Sec. Inflammation Pharmacology
Effects of Nigella sativa, Camellia sinensis, and Allium sativum as Food Additives on Metabolic Disorders, a Literature Review
- 1Department of Physiology, School of Medicine, Jiroft University of Medical Science, Jiroft, Iran
- 2Torbat Jam Faculty of Medical Sciences, Torbat Jam, Iran
- 3Cardiovascular Diseases Research Center, Birjand University of Medical Sciences, Birjand, Iran
- 4Applied Biomedical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
Objective: Metabolic disorders (MD) can disturb intracellular metabolic processes. A metabolic disorder can be resulted from enzyme deficits or disturbances in function of various organs including the liver, kidneys, pancreas, cardiovascular system, and endocrine system. Some herbs were used traditionally for spices, food additives, dietary, and medicinal purposes. Medicinal plants possess biological active compounds that enhance human health. We aimed to provide evidence about therapeutic effects of some medicinal herbs on MD.
Data Sources: PubMed, Scopus, and Google Scholar were explored for publications linked to MD until February 2021. The most literature reports that were published in the last 10 years were used. All types of studies such as animal studies, clinical trials, and in vitro studies were included. The keywords included “Metabolic disorders,” “Nigella sativa L.,” “Thymoquinone,” “White tea”OR “Camellia sinensis L.” “catechin,” and “Allium sativum L.” OR “garlic” were searched.
Results: Based on the results of scientific studies, the considered medicinal plants and their active components in this review have been able to exert the beneficial therapeutic effects on obesity, diabetes mellitus and non-alcoholic fatty liver disease.
Conclusions: These effects are obvious by inhibition of lipid peroxidation, suppression of inflammatory reactions, adjustment of lipid profile, reduction of adipogenesis and regulation of blood glucose level.
Nigella sativa L., Camellia sinensis L., and Allium sativum L. as a food additive showed therapeutic effects on metabolic disorders.
These plants and their active components inhibited release of inflammatory mediators and oxidant parameters.
These plants and their active components showed antidiabetic, anti-inflammatory, antioxidant, lipolysis, hepatoprotective, and cardioprotective effects.
Metabolic diseases are disturbances that affect a wide range of intracellular metabolic processes (Bertrand and Lehuen, 2019). These diseases can be an outcome of enzyme deficits (Barbagallo and Dominguez, 2007) or perturbation in the function of vital organs/systems of the human body, including the liver, kidneys, pancreas, and cardiovascular system and endocrine system (Rochlani et al., 2017). In recent decades, the prevalence of metabolic diseases has been significantly enhanced, and it is considered as a serious threat for human health (Fan and Pedersen, 2020). One of the most common metabolic diseases affecting human health is type 2 diabetes mellitus (NCD Risk Factor Collaboration, 2016). Rapid prevalence of this disease among men and women mostly is attributed to obesity and increment of body mass index (BMI) (Esser et al., 2014). In addition, inflammation followed by overstimulation of the immune system has been recognized as an important player in pathogenesis of metabolic diseases such as type 2 diabetes mellitus (Rea et al., 2018). Accumulating evidence confirms that inflammation triggered by obesity has a basic contribution in the reduction of insulin secretion and insulin resistance (Boulangé et al., 2016). It has been also revealed that obesity caused by inflammation affects various organs such as the liver, heart, and brain and disturbs hemostatic mechanisms in the body (Saltiel and Olefsky, 2017). Scientific findings also demonstrate a link between increased levels of inflammatory markers such as C-reactive protein and type 2 diabetes mellitus (Yang et al., 2020). Besides inflammation, the role of oxidative stress in pathogenesis of metabolic degasses has been confirmed (Mostafavinia et al., 2021).
Traditional medicine has been shown to have useful results in treatment of metabolic diseases (Zhang et al., 2020). Animal studies confirmed that extracts of some medicinal plants such as Rhinacanthus nasutus can modify overweight and lowered levels of glucose and lipids in rats (Ajmal Shah et al., 2017). Based on pharmacological research studies, flavonoids presented in the extract of plants such as Scutellaria baicalensis improved type 2 diabetes mellitus via attenuating inflammatory responses (Waisundara et al., 2008). It has been also documented that some varieties of tea also have potent effects in the improvement of nonalcoholic fatty liver disease (Mao et al., 2021). According to animal and clinical studies, plant alkaloids including berberine have also been suggested to have good therapeutic effects on obesity, type 2 diabetes mellitus, nonalcoholic fatty liver disease, and hyperlipidemia (Xu et al., 2020). Nigella sativa (N. sativa) and Allium sativum (A. sativum) are among the most commonly used medicinal plants in Persian traditional medicine (Khazdair et al., 2019). Traditionally, these plants have been used as dietary, food additives, spices, and various medicinal purposes for the treatment of different diseases (Gilani et al., 2004; Bathaie and Mousavi, 2010). Furthermore, Camellia sinensis is one of the most widely consumed functional beverages in the global population (Yi et al., 2019). Also, in this review article we documented the effects of some medicinal plants that were used as culinary and food additives on metabolic disorders. The selected medicinal plants and their active constituents are summarized in Figure 1.
THE Effects of Medicinal Plants on Metabolic Disorders
Black seed or Nigella sativa (N. sativa), a plant of the Ranunculaceae family, flourishes in different areas of the world and is used as food as well as a remedy in traditional medicine (Rusda et al., 2020). Thymoquinone (TQ), dithymoquinone (DTQ), thymol (THY), and thymohydroquinone (THQ) are main ingredients presented in the N. sativa extract (Figure 1). These compounds especially thymoquinone play an outstanding role in therapeutic effects of this plant (Randhawa and Al-Ghamdi, 2002). The oils of N. sativa are also rich in polyunsaturated fatty acids such as oleic, linoleic, and palmitic acids. In addition, carotenoids, sterols, tocols, and phenolics are present in oils of this plant (Ketenoglu et al., 2020).
A wide range of pharmacological effects such as modulation of immune system activity, suppression of inflammatory reactions, inhibition of oxidative stress, prevention of cancer cell proliferation, and death of germs have been attributed to N. sativa and its constituents (Adiban Fard et al., 2015; Mokhtari-Zaer et al., 2020). In addition, N. sativa has been demonstrated to cure disorders such as diabetes, dyslipidemia, and asthma (Namazi et al., 2018; Mortazavi Moghaddam et al., 2020). The effects of N. sativa in patients with metabolic syndrome illustrated that black seeds of N. sativa could improve body mass index (BMI), waist circumference, and fasting blood glucose. Co-administration of black seeds of N. sativa and turmeric also could ameliorate metabolic syndrome via the modification of BMI, waist circumference, fasting blood glucose, and lipid profile in patients (Ramadan, 2020). Anti-obesity of N. sativa and thymoquinone extracted from it has been also documented (Mahdavi et al., 2015). In addition, scientific evidence confirms that N. sativa regulates some of the membrane receptors involved in energy homeostasis including peroxisome proliferator–activated receptor gamma-2 (PPAR-γ2) (Benhaddou-Andaloussi et al., 2010). The potential molecular targets of the mentioned medicinal herbs on metabolic disorders are showed in Figure 2.
Effect of N. sativa and its Ingredient on Obesity
Obesity is a chronic metabolic disease which threatens human health. It can be a result of excessive accumulation of fat in adipocytes (Apovian, 2016). Obesity has been shown to affect the immune system for over-generation of pro-inflammatory cytokines including tumor necrosis factor alpha (TNF-α) (Ferrante, 2007). Obesity also can lead to the induction of nonalcoholic fatty liver disease. The beneficial effects of plant extracts in the improvement of MD have been documented. The researchers studied the effect of Livo-Pro-08 [N. sativa (250 mg/kg), Entada pursaetha (500 mg/kg) and Ficus glomerata (750 mg/kg)] on nonalcoholic fatty liver disease in rats. Based on results, the Liv-Pro-08 extract lowered the fasting blood glucose and insulin level. In addition, improvement of lipoprotein profiles and mitigation of liver enzymes such as alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALK-P) took place in rats treated by the extract (Vedanarayanan and Krishnan, 2011).
Thymoquinone (TQ) derived from the seeds and volatile oil of N. sativa has been suggested to be useful in blood glucose regulation and to ameliorate feeding disturbances (Mohtashami and Entezari, 2016). Uncoupling protein-1 (UCP-1) is an uncoupling molecule which disturbs the proton gradient in oxidative and phosphorylation in the mitochondria of brown adipose tissue (Dulloo et al., 2010). It has been understood that enhancing compounds of this protein are able to increase the metabolic energy consumption and reduce weight. In a study, the effect of TQ (100 mg/kg), hydroalcoholic (200 mg/kg), and hexane (300 mg/kg) extracts of N. sativa on the UCP-1 expression in brown adipose tissue was evaluated in mice. The results exhibited that TQ and both extracts augmented the expression of UCP-1. Based on results, TQ and extracts mitigated the level of cholesterol, low-density lipoprotein (LDL), and triglyceride (TG) and increased the concentration of high-density lipoprotein (HDL) in mice (Mahmoudi et al., 2018).
The ameliorative effect of TQ on the diabetic phenotype in a mice mold of diet-triggered obesity was investigated. In this study, the use of 20 mg/kg/day of this substance led to diminish the fasting blood glucose and insulin concentration and improve glucose tolerance and insulin sensitivity. In addition, the blood level of lipids including cholesterol and inflammatory mediators and liver TG decreased in animals treated by TQ. The fruitful effect of TQ on the diabetic phenotype was carried out through SIRT1-related pathways (Karandrea et al., 2017).
