Tingting Deng1
Jinxin Du1
Ying Yin2
Baorui Cao3
Zhiying Wang1
Zhongwen Zhang4
Meina Yang3,4*†
Jinxiang Han3,4*†- 1College of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China
- 2Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, China
- 3NHC Key Laboratory of Biotechnology Drugs (Shandong Academy of Medical Sciences), Biomedical Sciences College, Shandong First Medical University, Jinan, China
- 4Department of Endocrinology and Metabolism, The First Affiliated Hospital of Shandong First Medical University, Jinan, China
With the extension of life expectancy and changes in lifestyle, the prevalence of diabetes mellitus is increasing worldwide. Rheum palmatum L. a natural botanical medicine, has been used for thousands of years to prevent and treat diabetes mellitus in Eastern countries. Rhein, the main active component of rhubarb, is a 1, 8-dihydroxy anthraquinone derivative. Previous studies have extensively explored the clinical application of rhein. However, a comprehensive review of the antidiabetic effects of rhein has not been conducted. This review summarizes studies published over the past decade on the antidiabetic effects of rhein, covering the biological characteristics of Rheum palmatum L. and the pharmacological effects and pharmacokinetic characteristics of rhein. The review demonstrates that rhein can prevent and treat diabetes mellitus by ameliorating insulin resistance, possess anti-inflammatory and anti-oxidative stress properties, and protect islet cells, thus providing a theoretical basis for the application of rhein as an antidiabetic agent.
Introduction
The diabetes mellitus (DM) epidemic is a global public health problem that imposes a serious social and economic burden. According to the International Diabetes Federation, DM affects an estimated 537 million adults (aged 20–79 years) worldwide, resulting in 6.7 million deaths (International Diabetes Federation, 2021). The national cost of DM in the United States (US) in 2017 was more than $327 billion, up from $245 billion in 2012 (American Diabetes Association, 2018). Hyperglycemia can cause multiple complications, such as diabetic retinopathy, diabetic nephropathy, atherosclerosis, cardiovascular disease, obesity, hypertension, hyperlipidemia, cerebrovascular disease, skin complications, depression, and ultimately death. The United States National Vital Statistics System stated that DM was the 8TH leading cause of death in the United States in 2020 (Ahmad et al., 2021). Timely control of blood sugar with effective medications is important. In addition to traditional antidiabetic drugs and insulin therapy, natural compounds isolated from herbal medicines have unique advantages and great potential in preventing and treating DM (Yang et al., 2011). The World Ethnobotanical Inspection reports approximately 800 plant species that are used to treat DM (Deniyi et al., 2018; Khursheed et al., 2019).
Rhubarb is the root and rhizome of Rheum palmatum L. It has been widely used for treating obesity (Bati et al., 2020), DM (Cheng et al., 2019), chronic kidney disease (Dou et al., 2020), pneumonia (Shen et al., 2020), osteoarthritis (Ding et al., 2018), and constipation (Gao, 2021), among others. Rhein (4,5-dihydroxyanthraquinone-2-carboxylic acid) is an anthraquinone compound extracted from rhubarb, a traditional Chinese medicine. Rhein is commonly used to treat DM in Asian and European countries (Barreto and Sahebkar, 2021). The aim of this review was to elucidate the antidiabetic effects and pharmacological mechanisms of rhein.
Biological characteristics of Rheum palmatum L
Nomenclature of Rheum palmatum L
Rheum palmatum L. is a perennial herb that belongs to the Polygonaceae family. There are approximately 60 species worldwide, mainly distributed on mountain slopes or valley wetlands at an altitude of 1,500–4,400 m. The center of distribution of this genus is China, with 41 species and four varieties, accounting for approximately 75% of the total plants in the genus. Rhubarb has been used in medicine for over 1,000 years. The traditional Chinese medicine (TCM) theory holds that rhubarb is bitter and cold and has the function of reducing accumulation, clearing heat, and eliminating fire; cooling and detoxifying blood; and removing blood stasis and meridian obstruction (Peigen et al., 1984). The detailed characteristics of Rheum palmatum L. and rhubarb are shown in Figure 1.
FIGURE 1. Plant and Slice of root of Rheum palmatum L. The leaves of Rheum palmatum L. are palmately lobed to half-lobed, with the lobes mostly narrowly triangular; its flowers are small, purple-red or yellowish-white; its buds are inverted pyramidal; and its fruits are small. The outer skin of rhubarb is yellowish-brown or reddish-brown, with white-like reticulate texture and scattered stars, and its broken surface is light reddish-brown or yellowish-brown, showing granularity; it has a fresh aroma and a bitter and slightly astringent taste. (A) Rheum palmatum L. is a kind of herb with medicinal value. (B) prepared slices of Rhubarb, containing a variety of active pharmacological ingredients.
