Abstract
Metabolic syndrome (MetS), also known as syndrome X, is a significant risk factor for cardiovascular disease incidence and mortality. Increasing age, obesity, physical inactivity, smoking, and positive family history are the risk factors associated with MetS, which increases the risk of diabetes, cardiovascular disease, hypertension, hyperlipidemia, and obesity. Chemical compounds in the treatment of metabolic complications are associated with a lack of efficacy and severe side effects. Numerous studies have described the importance of herbs and natural products to treat human diseases. Therefore, nowadays, herbs-based diets and herbal medicines are recommended for the management of various diseases. The protective effects of several herbs have been reported against MetS such as rosemary, avocado, and silymarin. Eggplant (Solanum melongena) is a rich source of phenolic and alkaloid compounds. It possesses various pharmacological effects, including, anti-oxidant, antidiabetic, antihypertensive, and antihyperlipidemic, which has been supported by numerous investigations. In this review, we evaluated the effects of eggplant on MetS and its complications comprising diabetes, high blood pressure, hyperlipidemia, and obesity.
According to these studies, eggplant can control diabetes through the anti-oxidative properties and inhibition of α-amylase and α-glucosidase activity. Also, eggplant has exerted an antihypertensive effect via ACE inhibitory activity. Eggplant may have shown protective effects on hyperlipidemia and obesity via the induction of lipoprotein lipase activity and the reduction of pancreatic lipase activity.Eggplant can be useful in the treatment of MetS and its complications.
Key Words: Antihypertensive, Antihyperlipidemic, Aubergine, Diabetes, Eggplant, Metabolic syndrome, Solanum melongena
Introduction
Metabolic syndrome (MetS), also known as syndrome X, is not a disease in itself. Instead, patients with metabolic syndrome often develop diabetes, abdominal obesity, hyperlipidemia, and hypertension (1-3). MetS prevalence is the highest among the population over 60 years, and it is increasing among adolescents and children (4). The risk of cardiovascular disease will increase when MetS occurs (5, 6). Since the MetS has a high rate of mortality, thereby, lifestyle modification (calorie restriction, physical activity, and adequate sleep) and pharmacological therapy are essential (7, 8). Several studies have been conducted to assess the impact of medicinal plants or their extracts against MetS and its complications. For instance, in a review study published in 2017, it was concluded that mangosteen might help improve MetS and the quality of life (9). Moreover, rosemary (10), silymarin (11), avocado (12), cinnamon (13), and Abelmoschus esculentus (14) are herbs with protective effects against MetS.
Eggplant (Solanum melongena) is one of the common plants grow all around the world, especially in Asian countries, the Middle East, and around the Mediterranean basin (15, 16). Eggplant belongs to the Solanaceae family and the genus Solanum (17). Based on the fruit shape, eggplant has been classified into three types including, egg-shaped, long slender shape, and dwarf types (18). It also has known as aubergine and it is an important source of fiber, minerals (iron, calcium, potassium, magnesium, sodium, zinc, and phosphorus), vitamins C, thiamin, niacin, B6, B12, A, E, D, and K (19). Eggplant has been used in the treatment of several diseases, including asthma, bronchitis, diabetes, arthritis, and hypercholesterolemia (20, 21). The clinical use of eggplant is due to its phenolic and alkaloid contents (16). The delphinidin (an anthocyanin) and chlorogenic acid (a phenolic acid) are the main phenolic compounds in the skin and pulp of eggplant (18) (Figure 1).
Figure 1.
The structure of the main compounds in the skin, pulp, and root of eggplant
It has been reported that delphinidin can induce endothelial vasodilation by the activation of the nitric oxide (NO) pathway (22). Delphinidin also has shown antihypertensive effects via interrupting the renin (an aspartyl protease)-angiotensin system (RAS) signaling pathway (23). The overactivation of this system is one of the most important risk factors for the development of hypertension (24). Delphinidin reduces the expression and activation of the angiotensin-converting enzyme (ACE) (23). α-Amylase, as an enzyme in saliva and pancreas, plays an essential role in carbohydrate digestion. The inhibition of salivary and pancreatic α-amylase enzymes can reduce glucose uptake (25). Moreover, delphinidin has exhibited inhibitory properties against the α-amylase enzyme, and thereby it may be useful in the treatment of diabetes and its complications such as overweight and obesity, and cardiovascular disease (26).
Chlorogenic acid has been found to enhance NO status, improve endothelial function, and lower blood pressure (27). Also, chlorogenic acid has shown beneficial effects on type 2 diabetes mellitus by increasing the translocation of glucose transporter 4 (GLUT4) to the plasma membrane, enhancing glucose transport to skeletal muscle, and inhibiting gluconeogenesis, besides delaying intestinal glucose absorption (28). It has been suggested that chlorogenic acids exhibit anti-obesity and antihyperlipidemic activities by alleviating the levels of free fatty acids and triglycerides (TG) (29). Additionally, several studies have reported the pharmacologic aspects of eggplant, such as anti-oxidant (30), anti-inflammatory (31), antibacterial (32), antifungal (33), antidiabetic (34), antihypertensive (35), anti-obesity (36), hepatoprotective (37), and hypolipidemic (38) properties. Thus, the purpose of this study is to review the effects of eggplant on MetS.
In this review, various databases such as PubMed, Scopus, and Google Scholar have been involved. All the articles that have been chosen in this review were collected from the date of inception up to May 2020. The search keywords contained “eggplant”, “Solanum melongena”, “aubergine”, “metabolic syndrome”, “diabetes”, “hyperglycemia”, “insulin”, “hypoglycemic”, “antihyperglycemic”, “antidiabetic”, “blood glucose”, “hypertension”, “blood pressure”, “hypotensive”, “antihypertensive”, “dyslipidemia”, “hyperlipidemia”, “high cholesterol”, “high triglyceride”, “hypercholesterolemia”, “hypertriglyceridemia”, “atherogenic”, “atherosclerosis”, “obesity”, “overweight”, “appetite”, “anti-obesity” and “weight loss”.