Peroxisome proliferator-activated receptors (PPARs), in particular PPAR-γ, have been reported to suppress the production of inflammatory cytokines (Motawi et al., 2017). It has been found that capsules of N. sativa (1,000 mg) could increase the expression of PPAR-γ and decreased TNF-α in obese women (Razmpoosh et al., 2019). In a clinical test, the effect of N. sativa (two capsules 750 mg) in obese men was checked. In this experimental test, the subjects received two capsules of N. sativa daily. The results determined that the body weight, fasting blood sugar, and cholesterol decreased while adiponectin increased in the group treated by N. sativa with respect to the untreated group (Datau et al., 2010).
Effect of N. sativa and its Ingredients on Diabetes Mellitus
Diabetes mellitus is a chronic and intricate metabolic disease which has affected a large number of people all over the world (Roglic et al., 2005). Type 2 diabetes mellitus as the most common form of diabetes can result from overweight as well as genetic aspects (Mellitus, 2006). N. sativa possesses antidiabetic properties (Yimer et al., 2019). N. sativa oil (400 mg/kg) has been reported to protect myocardial cells against streptozotocin-diabetic rats. This protective effect of N. sativa was mediated via inhibiting apoptosis and enhancing antiapoptotic factors such as Bcl-2 (Altun et al., 2019). Administration of 2 mg/kg of N. sativa oil also lowered fasting blood sugar and elevated the blood level of insulin in rats. In addition, antioxidant effects of N. sativa oil were mediated via the amplification of the activity of antioxidant enzymes including catalase and glutathione peroxidase (Abdelrazek et al., 2018). Combined extracts of N. sativa and Cinnamomum cassia (100 and 200 mg/kg) balanced the blood glucose and lipid profile in rats. It has been suggested that these two plants can be considered as an adjunctive therapy for diabetes (Kaur et al., 2018).
N. sativa oil (100 mg/kg) also could exert antidiabetic activities via mitigating the insulin/insulin receptor ratio and tumor necrosis factor-α in rats (Balbaa et al., 2016). Oral use of the ethanol extract of N. sativa (300 mg/kg) for 30 days considerably lowered the blood level of insulin, glucose, and lipids and attenuated lipid peroxidation and elevated antioxidant enzymes such as superoxide dismutase and catalase in the kidney and liver in diabetic rats (Kaleem et al., 2006). It has been documented that N. sativa and its essential oils alleviated hyperglycemia and ameliorated antioxidant capacity in diabetes mellitus caused by streptozotocin in rats (Sultan et al., 2014). N. sativa also could improve diabetic rabbits via a significant reduction in glucose and MDA concentrations as well as enhancement of GSH and ceruloplasmin levels (Meral et al., 2001). The fruitful effects of N. sativa on type 1 diabetes mellitus have been also documented. In a study, researchers reported that N. sativa oil (0.2 ml/kg) saved the islet of Langerhans against damages caused by streptozotocin in rats (Hmza et al., 2013). Researchers reported that administration of 50 and 100 mg/kg/day of TQ could reduce the level of glucose, HOMA-IR, and food and water intake in diabetic rats. These effects of TQ were carried out through enhancing the endogenous level of glucagon-like peptide 1 (Lee et al., 2019).
In a study, the impact of N. sativa (5.45 g/day) and fenugreek seed–supplemented chapatis in individuals with overweight and type 2 diabetes mellitus was appraised. In this study, BMI, fasting blood sugar, LDL, VLDL, and TG decreased in treated subjects (Rao et al., 2020). Administration of 2 g/day of N. sativa for 12 weeks has been shown to ameliorate dyslipidemia and to prevent the cardiovascular problem in patients with type 2 diabetes mellitus (Kaatabi et al., 2012).
In a clinical trial, the therapeutic effect of oral administration of N. sativa (2 g daily for 1 year) on type 2 diabetic patients was evaluated. Results identified that N. sativa administration decreased TG, total cholesterol, LDL, systolic blood pressure, diastolic blood pressure, mean arterial pressure, and heart rate (Badar et al., 2017).
Researchers examined the impact of N. sativa oil (2.5 ml, daily) on chronic kidney disease stages 3 and 4 resulted from diabetic nephropathy. Based on evidence, in patients treated by N. sativa oil the serum level of glucose, creatine, and urea was lower, and the glomerular filtration rate was higher when they were compared with that of the control group (Ansari et al., 2017).
Effect of N. sativa and its Ingredients on Nonalcoholic Fatty Liver Disease
Nonalcoholic fatty liver disease (NAFLD) is a metabolic disorder related to inflammation. Traditional medicine has been demonstrated to improve the liver dysfunction (Nishiyama et al., 2020). Researchers reported that a mixture of aqueous extracts including N. sativa seeds and fenugreek (100 mg/kg) has an improving effect on nonalcoholic fatty liver disease in rats. In addition, this mixture of aqueous extract could modify hyperglycemia via elevating the level of insulin and regenerating β cells in the islets of Langerhans (Mohamed et al., 2015).
TQ extracted from N. sativa has been shown to reverse NAFLD followed by hypothyroidism in rats. Based on this study, 400 mg/kg of TQ improved liver damage associated with hypothyroidism by over-expression of the antioxidant CAT gene (Ayuob et al., 2019). Administration of low dose (10 mg/kg) and high dose (20 mg/kg) of TQ improved oxidative stress via decreasing MDA and alleviated inflammatory responses through deccreasing the level of TNF-α and enhancing the IL-10 concentration in a rat model of NAFLD. In this study, the protective effect of high dose of TQ was more noticeable than that of the low dose (Awad et al., 2016). It has been determined that N. sativa (1 g twice a day) ameliorated liver function in NAFLD patients through lessening BMI, body weight, and liver enzymes (Hussain et al., 2017).
In a placebo-controlled clinical trial, 2 g/day of N. sativa seed could decrease the plasma level of inflammatory cytokines such as TNF-α, C-reactive protein, and nuclear factor kappa-B (NF-κB) in patients with NAFLD (Darand et al., 2019b). In another clinical trial, 1 g of N. sativa oil lowered the fasting blood sugar, TG, LDL, VLDL, liver enzymes, hs-C reactive protein, IL-6, and TNF-α levels in patients with NAFLD (Rashidmayvan et al., 2019). In a study, the effect of N. sativa seed oil (2.5 ml) on 60 patients with NAFLD was evaluated. The results indicated that N. sativa seed oil lessened the grade of hepatic steatosis, plasma level of aminotransferases, LDL-C, and TG and enhanced the content of HDL-C. There was not any significant difference in the weight of the group treated with oil compared to the placebo group (Khonche et al., 2019). It has been reported that tablets of Dava Al-Balgham prepared from a combination of N. sativa (105 mg), Zataria multiflora (105 mg), Trachyspermum ammi (105), and Pistacia lentiscus (105) reduced the liver enzymes level and weight in NAFLD patients (Hormati et al., 2019). Use of N. sativa (5 g) and Melissa officinalis (5 g) could lower the blood level of liver enzymes including AST and ALT, BMI, and degree fatty liver in patients with NAFLD in a clinical trial (Hosseini et al., 2018).
Based on the results of the studies, daily consumption of 2 g of N. sativa associated with lifestyle modification is useful in improvement of hepatic steatosis and insulin resistance in NAFLD patients (Darand et al., 2019a). The effect of 100 mg–20 g of seed powder, 20–80 mg of seed oil, 35–25 mg of TQ, and seed extract of N. sativa on reduction of the plasma level of lipids including cholesterol, LDL-C, and TG has been shown (Asgary et al., 2015). Effects of N. sativa and its ingredients on obesity, diabetes mellitus, and nonalcoholic fatty liver disease have been summarized in Table 1.
TABLE 1. Effects of N. sativa and its ingredients on obesity, diabetes mellitus, and nonalcoholic fatty liver disease.
White Tea (Camellia sinensis L.)
White tea and other tea (green, oolong, and black) come from Camellia sinensis, or the tea plant. White tea prepared from young tea leaves is harvested only once a year in the spring (Rusak et al., 2008). The young tea leaves may be shielded from sunlight during growth for reducing chlorophyll formation and preparing white tea (Alcazar et al., 2007). The wide range of physiological and pharmacological properties for white tea including anticancer, anti-inflammatory and antioxidant (Dias, 2013), antiatherosclerotic and antihypertensive (Hodgson et al., 2005), and hypolipidemic and hypocholesterolemic effects (Huang and Lin, 2012) were reported. It has been suggested that oolong tea and dark tea could improve alcoholic fatty liver disease in mice by regulation of gut microbiota (Li et al., 2021). White tea contains proteins, minerals, and amino acids. Gallic acid, caffeine, and catechins are the main constituents of white tea (Ning et al., 2016) (Figure 1).
Effect of White Tea and its Constituent on Obesity
It has been reported that tea (white, green, and black) inhibited the pancreatic lipase activity. White tea was more effective than the other types. White and green teas have essentially equal amounts of flavan-3-ols. Green tea has high levels of flavonols. White tea also has high levels of 5-galloyl quinic acid, strictinin, trigalloyl glucose, and digalloyl glucose (Gondoin et al., 2010).