Botanical characteristics
Rheum palmatum L. is a tall stout herb, 1.5–2.0 m high, with thick woody roots and rhizomes. The stem is upright and hollow, and the leaves are nearly equal in length and width, up to 40–60 cm long. The apex is narrow and pointed, and the base is nearly heart-shaped, usually palmately hemi-5-lobed. The petiole is stout, cylindrical, nearly equal in length to the leaf, and densely covered with rusty papillary hairs. Cauline leaves get smaller upwards, while the stalks get shorter. The leaf sheath is large, up to 15 cm long, with a smooth inner surface and a rough exterior. The inflorescences are large, conical, branched, and more clustered, densely covered with coarse short hairs. The flowers are small, usually purple-red and sometimes yellowish white. The peduncle is 2.0–2.5 mm long, and the joints are located below the middle. The fruit is rounded, oval to rectangular, 8.0–9.0 mm long, and 7.0–7.5 mm wide. The seeds are broadly ovate and brownish black. The flowering period is June, and the fruiting period is August. Rhubarb is mainly distributed in the temperate and subtropical regions of Asia.
Rhein: The main therapeutic ingredient of rhubarb
Rhubarb contains a variety of biologically active ingredients, such as anthraquinone derivatives, anthracene derivatives, styrene, tannins, acyl glycosides, chromones, and phenylbutazone glycosides (Pharmacopoeia of the People’s Republic of China 2005). However, the main ones are rhein, emodin, aloe-emodin, chrysophanol, and emodin methyl ether (Ye et al., 2007). The chemical structures of these compounds are depicted in Figure 2. The extraction methods for the active ingredients include marinated extraction, heat reflux extraction (HRE), Soxhlet extraction (SE), and microwave-assisted extraction (MAE) (Sun and Liu, 2008; Huang et al., 2009). In the 21st century, rhubarb has been used in various medicinal and edible applications (Rhubarb, 2006). There is increasing evidence that rhein is effective against DM and its complications and can act on different anti-diabetic drug targets, indicating its potential as an anti-diabetic agent (Qi et al., 2010; Zeng et al., 2014; Chien et al., 2015; Zheng, 2020).
FIGURE 2. Chemical structures of the main active ingredients of Rhubarb. (A) chrysophanol, (B) rhein, (C) emodin, (D) aloe-emodin, (E) emodin methyl ether.
Extraction methods and quality control
The extraction methods of rhein include ultrasound-assisted extraction (UAE), HRE SE, and MAE (Sun and Liu, 2008; Huang et al., 2009). The UAE method has the advantages of high extraction efficiency, short consumption time, and low temperature. The HRE method is suitable for small amounts of drugs that aren’t easily destroyed by heat. The SE method is easy to operate, and the MAE method has the characteristics of uniform and selective heating.
In recent years, proton ionic liquids have been used as efficient solvents for MAE of rhein (Fan et al., 2019). A variety of qualitative and quantitative analytical methods have been developed for determining rhein content, including thin layer chromatography (Ma et al., 1989), high performance liquid chromatography (HPLC)-ultraviolet detection (Zhou et al., 2009), HPLC-mass spectrometry (Danielsen and Francis, 1994), high performance capillary electrophoresis (Hu, 2012), and capillary electrophoresis chromatography (Koyama et al., 2007). According to the provisions of the 2020 edition of the Chinese Pharmacopoeia (Chinese Pharmacopoeia Commission, 2020), the total ash content of medicinal materials should not exceed 10.0% (General Rule 2302). The total anthraquinone content was determined using HPLC (General Rule 0512), with the total amount of aloe emodin (C15H10O5), rhein (C15H8O6), emodin (C15H10O5), chrysophanol (C15H10O4), and emodin methyl ether (C16H12O5) not less than 1.5%. It shouldn’t be less than 25.0% according to the hot-dip method, which is a water-soluble extract determination method (General Rule 2201).
Pharmacological mechanisms of rhein on DM mellitus
Insulin resistance
Insulin resistance (IR) is a common risk factor for various endocrine, metabolic, and cardiovascular diseases (Zhang et al., 2019; Hill et al., 2021). Rhein can significantly improve IR associated with obesity (Ji and Gu, 2021) and non-alcoholic fatty liver disease (Sheng et al., 2011). Similarly, rhein can play a role in reducing IR, thereby inhibiting DM progression.
Insulin resistance prevents insulin from performing its normal physiological function, causing high blood glucose. This results in hyperinsulinism and a series of changes such as hyperglycemia and obesity. Rhein significantly improves glucose tolerance without regulating insulin secretion in streptozotocin (STZ)-induced diabetic mice (Choi et al., 2006). It was found to significantly reduce blood glucose, glycosylated hemoglobin, and glycosylated serum protein levels, increase the insulin sensitivity index, and decrease the IR index, Homeostatic Model Assessment for Insulin Resistance, effectively improving insulin sensitivity in diabetic rats (Jin, 2008). These findings confirm that rhein enhances insulin sensitivity.