Effects of eggplant on diabetes
Diabetes is a common metabolic disorder identified by abnormally high blood glucose levels and the insufficiency of secretion or function of endogenous insulin (39, 40). It is leading to major complications, such as diabetic retinopathy (41), neuropathy (42), nephropathy (43), micro-angiopathy (44), and cardiovascular diseases (45). It has been reported that several natural compounds such as green tea and garlic have improved health status in diabetes patients (46, 47). A study has investigated the efficacy of methanol extract of African eggplant leaves (100, 200, and 300 mg/kg, orally for 20 days) on alloxan-induced diabetes in rats. The results of this study showed that eggplant reduces high blood glucose levels in diabetic rats (48). The main mechanisms in the pathogenesis and progression of diabetes are free radicals production and oxidative stress. Oxidative stress can increase the development of diabetes-related complications including cardiovascular disease, neuropathy, and kidney disease (49). A significant protective pathway against oxidative stress is the activation of the nuclear erythroid 2-related factor 2 (Nrf2)/ anti-oxidant response element (ARE) signaling pathway. Nrf2 is a transcription factor that binds to the ARE and thereby up-regulates the anti-oxidant gene expression such as superoxide dismutase (SOD) and heme oxygenase-1 (HO-1) (50). The protein kinase C (PKC) and Kelch-like ECH-associated protein 1 (Keap1) are intracellular redox sensors. Under basal conditions, Keap1 inhibits the Nrf2/ARE signaling pathway through direct interaction with Nrf2. Under oxidative stress conditions, elevated ROS interacts with cysteine residues of Keap1 and dissociate it from Nrf2. ROS also regulate PKC activity and result in the phosphorylation and activation of Nrf2. Then Nrf2 translocates from the cytoplasm into the nucleus and induces the expression of the anti-oxidant enzyme genes such as SOD, heme oxygenase-1 (HO-1), and NAD (P) H quinone oxidoreductase 1 (NOQ1) (51). The imbalance between ROS production and anti-oxidant enzyme expression leads to β-cell dysfunction and insulin resistance (51, 52). Therefore, the Nrf2 signaling pathway is able to act as a potential therapeutic target in diabetes. Another study has reported that purple eggplant contains anthocyanin compounds that exerted anti-oxidant properties. The effect of the aqueous extract of purple eggplant (343, 686, and 1372 mg/kg, orally, for 14 days) has investigated on alloxan-induced diabetes (150 mg/kg, IP) in rats. The results of this study have shown that the extract of eggplant (686 and 1372 mg/kg) reduced the level of serum malondialdehyde (MDA) in diabetic rats (53). Several enzymes are involved in the absorption of glucose in the digestive organs, such as α-glucosidase (α-d-glucoside glucohydrolase) and α-amylase (α-1, 4-glucan-4- glucanohydrolases). α-glucosidase acts as the key enzyme in catalyzing the final level of carbohydrates digestion. Inhibiting these enzymes can delay glucose absorption and slows the elevation of blood glucose levels (54).
Numerous studies have reported that different phytochemicals can inhibit α-glucosidase activity (55-57). The phenolic, glycoalkaloids, and carotenoids compounds are found abundantly in eggplants (19). α-Amylase is secreted by the pancreas and salivary glands and plays an essential role in the digestion of starch and glycogen (58). Eggplant is an important source of flavonoids and has the potential to inhibit α-amylase activity (58, 59). A study has compared the total soluble phenolic content of the pulp and skin of eggplant varieties, including Purple, White, Graffiti, and Italian eggplants. This study has reported that the skin aqueous extract of Italian eggplant has the highest soluble phenolic content. Moreover, the results of this study exhibited that the skin of Italian eggplant had the highest anti-oxidant activity, followed by the pulp extract of White, Graffiti, and Purple. Also, the pulp and skin extracts of eggplant have shown an inhibitory effect on the intestinal α-glucosidase, except the Italian variety. Additionally, this study suggests that the eggplant varieties were moderate α-amylase inhibitors, except for Graffiti pulp (60). Therefore, eggplant has the potential to reduce glucose absorption in the intestine. An in vitro study has investigated the inhibitory effects of two eggplant species (S. melongena and S. macrocarpon) on starch hydrolyzing enzymes. The results of this study showed that the phenolic content of S. macrocarpon is higher than S. melongena extract and the methanolic extracts of both species inhibited α-glucosidase activity more than α-amylase activity in a dose-dependent manner (59). In another assessment, six phenolic compounds of the root of S. melongena were isolated (N-trans-feruloyl tyramine, N-trans-p-coumaroyl tyramine, N-cis-p-coumaroyl tyramine, Ferul aldehyde, 6, 7-Dimethoxycoumarin, and Ficusal) (Figure 1) and the inhibitory effect of these compounds against α-glucosidase was evaluated. The results of this study have shown that N-trans-feruloyl tyramine, N-trans-p-coumaroyl tyramine, and N-cis-p-coumaroyl tyramine have the highest inhibitory impact, besides Ferul aldehyde, 6,7-Dimethoxycoumarin, and Ficusal did not show any inhibitory activity (61).
Generally, these studies revealed that eggplant could manage/prevent diabetes and its complications through the anti-oxidative properties and inhibition of α-amylase and α-glucosidase activity (Figure 2).
Figure 2.
Main mechanisms of eggplant on high blood pressure, high blood glucose, and lipid levels
Effect of eggplant on high blood pressure
High blood pressure (BP), a common chronic condition, is created by the high force of the blood against artery walls and vascular dysfunction, which indirectly induces the risk of cardiovascular disease and type 2 diabetes (62, 63). The RAS plays a vital role in the regulation of body fluid volume and BP. Under physiological conditions, kidneys release renin into the circulation and convert angiotensinogen which is released from the liver to angiotensin I. Then, angiotensin I is converted to angiotensin II via the action of ACE, which bonds to the endothelium. Angiotensin II acts as a potent vasoconstrictor and regulates BP. Also, ACE can metabolize bradykinin (a vasodilator) and regulates BP. Therefore, the blockade of the RAS by ACE inhibitors is effective in managing high BP (64). To date, several natural compounds are identified to be effective in the treatment of high BP, such as rosemary and saffron (10, 65). A document compared ACE inhibitory activity of the pulp and skin of eggplant varieties, including Purple, White, Graffiti, and Italian eggplants. The pulp extract of White showed the highest ACE inhibitory activity in a dose-dependent manner, followed by the skin extract of White and pulp extract of Graffiti. The inhibition of this enzyme provides a robust biochemical basis for the management of high BP (60). Acetylcholine (ACh) is an endothelial-dependent vasodilator, which plays a significant role in the reduction of the pathogenesis of hypertension. Following the stimulation of muscarinic receptors located on the vascular endothelium by ACh, nitric oxide (NO) is released. NO relaxes arterial smooth muscle and causes a fall in arterial blood pressure (66).
S. melongena contains abundant ACh and can exert an antihypertensive effect. Also, it has been reported that oral administration of S. melongena (0.0650 and 0.821 mg/kg, for 28 days) reduced systolic blood pressure (SBP) and diastolic blood pressure (DBP) levels by ACh in rat thoracic aorta rings (67). The sympathetic nervous system (SNS) and the adrenal medulla play a significant role in BP regulation via the release of epinephrine and norepinephrine (68, 69). On the other hand, the excessive release of epinephrine and norepinephrine results in increased vascular resistance, cardiac contractility, and cardiac output (70). A study on the effect of aqueous extract of eggplant (0.001 to 1 mg/ml) on norepinephrine-stimulated guinea pig atria has shown that eggplant decreased the high BP probably via decreasing the cardiac output and myocardial contractility (71).
