PAH (Chang et al., 2019). After treatment, aloperine inhibits NF-κB pathway activation, resulting in an increase of p27kip1 and down-regulation of cyclin E1. On the other hand, aloperine decreases the expression of NOX-2 and NOX-4 and subsequently, oxidative stress induced vasoconstriction is abolished. Moreover, the PAH ameliorating effect can also be achieved through aloperine mediated inhibition of RhoA/ROCK signaling, which is crucial for the recruitment of myofibroblast (Wu et al., 2017b). Altogether, these studies support the idea that aloperine is helpful in hypertension treatment.
Myocardial Protection Effects of Aloperine
Accumulating studies have revealed the heart protection effect of aloperine. Mao et al. demonstrated that aloperine administration attenuates cardiac dysfunction induced by coronary micro-embolization, which is indicated by decreased serum cTnI and reduced myocardial infarction area. Such myocardial protection effect was related to the activation of PI3K/Akt signaling pathway and subsequent reduction of myocardial apoptosis (Mao et al., 2019). However, it is contradictory to the conclusion of other studies implying a PI3K/Akt inhibitory role of aloperine, and this discrepancy is possibly due to different cell types. In addition, it is reported that aloperine, at appropriate dose, may be useful in the treatment of cardiac arrhythmia via unknown mechanism (Zhao et al., 1986; Feng and Zhou, 2000; Li Y. et al., 2020). Given KCNQ5 is also expressed on myocardial cells, whether the anti-arrhythmic action is attributed to the activation of potassium channels remains to be determined. Taken together, aloperine exhibits potent cardiovascular protection effect by acting on multiple pathways (Figure 3). As a candidate drug, aloperine is worthy of in-depth researches in the future.
FIGURE 3. Cardiovascular-protection effects of aloperine. Aloperine exerts regulatory function on different cell types. Aloperine ameliorates endothelial damage by decreasing NOX2/4 and inhibiting NF-κB pathway. Aloperine alleviates hypertension-associated vascular remodeling via inhibiting proliferation and migration of vascular smooth muscle cells (VSMCs) and fibroblasts. In addition, aloperine directly binds with KCNQ5 expressed on VSMCs, leading to K+ influx and subsequent vessel dilation.
Anti-Oxidative Stress and Immune Regulatory Effect of Aloperine
Aloperine Attenuates Oxidative Stress
Oxidative stress impairs many cellular processes and plays critical role in disease conditions such as aging, diabetes and neurological disorders (Dandekar et al., 2015; Cabello-Verrugio et al., 2017). Published work demonstrated that aloperine could confer organ protective effect, which is attributed to its anti-oxidation and anti-inflammation characteristics.
Previous study found that aloperine alleviates neuropathic pain induced by chronic constriction injury, which is related to the reduction of reactive oxygen species (ROS) via suppression of NF-κB pathway (Xu et al., 2014). The up-regulation of TNF-α, IL-6 and IL-1β induced by chronic constriction injury in the dorsal spinal cord was remarkably reversed at the dosage of 80 mg/kg. In addition, Ma’s study showed that aloperine treatment (25, 50, and 100 mg/kg) attenuates neuronal damage induced by oxygen/glucose deprivation and reperfusion, evidenced by increased cell viability and decreased cell morphologic impairment (Ma et al., 2015). Mechanistically, aloperine reduces intracellular malondialdehyde content and bolsters the antioxidant enzymatic activity of catalases, including superoxide dismutase and glutathione peroxidase. Zhao et al. investigated the effect of aloperine on A β-induced neuronal oxidative insults in vitro. They found that aloperine treatment ameliorates oxidative stress in N2a/Swe.D9 cells by reducing the production of ROS and 4-HNE, both of which are important biomarkers in the brain of AD patients (Zhao et al., 2018). What’s more, another study showed that aloperine can ameliorate oxidative damage of early brain injury following subarachnoid hemorrhage, most likely through the Nrf2-ARE pathway (Song et al., 2018).
In our study conducted before, we identified that aloperine could protect mice against ischemia reperfusion induced renal injury via regulating mTOR pathway and AP-1 activity (Hu et al., 2016). Aloperine enhances superoxide dismutase expression to promote ROS detoxification and to correct the imbalance between Bcl-2 and Bax. Yin et al. showed that aloperine could significantly mitigate bleomycin-induced pulmonary fibrosis by attenuation of fibroblast proliferation and differentiation through repressing PI3K/AKT/mTOR and TGF-β/Smad signaling, respectively (Yin et al., 2018). Taken together, these results suggest that aloperine may act as an important therapeutic agent in oxidative stress related diseases.