Incubation of preadipocytes with white tea extract (0.1, 0.25, 0.5 and 0.75%) significantly decreased TG during adipogenesis without affecting cell viability. Tea extract also showed lipolytic activity by increasing the content of free glycerol (32 μg/ml) in trated as compared to control cells. Tea extract downregulated the ADD1/SREBP-1c protein expression during adipogenesis and decreased SIRT1 mRNA levels compared to control cells (Söhle et al., 2009). These results indicated that white tea effectively inhibits adipogenesis and stimulates lipolysis activity. White tea extract (2.5%) and its main constituent catechins reduced the glucose and cholesterol uptake and enhanced LDL receptor binding activity and HDL concentration. Also, tea extract has been revealed to have a potent inhibiting capacity against lipase activity and TG levels in HepG2 cell lines (Tenore et al., 2013). The aqueous extract of white tea (1.5%) for 30 days, significantly decreased serum levels of glucose, LDL, cholesterol, and TG, while increased levels of HDL compared to control diabetic rats (Amanzadeh et al., 2020).
The modulating effects of teas on the plasma bile acids (BAs) profile were investigated. The plasma levels of murocholic acid, glycocholic acid, taurochenodeoxycholic acid, glycodeoxycholic acid, tauromuricholic acid, tauroursodeoxycholic acid, taurodeoxycholic acid, and taurocholic acid were increased, whereas levels of isolithocholic acid and taurolithocholic acid were decreased after drinking white, green, and oolong tea compared with control (Sun et al., 2019). Teas altered the bile acids metabolism, and this change could be associated with the health benefit effects of teas. White tea extract (0.5%) in induced obesity, reduced blood TG in male mice fed with a high-fat diet. White tea extract also reduced oxidative stress in the liver and adipose tissue. Moreover, tea extract was not able to reduce the food intake and body weight in animals (Teixeira et al., 2012).
The effects of white tea polysaccharide and polyphenol (400 or 800 mg/kg) on rats fed with high-fat diet (for 6 weeks) were investigated. These components suppressed body weight increases and fat accumulation. Moreover, polyphenols and polysaccharides improved blood lipid and antioxidant index levels as well as the reduction of the serum leptin levels and gene expression levels of IL-6 and TNF-α. Polysaccharides and polyphenols also showed synergistic effects in the reduction of serum leptin levels (Xu et al., 2015). These results indicated that the polysaccharide combination with polyphenols might be a potential therapy against obesity.
Use of low or high fat supplemented fed diets (5 and 30% triglyceride, respectively) with catechin (0.1, 0.2, and 0.5%) for 1 month significantly reduced body weight, visceral, and liver fat accumulation as well as development of hyperinsulinemia and hyperleptinemia in mice. Furthermore, treatment with catechins significantly increased acyl-CoA oxidase and medium chain acyl-CoA dehydrogenase mRNA expression and β-oxidation activity in the liver (Murase et al., 2002).
Administration of catechins (118.5 and 483.0 mg/day) in healthy male subjects (27–47 years) for 12 weeks significantly decreased BMI, waist circumference, body fat ratio, abdominal fat, and total cholesterol, glucose and plasminogen activator inhibitor-1 (PAI-1) in the serum compared to the baseline (Hase et al., 2001).
Treatment of an overweight participant (n = 107) with a beverage containing (625 mg of catechins with 39 mg caffeine) induced loss of body weight compared with the control group (39 mg caffeine) for 12 weeks. Percentage changes in total abdominal fat, subcutaneous abdominal fat, and fasting serum TG were greater in the catechin group than those of the control group (Maki et al., 2009).
Effect of White Tea and its Constituent on Diabetes
Administration of aqueous extracts of white tea (0.5%) significantly increased the drink intake compared to the normal control or diabetic control rats. Tea extracts significantly decreased blood glucose concentration and improved glucose tolerance ability compared to that of the diabetic group. In addition, liver weight and liver glycogen were remarkably increased, while total cholesterol and LDL-cholesterol were significantly decreased in the white tea–treated group compared to that of the diabetic animals (Islam, 2011).
White tea consumption (1%) in prediabetic rats significantly increased mRNA and protein expression levels of glucose transporters (GLUT1 and GLUT3) in the heart tissue. Administration of white tea also significantly increased cardiac acetate and alanine contents, antioxidant power of ferric, and expression and activity of lactate dehydrogenase (LDH) (Alves et al., 2015). Daily administration of white tea (1%) ameliorated glucose tolerance and insulin sensitivity. Also, tea extract decreased the protein expression levels of GLUT 1 and GLUT3 in the cortex of prediabetic rats. In addition, tea extract increased antioxidant capacity and suppressed lipid peroxidation and protein oxidation in the cortex of prediabetic animals (Nunes et al., 2015).
Treatment of diabetic rats with white tea extract (2%) significantly increased glutathione peroxidase (GSH-px), superoxide dismutase (SOD), and catalase (CAT) activities in the serum and liver compared to the diabetic control group (Al-Shiekh et al., 2014). The effect of white tea ethanolic extract (WTE) on the reduction of fasting blood glucose levels in diabetic rats showed that administration of WTE (100 mg/kg, BW) for 14 days decreased fasting blood glucose levels in diabetic rats. These effects can be attributed to the presence of flavonoid compounds such as catechins in tea extract (Ardiana et al., 2018). The use of catechins (25 and 50 mg/kg) modified the body weight of diabetic rats. Catechins also significantly reduced heart hypertrophy, plasma glucose levels, and matrix metallopeptidase 9 (MMP-9) levels. Moreover, catechin improved oxidative stress parameters in the nerves (Addepalli and Suryavanshi, 2018). Administration of (+)-catechin (0.2, 1.0, and 5.0 mmol/L) for 16 weeks significantly ameliorated renal dysfunction in type 2 diabetic mice and exerted protective effects against structural nephropathies. Also, catechin downregulated the level of NF-κB p65 phosphorylation and lowered pro-inflammatory mediators such as TNF- α and IL-1β in diabetic mice (Zhu et al., 2014).
Treatment of type 2 diabetes patients with catechin-rich beverages (96.3 mg) per day for 12 weeks in a double-blind controlled trial significantly decreased waist circumference compared to the control group. Additionally, catechin significantly increased adiponectin and insulin levels compared to the control group (Nagao et al., 2009).
Consumption of beverages containing catechin (540–588 mg) for 12 weeks significantly reduced abdominal fat, visceral fat area, subcutaneous fat area, body weight, and waist circumference and improved blood pressure in six human trials (n = 921, 505 men) (Hibi et al., 2018). These results indicated that white tea and catechin can reduce the risk of metabolic syndrome (MetS) due to the reduction of abdominal fat. The effects of beverages containing catechin (615 mg/350 ml) per day for 4 weeks on postprandial hyperglycaemia and oxidative stress in healthy postmenopausal women lowered postprandial glucose levels (3%) and serum postprandial thioredoxin (5%) compared to the placebo group. Catechins also increased antioxidant capacity and inhibited protein oxidation (Nunes et al., 2015).
Effect of White Tea and Its Constituent on Nonalcoholic Fatty Liver Disease
Long term consumption of white tea (15 mg/d or 45 mg/d) improved antioxidant activity and modified fatty acid profiles in a model of hepatotoxicity-induced Adriamycin (Espinosa et al., 2015).
White tea extract (200 μg/ml) significantly downregulated apolipoprotein B (APOB) and microsomal TG transfer protein (MTTP) expression and reduced the production of very-low-density lipoprotein (VLDL) in HepG2 cells. Tea extract stimulated LDL-cholesterol (LDL-c) uptake through activating the LDL receptor (LDLR). Furthermore, this extract significantly downregulated TG synthesizing enzyme genes and reduced intracellular TG accumulation (Luo et al., 2020). It has been reported that the catechins such as epigallocatechin-3-gallate (EGCG) and epicatechin-3-gallate (ECG) are abundant in white tea extract and contribute to the regulation of cholesterol metabolism (Luo et al., 2020).
Dietary supplements of white tea extract (5%) significantly reduced water intake and food consumption and lowered the serum total LDLc and TG levels. The tea extracts also significantly reduced lipid synthesis and blood glucose level, but increased glucose tolerance in mice. Furthermore, administration of the tea extract prevented the fatty liver formation and restored the normal hepatic structure (Teng et al., 2018). These results indicated that white tea has the protective effects on nonalcoholic fatty liver disease and metabolic disorders.
Co-administration of epigallocatechin-3-gallate (40–160 mg/kg) and caffeine presented in tea suppressed body weight gain and reduced white adipose tissue and energy intake than single use. These effects may be due to the alteration in the serum lipid profile, oxidative stress, and inflammatory cytokines in rats with NAFLD (Yang et al., 2019).
Histopathology results demonstrated that treatment of animals with NAFLD by (-) epigallocatechin gallate (EGCG) (85% pure extract) reduced number of fatty scores, necrosis, and inflammatory foci in liver tissue. EGCG also reduced liver injury and decreased fibrosis with downregulation in the expression of oxidative parameters and pro-inflammatory markers (Xiao et al., 2014).
Treatment of 17 patients with NAFLD (20–70 years) with low or high doses of catechins (1,080 mg/700 ml or 200 mg/700, beverage, respectively) or a placebo for 12 weeks in a double-blind randomized study reduced body fat. Moreover, the level of alanine ALT and urinary 8-isoprostane excretion significantly decreased in the high dose of catechin compared to the placebo and low dose groups after 12 weeks (Sakata et al., 2013).
The beneficial effects of catechin on hepatic dysfunction through the reduction of intracellular redox distress and inhibition of inflammatory reactions resulted from the nuclear factor kappa-B (NFκB) pathway activity have been reported (Hodges et al., 2020). In (Hodges et al., 2020). Effects of white tea and catechin on obesity, diabetes and nonalcoholic fatty liver disease are shown in Table 2.