The hexosamine pathway (HBP) is an intracellular glucose metabolism pathway. Under normal circumstances, only 1%–3% of glucose enters the HBP. Changes in intracellular HBP activity are associated with the development of IR (Marshall et al., 1991; Cooksey et al., 1999). Studies have shown that rhein inhibits the development of DM mainly by inhibiting the overactivity of HBP. Specifically, after rhein stimulation, the activity of glutamine fructose-6-phosphate aminotransferase (GFAT) in the first step of the HBP decreases, and the formation of UDP-N- acetylglucosamine, the final product of HBP, decreases significantly (Liu et al., 2000; Liu et al., 2001a). Glucose transporter 1 (GLUT1) is the key glucose transporter in mesangial cells and is responsible for their basal metabolism; its expression level is often the main rate-limiting step in cellular glucose metabolism. Modern research has found that rhein can significantly reduce the glucose uptake rate of mesangial cells were transduced with the human GLUT1 gene (MCGT1) in a dose-dependent manner, correct the hypertrophic state of MCGT1, and reduce the cell volume of MCGT1 and the ratio of RNA/DNA and protein/DNA (Liu et al., 2001a; Li et al., 2001; Zhu et al., 2001).
In mesangial cells, transforming growth factor-β (TGF-β1) stimulates extracellular matrix (ECM) synthesis and cell hypertrophy as a result of high glucose concentrations (Masson et al., 2005; Masson et al., 2006). Rhein inhibits the overactivity of HBP in rat mesangial cells (MCGT1) transfected with the GLUT1 gene. It reduces the expression of TGF-β1, number of hypertrophic cells, and ECM synthesis (Liu et al., 2001b; Zheng et al., 2008). Rhein inhibits the upregulation of plasminogen activator inhibitor-1 (PAI-1) mRNA expression in TGF-β1-induced endothelial cells in a dose-dependent manner and the production of endothelial PAI-1 protein and has a significant inhibitory effect on the activity of phosphor-p44/p42 mitogen-activated protein kinase (MAPK) induced by TGF-β1 in human endothelial cells (Zhu et al., 2003). Rhein is transmitted through protein kinase C (PKC), and MAPK inhibits the abnormal increase in GLUT1 mRNA expression, thereby antagonizing the pathological effects of TGF-β1 on mesangial cells (Huang et al., 2007; Zhuang et al., 2019). GFAT is the key enzyme in HBP, and its activity intensity reflects the active state of HBP. Liu Q. found that rhein inhibits the activity and expression of GFAT in the skeletal muscle of IR mice, 3T3 L1 adipocytes, and C2C12 myoblast models of IR induced by high glucose and insulin levels, thereby inhibiting HBP flow and downregulating the glycosylation modification level of the protein O-linked N-acetylglucosamine. It increases the responsiveness of the whole body and insulin target tissues to insulin (Liu Q., 2009). The pharmacological mechanisms by which rhein improves IR in DM by inhibiting HBP overactivity are shown in Figure 3.
FIGURE 3. The pharmacological mechanisms of rhein in improving IR in DM by inhibiting HBP overactivity. PAGM, Phosphoacetllucosaminemutase; ATP, adenosine triphosphate; ADP, adenosine diphosphate; UDP, uridine diphosphate; UTP, uridine triphosphate.
In addition, rhein can increase the expression of SIRT1 in the renal tissue, improve insulin sensitivity and glucose and lipid metabolism disorders, and reduce the IR index in diabetic rats (Chen et al., 2015). A study found that argirein synthesized by hydrogen bonding of rhein and L-arginine inhibits the activation of NOX4-dependent O2− in rat aortic endothelial cells triggered by palmitic acid, thereby inhibiting endothelial IR and improving vascular function (Li et al., 2018). Rhein significantly reduces blood glucose levels in diabetic mice and upregulates peroxisome proliferator-activated receptor γ (PPARγ) expression, thus improving metabolic disorders and reversing IR (Huang et al., 2004; Chi et al., 2008).
Inflammation
The risk of developing DM is positively associated with inflammation (Navarro and Mora, 2005; Shoelson et al., 2006). Rhein exhibits significant anti-inflammatory properties in colitis (Dong et al., 2022; Zhou et al., 2022), acute pancreatitis (Yang D et al., 2022), and obesity (Fang et al., 2022), among other conditions. Similarly, rhein exerts anti-inflammatory effects by inhibiting DM development. Inflammation induces the release of chemicals called inflammatory cytokines from damaged cells; these cytokines regulate various inflammatory responses. Studies have shown that rhein inhibits the development of DM primarily by inhibiting the release of inflammatory cytokines. In the KK/HlJ diabetic mouse model, rhein lysinate reduces the levels of blood glucose and significantly decreases the expression of tumor necrosis factor alpha (TNF-α) and interleukin 6 (IL-6) (Wei et al., 2016). Another study reported that Rhein@OR-S gel can inhibit reactive oxygen species (ROS) and NO overproduction and has excellent efficiency in suppressing diabetic wound inflammation, bringing forward the transition from the inflammatory phase to the proliferative phase (Zhao et al., 2020).