Immune Regulatory Function of Aloperine
Based on TCM theory, bitter food or medication, such as snake gall and coptis, possess anti-inflammatory function. This is also the case on aloperine, which displays excellent immune modulatory property (Zhou et al., 1989; Lin and Lin, 2011). Wang et al. revealed that aloperine attenuates allergic airway inflammation by lowering inflammatory cell infiltration, down-regulating IL-4, IL-5 and IL-13 expression, and reducing goblet cell hyperplasia (Wang et al., 2018). In addition, aloperine directly abrogates LPS-induced NO and PGE2 production in RAW264.7 cells by suppressing iNOS and COX-2 activity (Ye et al., 2020). Allergic contact dermatitis is a delayed-type hypersensitivity reaction mediated by hapten-specific T cells. Guo’s group demonstrated that topical 1% aloperine cream treatment suppresses 2, 4-dinitrofluorobenzene induced ear swelling, ear erythema as well as the secretion of inflammatory cytokines like TNF-α, IL-1β and IL-6 (Yuan et al., 2010; Yuan et al., 2011).
Regulatory function of natural plant derived small molecules on immune cells, especially T cells, is an interesting research area. Previous study revealed that total alkaloids of Sophora alopecuroides could increase CD4+CD25+Treg cell proportion and IL-10 level in rats, indicating a potential immunomodulatory capacity of aloperine (Zhou et al., 2010). Next, it is verified that aloperine promotes the expression of key Treg transcription factor Foxp3 via suppressing PI3K/Akt/mTOR signaling and glycolysis pathway in dextran sodium sulfate elicited colitis model (Fu et al., 2017). However, additional possible regulatory roles of aloperine on T cell biology still requires further study.
In conclusion, these studies proved that aloperine possesses excellent anti-oxidation and anti-inflammation properties, indicating its potential use for prevention or treatment of various associated disorders in clinic.
Discussion
During past decades, modern medical technology has brought unprecedented advance to folk medicine research. Importantly, it is a good method to screen appropriate and effective drugs through combination of the theory of TCM and modern understanding of different diseases, and the shining example is artemisinin. Interest in the alkaloids stems from the wide variety of physiological effects it produces in humans and other organisms. In the present review, we concluded the pharmacological effects and associated mechanisms of aloperine, which make it a potential candidate for the treatment of cancer, infectious diseases, cardiovascular complications and inflammation-related disorders (Figure 4).
FIGURE 4. Schematic representation of pharmacological activities of aloperine.
Like many other alkaloids, evidence suggests that aloperine exerts therapeutic effect on various cancer types such as colon cancer, prostate cancer, thyroid cancer and breast cancer etc. Mechanistically, aloperine induces cell apoptosis and suppresses tumor migration through various signaling pathways including Ras/Erk, PI3K/Akt and MMPs. Intriguingly, Zhang et al. found that, SA-49, a novel sulfonyl-substituted aloperine analogue, down-regulated the protein level of PD-L1 in non-small cell lung cancer cells by promoting melanogenesis associated transcription factor mediated lysosomal proteolysis via PKCα-GSK3β signal pathway. Besides, SA-49 enhances the tumor cell killing capacity of T and NK cells, as determined in C57BL/6 mice bearing Lewis tumor xenografts. Altogether, aloperine serves as an effective anti-tumor agent which has multifaceted roles in cancer treatment. As for CVD, aloperine administration ameliorates cardiac dysfunction caused by coronary micro-embolization partially through the inhibition of myocardial apoptosis. Further study revealed that aloperine suppresses isoprenaline induced cardiac hypertrophy and the mechanism is related to its antioxidant property (Cao et al., 2000). In addition, by systematic network pharmacology analysis, Zhu’s group unveiled that the anti-CVD effect of aloperine may also be related to the modulation of nitrogen metabolism (Huang et al., 2020). Good blood pressure management is essential to reduce morbidity and mortality in CVD patients. Conventional antihypertensive drugs including ACE inhibitors, alpha blockers, diuretics, calcium channel blockers, angiotensin II receptor antagonists and vasodilators are developed with distinct physiological mechanisms and accompanying side effects, respectively. Therefore, it is worthy to note that a great many folk medicines have been used to treat hypertension while the underlying mechanisms are not clear. Recently, Abbott identified aloperine as an activator of KCNQ5 potassium channel. Aloperine could bind to KCNQ5 R212 site and exert vasodilation effect by reducing cell membrane depolarization. Moreover, other tested materials extracted from hypotensive plants such as Lavandula angustifolia, Matricaria chamomilla, and Thymus vulgaris can work in a similar manner. This discovery paves a new avenue for the identification of potential antihypertensive drugs, and perhaps, more specific and efficient aloperine-derived small molecules would be developed with ideal clinical implications.