TABLE 2. Effects of white tea and its ingredients on obesity, diabetes mellitus, and nonalcoholic fatty liver disease.
Garlic (Allium sativum L.)
Garlic (Allium sativum L.) belongs to the Amaryllidaceae family. Garlic is a bulbous and aromatic plant that is used as food and traditional remedy for various diseases worldwide (Bayan et al., 2014). This medicinal plant possesses bioactive ingredients with anti-inflammatory and antioxidant properties (Shang et al., 2019). The use of garlic has been recommended to aid respiration and digestion as well as treatment of leprosy and parasitic infection in ancient Chinese and Indian medicine (El-Saber Batiha et al., 2020). Bulbs of garlic possess the several phytochemicals including ajoenes, allicin (allyl 2-propenethiosulfinate or diallyl thiosulfinate), and sulfides [diallyl disulfide (DADS Al-Snafi, 2013] (Figure 1). Several biological and pharmacological activities for garlic and its related compounds including anticarcinogenic, antioxidant, antibacterial, antifungal, antidiabetic, anti-atherosclerotic, and antihypertensive renoprotective activities have been reported (Rahman and Lowe, 2006).
Effects of Garlic and Its Ingredients on Diabetes
Treatment of alloxan-diabetic rats by A. sativum decreased their blood glucose levels (Sheela et al., 1995). Liu et al. investigated the effects of garlic oil and diallyltrisulfide on glycemic control in STZ-diabetic rats. Diabetic rats received garlic oil and diallyltrisulfide for 3 weeks at a dose of 100 and 40 mg/kg body weight. The administration of garlic oil and diallyltrisulfide led to rise in basal insulin concentration and improved glucose tolerance. Both garlic oil and diallyltrisulfide ameliorated the increased level of blood glucose in diabetic rats through the increase of insulin secretion and enhancement of insulin sensitivity (Liu et al., 2005).
Albajali et al. assessed the effects of A. sativa (100 mg/kg/day) on glucose level, insulin concentration in streptozotocin-diabetic animals. Results showed a significant decrease in the serum level of glucose and a remarkable enhancement in blood insulin concentration (Osman et al., 2012). Garlic has been also revealed to decrease the TNF-α level and to increase the IL-10 production in alloxan-diabetic rats (Hashem et al., 2008). Hashem et al. examined the dose-dependent protective effect of garlic against streptozotocin-induced oxidative stress in hepatic and intestinal tissues. Findings showed that garlic administration (250 and 500 mg/kg) significantly normalized the blood glucose in diabetic rats (Kanth et al., 2008).
The effects of garlic oil and diallyl disulfide on blood glucose regulation and renal function showed that the administration of garlic oil (100 mg/kg) and DADS (40 or 80 mg/kg) until 16 weeks after the induction of diabetes stimulated insulin secretion in STZ-diabetic rats. Researchers suggested that the long-term treatment with garlic oil can improve glucose tolerance and renal function in diabetic rats (Liu et al., 2006). Short-term use of garlic in diabetic rabbits by alloxan also reduced the blood sugar levels as effectively as tolbutamide (Augusti, 1975).
Garlic ethanolic extract administration (0.1, 0.25 and 0.5 g/kg body wt.) in STZ-diabetic rats for 14 days significantly decreased the glucose, total cholesterol, triglycerides, urea, uric acid, creatinine, AST, and ALT levels and also increased serum concentration of insulin. Garlic extract has also been shown to have better antidiabetic effect than glibenclamide (Eidi et al., 2006). Musabayane et al. indicated that the garlic extract reduced blood glucose through increasing the insulin level. Also, the garlic extracts and metformin did not affect serum concentration of insulin in nondiabetic rats, while glibenclamide increased the blood level of insulin (Musabayane et al., 2006). The administration of aged garlic extract (AGE) (5 and 10 ml/kg, p.o.) significantly prevented adrenal hypertrophy, hyperglycemia, and elevated corticosterone levels in mice (Kasuga et al., 1999).
Mariee et al. studied the effects of garlic on diabetic nephropathy and oxidative stress induced by STZ in rats. The data revealed that fresh garlic homogenate reduced the serum level of glucose, total triglyceride, and total cholesterol and prevented STZ-induced diabetic nephropathy possibly through the inhibition of kidney oxidative damage and increase of nitric oxide bioavailability (Mariee et al., 2009). In another study, diabetic patients received 3 cloves of raw garlic (1 clove = 1.2 g) daily in the morning in fasting condition (12–14 h) for 30 days. The results showed that raw garlic has a potent antidiabetic effect (Mirunalini et al., 2011). The metabolic effects of time-released garlic powder tablets in patients with type 2 diabetes mellitus indicated that garlic reduced cardiovascular disease risks (Sobenin et al., 2008).
Also, many studies confirmed that the garlic as an adjunct can be useful for treatment of hyperlipidemia in patients with type 2 diabetes by inhibiting lipogenesis and promoting lipolysis (Afkhami-Ardekani et al., 2006). In a study, the effect of raw crushed garlic on metabolic syndrome was investigated. The patients were treated with 100 mg/kg of raw crushed garlic two times a day. Raw crushed garlic significantly reduced blood pressure, TG, and fast blood glucose compared to the control subjects (Choudhary et al., 2018).
Effects of Garlic and Its Ingredients on Nonalcoholic Fatty Liver Disease
The hypoglycemic, hypercholesterolemia, and hypotriglyceridaemic effects of garlic were studied in STZ-diabetic rats. Administration of garlic extract (500 mg/kg) for 7 weeks reduced the serum level of glucose, cholesterol, and TG levels. These results suggested that garlic could be effective in managing the side effects of diabetes (Thomson et al., 2007). In another study, the cardiovascular effects of aqueous garlic extracts (5–20 mg/kg) on normotensive and hypertensive rats decreased the mean arterial blood pressure (MAP), heart rate (HR), and systolic and diastolic blood pressure in hypertensive rats as well as in normotensive rats compared to the basal levels (Nwokocha et al., 2011). The effects of garlic on alloxan-induced diabetic male rabbits lowered serum glucose levels [38.88%] and serum cholesterol [57%], after 30 days of treatment compared to the control group. These results indicated that garlic could be a beneficial anti-hyperglycemic effect in alloxan-induced diabetic rabbits (Mahesar et al., 2010).
Marc et al. showed that aged garlic extract (AGE) had no significant effect on insulin resistance. They also revealed that treatment with AGE also had no significant effect on oxidative stress or inflammation (Atkin et al., 2016). Also, the A. sativum aqueous extract on heavy metal improved the lipid profile via the regulation of low-density lipoprotein-cholesterol (LDL-C), very-low-density lipoprotein-cholesterol (VLDL-C), and TG level (Gupta et al., 2008). The antihypertensive effect of garlic aqueous extract in the two–kidney–one–clip (2K-1C) Goldblatt model showed that the single dose of garlic (50 mg/kg) had a maximum antihypertensive effect 2–6 h after administration. They suggest that garlic does have an effective antihypertensive ability (Al-Qattan et al., 1999). Intraperitoneal administration of the A. sativum aqueous extract (500 mg/kg) for 3 weeks significantly increased serum antioxidant levels compared to the pretreatment levels in both diabetic and hypertensive rats. In addition, the A. sativum extract decreased serum glucose and systolic blood pressure in diabetic and hypertensive rats, respectively (Drobiova et al., 2011).
Chan Wok Sohn et al. examined the effect of high temperature/high pressure–processed garlic on plasma lipid profiles in rats. They suggested that high temperature/high pressure–processed garlic may be useful as a functional food to improve the lipid profile (Sohn et al., 2012). Black garlic extracts (0.5 and 1.5%) downregulated lipid and cholesterol metabolism in rats fed by a high fat diet. As a result, the blood levels of total lipids, triglyceride, and cholesterol were decreased (Ha et al., 2015). It has been reported that S-allyl cysteine sulphoxide (SACS), a sulfur-containing amino acid of garlic, has significant antidiabetic effects in alloxan-induced diabetic rats. Administration of allicin at a dose of 200 mg/kg decreased the concentration of blood glucose and ameliorated diabetic condition and increased liver and intestinal HMG CoA reductase activity and liver hexokinase activity (Sheela and Augusti, 1992).
The effects of garlic tablet (300 mg), containing (1.3% allicin) twice daily in patients with type 2 diabetes mellitus for 12 weeks significantly reduced total cholesterol, LDL-C, while significantly increased HDL cholesterol in patients treated with garlic compared to the placebo-treated group (Ashraf et al., 2004). In a study, the patients with type 2 diabetes mellitus received garlic tablets at doses of 300, 600, 900, 1,200, and 1,500 mg per day, respectively, for 24 weeks. Based on results, a significant reduction in FBS and HbA1c was observed when compared with placebo (Khan, 2011; Mirunalini et al., 2011; Aslani et al., 2016). Treatment of diabetic patients with three small cloves of raw garlic (1 clove = 1.2 g) daily in fasting condition for 30 days significantly reduced the blood glucose level, serum cholesterol, TG, and LDL while increased the HDL fraction. Furthermore, garlic significantly improved SOD, catalase (CAT) and glutathione peroxidase (GPx) in erythrocytes of diabetic patients compared to the control group (Khan, 2011; Mirunalini et al., 2011; Aslani et al., 2016).