Nuclear factor-kappa B (NF-κB) is a sequence-specific DNA-binding protein with pleiotropic transcriptional regulation, regulating the expression of multiple target genes encoding cytokines and inflammatory mediators. The NF-κB signaling pathway plays an important role in the molecular mechanisms of IR. After stimulation by exogenous substances, such as TNF-α, IL-1β, and LPS, IκB-α in the cytoplasm is phosphorylated, undergoes ubiquitination and degradation, and is released into p65 into the nucleus. In turn, p65 binds to specific response element sequences on target genes and activates their transcription (Pires et al., 2018). Rhein plays an anti-inflammatory role by inhibiting the NF-κB signaling pathway through the degradation of IκB-α and nuclear translocation of p65 (Li and Verma, 2002; Tobar et al., 2011; Zheng et al., 2019; He et al., 2021). Macrophages exacerbate inflammatory responses by releasing inflammatory factors. Rhein plays a dual role in lipopolysaccharide-activated macrophages by inhibiting IKKβ. On the one hand, by inhibiting the standard IKKβ-mediated NF-κB activation sequence (IKKβ axis), rhein suppresses downstream NO and IL-6 levels; on the other hand, rhein enhances caspase-1 activity by inhibiting NF-κB-independent IKKβ itself, which in turn increases the release of IL-1β and HMGB1 (Gao et al., 2014). PPARγ is a significant protein involved in insulin activity. PPAR-γ ligand downregulates the expression of TNF-α in macrophages PPAR-γ (Bermudez et al., 2017). C-Jun N-terminal kinase (JNK) is a member of the mitogen-activated protein kinase (MAPK) family, which is a critical component of the death pathway caused by inflammation and oxidative stress. Rhein can regulate the PPARγ signaling pathway in a dose-dependent manner, effectively improving the protein expression of PPARγ, and inhibiting NF-κB expression and p-JNK activation. These changes effectively inhibit the inflammatory response of renal mesangial cells and enhance insulin sensitivity (Duan S. F. et al., 2016; Ji and Gu, 2021).
The Wnt/β-catenin signaling pathway activated by high glucose levels is involved in the pathogenesis of DM (Park et al., 2011; García-Jiménez et al., 2013). ß-Catenin is mainly responsible for mediating intercellular adhesion and related signaling. Stimulation of the Wnt signaling pathway is the only mechanism that enhances ß-catenin stability (Lin, 2004). When the Wnt signaling pathway is activated, the Wnt protein binds to the receptor, thereby inhibiting the activity of GSK-3β. Thus, ß-catenin cannot be phosphorylated and degraded, then accumulates in the cytoplasm, and integrates into the nucleus to initiate the expression of downstream target genes. Rhein can downregulate the expression of ß-catenin protein, promote the expression of GSK-3β, reduce the secretion of TGF-β1, and play a role in inhibit the Wnt/β-catenin signaling pathway (Zhang et al., 2015; Duan S. et al., 2016). The NLRP3 inflammasome is involved in inflammation and glucose homeostasis, and its activation can induce immune cells to produce proinflammatory cytokines, thereby exacerbating IR. NLRP3 inflammasome provides a platform for the production of IL-1β. IL-1β directly inhibits the insulin signaling pathway by decreasing insulin receptor substrate-1 (IRS-1) tyrosine phosphorylation and negatively regulating IRS-1 gene expression (Ding et al., 2019). Rhein inhibits NLRP3 inflammasome activation (Ge et al., 2017).
Rhein analogs may also improve diabetic symptoms by reducing the production of pro-inflammatory cytokines and inhibiting the expression of TGF-β1. Rhein lysinate (RHL), a water-soluble rhein derivative, can reduce the expression of TNF-α and NF-κB, and inhibits the immune response by directly or indirectly blocking the TNF–NF-κB biochemical pathway (Lin et al., 2015; Lin et al., 2017; Chueakula et al., 2018). Diacerhein is completely metabolized in the human body, resulting in rhein production, which exerts anti-inflammatory properties locally, decreases the expression of pro-inflammatory cytokines such as IL-1β, TNF-α, IFN-γ, and IL-12, thereby interfering with the occurrence of DM (Malaguti et al., 2008). Diacerein can reduce the level of TNF-α in patients with DM and improve metabolic control (Piovesan et al., 2017; Tres et al., 2018). The experimental details of the anti-inflammatory mechanisms of rhein are presented in Table 1.