In these studies, ACh has been introduced as the main compound responsible for the antihypertensive effect of eggplant. Also, eggplant has exerted an antihypertensive effect via ACE inhibitory activity. Therefore, eggplant has been suggested as useful food for the management of hypertension and its complications in daily life (Figure 2).
Effect of eggplant on hyperlipidemia
Hyperlipidemia is abnormally elevated levels of lipids, including fat, cholesterol, and TGs in the blood, which is commonly known as the main risk factor for cardiovascular disease and is one of the leading causes of mortality worldwide (72, 73). Eggplant is rich in dietary fiber and possibility can positively modify the lipid profile, including total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), very low-density lipoprotein cholesterol (VLDL-C), total triglyceride (TG), in addition to apolipoprotein (Apo) A and B (74). In a clinical study, the influence of eggplant on lipid profile (TC, TC, LDL-C, HDL-C, and TG) was examined in 19 healthy subjects with a mean age of 26 years (11 females and 8 males) for three weeks. The obtained results revealed that 200 ml orange juice with fresh unpeeled eggplant did not modify lipid profiles in the study population (75). In another research, the effects of ingesting eggplant infusion on TC and TG in the serum of 38 hypercholesterolemic patients with the mean age of 43.7 years were assessed for five weeks. The results of this study displayed that eggplant has a modest and transitory effect on the parameters analyzed, including TC, LDL-C, HDL-C, VLDL-C, TG, Apo A, and Apo B (21). Furthermore, the effect of eggplant on serum lipid profile with lovastatin was compared in 21 individuals (both sexes) with TC levels of more than 200 mg/dl. In this study, eggplant did not show a significant effect on TC, LDL-C, and HDL-C levels after six weeks. Therefore, eggplant cannot be considered as an alternative to lovastatin in decreasing cholesterol serum levels (76). Additionally, the effects of eggplant (capsules 450 mg of dried powdered fruits, twice daily, for three months) were evaluated on 41 hyperlipidemic patients. The data revealed that eggplant decreased the serum levels of TC and LDL-C (77).
In an animal study, the influence of eggplant on cholesterol metabolism in rats fed with diets containing 1 % eggplant has been reported. The results illustrated that the leaf and fruit of eggplant could not lower the cholesterol pool of the serum and liver in rats. However, it was reported that eggplant reduced the absorption of a single dietary dose of cholesterol, probably via binding the bile salts to cholesterol (78). Besides, the effect of eggplant (free access to extract, orally, for 12 weeks) on cholesterol metabolism and atherosclerosis has been studied in LDL receptor knockout mice. In this study, eggplant did not decrease total cholesterol and atherogenic lipoprotein levels (79). In another study, the hypolipidemic effect of the isolated flavonoids from eggplant (dose of 1 mg/100 g BW, orally) was tested in cholesterol-fed rats. It was observed that eggplant stimulated lipoprotein lipase activity, and attenuated the concentration of TG in serum. Moreover, eggplant decreased serum cholesterol concentration and triggered 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase activity (80). HMG-CoA reductase is an enzyme in the liver that catalyzes the formation of cholesterol from HMG-CoA (81). Therefore, it might be suggested that eggplant reduced cholesterol levels via some other mechanisms, including the enhancement rate of degradative processes of elimination of cholesterol and the effective reduction in its absorption from the intestine (82). Also, the effects of eggplant (a diet containing 61.62%, orally, for 28 days) on serum and hepatic TC and TG have been investigated in cholesterol-fed rats. It was indicated that eggplant aqueous extract decreased hepatic TC, while it had little effect on serum and hepatic TG (83). In rats treated by the high-fat diet, assessing the effect of eggplant peels powder (a diet containing 4 % eggplant for four weeks) on lipid profiles revealed that eggplant modified TC, LDL-C, HDL-C, and VLDL-C levels (84). Administration of methanol extract of African eggplant leaves (100, 200, and 300 mg/kg, orally) to diabetic rats resulted in a significant reduction in the TC, LDL-C, HDL-C, and TG values (48). Also, the eggplant core reduced the plasma concentration of TC, LDL-C, and HDL-C in guinea pigs fed a hypercholesterolemic diet (85). In an experiment in hypercholesterolemic rabbits, the treatment of 10 ml eggplant juice daily for 2 weeks significantly reduced weight and plasma cholesterol levels (86).
Generally, in these studies, the possible mechanisms of action of eggplant on cholesterol metabolism and lipid profile have not been clarified. Since the eggplant has induced HMG-CoA reductase activity, eggplant may have shown protective effects on hyperlipidemia via the enhancement rate of degradative processes of cholesterol or induction of lipoprotein lipase activity, and the effective reduction in lipids absorption from the intestine (Figure 2). Although experimental animal studies have demonstrated the hypolipidemia effect of eggplant, clinical studies suggested a small transient effect of eggplant on hyperlipidemia, which might be due to the small number of individuals in studies and the use of low eggplant doses to induce hypolipidemic effects.
Effect of eggplant on obesity
Obesity is a medical problem in which excess body fat has accumulated to the extent that it may harm health and is defined by body mass index (BMI), an indicator of the measure of high body fatness (87, 88). It acts as a risk factor for several diseases such as type 2 diabetes (89), hypertension (90), cardiovascular (91), and respiratory diseases (92). The anti-oxidant status and ROS formation are involved in metabolic disorders associated with obesity (93). Several studies have shown that the plasma levels of anti-oxidant markers (SOD, GSH) are decreased in obese patients (93-95). The anti-oxidant compounds are used in the treatment of obesity and its complications (96, 97). The pancreatic lipase acts as a key enzyme in intestinal fat digestion. Therefore, pancreatic lipase inhibitors such as saponins and phenolic compounds might be introduced as therapeutic targets in controlling obesity (98-100). An in vitro study investigated the inhibitory effect of eggplant on pancreatic lipase activity. The saponins isolated from the methanol extract of eggplant have shown an inhibitory effect on porcine pancreatic lipase activity (the titrimetric method) (Figure 1) (101).
A randomized clinical trial has reported the effects of eggplant flour (13 g, orally) on anti-oxidant status and body fat in 97 overweight women (the mean age of 47.5 years) for four months. This study has shown that eggplant increased the anti-oxidant capacity in plasma and reduced the body fat mass in volunteers (36).
Because eggplant has the potential to reduce pancreatic lipase activity (Figure 2), future studies can investigate the anti-obesity effects of eggplant.
Table 1.