Treatment of hyperlipidemic patients (n = 112) with garlic (20 g) daily with 1 tablespoon lemon juice significantly decreased the total cholesterol, LDL-cholesterol, and fibrinogen compared to the control groups (Khan, 2011; Mirunalini et al., 2011; Aslani et al., 2016). Aged garlic extract did not affect blood glucose but TG concentrations declined after 3 months of intervention. Aged garlic extract intake also reduced hydroperoxide as an indicator of oxidative stress (Ahmed et al., 2012). These findings suggest that dietary supplementation of garlic may be beneficial in reducing blood pressure and oxidative stress in hypertensive individuals. Effects of garlic and its ingredients on diabetes and nonalcoholic fatty liver disease are summarized in Table 3.
TABLE 3. Effects of garlic and its ingredients on obesity, diabetes mellitus, and nonalcoholic fatty liver disease.
Based on the results of animal and clinical trial studies, the mentioned medicinal herbs and their effective ingredients have beneficial therapeutic effects on metabolic diseases including obesity, diabetes mellitus, and fatty liver. These therapeutic properties are mainly associated with the modification of lipid profile, reduction of serum level of glucose, improvement of oxidative stress, and inhibition of inflammatory responses.
AA and HS helped in study design, search in literature, and helped in the preparation of the manuscript. MK, made substantial contributions to the study design, search in literature, and designed the study and critically revised the manuscript. All authors read and approved the final version of the manuscript.
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.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Abdelrazek, H., Kilany, O. E., Muhammad, M. A., Tag, H. M., and Abdelazim, A. M. (2018). Black Seed Thymoquinone Improved Insulin Secretion, Hepatic Glycogen Storage, and Oxidative Stress in Streptozotocin-Induced Diabetic Male Wistar Rats. Oxid. Med. Cell. Longev. 2018, 8104165. doi:10.1155/2018/8104165
Addepalli, V., and Suryavanshi, S. V. (2018). Catechin Attenuates Diabetic Autonomic Neuropathy in Streptozotocin Induced Diabetic Rats. Biomed. Pharmacother. 108, 1517–1523. doi:10.1016/j.biopha.2018.09.179
Adiban Fard, F., Tork Zahrani, S., Akbarzadeh Bagheban, A., and Mojab, F. (2015). Therapeutic Effects of Nigella Sativa linn (Black Cumin) on Candida Albicans Vaginitis. Arch. Clin. Infect. Dis. 10 (1–5), e22991. doi:10.5812/archcid.22991
Afkhami-Ardekani, M., Kamali-Ardekani, A.-R., and Shojaoddiny-Ardekani, A. (2006). Effects of Garlic on Serum Lipids and Blood Glucose of Type 2 Diabetic Patients. Int. J. Diab. Dev. Ctries 26 (2), 86–88. doi:10.4103/0973-3930.28279
Ajmal Shah, M., Khalil, R., Ul-Haq, Z., and Panichayupakaranant, P. (2017). α-Glucosidase Inhibitory Effect of Rhinacanthins-Rich Extract from Rhinacanthus Nasutus Leaf and Synergistic Effect in Combination with Acarbose. J. Funct. Foods 36, 325–331. doi:10.1016/j.jff.2017.07.021
Al-Qattan, K. K., Alnaqeeb, M. A., and Ali, M. (1999). The Antihypertensive Effect of Garlic (Allium Sativum) in the Rat Two-Kidney-OoneCclip Goldblatt Model. J. Ethnopharmacol. 66 (2), 217–222. doi:10.1016/S0378-8741(98)00173-1
Al-Shiekh, A., Al-Shati, A., and Sarhan, M. (2014). Effect of White Tea Extract on Antioxidant Enzyme Activities of Streptozotocin -Induced Diabetic Rats. Egypt. Acad. J. Biol. Sci. C Physiol. Mol. Biol. 6 (2), 17–30. doi:10.21608/eajbsc.2014.13710
Alcázar, A., Ballesteros, O., Jurado, J. M., Pablos, F., Martín, M. J., Vilches, J. L., et al. (2007). Differentiation of green, white, Black, Oolong, and Pu-Erh Teas According to Their Free Amino Acids Content. J. Agric. Food Chem. 55 (15), 5960–5965. doi:10.1021/jf070601a
Altun, E., Avci, E., Yildirim, T., and Yildirim, S. (2019). Protective Effect of Nigella Sativa Oil on Myocardium in Streptozotocin-Induced Diabetic Rats. Acta Endocrinol. (Buchar) 15 (3), 289–294. doi:10.4183/aeb.2019.289
Alves, M. G., Martins, A. D., Teixeira, N. F., Rato, L., Oliveira, P. F., and Silva, B. M. (2015). White tea Consumption Improves Cardiac Glycolytic and Oxidative Profile of Prediabetic Rats. J. Funct. Foods 14, 102–110. doi:10.1016/j.jff.2015.01.019
Ansari, Z. M., Nasiruddin, M., Khan, R. A., and Haque, S. F. (2017). Protective Role of Nigella Sativa in Diabetic Nephropathy: A Randomized Clinical Trial. Saudi J. Kidney Dis. Transpl. 28 (1), 9–14. doi:10.4103/1319-2442.198093
Ardiana, L., Sauriasari, R., and Elya, B. (2018). Antidiabetic Activity Studies of white tea (Camellia Sinensis (L.) O. Kuntze) Ethanolic Extracts in Streptozotocin-Nicotinamide Induced Diabetic Rats. Pharmacognosy J. 10 (1), 186. doi:10.5530/pj.2018.1.31
Aslani, N., Entezari, M. H., Askari, G., Maghsoudi, Z., and Maracy, M. R. (2016). Effect of Garlic and Lemon Juice Mixture on Lipid Profile and Some Cardiovascular Risk Factors in People 30-60 Years Old with Moderate Hyperlipidaemia: A Randomized Clinical Trial. Int. J. Prev. Med. 7, 95. doi:10.4103/2008-7802.187248
Atkin, M., Laight, D., and Cummings, M. H. (2016). The Effects of Garlic Extract upon Endothelial Function, Vascular Inflammation, Oxidative Stress and Insulin Resistance in Adults with Type 2 Diabetes at High Cardiovascular Risk. A Pilot Double Blind Randomized Placebo Controlled Trial. J. Diabetes Complications 30 (4), 723–727. doi:10.1016/j.jdiacomp.2016.01.003
Awad, A. S., Abd Al Haleem, E. N., El-Bakly, W. M., and Sherief, M. A. (2016). Thymoquinone Alleviates Nonalcoholic Fatty Liver Disease in Rats via Suppression of Oxidative Stress, Inflammation, Apoptosis. Naunyn Schmiedebergs Arch. Pharmacol. 389 (4), 381–391. doi:10.1007/s00210-015-1207-1
Ayuob, N. N., Abdel-Hamid, A. A. H. M., Helal, G. M. M., and Mubarak, W. A. (2019). Thymoquinone Reverses Nonalcoholic Fatty Liver Disease (NAFLD) Associated with Experimental Hypothyroidism. Rom. J. Morphol. Embryol. 60 (2), 479–486.
Badar, A., Kaatabi, H., Bamosa, A., Al-Elq, A., Abou-Hozaifa, B., Lebda, F., et al. (2017). Effect of Nigella Sativa Supplementation over a One-Year Period on Lipid Levels, Blood Pressure and Heart Rate in Type-2 Diabetic Patients Receiving Oral Hypoglycemic Agents: Nonrandomized Clinical Trial. Ann. Saudi Med. 37 (1), 56–63. doi:10.5144/0256-4947.2017.56
Balamash, K., Albar, O., Wang, Q., and Ahmed, N. (2012). Effect of Kyolic Aged Garlic Extract on Glycaemia, Lipidaemia and Oxidative Stress in Patients with Type 2 Diabetes Mellitus. J. Diab Res. Clin. Met. 1, 18. doi:10.7243/2050-0866-1-18
Balbaa, M., El-Zeftawy, M., Ghareeb, D., Taha, N., and Mandour, A. W. (2016). Nigella Sativa Relieves the Altered Insulin Receptor Signaling in Streptozotocin-Induced Diabetic Rats Fed with a High-Fat Diet. Oxid. Med. Cell. Longev. 2016, 2492107. doi:10.1155/2016/2492107
Barbagallo, M., and Dominguez, L. J. (2007). Magnesium Metabolism in Type 2 Diabetes Mellitus, Metabolic Syndrome and Insulin Resistance. Arch. Biochem. Biophys. 458 (1), 40–47. doi:10.1016/j.abb.2006.05.007
Bathaie, S. Z., and Mousavi, S. Z. (2010). New Applications and Mechanisms of Action of Saffron and its Important Ingredients. Crit. Rev. Food Sci. Nutr. 50 (8), 761–786. doi:10.1080/10408390902773003
Benhaddou-Andaloussi, A., Martineau, L. C., Vallerand, D., Haddad, Y., Afshar, A., Settaf, A., et al. (2010). Multiple Molecular Targets Underlie the Antidiabetic Effect of Nigella Sativa Seed Extract in Skeletal Muscle, Adipocyte and Liver Cells. Diabetes Obes. Metab. 12 (2), 148–157. doi:10.1111/j.1463-1326.2009.01131.x
Boulangé, C. L., Neves, A. L., Chilloux, J., Nicholson, J. K., and Dumas, M. E. (2016). Impact of the Gut Microbiota on Inflammation, Obesity, and Metabolic Disease. Genome Med. 8 (1), 42–12. doi:10.1186/s13073-016-0303-2
Choudhary, P. R., Jani, R. D., and Sharma, M. S. (2018). Effect of Raw Crushed Garlic (Allium Sativum L.) on Components of Metabolic Syndrome. J. Diet. Suppl. 15 (4), 499–506. doi:10.1080/19390211.2017.1358233
NCD Risk Factor Collaboration (2016). Trends in Adult Body-Mass index in 200 Countries from 1975 to 2014: a Pooled Analysis of 1698 Population-Based Measurement Studies with 19·2 Million Participants. Lancet 387 (10026), 1377–1396. doi:10.1016/S0140-6736(16)30054-X
Darand, M., Darabi, Z., Yari, Z., Hedayati, M., Shahrbaf, M. A., Khoncheh, A., et al. (2019a). The Effects of Black Seed Supplementation on Cardiovascular Risk Factors in Patients with Nonalcoholic Fatty Liver Disease: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial. Phytother Res. 33 (9), 2369–2377. doi:10.1002/ptr.6424
Darand, M., Darabi, Z., Yari, Z., Saadati, S., Hedayati, M., Khoncheh, A., et al. (2019b). Nigella Sativa and Inflammatory Biomarkers in Patients with Non-alcoholic Fatty Liver Disease: Results from a Randomized, Double-Blind, Placebo-Controlled, Clinical Trial. Complement. Ther. Med. 44, 204–209. doi:10.1016/j.ctim.2019.04.014
Das Gupta, A., Das, S. N., Dhundasi, S. A., and Das, K. K. (2008). Effect of Garlic (Allium Sativum) on Heavy Metal (Nickel II and Chromium VI) Induced Alteration of Serum Lipid Profile in Male Albino Rats. Int. J. Environ. Res. Public Health 5 (3), 147–151. doi:10.3390/ijerph2008050020
Datau, E. A., Wardhana, E. E., Surachmanto, E. E., Pandelaki, K., Langi, J. A., and Fias, W. (2010). Efficacy of Nigella Sativa on Serum Free Testosterone and Metabolic Disturbances in central Obese Male. Acta Med. Indones 42 (3), 130–134.