TABLE 1. Experiments on the anti-inflammatory mechanism of rhein in diabetes mellitus.
Oxidative stress
Under high glucose conditions, autoxidation of glucose, non-enzymatic glycosylation of glucose and other biomolecules, and enhancement of polyol metabolic pathways results in the production of large amounts of ROS in the body. The inhibition of antioxidants (vitamin C, vitamin E, etc.,) and antioxidant enzymes (SOD, glutathione (GSH, catalase, etc.,) used to scavenge ROS in the body leads to the accumulation of lipid peroxidation products (e.g., MDA) and a long-term imbalance between the production of highly reactive molecules and antioxidant effects, resulting in oxidative stress, which in turn activates the polyol, AGEs, and PKC pathways, causing IR and impairment of islet ß-cell function (Scott and King, 2004; Pitocco et al., 2010).
Rhein has a unique structure containing carboxyl and hydroxyl groups, including two hydroxyl radicals, which confer antioxidant properties. Rhein inhibits OS in histiocytes by inhibiting antioxidant enzymes and reducing coenzyme II (NADPH) oxidase, reducing peroxisomes such as ROS in vivo, and has a protective effect on islet function and renal histiocytes. Huang et al. applied rhein to treat STZ-induced DM rats and found that rhein could antagonize the effect of Ang II and inhibit the signaling pathway of Ang II receptor, significantly inhibit the mRNA expression of renal NADPH oxidase subunits p47phox and p22phox. This reduces the production of ROS, which increases the antioxidant capacity of kidney tissue in DM and inhibits the oxidative emergency of kidney tissue (Huang et al., 2012). Huang et al. reported that rhein could reduce the expression of 8-OHdG, a marker of DNA damage, significantly inhibit OS injury in islet cells, and protect islet function (Huang et al., 2013). Rhein inhibited the increase in MDA content, increased SOD activity, and significantly inhibited OS damage in pancreatic islet cells (Wang J B et al., 2011; Li and Zhen, 2017). The pharmacological mechanism of rhein in inhibition of oxidative stress in DM are shown in Figure 4.
FIGURE 4. Pharmacological mechanism of rhein in inhibition of oxidative stress in diabetes mellitus. Drpl, dynamin-relatedprotein 1; Nrf2, nuclea factor erythroid-2-related factor 2; MDA,malonaldehyde; ROS, reactive oxygen species; SOD,superoxide dismutase; HO-1, Heme Oxygenase-1; CAT,catalase; GPX, glutathione peroxidase; GSH, glutathione,reduced; GSSG glutathione,oxydized; GR, gluathione reductase; NADPH, nicotinamide adenine dinucleotide phosphate; G-6-PDH,glucose-6-phosphate dehydrogenase; G-6-P, glucose-6-phosphate; GPI, phosphohexose isomerase; F-6-P, fructose-6-phosphate; PEK, Phosphofructokinase; PGAL, glyceraldehyde-3-phosphate; 1,3 BPG, 1,3 Biphosphoglycerate; TCA cycle, tricarboxylicacidcycle.
Gut microbiota
Gut microbiota dysbiosis leads to an increase in the proportion of G-bacteria, which, through the production and uptake of more LPS, activates a low-grade chronic inflammatory response, exacerbates IR, and impairs ß-cell function (Larsen et al., 2010). A two-stage metagenome-wide association study based on deep next-generation shotgun sequencing of gut microbial DNA extracted from 345 individuals identified alterations in vitamin and cofactor synthesis-related, butyrate-producing, sulfate-reducing, and mucin-degrading bacteria in the gut of patients with DM. The gut environment of patients with DM is one that stimulates bacterial defense mechanisms against OS (Qin et al., 2012). The ratio of Bacteroidetes to Firmicutes was positively correlated with blood glucose concentration. Rhein significantly enriched the gut microbiota, increased the relative abundance of Bacteroides, reversed the ratio of Bacteroides and Firmicutes, maintained the diversity of the gut microbiota to improve glucose metabolism, and exerted a hypoglycemic effect (Wang et al., 2016; 2018). Rhein significantly increased the number of terminal ileal L cells in db/db mice, which increased glucagon-like tide-l (GLP-1) release, which in turn stimulated increased insulin secretion by islet ß-cells and inhibited glucagon secretion by α-cells, thus improving glucose homeostasis (Wang et al., 2016).