The core structure of aloperine is the quinolizidine ring (Figure 1B) belonging to a rare family of C15 lupine alkaloid. For this reason, aloperine provides a skeletal structure that can be easily modified for further optimization. Danie li’s group developed a practical protocol for synthesis of aloperine in 12 steps starting from the commercially available piperidine-2-ethanol (Passarella et al., 2002). It is reported that the aloperine derivative with either an N-(1-butyl) 4-trifluoromethoxy benzamide side chain or the introduction of trifluoromethane sulfonyl group shows more potent anti-HIV activity. Besides, addition of a sulfonyl moiety on the N12 atom results in an enhanced potency against both wild type and direct-acting antiviral agents-resistant HCV variants with more satisfying pharmacokinetic and safety profile. SA-49, a derivative of aloperine, could induce melanogenesis associated transcription factor dependent lysosomal degradation of PD-L1, thus disrupting immune tolerant tumor microenvironment. The reported modifications of aloperine and its improved activities are summarized in detail (Table 2). From the perspective of recognition to practice, modification of aloperine not only gives the drug a chance for better performance, but also provides a deeper understanding of the structure-function interrelationship.
In spite of these excellent properties, clinical application of aloperine has been limited by some inherent shortcomings. One issue to concern falls into the toxicity of aloperine. A recent study by Qiu M et al. pointed out that intraperitoneal (i.p.) aloperine administration induces damage in liver and kidney at the dosage of 16 mg/kg, manifested by cytoplasm vacuolization and swelling respectively (Qiu et al., 2020a). However, after withdrawing aloperine, mice would partially recover at 1 week and fully recover at 4 weeks, which indicates that the kidney and liver injury induced by high dose i.p injection of aloperine is reversible. On our hand, we found that no cytotoxicity was observed until the dosage reaches 150 mg/kg by oral gavage for consecutive 7 days (Hu et al., 2016). Moreover, several studies showed that injection of total alkaloids of Sophora alopecuroides is effective in treating diseases including psoriasis and internal hemorrhoid without obvious side effect. Nevertheless, the pharmacokinetic properties of aloperine remain to be determined in vivo. Another drawback comes to its poor solubility in aqueous solvents. The increased dosage attributed to compromised bioavailability would exaggerate the toxicity to body system. Thus, strategies for improving aloperine water-solubility are demanded. Theoretically, the modification of parent structure of aloperine would directly improve the hydrophilicity, for example, the introduction of a hydrophile component. However, till now, the related studies are scarce and no feasible solution is proposed. Specific drug delivery systems may be an alternative option to overcome these obstacles and to increase the efficacy at the target location (Liu and Feng, 2015; Xu et al., 2015; Vader et al., 2016). Among them, nano-capsule based technology gains increasing attention. Many materials such as polyethylene glycol, polysaccharide, chitosan and liposome were used as nano-capsules to efficiently encapsulate the purified bioactive cargo for drug delivery through intravenous injection or oral administration (Kolate et al., 2014; Li et al., 2019). Altogether, tremendous efforts are needed to improve the solubility and selectivity of aloperine for future clinical application.
In conclusion, aloperine holds the potential to be developed into a novel multifunctional drug due to its various bioactivities and safety. However, more scientific evidence based on clinical and animal studies is eagerly needed.
Author Contributions
HZ, JL, and FS proposed and wrote the manuscript. FW, ML, and YD collected and analyzed the information. DH and HF supervised the conception and writing of the article.
Funding
The research was supported by the National Natural Science Foundation of China (Grant No. 31770983, 81974249).
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
Altorki, N., Markowitz, G., Gao, D., Port, J., Saxena, A., Stiles, B., et al. (2019). The lung microenvironment: an important regulator of tumour growth and metastasis. Nat. Rev. Cancer 19 (1), 9–31. doi: 10.1038/s41568-018-0081-9
Aly, S., Elissawy, A., Eldahshan, O., Elshanawany, M., Efferth, T., and Singab, A. (2019). The pharmacology of the genus Sophora (Fabaceae): an updated review. Phytomedicine 64, 153070. doi: 10.1016/j.phymed.2019.153070
Brosius, A., and Overman, L. (1997). Aloperine: stereocontrolled synthesis of two stereoisomers and determination of absolute configuration. J. Org. Chem. 62 (3), 440–441. doi: 10.1021/jo9621231
Brosius, A., Ziller, J., and Zhang, Q. (1997). Relative and absolute configuration of aloperine. Acta Crystallogr. Sect. C. Cryst. Struct. Commun. 53(Pt 10), 1510–1512. doi: 10.1107/s0108270197009244
Brown, I., Diederich, L., Good, M., DeLalio, L., Murphy, S., Cortese-Krott, M., et al. (2018). Vascular smooth muscle remodeling in conductive and resistance arteries in hypertension. Arterioscler. Thromb. Vasc. Biol. 38 (9), 1969–1985. doi: 10.1161/atvbaha.118.311229
Cabello-Verrugio, C., Simon, F., Trollet, C., and Santibañez, J. (2017). Oxidative stress in disease and aging: mechanisms and therapies 2016. Oxid. Med. Cell. Longevity 2017, 4310469. doi: 10.1155/2017/4310469
Cao, L., Mao, Y., and Tan, H. (2000). Effects of isoprenaline on apoptosis related gene expression in rat myocardium cells. Yaoxue Xuebao 35 (11), 801–805 [in Chinese].