Drobiova, H., Thomson, M., Al-Qattan, K., Peltonen-Shalaby, R., Al-Amin, Z., and Ali, M. (2011). Garlic Increases Antioxidant Levels in Diabetic and Hypertensive Rats Determined by a Modified Peroxidase Method. Evid. Based Complement. Alternat. Med. 2011, 703049. doi:10.1093/ecam/nep011
Dulloo, A. G., Jacquet, J., Solinas, G., Montani, J. P., and Schutz, Y. (2010). Body Composition Phenotypes in Pathways to Obesity and the Metabolic Syndrome. Int. J. Obes. (Lond) 34 (2), S4–S17. doi:10.1038/ijo.2010.234
Eidi, A., Eidi, M., and Esmaeili, E. (2006). Antidiabetic Effect of Garlic (Allium Sativum L.) in normal and Streptozotocin-Induced Diabetic Rats. Phytomedicine 13 (9-10), 624–629. doi:10.1016/j.phymed.2005.09.010
El-Saber Batiha, G., Magdy Beshbishy, A., G. Wasef, L., Elewa, Y. H. A., A. Al-Sagan, A., Abd El-Hack, M. E., et al. (2020). Chemical Constituents and Pharmacological Activities of Garlic (Allium Sativum L.): A Review. Nutrients 12 (3), 872. doi:10.3390/nu12030872
Espinosa, C., González-Silvera, D., Pérez-Llamas, F., López-Jiménez, J. Á., and Zamora, S. (2015). Effect of Long Term Intake of white tea on Acute Oxidative Stress in Rats. Nutr. Hosp. 32 (2), 749–756. doi:10.3305/nh.2015.32.2.9270
Esser, N., Legrand-Poels, S., Piette, J., Scheen, A. J., and Paquot, N. (2014). Inflammation as a Link between Obesity, Metabolic Syndrome and Type 2 Diabetes. Diabetes Res. Clin. Pract. 105 (2), 141–150. doi:10.1016/j.diabres.2014.04.006
Gondoin, A., Grussu, D., Stewart, D., and McDougall, G. J. (2010). White and green tea Polyphenols Inhibit Pancreatic Lipase In Vitro. Food Res. Int. 43 (5), 1537–1544. doi:10.1016/j.foodres.2010.04.029
Ha, A. W., Ying, T., and Kim, W. K. (2015). The Effects of Black Garlic (Allium Satvium) Extracts on Lipid Metabolism in Rats Fed a High Fat Diet. Nutr. Res. Pract. 9 (1), 30–36. doi:10.4162/nrp.2015.9.1.30
Hashem, R. M., Mahmoud, M. F., EL-Moselhy, M. A., and Soliman, H. M. (2008). Interleukin-10 to Tumor Necrosis Factor-Alpha Ratio Is a Predictive Biomarker in Nonalcoholic Fatty Liver Disease: Interleukin-10 to Tumor Necrosis Factor-Alpha Ratio in Steatohepatitis. Eur. J. Gastroenterol. Hepatol. 20 (10), 995–1001. doi:10.1097/MEG.0b013e3282fdf65f
Hibi, M., Takase, H., Iwasaki, M., Osaki, N., and Katsuragi, Y. (2018). Efficacy of tea Catechin-Rich Beverages to Reduce Abdominal Adiposity and Metabolic Syndrome Risks in Obese and Overweight Subjects: a Pooled Analysis of 6 Human Trials. Nutr. Res. 55, 1–10. doi:10.1016/j.nutres.2018.03.012
Hmza, A. J. A., Omar, E., Adnan, A., and Osman, M. T. (2013). Nigella Sativa Oil Has Significant Repairing Ability of Damaged Pancreatic Tissue Occurs in Induced Type 1 Diabetes Mellitus. Glob. J. Pharmacol. 7 (1), 14–19. doi:10.5829/idosi.gjp.2013.7.1.7383
Hodges, J. K., Sasaki, G. Y., and Bruno, R. S. (2020). Anti-inflammatory Activities of green tea Catechins along the Gut-Liver axis in Nonalcoholic Fatty Liver Disease: Lessons Learned from Preclinical and Human Studies. J. Nutr. Biochem. 85, 108478. doi:10.1016/j.jnutbio.2020.108478
Hodgson, J. M., Burke, V., and Puddey, I. B. (2005). Acute Effects of tea on Fasting and Postprandial Vascular Function and Blood Pressure in Humans. J. Hypertens. 23 (1), 47–54. doi:10.1097/00004872-200501000-00012
Hormati, A., Tooiserkany, F., Mohammadbeigi, A., Aliasl, F., and Moradi Dehnavi, H. (2019). Effect of an Herbal Product on the Serum Level of Liver Enzymes in Patients with Non-Alcoholic Fatty Liver Disease: A Randomized, Double-Blinded, Placebo-Controlled Trial. Iranian Red Crescent Med. J. 21 (1–7), e91024. doi:10.5812/ircmj.91024
Hosseini, S. M. R., Razmgah, G. R. G., Nematy, M., Esmaily, H., Yousefi, M., Kamalinejad, M., et al. (2018). Efficacy of Black Seed (Nigella Sativa) and Lemon Balm (melissa Officinalis) on Non-alcoholic Fatty Liver Disease: A Randomized Controlled Clinical Trial. Iranian Red Crescent Med. J. 20 (1–9), e59183. doi:10.5812/ircmj.59183
Huang, H. C., and Lin, J. K. (2012). Pu-erh tea, green tea, and Black tea Suppresses Hyperlipidemia, Hyperleptinemia and Fatty Acid Synthase through Activating AMPK in Rats Fed a High-Fructose Diet. Food Funct. 3 (2), 170–177. doi:10.1039/c1fo10157a
Hussain, M., Tunio, A. G., Akhtar, L., and Shaikh, G. S. (2017). Effects of Nigella Sativa on Various Parameters in Patients of Non-alcoholic Fatty Liver Disease. J. Ayub Med. Coll. Abbottabad 29 (3), 403–407.