Dyslipidemia
Diabetic dyslipidemia, which comprises very-low-density lipoprotein (VLDL), triacylglycerol (TG), small dense low-density lipoprotein, low-density lipoprotein (LDL), and high-density lipoprotein (HDL), is common in patients with DM (Bahiru et al., 2021). Multiple polymorphic studies have confirmed that hyperglycemia and elevated plasma triglycerides are associated with hepatic steatosis (Liang et al., 2015; Zhu et al., 2020). 3-hydroxy-3-methyl glutaryl coenzyme A (HMG-CoA), a rate-limiting enzyme in cholesterol synthesis by hepatocytes, catalyzes the formation of mevalonate. Gao et al. found that rhein inhibits HMG-CoA reductase, thereby inhibiting cholesterol synthesis (Gao et al., 2010). Wu et al. found that rhein significantly reduced the contents of TG and TC in L02 hepatic steatosis cells, and significantly reduced the fat granules around the nucleus (Wu et al., 2022). Rhein can downregulate the expression of resistin in the adipose tissue of obese diabetic rats, thereby reducing plasma free fatty acid levels and inhibiting signal transduction to insulin (Liu et al., 2011). Under pathological conditions such as DM and fatty liver, oxidized low-density lipoprotein can induce an increase in PPAR-γ through the PKC-α/ERK/PPAR-γ pathway (Hashimoto et al., 2000; Neuschwander-Tetri and Caldwell, 2003), which can inhibit the susceptibility of PPAR-γ and the expression of its target genes in a dose-dependent manner (Cen et al., 2013). Rhein can reduce serum total cholesterol (TC) levels, increase HDL levels, reduce LDL and VLDL levels, and prevent excessive oxidation of LDL in mice (Xie and Shang, 2014).
Mitochondrial dysfunction
When the inner and outer mitochondrial membrane proton gradients are high and oxygen consumption is low, ROS generation in the body increases. Excessive ROS damage mitochondrial proteins, mtDNA, and lipids on the mitochondrial membrane, thereby causing mitochondrial damage. Sustained and high-yield ROS generation caused by mitochondrial function damage reduces ATP generation, damages ß cells and inhibits insulin release (Hodgin et al., 2013). ROS prevents IRS-1 from binding to the insulin receptor by activating IKKβ, which phosphorylates the IRS-1 SER site, thereby preventing the transmission of insulin signals and causing insulin resistance (Nishikawa, 2007). Rhein is localized in the mitochondria of pancreatic ß-cells, and it can maintain mitochondrial ultrastructure by reducing the ROS content in mitochondria, thereby inhibiting the expression of dynamin related protein 1 (Drp1) and preventing ß-cell apoptosis induced by hyperglycemia (Lin et al., 2007; Liu et al., 2013). AMP-activated protein kinase (AMPK) is an important protein that regulates mitochondrial biosynthesis (Jager et al., 2007). Studies have shown that rhein can activate the AMPK-Sirt1 pathway to promote the translocation of the α-subunit of ATPase to the plasma membrane, promote mitochondrial biosynthesis, improve mitochondrial respiratory function, and ultimately improve insulin resistance (Tu et al., 2017; Rhein et al., 2021).
β-cell failure
Insufficient relative or absolute insulin secretion due to an insufficient number of pancreatic ß-cells causes hyperglycemia (Wajchenberg, 2007). Type 2 DM is the result of progressive loss of pancreatic ß-cell number and secretion function (Park et al., 2012). The main mechanism for the decrease in ß-cell numbers is an increase in ß-cell apoptosis rather than a decrease in proliferation or replication (Lupi and Del Prato, 2008). Hu et al. applied H2O2 treatment to NIT-1 cells as a model of pancreatic cell damage and found that RHL increased the expression level of anti-apoptotic protein Bcl-2, decreased the expression level of pro-apoptotic protein Bax, and increased the Bcl-2/Bax ratio, which partially blocked NIT-1 cell apoptosis induced by H2O2 and protected pancreatic ß cells, thus exerting a pancreatic protective effect (Hu et al., 2014). Rhein significantly inhibited the reduction of ß-cell mass and reduced ß-cell apoptosis, which improved the glucose-dependent and glucose-independent secretion of insulin by improving ß-cell function (Du et al., 2012; Liu et al., 2013). The pharmacological mechanisms of rhein in DM are presented in Figure 5.
FIGURE 5. Pharmacological mechanisms of rhein in diabetes mellitus. Rhein maintains glucose homeostasis by anti-inflammation, alleviating renal lesions, improving insulin resistance, improving lipid metabolism, anti-oxidative stress, maintaining mitochondrial respiratory function, improving gut microbiota, and improving β -cell functional. GSK-3 β, Glycogen synthase kinase 3 β; PPAR- γ ,peroxisome proliferator-activated receptor γ ; NF-κ B, nuclear factor kappa-B; HDAC3, histone deacetylase 3; NLRP3, NOD-like receptor thermal protein domain associated protein 3; IL-6, Interleukin-6; IL-1 β ,Interleukin-1 β ; TNF- α ,tumor necrosis factor α ; IKK β ,inhibitor of kappa B kinase β ;Foxo3 α, Forkhead box 03 α ; SIRT1, sirtuin 1; HBP, Hexosamine pathway; TC, Serum total cholesterol; HDL-C,High density liptein cholesterol; TG, triacylglycerol; LDL-C, Low-Density Lipoprotein Cholesterol; VLDL,very low-density lipoprotein; SOD, Superoxide dismutase; CAT,Catalase from micrococcus lysodeiktic; GSH,glutathione,reduced; GSSG, glutathione, oxydized; MDA, malonaldehyde; ROS, reactive oxygen species; Drpl,Dynamin-related protein 1; AMPK,Adenosine 5' -monophosphate (AMP)-activated protein kinase; GLP-1,glucagon-like peptide-1; Bcl-2,B-cell lymphoma-2; BAX,BCL2-Associated X.