Chang, Z., Zhang, P., Zhang, M., Jun, F., Hu, Z., Yang, J., et al. (2019). Aloperine suppresses human pulmonary vascular smooth muscle cell proliferation via inhibiting inflammatory response. Chin. J. Physiol. 62 (4), 157–165. doi: 10.4103/cjp.cjp_27_19
Chen, S., Jin, Z., Dai, L., Wu, H., Wang, J., Wang, L., et al. (2018). Aloperine induces apoptosis and inhibits invasion in MG-63 and U2OS human osteosarcoma cells. Biomed. Pharmacother. 97, 45–52. doi: 10.1016/j.biopha.2017.09.066
Cianciosi, D., Varela-Lopez, A., Forbes-Hernandez, T., Gasparrini, M., Afrin, S., Reboredo-Rodriguez, P., et al. (2018). Targeting molecular pathways in cancer stem cells by natural bioactive compounds. Pharmacol. Res. 135, 150–165. doi: 10.1016/j.phrs.2018.08.006
Dandekar, A., Mendez, R., and Zhang, K. (2015). Cross talk between ER stress, oxidative stress, and inflammation in health and disease. Methods Mol. Biol. 1292, 205–214. doi: 10.1007/978-1-4939-2522-3_15
Dang, Z., Jung, K., Zhu, L., Lai, W., Xie, H., Lee, K., et al. (2014). Identification and synthesis of quinolizidines with anti-influenza a virus activity. ACS Med. Chem. Lett. 5 (8), 942–946. doi: 10.1021/ml500236n
Dang, Z., Xie, H., Zhu, L., Zhang, Q., Li, Z., Huang, L., et al. (2017). Structure optimization of aloperine derivatives as HIV-1 entry inhibitors. ACS Med. Chem. Lett. 8 (11), 1199–1203. doi: 10.1021/acsmedchemlett.7b00376
Feng, H., and Zhou, Y. (2000). Overview of research on antiarrhythmic action of eight alkaloids from Kudouzi. Zhongyao Yaoli Yu Linchuang 16 (3), 47–49. doi: 10.13412/j.cnki.zyyl.2000.03.029
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. Mediat. Inflamm. 2017, 5706152. doi: 10.1155/2017/5706152
Gao, H., Li, G., and Wang, J. (2011). Studies on the dynamic accumulations of Sophora alopecuroides L. alkaloids in different harvest times and the appropriate harvest time. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 879, 1121–1125. doi: 10.1016/j.jchromb.2011.03.031
Harvey, A., Montezano, A., Lopes, R., Rios, F., and Touyz, R. (2016). Vascular fibrosis in aging and hypertension: molecular mechanisms and clinical implications. Can. J. Cardiol. 32 (5), 659–668. doi: 10.1016/j.cjca.2016.02.070
He, X., Fang, J., Huang, L., Wang, J., and Huang, X. (2015). Sophora flavescens Ait.: traditional usage, phytochemistry and pharmacology of an important traditional Chinese medicine. J. Ethnopharmacol. 172, 10–29. doi: 10.1016/j.jep.2015.06.010
Herrington, W., Lacey, B., Sherliker, P., Armitage, J., and Lewington, S. (2016). Epidemiology of atherosclerosis and the potential to reduce the global burden of atherothrombotic disease. Circ. Res. 118 (4), 535–546. doi: 10.1161/circresaha.115.307611
Ho, M., Huang, L., Goodwin, J., Dong, X., Chen, C., and Xie, H. (2016). Two small molecules block oral epithelial cell invasion by Porphyromons gingivalis. PLoS One 11 (2), e0149618. doi: 10.1371/journal.pone.0149618
Hu, S., Zhang, Y., Zhang, M., Guo, Y., Yang, P., Zhang, S., et al. (2016). Aloperine protects mice against ischemia-reperfusion (IR)-induced renal injury by regulating PI3K/AKT/mTOR signaling and AP-1 activity. Mol. Med. 21 (1), 912–923. doi: 10.2119/molmed.2015.00056
Huang, B., Xiong, J., Zhao, X., Zheng, Y., and Zhu, N. (2020). Network pharmacology-based analysis of the pharmacological mechanisms of aloperine on cardiovascular disease. Evid. Based Complement. Alternat. Med. 2020, 5180716. doi: 10.1155/2020/5180716
Joseph, P., Leong, D., McKee, M., Anand, S., Schwalm, J., Teo, K., et al. (2017). Reducing the global burden of cardiovascular disease, part 1: the epidemiology and risk factors. Circ. Res. 121 (6), 677–694. doi: 10.1161/circresaha.117.308903