The protective effects of eggplant on metabolic syndrome
Pharmacological effects | Compound | Study design | Results | Ref |
---|---|---|---|---|
Anti-diabetic | Leaves, 100, 200, and 300 mg/kg, orally, for 20 days | Rats, alloxan | ↓BG | (48) |
Aqueous extract of purple eggplant, 343, 686, and 1372 mg/kg, orally, for 14 days | Rats, alloxan | ↓BG | (53) | |
Skin and pulp aqueous extracts | In vitro | ↓Oxidative stress ↓α-glucosidase activity |
(60) | |
Methanolic extracts | In vitro | ↓α-glucosidase activity ↓α-amylase activity |
(59) | |
Root ethanolic extract | In vitro | ↓α-glucosidase activity | (61) | |
Anti-hypertensive | Skin and pulp aqueous extracts | In vitro | ↓ACE activity | (60) |
Calyx, 0.0650 and 0.821 mg/kg, orally | Spontaneously hypertensive rats | ↓BP | (67) | |
Unripe fruits aqueous extracts | Guinea pig atria, norepinephrine | ↓BP | ||
Anti-hyperlipidemic | 2% (w/v) infusion | Human (11 men and 27 women), a RCT | ↓TC and LDL-C levels ↓Apo B |
(21) |
The eggplant and orange blended juice | Human (8 men and 11 women), a RCT | Lipid profile was not modified | (75) | |
_ | Human (9 men and 12 women) | Lipid profile was not modified | (76) | |
Capsules 450 mg | Human (41 women), a double-blind placebo-controlled study | ↓TC and LDL-C levels | (77) | |
Leaf or fruit powder | Rats | Lipid profile was not modified ↓Absorption of cholesterol |
(78) | |
Fruit aqueous extract | LDL receptor knock out mice | Lipid profile was not modified | (79) | |
1 mg/100 g bw, orally | Cholesterol-fed rats | ↑lipoprotein lipase activity ↓TG and TC levels ↑ HMG CoA reductase activity |
(80) | |
Aqueous extract | Cholesterol-fed rats | ↓TC | (83) | |
Peels | High fat-diet in rats | ↓TC, LDL-C, HDL-C, and VLDL-C levels | (84) | |
Leaves, 100, 200, and 300 mg | Rats, alloxan | ↓TC, LDL-C, HDL-C, and VLDL-C levels | (48) | |
Core | Hypercholesterolemic guinea pigs | ↓TC, LDL-C, and HDL-C levels | (85) | |
Fruit juice/day, for 2 weeks | Hypercholesterolemic rabbits | ↓TC, LDL-C, and HDL-C levels | (86) | |
Anti-obesity | Flour | Human(97 women), a RCT | ↓Oxidative stress ↓Body fat ↓Waist circumference |
(36) |
Methanolic extracts | In vitro | ↓Pancreatic lipase activity | (101) |
ACE: angiotensin-converting enzyme; Apo B: apolipoprotein B; BG: blood glucose; BP: blood pressure; HDL-C: high- density lipoprotein cholesterol; HMG CoA: 3-hydroxy-3-methylglutaryl-coenzyme A; LDL-C: low-density lipoprotein cholesterol; RCT: randomized clinical trial; TC: total cholesterol; TG: triglyceride
Conclusion
Metabolic syndrome is characterized by the co-occurrence of multiple changes in high blood glucose, hypertension, hyperlipidemia, and obesity, correlated with an enhanced risk of developing cardiovascular diseases and mortality. Eggplant (S. melongena) can be useful in the treatment of MetS and its complications due to possessing delphinidin (an anthocyanin), and chlorogenic acid (a phenolic acid). There have been several studies reporting that eggplant has antidiabetic properties because of its anti-oxidant effects and lowering the absorption of glucose in the digestive organs via inhibiting α-glucosidase and α-amylase activity.
On the other hand, eggplant contains abundant ACh and can act as an antihypertensive agent. Also, eggplant inhibits ACE activity and thereby can reduce high blood pressure. Clinical and animal studies have documented that eggplant has little effect on the lipid profile. Nevertheless, its inhibitory effect on pancreatic lipase activity and anti-obesity effect of eggplant have been shown.
Generally, eggplant has shown protective effects on MetS and its complications. However, further studies on the most representative compounds of eggplant are necessary to deeply understand the mechanisms of action of this plant.
Acknowledgment
The authors are thankful to Mashhad University of Medical Sciences, Mashhad, Iran.
Conflicts of Interest
The authors express no conflict of interest.
References
- 1.Obunai K, Jani S, Dangas GD. Cardiovascular morbidity and mortality of the metabolic syndrome. Med Clin North Am. 2007;91:1169–1184. doi: 10.1016/j.mcna.2007.06.003. [DOI] [PubMed] [Google Scholar]
- 2.Sanati S, Razavi BM, Hosseinzadeh H. A review of the effects of Capsicum annuum L and its constituent, capsaicin, in metabolic syndrome. Iran J Basic Med Sci. 2018;21:439–448. doi: 10.22038/IJBMS.2018.25200.6238. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Mahdian D, Abbaszadeh-Goudarzi K, Raoofi A, Dadashizadeh G, Abroudi M, Zarepour E, et al. Effect of Boswellia species on the metabolic syndrome: a review. Iran J Basic Med Sci. 2020;23:1374–1381. doi: 10.22038/ijbms.2020.42115.9957. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Zimmet P, Alberti G, Kaufman F, Tajima N, Silink M, Arslanian S, et al. The metabolic syndrome in children and adolescents. Lancet. 2007;369:2059–2061. doi: 10.1016/S0140-6736(07)60958-1. [DOI] [PubMed] [Google Scholar]
- 5.Bray GA, Bellanger T. Epidemiology, trends, and morbidities of obesity and the metabolic syndrome. Endocrine. 2006;29:109–117. doi: 10.1385/ENDO:29:1:109. [DOI] [PubMed] [Google Scholar]
- 6.Eisvand F, Razavi BM, Hosseinzadeh H. The effects of Ginkgo biloba on metabolic syndrome: a review. Phytother Res. 2020;34:1798–1811. doi: 10.1002/ptr.6646. [DOI] [PubMed] [Google Scholar]
- 7.Takahara M, Shimomura I. Metabolic syndrome and lifestyle modification. Rev Endocr Metab Disord. 2014;15:317–327. doi: 10.1007/s11154-014-9294-8. [DOI] [PubMed] [Google Scholar]