Toxicology of rhein
In recent years, increasing adverse reactions due to high doses or long-term administration of rhubarb and its preparations have caused global concern (Wang M et al., 2011; Zeng et al., 2013; Cao et al., 2019). Therefore, it is crucial to determine its toxic components. Studies have shown that rhein exhibits hepatotoxicity and nephrotoxicity (Hu et al., 2019; Yang X et al., 2022). Rhein can inhibit HepaRG cell viability and induce cell death by blocking the S-phase cell cycle and activating the Fas- and mitochondria-mediated apoptotic pathways (You et al., 2018). Rhein affects the accumulation of Rh123 in hepatocyte mitochondria, thereby altering the mitochondrial membrane potential and affecting mitochondrial membrane permeability; mitochondrial dysfunction causes changes in Ca2+ homeostasis and ATP depletion, ultimately leading to cell death (Bironaite and Ollinger, 1997). He et al. found that CYP2C19 could activate rhein to reactive metabolites (RMs), and RMs can covalently bind to intracellular mitochondria, resulting in ROS overproduction, respiratory chain dysfunction, liver function impairment (increased aspartate aminotransferase and lactate dehydrogenase), and cell death. In addition, RM overproduction depletes GSH, leading to hepatotoxicity (He et al., 2015). Mao et al. demonstrated that rhein can induce apoptosis in HK-2 cells by activating caspase-3 and caspase-9, which are involved in the ROS-dependent mitochondrial pathway (Sun et al., 2015; Mao et al., 2017). Rhein induces apoptosis by activating caspase-3 expression, resulting in pathological changes in renal histology, mainly manifested as protein casts in the lumen of renal tubules, capillary congestion in glomeruli and renal interstitium, swelling of renal tubule epithelial cells, and small focal proliferation of lymphocytes (Hu et al., 2019). Repeated administration of rhein for 75 days resulted in obvious steatosis and cell swelling in the liver, as well as varying degrees of inflammation, swelling, and necrosis in the kidney and colon cells, associated with competitive binding of rhein to multidrug resistance-associated protein 2 (MRP2) protein sites. Reduced expression of MRP2 protein blocked cellular oxidative stress substance expulsion, causing increased oxidative stress, impaired mitochondrial function, and stimulation of the release of caspase 3, a downstream factor of apoptosis, thus exhibiting cytotoxicity (Yang, 2022).
Pharmacokinetics of rhein
The HPLC-fluorescence detector method has been used to study the absorption of rhein in rats after oral administration, and the results showed that rhein is mainly distributed in the stomach, kidney, liver, and intestine, had good biocompatibility with them, and could pass the blood-brain barrier (Zhao et al., 2021). Rhein is mainly metabolized by the kidneys. The cumulative excretion rate in urine is 6.0 ± .6% within 24 h after oral administration of 70 mg/kg rhein, and the renal clearance of rhein is 21.3 ± 5.47 mL/h/kg (Hao et al., 2014). In total, 20% of rhein is excreted in its natural form in urine, 60% as thiourea acid ester conjugates, and 20% as sulfates (Dahms et al., 1997). Rhein is the only anthraquinone component of rhubarb that is absorbed into the blood in the human body (Lee et al., 2003).
Takizawa et al., 2003 used HPLC-ultraviolet detection to determine the plasma levels of rhein, which rapidly reached the maximum level after oral administration. In addition, the plasma concentration-time curve revealed secondary peaks, indicating enterohepatic recirculation of rhein. Zhang et al. (2013) used liquid chromatograph mass spectrometer to compare the pharmacokinetics of rhein in rat plasma after oral administration of rhubarb peony decoction (RPD) and rhubarb extract and found that the Cmax of rhein in RPD was significantly lower than that after administration of rhubarb, indicating that the absorption of rhein in rats was inhibited after oral administration of RPD. Hou et al. (2014) applied Ultra-high performance liquid chromatography-tandem mass spectrometry to simultaneously quantify the active ingredients in commercial ready-to-use pharmaceutical herbal products to investigate the pharmacokinetics of rhein, rhubarb, and San-Huang-Xie-Xin-Tang (SHXXT) in rats and found that Cmax and area under the curve (AUC) in the SHXXT group, compared with the rhein administration group, were significantly increased by 17-fold and 9-fold, respectively, indicating that the absorption rate of rhein via SHXXT was significantly higher than that of pure rhein. Based on the pharmacokinetic parameters of rhein, herbal formulations containing different components may have a synergistic or antagonistic effect on rhein absorption. Considering its hepatotoxicity and nephrotoxicity, it is crucial to ensure that herbs rich in rhein are used in the appropriate formulations in TCM.