Kolate, A., Baradia, D., Patil, S., Vhora, I., Kore, G., and Misra, A. (2014). PEG - a versatile conjugating ligand for drugs and drug delivery systems. J. Contr. Release 192, 67–81. doi: 10.1016/j.jconrel.2014.06.046
Laurent, S. (2017). Antihypertensive drugs. Pharmacol. Res. 124, 116–125. doi: 10.1016/j.phrs.2017.07.026
Lee, Y., Chen, S., Lin, C., Chao, W., Lim, Y., Yu, H., et al. (2018). In Vitro antitumor activity of aloperine on human thyroid cancer cells through caspase-dependent apoptosis. Int. J. Mol. Sci. 19 (1), 312. doi: 10.3390/ijms19010312
Li, B., Xu, X., Wang, X., Yu, H., Li, X., Tao, W., et al. (2012). A systems biology approach to understanding the mechanisms of action of Chinese herbs for treatment of cardiovascular disease. Int. J. Mol. Sci. 13 (10), 13501–13520. doi: 10.3390/ijms131013501
Li, J., Sun, F., Zhou, H., Yang, J., Huang, C., and Fan, H. (2019). A systematic review exploring the anticancer activity and mechanisms of glucomannan. Front. Pharmacol. 10, 930. doi: 10.3389/fphar.2019.00930
Li, K., Tay, F., and Yiu, C. (2020). The past, present and future perspectives of matrix metalloproteinase inhibitors. Pharmacol. Ther. 207, 107465. doi: 10.1016/j.pharmthera.2019.107465
Li, W., Li, Y., Zhao, Y., and Ren, L. (2020). The protective effects of aloperine against ox-LDL-induced endothelial dysfunction and inflammation in HUVECs. Artif. Cells, Nanomed., Biotechnol. 48 (1), 107–115. doi: 10.1080/21691401.2019.1699816
Li, Y., Wang, G., Liu, J., and Ouyang, L. (2020). Quinolizidine alkaloids derivatives from Sophora alopecuroides Linn: bioactivities, structure-activity relationships and preliminary molecular mechanisms. Eur. J. Med. Chem. 188, 111972. doi: 10.1016/j.ejmech.2019.111972
Lin, W., and Lin, J. (2011). Five bitter compounds display different anti-inflammatory effects through modulating cytokine secretion using mouse primary splenocytes in vitro. J. Agric. Food Chem. 59 (1), 184–192. doi: 10.1021/jf103581r
Lin, Z., Huang, C., Liu, X., and Jiang, J. (2011). In vitro anti-tumour activities of quinolizidine alkaloids derived from Sophora flavescens Ait. Basic Clin. Pharmacol. Toxicol. 108 (5), 304–309. doi: 10.1111/j.1742-7843.2010.00653.x
Ling, Z., Guan, H., You, Z., Wang, C., Hu, L., Zhang, L., et al. (2018). Aloperine executes antitumor effects through the induction of apoptosis and cell cycle arrest in prostate cancer in vitro and in vivo. OncoTargets Ther. 11, 2735–2743. doi: 10.2147/ott.s165262
Little, W., and Cheng, C. (1994). Vascular versus myocardial effects of calcium antagonists. Drugs 47, 41–45; discussion 45–46. doi: 10.2165/00003495-199400474-00007
Liu, C., and Huang, Y. (2016). Chinese herbal medicine on cardiovascular diseases and the mechanisms of action. Front. Pharmacol. 7, 469. doi: 10.3389/fphar.2016.00469
Liu, J., Huo, C., Cao, H., Fan, C., Hu, J., Deng, L., et al. (2019). Aloperine induces apoptosis and G2/M cell cycle arrest in hepatocellular carcinoma cells through the PI3K/Akt signaling pathway. Phytomedicine 61, 152843. doi: 10.1016/j.phymed.2019.152843
Liu, L., Alam, M., Hirata, K., Matsuda, K., and Ozoe, Y. (2008). Actions of quinolizidine alkaloids on Periplaneta americana nicotinic acetylcholine receptors. Pest Manag. Sci. 64 (12), 1222–1228. doi: 10.1002/ps.1622
Liu, X., and Chen, H. (2014). Effects of compound Kudouzi on blood pressure, blood lipids and body weight in rats with spontaneously hypertension combined with hyperlipidemia. Xian Dai Yu Fang. Yi Xue 41 (23), 4350–4353.