Kaatabi, H., Bamosa, A. O., Lebda, F. M., Al Elq, A. H., and Al-Sultan, A. I. (2012). Favorable Impact of Nigella Sativa Seeds on Lipid Profile in Type 2 Diabetic Patients. J. Fam. Community Med. 19 (3), 155–161. doi:10.4103/2230-8229.102311
Karandrea, S., Yin, H., Liang, X., Slitt, A. L., and Heart, E. A. (2017). Thymoquinone Ameliorates Diabetic Phenotype in Diet-Induced Obesity Mice via Activation of SIRT-1-dependent Pathways. PloS one 12 (9), e0185374. doi:10.1371/journal.pone.0185374
Kasuga, S., Ushijima, M., Morihara, N., Itakura, Y., and Nakata, Y. (1999). Effect of Aged Garlic Extract (AGE) on Hyperglycemia Induced by Immobilization Stress in Mice. Nihon Yakurigaku Zasshi 114 (3), 191–197. doi:10.1254/fpj.114.191
Kaur, G., Invally, M., Khan, M. K., and Jadhav, P. (2018). A Nutraceutical Combination of Cinnamomum cassia &Nigella Sativa for Type 1 Diabetes Mellitus. J. Ayurveda Integr. Med. 9 (1), 27–37. doi:10.1016/j.jaim.2017.02.005
Ketenoglu, O., Kiralan, S. S., Kiralan, M., Ozkan, G., and Ramadan, M. F. (2020). “Cold Pressed Black Cumin (Nigella Sativa L.) Seed Oil,” in Cold Pressed Oils (Çankırı, Turkey: Elsevier), 53–64. doi:10.1016/b978-0-12-818188-1.00006-2
Khazdair, M. R., Anaeigoudari, A., Hashemzehi, M., and Mohebbati, R. (2019). Neuroprotective Potency of Some Spice Herbs, a Literature Review. J. Tradit. Complement. Med. 9 (2), 98–105. doi:10.1016/j.jtcme.2018.01.002
Khonche, A., Huseini, H. F., Gholamian, M., Mohtashami, R., Nabati, F., and Kianbakht, S. (2019). Standardized Nigella Sativa Seed Oil Ameliorates Hepatic Steatosis, Aminotransferase and Lipid Levels in Non-alcoholic Fatty Liver Disease: A Randomized, Double-Blind and Placebo-Controlled Clinical Trial. J. Ethnopharmacol. 234, 106–111. doi:10.1016/j.jep.2019.01.009
Lee, S. P., Kuo, F. Y., Cheng, J. T., and Wu, M. C. (2019). GLP-1 Mediates the Modulating Effect of Thymoquinone on Feeding Behaviors in Diabetic Rats. Diabetes Metab. Syndr. Obes. 12, 873–881. doi:10.2147/DMSO.S207596
Li, B., Mao, Q., Zhou, D., Luo, M., Gan, R., Li, H., et al. (2021). Effects of Tea against Alcoholic Fatty Liver Disease by Modulating Gut Microbiota in Chronic Alcohol-Exposed Mice. Foods 10 (6), 1232. doi:10.3390/foods10061232
Liu, C. T., Hse, H., Lii, C. K., Chen, P. S., and Sheen, L. Y. (2005). Effects of Garlic Oil and Diallyl Trisulfide on Glycemic Control in Diabetic Rats. Eur. J. Pharmacol. 516 (2), 165–173. doi:10.1016/j.ejphar.2005.04.031
Liu, C. T., Wong, P. L., Lii, C. K., Hse, H., and Sheen, L. Y. (2006). Antidiabetic Effect of Garlic Oil but Not Diallyl Disulfide in Rats with Streptozotocin-Induced Diabetes. Food Chem. Toxicol. 44 (8), 1377–1384. doi:10.1016/j.fct.2005.07.013
Luo, K., Ma, C., Xing, S., An, Y., Feng, J., Dang, H., et al. (2020). White tea and its Active Polyphenols Lower Cholesterol through Reduction of Very-Low-Density Lipoprotein Production and Induction of LDLR Expression. Biomed. Pharmacother. 127, 110146. doi:10.1016/j.biopha.2020.110146
Mahdavi, R., Namazi, N., Alizadeh, M., and Farajnia, S. (2015). Effects of Nigella Sativa Oil with a Low-Calorie Diet on Cardiometabolic Risk Factors in Obese Women: a Randomized Controlled Clinical Trial. Food Funct. 6 (6), 2041–2048. doi:10.1039/c5fo00316d
Mahmoudi, A., Ghatreh Samani, K., Farrokhi, E., and Heidarian, E. (2018). Effects of Nigella Sativa Extracts on the Lipid Profile and Uncoupling Protein-1 Gene Expression in Brown Adipose Tissue of Mice. Adv. Biomed. Res. 7, 121. doi:10.4103/abr.abr_91_18
Maki, K. C., Reeves, M. S., Farmer, M., Yasunaga, K., Matsuo, N., Katsuragi, Y., et al. (2009). Green tea Catechin Consumption Enhances Exercise-Induced Abdominal Fat Loss in Overweight and Obese Adults. J. Nutr. 139 (2), 264–270. doi:10.3945/jn.108.098293
Mao, Q. Q., Li, B. Y., Meng, J. M., Gan, R. Y., Xu, X. Y., Gu, Y. Y., et al. (2021). Effects of Several tea Extracts on Nonalcoholic Fatty Liver Disease in Mice Fed with a High‐fat Diet. Food Sci. Nutr. 9, 2954. doi:10.1002/fsn3.2255
Mariee, A. D., Abd-Allah, G. M., and El-Yamany, M. F. (2009). Renal Oxidative Stress and Nitric Oxide Production in Streptozotocin-Induced Diabetic Nephropathy in Rats: the Possible Modulatory Effects of Garlic (Allium Sativum L.). Biotechnol. Appl. Biochem. 52 (3), 227–232. doi:10.1042/BA20080086
Meral, I., Yener, Z., Kahraman, T., and Mert, N. (2001). Effect of Nigella Sativa on Glucose Concentration, Lipid Peroxidation, Anti-oxidant Defence System and Liver Damage in Experimentally-Induced Diabetic Rabbits. J. Vet. Med. A. Physiol. Pathol. Clin. Med. 48 (10), 593–599. doi:10.1046/j.1439-0442.2001.00393.x
Mohamed, W. S., Mostafa, A. M., Mohamed, K. M., and Serwah, A. H. (2015). Effects of Fenugreek, Nigella, and Termis Seeds in Nonalcoholic Fatty Liver in Obese Diabetic Albino Rats. Arab J. Gastroenterol. 16 (1), 1–9. doi:10.1016/j.ajg.2014.12.003
Mohtashami, A., and Entezari, M. H. (2016). Effects of Nigella Sativa Supplementation on Blood Parameters and Anthropometric Indices in Adults: A Systematic Review on Clinical Trials. J. Res. Med. Sci. 21, 3. doi:10.4103/1735-1995.175154
Mokhtari-Zaer, A., Norouzi, F., Askari, V. R., Khazdair, M. R., Roshan, N. M., Boskabady, M., et al. (2020). The Protective Effect of Nigella Sativa Extract on Lung Inflammation and Oxidative Stress Induced by Lipopolysaccharide in Rats. J. Ethnopharmacol. 253, 112653. doi:10.1016/j.jep.2020.112653
Mortazavi Moghaddam, S. G., Kianmehr, M., and Khazdair, M. R. (2020). The Possible Therapeutic Effects of Some Medicinal Plants for Chronic Cough in Children. Evidence-Based Complement. Altern. Med. 2020, 2149328. doi:10.1155/2020/2149328
Mostafavinia, A., Ahmadi, H., Amini, A., Roudafshani, Z., Hamblin, M. R., Chien, S., et al. (2021). The Effect of Photobiomodulation Therapy on Antioxidants and Oxidative Stress Profiles of Adipose Derived Mesenchymal Stem Cells in Diabetic Rats. Spectrochim. Acta A: Mol. Biomol. Spectrosc. 262, 120157. doi:10.1016/j.saa.2021.120157
Motawi, T. K., Shaker, O. G., Ismail, M. F., and Sayed, N. H. (2017). Peroxisome Proliferator-Activated Receptor Gamma in Obesity and Colorectal Cancer: the Role of Epigenetics. Sci. Rep. 7 (1), 10714–10718. doi:10.1038/s41598-017-11180-6
Murase, T., Nagasawa, A., Suzuki, J., Hase, T., and Tokimitsu, I. (2002). Beneficial Effects of tea Catechins on Diet-Induced Obesity: Stimulation of Lipid Catabolism in the Liver. Int. J. Obes. Relat. Metab. Disord. 26 (11), 1459–1464. doi:10.1038/sj.ijo.0802141
Musabayane, C. T., Bwititi, P. T., and Ojewole, J. A. (2006). Effects of Oral Administration of Some Herbal Extracts on Food Consumption and Blood Glucose Levels in normal and Streptozotocin-Treated Diabetic Rats. Methods Find Exp. Clin. Pharmacol. 28 (4), 223–228. doi:10.1358/mf.2006.28.4.990202
Nagao, T., Meguro, S., Hase, T., Otsuka, K., Komikado, M., Tokimitsu, I., et al. (2009). A Catechin-Rich Beverage Improves Obesity and Blood Glucose Control in Patients with Type 2 Diabetes. Obesity (Silver Spring) 17 (2), 310–317. doi:10.1038/oby.2008.505
Namazi, N., Larijani, B., Ayati, M. H., and Abdollahi, M. (2018). The Effects of Nigella Sativa L. On Obesity: A Systematic Review and Meta-Analysis. J. Ethnopharmacol. 219, 173–181. doi:10.1016/j.jep.2018.03.001
Ning, J.-M., Ding, D., Song, Y.-S., Zhang, Z.-Z., Luo, X., and Wan, X.-C. (2016). Chemical Constituents Analysis of white tea of Different Qualities and Different Storage Times. Eur. Food Res. Technol. 242 (12), 2093–2104. doi:10.1007/s00217-016-2706-0
Nishiyama, M., Ohtake, N., Kaneko, A., Tsuchiya, N., Imamura, S., Iizuka, S., et al. (2020). Increase of Akkermansia Muciniphila by a Diet Containing Japanese Traditional Medicine Bofutsushosan in a Mouse Model of Non-Alcoholic Fatty Liver Disease. Nutrients 12 (3), 839. doi:10.3390/nu12030839
Nunes, A. R., Alves, M. G., Tomás, G. D., Conde, V. R., Cristóvão, A. C., Moreira, P. I., et al. (2015). Daily Consumption of white tea (Camellia Sinensis (L.)) Improves the Cerebral Cortex Metabolic and Oxidative Profile in Prediabetic Wistar Rats. Br. J. Nutr. 113 (5), 832–842. doi:10.1017/S0007114514004395
Nwokocha, C. R., Ozolua, R. I., Owu, D. U., Nwokocha, M. I., and Ugwu, A. C. (2011). Antihypertensive Properties of Allium Sativum (Garlic) on Normotensive and Two Kidney One Clip Hypertensive Rats. Niger. J. Physiol. Sci. 26 (2), 213–218.