Researchers have begun to improve the absorption efficiency and bioavailability of rhein by altering the drug delivery route, using liposomes, nanoparticles, solid lipid nanoparticles, polymeric micelles, and hydrogels, among others (Cheng et al., 2021; Li et al., 2022). F127 modified liposomal rhein (F127-RPC-Lip) exhibits longer systemic circulation time, better drug distribution, and reduced pancreatic injury after complexation with lipids via non-covalent interactions. Wei et al. used an emulsification solvent evaporation technique to encapsulate rhein, which has poor water solubility, in mPEG-PLA NPs. RH-NPs significantly increase the plasma AUC of rhein, improve the biological half-life of rhein, increase the circulation time of rhein, and enhance renal permeability (Wei et al., 2017). Rhein (1.5%), Precrol ATO5 (2%), and lecinol (.5%) were prepared by hot homogenization followed by ultrasonication after co-solubilization in a mixture of organic solvent consisting of acetone/ethanol (1:1) to Rhein-SLNs. The AUC0-t of rhein in the case of Rhein-SLNs was 2.06 times higher than that of the suspension group (Feng et al., 2017). DOX/RHE-loaded polymeric micelle, assembled by DSPE -PEG2000 and TPGS1000, released rhein in a rapid and targeted manner until 10 h to increase the distribution of rhein in tumor tissues (Han et al., 2018). Rhein hydrogel, directly self-assembled from rhein via intermolecular π–π interactions and hydrogen bonds, readily binds to Toll-like receptor four and then significantly dephosphorylates IκBα to inhibit the nuclear translocation of p65 in the NF-κB signaling pathway (Zheng et al., 2019). These new delivery systems improve the stability, absorption efficiency, and bioavailability of rhein.
Concluding remarks
The effects of rhein on DM have been studied extensively. Rhein ameliorates IR by inhibiting the overactivity of HBP and the production of inflammatory cytokines through signaling pathways such as those of NF-κB and Wnt/β-catenin. Rhein inhibits ROS overproduction, thereby preventing oxidative stress in cells. It maintains the diversity of the gut microbiota to improve glucose metabolism. Moreover, it improves lipid metabolism, mitochondrial respiratory function, and pancreatic ß-cell function. The toxicology and pharmacokinetics of rhein have been studied in detail. In view of the low bioavailability and solubility of rhein, further structural modification studies can be conducted to search for derivatives with low toxicity and better efficacy that can be better applied in the treatment of DM.
Author contributions
TD and JH: the conception and design of the study. MY: the conception and design of the study and drafting the article. JD: drafting the article. BC, ZW and ZZ: revising the article critically. YY and MY: revising the article. All authors contributed to the article and approved the submitted version.
Funding
This study was financially supported by the Natural Science Foundation of China (No. 82004212), the Key Research and Development Plan of Shandong Province (No. 2019GSF108168, No. 2019LYXZ037), and the Academic Promotion Program of Shandong First Medical University (No. 2019LJ001).
Acknowledgments
Thanks to Plant Photo Bank of China for the figures materials.
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.
Publisher’s note
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Keywords: rhein (PubChem CID: 10168), Rheum palmatum L. (dahuang), diabetes, blood glucose, inflammatory, oxidative stress
Citation: Deng T, Du J, Yin Y, Cao B, Wang Z, Zhang Z, Yang M and Han J (2023) Rhein for treating diabetes mellitus: A pharmacological and mechanistic overview. Front. Pharmacol. 13:1106260. doi: 10.3389/fphar.2022.1106260
Received: 23 November 2022; Accepted: 26 December 2022;
Published: 09 January 2023.
Edited by:
Sadiq Umar, University of Illinois at Chicago, United StatesReviewed by:
Farhath Sultana, Icahn School of Medicine at Mount Sinai, United StatesJatin Tulsulkar, Moffitt Cancer Center, United States
Copyright © 2023 Deng, Du, Yin, Cao, Wang, Zhang, Yang and Han. 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: Meina Yang, bWVpbmE4NjEwMTBAMTYzLmNvbQ==; Jinxiang Han, c2Ftc2hqeEBzaW5hLmNvbQ==
†These authors have contributed equally to this work