Liu, Y., and Feng, N. (2015). Nanocarriers for the delivery of active ingredients and fractions extracted from natural products used in traditional Chinese medicine (TCM). Adv. Colloid Interface Sci. 221, 60–76. doi: 10.1016/j.cis.2015.04.006
Lv, W., Liu, Q., An, J., and Song, X. (2020). Aloperine prevents hypoxia-induced epithelial-mesenchymal transition in bladder cancer cells through regulating the mTOR/p70S6K/4E-BP1 pathway. doi: 10.21203/rs.3.rs-15917/v1
Lv, X., Zou, L., Tan, J., Li, H., Li, J., Liu, N., et al. (2020). Aloperine inhibits hepatitis C virus entry into cells by disturbing internalisation from endocytosis to the membrane fusion process. Eur. J. Pharmacol.,883, 173323. doi: 10.1016/j.ejphar.2020.173323
Ma, N., Zhou, R., Chang, R., Hao, Y., Ma, L., Jin, S., et al. (2015). Protective effects of aloperine on neonatal rat primary cultured hippocampal neurons injured by oxygen-glucose deprivation and reperfusion. J. Nat. Med. 69 (4), 575–583. doi: 10.1007/s11418-015-0928-2
Manville, R., van der Horst, J., Redford, K., Katz, B., Jepps, T., and Abbott, G. (2019). KCNQ5 activation is a unifying molecular mechanism shared by genetically and culturally diverse botanical hypotensive folk medicines. Proc. Natl. Acad. Sci. U.S.A. 116 (42), 21236–21245. doi: 10.1073/pnas.1907511116
Mao, Q., Guo, F., Liang, X., Wu, Y., and Lu, Y. (2019). Aloperine activates the PI3K/akt pathway and protects against coronary microembolisation-induced myocardial injury in rats. Pharmacology 104, 90–97. doi: 10.1159/000500761
Montezano, A., Tsiropoulou, S., Dulak-Lis, M., Harvey, A., Camargo, L. L., and Touyz, R. (2015). Redox signaling, Nox5 and vascular remodeling in hypertension. Curr. Opin. Nephrol. Hypertens. 24 (5), 425–433. doi: 10.1097/mnh.0000000000000153
Muhammad, T., Sakhawat, A., Khan, A., Huang, H., Khan, H., Huang, Y., et al. (2020). Aloperine in combination with therapeutic adenoviral vector synergistically suppressed the growth of non-small cell lung cancer. J. Canc. Res. Clin. Oncol. 146 (4), 861–874. doi: 10.1007/s00432-020-03157-2
Paier, C., Maranhão, S., Carneiro, T., Lima, L., Rocha, D., Santos, R., et al. (2018). Natural products as new antimitotic compounds for anticancer drug development. Clinics (Sao Paulo) 73, e813s. doi: 10.6061/clinics/2018/e813s
Passarella, D., Angoli, M., Giardini, A., Lesma, G., Silvani, A., and Danieli, B. (2002). Concise total synthesis of (+/-)-aloperine and 6-epi-aloperine. Org. Lett. 4 (17), 2925–2928. doi: 10.1021/ol0263144
Pu, Q., Li, Y., Yang, J., and Yan, S. (1987). Study on mass spectra of alkaloids from Sophora alopecuroides L. Yaoxue Xuebao 22 (6), 438–444 [in Chinese].
Qiu, M., Liu, J., Feng, P., Su, Y., Guo, R., Shi, F., et al. (2020a). 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
Qiu, M., Liu, J., Su, Y., Liu, J., Wu, C., and Zhao, B. (2020b). Aloperine induces apoptosis by a reactive oxygen species activation mechanism in human ovarian cancer cells. Protein Pept. Lett. 27 (9), doi: 10.2174/0929866527666200320094313
Ren, J., Wang, D., Lei, L., Kang, L., and Liu, J. (2017). Preliminary analysis on relationship between traditional efficacy of Chinese medicine and modern pharmacological action. Zhongguo Zhongyao Zazhi 42 (10), 1979–1983 [in Chinese]. doi: 10.19540/j.cnki.cjcmm.20170307.002
Roth, G., Johnson, C., Abajobir, A., Abd-Allah, F., Abera, S., Abyu, G., et al. (2017). Global, regional, and national burden of cardiovascular diseases for 10 causes, 1990 to 2015. J. Am. Coll. Cardiol. 70 (1), 1–25. doi: 10.1016/j.jacc.2017.04.052
Shi, Q., Han, X., and Jiang, A. (2003). Experimental observation on germicidal efficacy and toxicity of aloperine disinfectant solution. Zhongguo Xiaoduxue Zazhi 20 (4), 250–253. doi: 10.3969/j.issn.1001-7658.2003.04.003
Song, S., Chen, Y., Han, F., Dong, M., Xiang, X., Sui, J., et al. (2018). Aloperine activates the Nrf2-ARE pathway when ameliorating early brain injury in a subarachnoid hemorrhage model. Exp. Ther. Med. 15 (4), 3847–3855. doi: 10.3892/etm.2018.5896