- 8.Koren D, Dumin M, Gozal D. Role of sleep quality in the metabolic syndrome. Diabetes Metab Syndr Obes. 2016;9:281–310. doi: 10.2147/DMSO.S95120. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Tousian Shandiz H, Razavi BM, Hosseinzadeh H. Review of Garcinia mangostana and its xanthones in metabolic syndrome and related complications. Phytother Res. 2017;31:1173–1182. doi: 10.1002/ptr.5862. [DOI] [PubMed] [Google Scholar]
- 10.Hassani FV, Shirani K, Hosseinzadeh H. Rosemary (Rosmarinus officinalis) as a potential therapeutic plant in metabolic syndrome: a review. Naunyn-Schmiedeberg’s Arch Pharmacol. 2016;389:931–949. doi: 10.1007/s00210-016-1256-0. [DOI] [PubMed] [Google Scholar]
- 11.Vahabzadeh M, Amiri N, Karimi G. Effects of silymarin on metabolic syndrome: a review. J Sci Food Agr. 2018;98:4816–4823. doi: 10.1002/jsfa.9115. [DOI] [PubMed] [Google Scholar]
- 12.Tabeshpour J, Razavi BM, Hosseinzadeh H. Effects of avocado (Persea americana) on metabolic syndrome: a comprehensive systematic review. Phytother Res. 2017;31:819–837. doi: 10.1002/ptr.5805. [DOI] [PubMed] [Google Scholar]
- 13.Mollazadeh H, Hosseinzadeh H. Cinnamon effects on metabolic syndrome: A review based on its mechanisms. Iran J Basic Med Sci. 2016;19:1258–1270. doi: 10.22038/ijbms.2016.7906. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Esmaeilzadeh D, Razavi BM, Hosseinzadeh H. Effect of Abelmoschus esculentus (okra) on metabolic syndrome: A review. Phytother Res. 2020;34:2192–2202. doi: 10.1002/ptr.6679. [DOI] [PubMed] [Google Scholar]
- 15.Cericola F, Portis E, Toppino L, Barchi L, Acciarri N, Ciriaci T, et al. The population structure and diversity of eggplant from Asia and the Mediterranean basin. PLoS One. 2013;8:e73702. doi: 10.1371/journal.pone.0073702. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Daunay MC. Vegetables II. New York: Springer; 2008. Eggplant; pp. 163–220. [Google Scholar]
- 17.Sukprasansap M, Sridonpai P, Phiboonchaiyanan PP. Eggplant fruits protect against DNA damage and mutations. Mutat Res. 2019;813:39–45. doi: 10.1016/j.mrfmmm.2018.12.004. [DOI] [PubMed] [Google Scholar]
- 18.Niño-Medina G, Urías-Orona V, Muy-Rangel MD, Heredia JB. Structure and content of phenolics in eggplant (Solanum melongena) - a review. S Afr J Bot. 2017;111:161–169. [Google Scholar]
- 19.Gürbüz N, Uluişik S, Frary A, Frary A, Doğanlar S. Health benefits and bioactive compounds of eggplant. Food Chem. 2018;268:602–610. doi: 10.1016/j.foodchem.2018.06.093. [DOI] [PubMed] [Google Scholar]
- 20.Magioli C, Mansur E. Eggplant (Solanum melongena L ): tissue culture, genetic transformation and use as an alternative model plant. Acta Bot Bras. 2005;19:139–148. [Google Scholar]
- 21.Guimarães P, Galvão A, Batista C, Azevedo G, Oliveira R, Lamounier R, et al. Eggplant (Solanum melongena) infusion has a modest and transitory effect on hypercholesterolemic subjects. Braz J Med Biol Res. 2000;33:1027–1036. doi: 10.1590/s0100-879x2000000900006. [DOI] [PubMed] [Google Scholar]
- 22.Patel K, Jain A, Patel DK. Medicinal significance, pharmacological activities, and analytical aspects of anthocyanidins ‘delphinidin’: a concise report. J Acute Dis. 2013;2:169–178. [Google Scholar]
- 23.Parichatikanond W, Pinthong D, Mangmool S. Blockade of the renin-angiotensin system with delphinidin, cyanin, and quercetin. Planta Med. 2012;78:1626–1632. doi: 10.1055/s-0032-1315198. [DOI] [PubMed] [Google Scholar]
- 24.Gonzalez AA, Salinas-Parra N, Cifuentes-Araneda F, Reyes-Martinez C. Vasopressin actions in the kidney renin angiotensin system and its role in hypertension and renal disease. Vitam Horm. 2020;113:217–238. doi: 10.1016/bs.vh.2019.09.003. [DOI] [PubMed] [Google Scholar]
- 25.Morais FS, Canuto KM, Ribeiro PR, Silva AB, Pessoa OD, Freitas CD, et al. Chemical profiling of secondary metabolites from Himatanthus drasticus (Mar Plumel latex with inhibitory action against the enzymes α-amylase and α-glucosidase: invitro and in silico assays. J Ethnopharmacol. 2020;253:112644–112652. doi: 10.1016/j.jep.2020.112644. [DOI] [PubMed] [Google Scholar]
- 26.Demir Y, Durmaz L, Taslimi P, Gulçin İ. Antidiabetic properties of dietary phenolic compounds: inhibition effects on α-amylase, aldose reductase, and α-glycosidase. Biotechnol Appl Biochem. 2019;66:781–786. doi: 10.1002/bab.1781. [DOI] [PubMed] [Google Scholar]
- 27.Mubarak A, Bondonno CP, Liu AH, Considine MJ, Rich L, Mas E, et al. Acute effects of chlorogenic acid on nitric oxide status, endothelial function, and blood pressure in healthy volunteers: a randomized trial. J Agr Food Chem. 2012;60:9130–9136. doi: 10.1021/jf303440j. [DOI] [PubMed] [Google Scholar]
- 28.Ong KW, Hsu A, Tan BKH. Chlorogenic acid stimulates glucose transport in skeletal muscle via AMPK activation: a contributor to the beneficial effects of coffee on diabetes. PloS One. 2012;7:32718–32729. doi: 10.1371/journal.pone.0032718. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Sudeep H, Venkatakrishna K, Patel D, Shyamprasad K. Biomechanism of chlorogenic acid complex mediated plasma free fatty acid metabolism in rat liver. BMC Complement Altern Med. 2016;16:274–279. doi: 10.1186/s12906-016-1258-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Kaur C, Kapoor HC. Anti-oxidant activity and total phenolic content of some Asian vegetables. Int J Food Sci Tech. 2002;37:153–161. [Google Scholar]
- 31.Im K, Lee JY, Byeon H, Hwang KW, Kang W, Whang WK, et al. Invitro anti-oxidative and anti-inflammatory activities of the ethanol extract of eggplant (Solanum melongena) stalks in macrophage RAW 264 7 cells. Food Agr Immunol. 2016;27:758–771. [Google Scholar]
- 32.Gubarev MI, Enioutina EY, Taylor JL, Visic DM, Daynes RA. Plant-derived glycoalkaloids protect mice against lethal infection with Salmonella typhimurium. Phytother Res. 1998;12:79–88. [Google Scholar]
- 33.Das J, Lahan J, Srivastava R. Solanum melongena: a potential source of antifungal agent. Indian J Microbiol. 2010;50:62–69. doi: 10.1007/s12088-010-0004-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Qonita NR, Zulhaidah M, Tjahjono HA. The effect of eggplant (Solanum melongena L ) extract peroal against blood glucose level of white rat (Ratus novergicus) wistar strain diabetic model. Int J Pediatr Endocrinol. 2013;2013:O33. [Google Scholar]
- 35.Yamaguchi S, Matsumoto K, Koyama M, Tian S, Watanabe M, Takahashi A, et al. Antihypertensive effects of orally administered eggplant (Solanum melongena) rich in acetylcholine on spontaneously hypertensive rats. Food Chem. 2019;276:376–382. doi: 10.1016/j.foodchem.2018.10.017. [DOI] [PubMed] [Google Scholar]
- 36.Scorsatto M, Rosa G, Raggio Luiz R, da Rocha Pinheiro Mulder A, Junger Teodoro A, Moraes de Oliveira GM. Effect of eggplant flour (Solanum melongena associated with hypoenergetic diet on anti-oxidant status in overweight women-a randomised clinical trial. Int J Food Sci Technol. 2019;54:2182–2189. [Google Scholar]
- 37.Komara N, Sastramihardja H, Afiati A. Hepatoprotective effect of Solanum melongena/eggplant against acute hepatitis. Althea Med J. 2015;2:68–72. [Google Scholar]
- 38.Audu A, Egwim EC, Adeyemi HY. Hypolipidemic properties of four varieties of eggplants (Solanum melongena L ) Int J Pharma Sci Invent. 2014;3:47–54. [Google Scholar]
- 39.Cohrs CM, Panzer JK, Drotar DM, Enos SJ, Kipke N, Chen C, et al. Dysfunction of persisting β cells is a key feature of early type 2 diabetes pathogenesis. Cell Rep. 2020;31:107469–107482. doi: 10.1016/j.celrep.2020.03.033. [DOI] [PubMed] [Google Scholar]
- 40.Dehghani S, Mehri S, Hosseinzadeh H. The effects of Crataegus pinnatifida (Chinese hawthorn) on metabolic syndrome: a review. Iran J Basic Med Sci. 2019;22:460–468. doi: 10.22038/IJBMS.2019.31964.7678. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Wang W, Liu S, Qiu Z, He M, Wang L, Li Y, et al. Choroidal thickness in diabetes and diabetic retinopathy: a swept source OCT study. Investig Ophthalmol Vis Sci. 2020;61:29–38. doi: 10.1167/iovs.61.4.29. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Pop-Busui R, Boulton AJ, Feldman EL, Bril V, Freeman R, Malik RA, et al. Diabetic neuropathy: a position statement by the american diabetes association. Diabetes Care. 2017;40:136–154. doi: 10.2337/dc16-2042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Umanath K, Lewis JB. Update on diabetic nephropathy: core curriculum 2018. Am J Kidney Dis. 2018;71:884–895. doi: 10.1053/j.ajkd.2017.10.026. [DOI] [PubMed] [Google Scholar]
- 44.Huang L, Xie Y, Dai S, Zheng H. Neutrophil-to-lymphocyte ratio in diabetic microangiopathy. Int J Clin Exp Pathol. 2017;10:1223–1232. [Google Scholar]
- 45.Xie X-r, Yan L-z, Bai X-s. Peripheral neuropathy and the risk of cardiovascular events in type 2 diabetes mellitus. Heart. 2014;100:1837–1843. doi: 10.1136/heartjnl-2014-305657. [DOI] [PubMed] [Google Scholar]
- 46.Razavi BM, Lookian F, Hosseinzadeh H. Protective effects of green tea on olanzapine-induced-metabolic syndrome in rats. Biomed Pharmacother. 2017;92:726–731. doi: 10.1016/j.biopha.2017.05.113. [DOI] [PubMed] [Google Scholar]
- 47.Hosseini A, Hosseinzadeh H. A review on the effects of Allium sativum (Garlic) in metabolic syndrome. J Endocrinol Investig. 2015;38:1147–1157. doi: 10.1007/s40618-015-0313-8. [DOI] [PubMed] [Google Scholar]
- 48.Onuora EEO, Okafor CN. Efficacy of extracts of African eggplant and Okra leaves on alloxan-induced diabetes mellitus adult male albino rats. Pak J Nutr. 2016;15:551–555. [Google Scholar]
- 49.Maritim AC, Sanders RA, Watkins J. Diabetes, oxidative stress, and anti-oxidants: a review. J Biochem Mol Toxicol. 2003;17:24–38. doi: 10.1002/jbt.10058. [DOI] [PubMed] [Google Scholar]
- 50.Wang H, Liu K, Geng M, Gao P, Wu X, Hai Y, et al. RXRα inhibits the NRF2-ARE signaling pathway through a direct interaction with the Neh7 domain of NRF2. Cancer Res. 2013;73:3097–3108. doi: 10.1158/0008-5472.CAN-12-3386. [DOI] [PubMed] [Google Scholar]
- 51.Zhang P, Li T, Wu X, Nice EC, Huang C, Zhang Y. Oxidative stress and diabetes: anti-oxidative strategies. Front Med. 2020;14:583–600. doi: 10.1007/s11684-019-0729-1. [DOI] [PubMed] [Google Scholar]
- 52.Kaneto H, Nakatani Y, Kawamori D, Miyatsuka T, Matsuoka T-a, Matsuhisa M, et al. Role of oxidative stress, endoplasmic reticulum stress, and c-Jun N-terminal kinase in pancreatic β-cell dysfunction and insulin resistance. Int J Biochem Cell Biol. 2005;37:1595–1608. doi: 10.1016/j.biocel.2005.04.003. [DOI] [PubMed] [Google Scholar]
- 53.Nugraheni ES, Tjahjono HA. Extracts giving of purple eggplant (Solanum melongena L ) orally can lower blood serum levels of malondialdehide of white rat (Rattus novergicus) wistar diabetes mellitus induced by aloxan. Int J Pediatr Endocrinol. 2013;2013:O48. [Google Scholar]