Tabassum, N., and Ahmad, F. (2011). Role of natural herbs in the treatment of hypertension. Phcog. Rev. 5 (9), 30–40. doi: 10.4103/0973-7847.79097
Tian, D., Li, Y., Li, X., and Tian, Z. (2018). Aloperine inhibits proliferation, migration and invasion and induces apoptosis by blocking the Ras signaling pathway in human breast cancer cells. Mol. Med. Rep. 18 (4), 3699–3710. doi: 10.3892/mmr.2018.9419
Vader, P., Mol, E., Pasterkamp, G., and Schiffelers, R. (2016). Extracellular vesicles for drug delivery. Adv. Drug Deliv. Rev. 106, 148–156. doi: 10.1016/j.addr.2016.02.006
Van Kleef, M., and Spiering, W. (2017). Hypertension: overly important but under-controlled. Eur J. Prev Cardiol. 24, 36–43. doi: 10.1177/2047487317709116
Wan, L., Pantel, K., and Kang, Y. (2013). Tumor metastasis: moving new biological insights into the clinic. Nat. Med. 19 (11), 1450–1464. doi: 10.1038/nm.3391
Wang, C., Choi, Y., Xian, Z., Zheng, M., Piao, H., and Yan, G. (2018). Aloperine suppresses allergic airway inflammation through NF-κB, MAPK, and Nrf2/HO-1 signaling pathways in mice. Int. Immunopharm. 65, 571–579. doi: 10.1016/j.intimp.2018.11.003
Wang, H., Yang, S., Zhou, H., Sun, M., Du, L., Wei, M., et al. (2015). Aloperine executes antitumor effects against multiple myeloma through dual apoptotic mechanisms. J. Hematol. Oncol. 8, 26. doi: 10.1186/s13045-015-0120-x
Wang, L., Ma, R., Liu, C., Liu, H., Zhu, R., Guo, S., et al. (2017). Salvia miltiorrhiza: a potential red light to the development of cardiovascular diseases. Curr. Pharmaceut. Des. 23 (7), 1077–1097. doi: 10.2174/1381612822666161010105242
Wang, M., and Chen, H. (2006). Effects of KUDOUZI on lipid of hyperlipidemia Coturnix. Shihezi Daxue Xuebao Ziran Kexueban 24 (2), 158–160.
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
Wu, F., Hao, Y., Yang, J., Yao, W., Xu, Y., Yan, L., et al. (2017a). Protective effects of aloperine on monocrotaline-induced pulmonary hypertension in rats. Biomed. Pharmacother. 89, 632–641. doi: 10.1016/j.biopha.2017.02.033
Wu, F., Yao, W., Yang, J., Zhang, M., Xu, Y., Hao, Y., et al. (2017b). Protective effects of aloperin on monocroline-induced pulmonary hypertension via regulation of Rho A/Rho kinsase pathway in rats. Biomed. Pharmacother. 95, 1161–1168. doi: 10.1016/j.biopha.2017.08.126
Wu, T., and Dai, Y. (2017). Tumor microenvironment and therapeutic response. Canc. Lett. 387, 61–68. doi: 10.1016/j.canlet.2016.01.043
Wu, Y., Guo, R., Cao, N., Sun, X., Sui, Z., and Guo, Q. (2018). A systematical rheological study of polysaccharide from Sophora alopecuroides L. seeds. Carbohydr. Polym. 180, 63–71. doi: 10.1016/j.carbpol.2017.10.007
Xu, Q., Bauer, R., Hendry, B., Fan, T., Zhao, Z., Duez, P., et al. (2013). The quest for modernisation of traditional Chinese medicine. BMC Compl. Alternat. Med. 13, 132. doi: 10.1186/1472-6882-13-132
Xu, W., Xing, F., Dong, K., You, C., Yan, Y., Zhang, L., et al. (2015). Application of traditional Chinese medicine preparation in targeting drug delivery system. Drug Deliv. 22 (3), 258–265. doi: 10.3109/10717544.2014.892545
Xu, Y., Jin, S., Liu, N., Li, Y., Zheng, J., Ma, L., et al. (2014). Aloperine attenuated neuropathic pain induced by chronic constriction injury via anti-oxidation activity and suppression of the nuclear factor kappa B pathway. Biochem. Biophys. Res. Commun. 451 (4), 568–573. doi: 10.1016/j.bbrc.2014.08.025
Xu, Z., Wang, X., Chen, X., Zeng, S., Qian, L., Wei, J., et al. (2019). Identification of aloperine as an anti-apoptotic Bcl2 protein inhibitor in glioma cells. PeerJ 7, e7652. doi: 10.7717/peerj.7652
Yamauchi, S., and Omi, Y. (2005). Synthesis of an optically pure synthetic intermediate of aloperine from a yeast-reductive product. Biosci. Biotechnol. Biochem. 69 (8), 1589–1594. doi: 10.1271/bbb.69.1589
Yang, C., Yu, Y., Wu, F., Wu, Y., Feng, J., Yan, L., et al. (2018). Vasodilatory effects of aloperine in rat aorta and its possible mechanisms. Chin. J. Physiol. 61 (5), 293–301. doi: 10.4077/cjp.2018.bah609