- 54.Kumar S, Narwal S, Kumar V, Prakash O. α-glucosidase inhibitors from plants: a natural approach to treat diabetes. Pharmacogn Rev. 2011;5:19–29. doi: 10.4103/0973-7847.79096. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Brown A, Anderson D, Racicot K, Pilkenton SJ, Apostolidis E. Evaluation of phenolic phytochemical enriched commercial plant extracts on the invitro inhibition of α-glucosidase. Front Nutr. 2017;4:56–64. doi: 10.3389/fnut.2017.00056. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Ifie I, Ifie BE, Ibitoye DO, Marshall LJ, Williamson G. Seasonal variation in Hibiscus sabdariffa (Roselle) calyx phytochemical profile, soluble solids and α-glucosidase inhibition. Food Chem. 2018;261:164–168. doi: 10.1016/j.foodchem.2018.04.052. [DOI] [PubMed] [Google Scholar]
- 57.Ifie I, Abrankó L, Villa-Rodriguez JA, Papp N, Ho P, Williamson G, et al. The effect of ageing temperature on the physicochemical properties, phytochemical profile and α-glucosidase inhibition of Hibiscus sabdariffa (roselle) wine. Food Chem. 2018;267:263–270. doi: 10.1016/j.foodchem.2017.05.044. [DOI] [PubMed] [Google Scholar]
- 58.Sales PM, Souza PM, Simeoni LA, Magalhães PO, Silveira D. α-Amylase inhibitors: a review of raw material and isolated compounds from plant source. J Pharm Pharm Sci. 2012;15:141–183. doi: 10.18433/j35s3k. [DOI] [PubMed] [Google Scholar]
- 59.Nwanna EE, Ibukun EO, Oboh G. Inhibitory effects of methanolic extracts of two eggplant species from south-western Nigeria on starch hydrolysing enzymes linked to type-2 diabetes. Afr J Pharm Pharmaco. 2013;7:1575–1584. [Google Scholar]
- 60.Kwon Y-I, Apostolidis E, Shetty K. In vitro studies of eggplant (Solanum melongena) phenolics as inhibitors of key enzymes relevant for type 2 diabetes and hypertension. Bioresource Technol. 2008;99:2981–2988. doi: 10.1016/j.biortech.2007.06.035. [DOI] [PubMed] [Google Scholar]
- 61.Liu X, Luo J, Kong L. Phenylethyl cinnamides as potential α-Glucosidase inhibitors from the roots of Solanum Melongena. Nat Prod Commu. 2011;6:851–853. [PubMed] [Google Scholar]
- 62.Martinez-Quinones P, McCarthy CG, Watts SW, Klee NS, Komic A, Calmasini FB, et al. Hypertension induced morphological and physiological changes in cells of the arterial wall. Am J Hypertens. 2018;31:1067–1078. doi: 10.1093/ajh/hpy083. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Mancia G, Grassi G. Blood pressure targets in type 2 diabetes. Evidence against or in favour of an aggressive approach. Diabetologia. 2018;61:517–525. doi: 10.1007/s00125-017-4537-3. [DOI] [PubMed] [Google Scholar]
- 64.Shirani J, Loredo ML, Eckelman WC, Jagoda EM, Dilsizian V. Imaging the renin-angiotensin-aldosterone system in the heart. Curr Heart Fail Rep. 2005;2:78–86. doi: 10.1007/s11897-005-0013-3. [DOI] [PubMed] [Google Scholar]
- 65.Razavi BM, Hosseinzadeh H. Saffron: a promising natural medicine in the treatment of metabolic syndrome. J Sci Food Agr. 2017;97:1679–1685. doi: 10.1002/jsfa.8134. [DOI] [PubMed] [Google Scholar]
- 66.Taddei S, Virdis A, Mattei P, Salvetti A. Vasodilation to acetylcholine in primary and secondary forms of human hypertension. Hypertension. 1993;21:929–933. doi: 10.1161/01.hyp.21.6.929. [DOI] [PubMed] [Google Scholar]
- 67.Yamaguchi S, Matsumoto K, Koyama M, Tian S, Watanabe M, Takahashi A, et al. Antihypertensive effects of orally administered eggplant (Solanum melongena) rich in acetylcholine on spontaneously hypertensive rats. Food Chem. 2019;276:376–382. doi: 10.1016/j.foodchem.2018.10.017. [DOI] [PubMed] [Google Scholar]
- 68.Philipp T, Distler A, Cordes U. Sympathetic nervous system and blood-pressure control in essential hypertension. Lancet. 1978;312:959–963. doi: 10.1016/s0140-6736(78)92526-6. [DOI] [PubMed] [Google Scholar]
- 69.Champlain J, Ameringen MR. Regulation of blood pressure by sympathetic nerve fibers and adrenal medulla in normotensive and hypertensive rats. Circ Res. 1972;31:617–628. doi: 10.1161/01.res.31.4.617. [DOI] [PubMed] [Google Scholar]
- 70.Guyenet PG. The sympathetic control of blood pressure. Nat Rev Neurosci. 2006;7:335–346. doi: 10.1038/nrn1902. [DOI] [PubMed] [Google Scholar]
- 71.Bipat R, Toelsie J, Joemmanbaks R, Gummels J, Klaverweide J, Jhanjan N, et al. Effects of plants popularly used against hypertension on norepinephrine-stimulated guinea pig atria. Pharmacogn Mag. 2008;4:12–19. [Google Scholar]
- 72.Mueller M, Beck V, Jungbauer A. PPARalpha activation by culinary herbs and spices. Planta Med. 2011;77:497–504. doi: 10.1055/s-0030-1250435. [DOI] [PubMed] [Google Scholar]
- 73.Galavi A, Hosseinzadeh H, Razavi BM. The effects of Allium cepa (onion) and its active constituents on metabolic syndrome: a review. Iran J Basic Med Sci. 2020;23:1–14. doi: 10.22038/ijbms.2020.46956.10843. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 74.El-Dashlouty MS, El-Sherif FE-ZA, Shalaby MA, El-Din MF, El-Mosselhy SE-M. Round black, long white eggplant diets for clinical nutrition of fructose induced hypertensiona, hyperglycemia and hyperlipidemia. Alexandria J Agr Sci. 2016;61:139–151. [Google Scholar]
- 75.Kakuda C, Aoki L, Ferrari M, Lotierzo P, Caramelli B. Influence of an eggplant and orange juice on lipids and fibrinogen. Atherosclerosis. 1997;1:325–325. [Google Scholar]
- 76.Praça JM, Thomaz A, Caramelli B. Eggplant (Solanum melongena) extract does not alter serum lipid levels. Arq Bras Cardiol. 2004;82:269–276. [PubMed] [Google Scholar]
- 77.Silva GE, Takahashi MH, Eik Filho W, Albino CC, Tasim GE, Serri Lde A, et al. Absence of hypolipidemic effect of Solanum melongena L (eggplant) on hyperlipidemic patients. Arq Bras Endocrinol Metabol. 2004;48:368–373. doi: 10.1590/s0004-27302004000300006. [DOI] [PubMed] [Google Scholar]
- 78.Kritchevsky D, Tepper S, Story J. Influence of an eggplant (Solanum melongena) preparation on cholesterol metabolism in rats. Experimentelle Pathol. 1975;10:180–183. doi: 10.1016/s0014-4908(75)80021-4. [DOI] [PubMed] [Google Scholar]
- 79.Botelho FV, Enéas LR, Cesar GC, Bizzotto CS, Tavares É, Oliveira FcA, et al. Effects of eggplant (Solanum melongena) on the atherogenesis and oxidative stress in LDL receptor knock out mice (LDLR−/−) Food Chem Toxicol. 2004;42:1259–1267. doi: 10.1016/j.fct.2004.03.007. [DOI] [PubMed] [Google Scholar]
- 80.Sudheesh S, Presannakumar G, Vijayakumar S, Vijayalakshmi NR. Hypolipidemic effect of flavonoids from Solanum melongena. Plant Foods Human Nutrition. 1997;51:321–330. doi: 10.1023/a:1007965927434. [DOI] [PubMed] [Google Scholar]
- 81.Ressaissi A, Attia N, Falé L P, Pacheco R, Victor B, Machuqueiro M, et al. Isorhamnetin dervatives and piscidic acid for hypercholestrolemia: cholesterol permeability, HMG-CoA reductase inhibition, and docking studies. Arch Pharm Res. 2017;40:1278–1286. doi: 10.1007/s12272-017-0959-1. [DOI] [PubMed] [Google Scholar]
- 82.Sudheesh S, Presannakumar G, Vijayakumar S, Vijayalakshmi NR. Hypolipidemic effect of flavonoids from Solanum melongena. Plant Foods Hum Nutr. 1997;51:321–330. doi: 10.1023/a:1007965927434. [DOI] [PubMed] [Google Scholar]
- 83.Silva ME, Santos RC, O’Leary MC, Santos RS. Effect of aubergine (Solanum melongena) on serum and hepatic cholesterol and triglycerides in rats. Braz Arch Biol Technol. 1999;42:339–342. [Google Scholar]
- 84.Zaki AN. Hypolipidemic effect of eggplant peels (Solanum melongena, L) powder on obese rats. Nutr Food Sci. 2018;1:1783–1798. [Google Scholar]
- 85.Cherem ADR, Tramonte VLCG, Fett R, Dokkum W. The effect of the eggplant core on blood lipid concentrations in hypercholesterolemic guinea pigs (Cavia porcellus) Rev Bras Plantas Med. 2007;9:51–60. [Google Scholar]
- 86.Jorge P, Neyra LC, Osaki RM, de Almeida E, Bragagnolo N. Effect of eggplant on plasma lipid levels, lipidic peroxidation and reversion of endothelial dysfunction in experimental hypercholesterolemia. Arq Bras Cardiol. 1998;70:87–91. doi: 10.1590/s0066-782x1998000200004. [DOI] [PubMed] [Google Scholar]
- 87.Razavi BM, Abazari AR, Rameshrad M, Hosseinzadeh H. Carnosic acid prevented olanzapine-induced metabolic disorders through AMPK activation. Mol Biol Rep. 2020;47:7583–7592. doi: 10.1007/s11033-020-05825-5. [DOI] [PubMed] [Google Scholar]
- 88.Malekzadeh S, Heidari MR, Razavi BM, Rameshrad M, Hosseinzadeh H. Effect of safranal, a constituent of saffron, on olanzapine (an atypical antipsychotic) induced metabolic disorders in rat. Iran J Basic Med Sci. 2019;22:1476–1482. doi: 10.22038/IJBMS.2019.13992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 89.Bhupathiraju SN, Hu FB. Epidemiology of obesity and diabetes and their cardiovascular complications. Circ Res. 2016;118:1723–1735. doi: 10.1161/CIRCRESAHA.115.306825. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 90.Jiang SZ, Lu W, Zong XF, Ruan HY, Liu Y. Obesity and hypertension. Exp Ther Med. 2016;12:2395–2399. doi: 10.3892/etm.2016.3667. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 91.Ortega FB, Lavie CJ, Blair SN. Obesity and cardiovascular disease. Circ Res. 2016;118:1752–1770. doi: 10.1161/CIRCRESAHA.115.306883. [DOI] [PubMed] [Google Scholar]
- 92.Xanthopoulos M, Tapia IE. Obesity and common respiratory diseases in children. Paediatr Respir Rev. 2017;23:68–71. doi: 10.1016/j.prrv.2016.10.002. [DOI] [PubMed] [Google Scholar]
- 93.Malti N, Merzouk H, Merzouk SA, Loukidi B, Karaouzene N, Malti A, et al. Oxidative stress and maternal obesity: feto-placental unit interaction. Placenta. 2014;35:411–416. doi: 10.1016/j.placenta.2014.03.010. [DOI] [PubMed] [Google Scholar]
- 94.Madhikarmi N, Murthy K, Rajagopal G, Singh P. Lipid peroxidation and anti-oxidant status in patients with type 2 diabetes in relation to obesity in Pokhara-Nepal. J Diabetol. 2013;4:5–12. [Google Scholar]
- 95.Molnár D, Decsi T, Koletzko B. Reduced anti-oxidant status in obese children with multimetabolic syndrome. Int J Obes. 2004;28:1197–1202. doi: 10.1038/sj.ijo.0802719. [DOI] [PubMed] [Google Scholar]
- 96.You JS, Lee YJ, Kim KS, Kim SH, Chang KJ. Ethanol extract of lotus (Nelumbo nucifera) root exhibits an anti-adipogenic effect in human pre-adipocytes and anti-obesity and anti-oxidant effects in rats fed a high-fat diet. Nutr Res. 2014;34:258–267. doi: 10.1016/j.nutres.2014.01.003. [DOI] [PubMed] [Google Scholar]
- 97.Qian Y, Zhong P, Liang D, Xu Z, Skibba M, Zeng C, et al. A newly designed curcumin analog Y20 mitigates cardiac injury via anti-inflammatory and anti-oxidant actions in obese rats. PLoS One. 2015;10:e0120215. doi: 10.1371/journal.pone.0120215. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 98.Han L-K, Zheng Y-N, Xu B-J, Okuda H, Kimura Y. Saponins from Platycodi Radix ameliorate high fat diet–induced obesity in mice. J Nut. 2002;132:2241–2245. doi: 10.1093/jn/132.8.2241. [DOI] [PubMed] [Google Scholar]
- 99.Kim JH, Hahm DH, Yang DC, Kim JH, Lee HJ, Shim I. Effect of crude saponin of Korean red ginseng on high fat diet-induced obesity in the rat. J Pharmacol Sci. 2005;97:124–131. doi: 10.1254/jphs.fp0040184. [DOI] [PubMed] [Google Scholar]
- 100.Buchholz T, Melzig MF. Polyphenolic compounds as pancreatic lipase inhibitors. Planta Med. 2015;81:771–783. doi: 10.1055/s-0035-1546173. [DOI] [PubMed] [Google Scholar]
- 101.Zakiyaturrodliyah L, Brotosudarmo TH, editors Saponin from purple eggplant (Solanum melongena L ) and their activity as pancreatic lipase inhibitor. Mater Sci Eng C. 2019;509:012139. [Google Scholar]