Ye, Y., Wang, Y., Yang, Y., and Tao, L. (2020). Aloperine suppresses LPS-induced macrophage activation through inhibiting the TLR4/NF-κB pathway. Inflamm. Res. 69 (4), 375–383. doi: 10.1007/s00011-019-01313-0
Yugang, H., and Hao, Z. (2013). Research progress on the bioactive alkaloids from Kudouzi. Med. Front. 33, 357–358. doi: 10.3969/j.issn.2095-1752.2013.33.444
Yin, W., Han, J., Zhang, Z., Han, Z., and Wang, S. (2018). Aloperine protects mice against bleomycin-induced pulmonry fibrosis by attenuating fibroblast proliferation and differentiation. Sci. Rep. 8 (1), 6265. doi: 10.1038/s41598-018-24565-y
Yuan, X., Liu, W., Zhang, P., Wang, R., and Guo, J. (2010). Effects and mechanisms of aloperine on 2, 4-dinitrofluorobenzene-induced allergic contact dermatitis in BALB/c mice. Eur. J. Pharmacol. 629, 147–152. doi: 10.1016/j.ejphar.2009.12.007
Yuan, X., Ma, H., Li, R., Wang, R., Liu, W., and Guo, J. (2011). Topical application of aloperine improves 2,4-dinitrofluorobenzene-induced atopic dermatitis-like skin lesions in NC/Nga mice. Eur. J. Pharmacol. 658, 263–269. doi: 10.1016/j.ejphar.2011.02.013
Zhang, L., Zheng, Y., Deng, H., Liang, L., and Peng, J. (2014). Aloperine induces G2/M phase cell cycle arrest and apoptosis in HCT116 human colon cancer cells. Int. J. Mol. Med. 33 (6), 1613–1620. doi: 10.3892/ijmm.2014.1718
Zhang, N., Dou, Y., Liu, L., Zhang, X., Liu, X., Zeng, Q., et al. (2019). SA-49, a novel aloperine derivative, induces MITF-dependent lysosomal degradation of PD-L1. EBioMedicine 40, 151–162. doi: 10.1016/j.ebiom.2019.01.054
Zhang, X., Liu, Q., Zhang, N., Li, Q., Liu, Z., Li, Y., et al. (2018a). Discovery and evolution of aloperine derivatives as novel anti-filovirus agents through targeting entry stage. Eur. J. Med. Chem. 149, 45–55. doi: 10.1016/j.ejmech.2018.02.061
Zhang, X., Lv, X., Tang, S., Mei, L., Li, Y., Zhang, J., et al. (2018b). Discovery and evolution of aloperine derivatives as a new family of HCV inhibitors with novel mechanism. Eur. J. Med. Chem. 143, 1053–1065. doi: 10.1016/j.ejmech.2017.12.002
Zhao, D., Li, Z., Yang, X., and Sheng, B. (1986). The antiarrhythmic effect of aloperine. Chin. Herb. Med. 17 (04), 26–27.
Zhao, D., Liu, J., Wang, M., Zhang, X., and Zhou, M. (2019). Epidemiology of cardiovascular disease in China: current features and implications. Nat. Rev. Cardiol. 16 (4), 203–212. doi: 10.1038/s41569-018-0119-4
Zhao, J., Zhang, G., Li, M., Luo, Q., Leng, Y., and Liu, X. (2018). Neuro-protective effects of aloperine in an Alzheimer’s disease cellular model. Biomed. Pharmacother. 108, 137–143. doi: 10.1016/j.biopha.2018.09.008
Zhou, C., Gao, H., Sun, X., Shi, H., Liu, W., Yuan, H., et al. (1989). Anti-inflammatory and anti-allergic action of aloperine. Zhongguo Yaoli Xuebao 10 (4), 360–365 [in Chinese].
Zhou, Y., Wang, H., Liang, L., Zhao, W., Chen, Y., and Deng, H. (2010). Total alkaloids of Sophora alopecuroides increases the expression of CD4+ CD25+ Tregs and IL-10 in rats with experimental colitis. Am. J. Chin. Med. 38 (2), 265–277. doi: 10.1142/s0192415x1000783x
Keywords: Sophora genus phytomedicine, traditional herbal medicine, pharmacological effects, biological mechanisms, aloperine
Citation: Zhou H, Li J, Sun F, Wang F, Li M, Dong Y, Fan H and Hu D (2020) A Review on Recent Advances in Aloperine Research: Pharmacological Activities and Underlying Biological Mechanisms. Front. Pharmacol. 11:538137. doi: 10.3389/fphar.2020.538137
Received: 13 March 2020; Accepted: 21 September 2020;
Published: 29 October 2020.
Edited by:
Michał Tomczyk, Medical University of Bialystok, PolandReviewed by:
Tan Loh Teng Hern, Guangdong University of Technology, ChinaMuhammad Ayaz, University of Malakand, Pakistan
Copyright © 2020 Li, Sun, Zhou, Wang, Dong, Li, Fan and Hu. This is an open-access article distributed under the terms of the . 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: Heng Fan, fanheng009@aliyun.com, Desheng Hu, desheng.hu@hust.edu.cn