Osman, M., Adnan, A., Salmah Bakar, N., and Alashkham, F. (2012). Allicin Has Significant Effect on Autoimmune Anti-islet Cell Antibodies in Type 1 Diabetic Rats. Pol. J. Pathol. 63 (4), 248–254. doi:10.5114/pjp.2012.32772
Rajani Kanth, V., Uma Maheswara Reddy, P., and Raju, T. N. (2008). Attenuation of Streptozotocin-Induced Oxidative Stress in Hepatic and Intestinal Tissues of Wistar Rat by Methanolic-Garlic Extract. Acta Diabetol. 45 (4), 243–251. doi:10.1007/s00592-008-0051-x
Ramadan, M. F. (2020). Black Cumin (Nigella Sativa) Seeds: Chemistry, Technology, Functionality, and Applications. Zagazig, Egypt: Springer Nature Press, 53–64. ISBN 9780128181881. doi:10.1016/B978-0-12-818188-1.00006-2
Rao, A. S., Hegde, S., Pacioretty, L. M., DeBenedetto, J., and Babish, J. G. (2020). Nigella Sativa and Trigonella Foenum-Graecum Supplemented Chapatis Safely Improve HbA1c, Body Weight, Waist Circumference, Blood Lipids, and Fatty Liver in Overweight and Diabetic Subjects: A Twelve-Week Safety and Efficacy Study. J. Med. Food 23 (9), 905–919. doi:10.1089/jmf.2020.0075
Rashidmayvan, M., Mohammadshahi, M., Seyedian, S. S., and Haghighizadeh, M. H. (2019). The Effect of Nigella Sativa Oil on Serum Levels of Inflammatory Markers, Liver Enzymes, Lipid Profile, Insulin and Fasting Blood Sugar in Patients with Non-alcoholic Fatty Liver. J. Diabetes Metab. Disord. 18 (2), 453–459. doi:10.1007/s40200-019-00439-6
Razmpoosh, E., Safi, S., Mazaheri, M., Salehi-Abargouei, A., Abdollahi, N., Nazari, M., et al. (2019). Effects of Oral Nigella Sativa Oil on the Expression Levels and Serum Concentrations of Adiponectin, PPAR-γ, and TNF-α in Overweight and Obese Women: a Study Protocol for a Crossover-Designed, Double-Blind, Placebo-Controlled Randomized Clinical Trial. Trials 20 (1), 512–518. doi:10.1186/s13063-019-3568-0
Rea, I. M., Gibson, D. S., McGilligan, V., McNerlan, S. E., Alexander, H. D., and Ross, O. A. (2018). Age and Age-Related Diseases: Role of Inflammation Triggers and Cytokines. Front. Immunol. 9, 586. doi:10.3389/fimmu.2018.00586
Rochlani, Y., Pothineni, N. V., Kovelamudi, S., and Mehta, J. L. (2017). Metabolic Syndrome: Pathophysiology, Management, and Modulation by Natural Compounds. Ther. Adv. Cardiovasc. Dis. 11 (8), 215–225. doi:10.1177/1753944717711379
Roglic, G., Unwin, N., Bennett, P. H., Mathers, C., Tuomilehto, J., Nag, S., et al. (2005). The burden of Mortality Attributable to Diabetes: Realistic Estimates for the Year 2000. Diabetes Care 28 (9), 2130–2135. doi:10.2337/diacare.28.9.2130
Rusak, G., Komes, D., Likić, S., Horžić, D., and Kovač, M. (2008). Phenolic Content and Antioxidative Capacity of green and white tea Extracts Depending on Extraction Conditions and the Solvent Used. Food Chem. 110 (4), 852–858. doi:10.1016/j.foodchem.2008.02.072
Rusda, M., Ganis Siregar, M. F., Lelo, A., Ilyas, S., Akbari Ganie, R., Effendi, Y., et al. (2020). A Therapeutic Effect of Nigella Sativa Extract on Female Wistar Rats Vulvovaginal Candidiasis Model. Med. Glas (Zenica) 17 (2), 472–476. doi:10.17392/1112-20
Sakata, R., Nakamura, T., Torimura, T., Ueno, T., and Sata, M. (2013). Green tea with High-Density Catechins Improves Liver Function and Fat Infiltration in Non-alcoholic Fatty Liver Disease (NAFLD) Patients: a Double-Blind Placebo-Controlled Study. Int. J. Mol. Med. 32 (5), 989–994. doi:10.3892/ijmm.2013.1503
Shang, A., Cao, S. Y., Xu, X. Y., Gan, R. Y., Tang, G. Y., Corke, H., et al. (2019). Bioactive Compounds and Biological Functions of Garlic (Allium Sativum L.). Foods 8 (7), 246. doi:10.3390/foods8070246
Sobenin, I. A., Nedosugova, L. V., Filatova, L. V., Balabolkin, M. I., Gorchakova, T. V., and Orekhov, A. N. (2008). Metabolic Effects of Time-Released Garlic Powder Tablets in Type 2 Diabetes Mellitus: the Results of Double-Blinded Placebo-Controlled Study. Acta Diabetol. 45 (1), 1–6. doi:10.1007/s00592-007-0011-x
Söhle, J., Knott, A., Holtzmann, U., Siegner, R., Grönniger, E., Schepky, A., et al. (2009). White Tea Extract Induces Lipolytic Activity and Inhibits Adipogenesis in Human Subcutaneous (Pre)-adipocytes. Nutr. Metab. (Lond) 6 (1), 20–10. doi:10.1186/1743-7075-6-20
Sohn, C. W., Kim, H., You, B. R., Kim, M. J., Kim, H. J., Lee, J. Y., et al. (2012). High Temperature- and High Pressure-Processed Garlic Improves Lipid Profiles in Rats Fed High Cholesterol Diets. J. Med. Food 15 (5), 435–440. doi:10.1089/jmf.2011.1922
Sultan, M. T., Butt, M. S., Karim, R., Iqbal, S. Z., Ahmad, S., Zia-Ul-Haq, M., et al. (2014). Effect of Nigella Sativa Fixed and Essential Oils on Antioxidant Status, Hepatic Enzymes, and Immunity in Streptozotocin Induced Diabetes Mellitus. BMC Complement. Altern. Med. 14 (1), 193. doi:10.1186/1472-6882-14-193
Sun, L., Xu, H., Ye, J., and Gaikwad, N. W. (2019). Comparative Effect of Black, green, Oolong, and white tea Intake on Weight Gain and Bile Acid Metabolism. Nutrition 65, 208–215. doi:10.1016/j.nut.2019.02.006
Suriyavathana Vedanarayanan, M., and Krishnan, N. (2011). Ayurvedic Formulation of Liv-Pro-08 Reduces Nonalcoholic Fatty Liver Disease in Rats Fed with High-Fat Diet. J. Acupunct. Meridian Stud. 4 (4), 236–241. doi:10.1016/j.jams.2011.09.014
Teixeira, L. G., Lages, P. C., Jascolka, T. L., Aguilar, E. C., Soares, F. L. P., Pereira, S. S., et al. (2012). White tea (Camellia Sinensis) Extract Reduces Oxidative Stress and Triacylglycerols in Obese Mice. Food Sci. Technol. 32 (4), 733–741. doi:10.1590/s0101-20612012005000099
Teng, Y., Li, D., Guruvaiah, P., Xu, N., and Xie, Z. (2018). Dietary Supplement of Large Yellow tea Ameliorates Metabolic Syndrome and Attenuates Hepatic Steatosis in Db/db Mice. Nutrients 10 (1), 75. doi:10.3390/nu10010075
Tenore, G. C., Stiuso, P., Campiglia, P., and Novellino, E. (2013). In Vitro hypoglycaemic and Hypolipidemic Potential of white tea Polyphenols. Food Chem. 141 (3), 2379–2384. doi:10.1016/j.foodchem.2013.04.128
Thomson, M., Al-Amin, Z. M., Al-Qattan, K. K., Shaban, L. H., and Ali, M. (2007). Anti-diabetic and Hypolipidaemic Properties of Garlic (Allium Sativum) in Streptozotocin-Induced Diabetic Rats. Int. J. Diabetes Metab. 15 (3), 108–115.
Waisundara, V. Y., Hsu, A., Huang, D., and Tan, B. K. (2008). Scutellaria Baicalensis Enhances the Anti-diabetic Activity of Metformin in Streptozotocin-Induced Diabetic Wistar Rats. Am. J. Chin. Med. 36 (03), 517–540. doi:10.1142/S0192415X08005953
Xiao, J., Ho, C. T., Liong, E. C., Nanji, A. A., Leung, T. M., Lau, T. Y., et al. (2014). Epigallocatechin Gallate Attenuates Fibrosis, Oxidative Stress, and Inflammation in Non-alcoholic Fatty Liver Disease Rat Model through TGF/SMAD, PI3 K/Akt/FoxO1, and NF-Kappa B Pathways. Eur. J. Nutr. 53 (1), 187–199. doi:10.1007/s00394-013-0516-8
Xu, X., Yi, H., Wu, J., Kuang, T., Zhang, J., Li, Q., et al. (2020). Therapeutic Effect of Berberine on Metabolic Diseases: Both Pharmacological Data and Clinical Evidence. Biomed. Pharmacother. 133, 110984. doi:10.1016/j.biopha.2020.110984
Xu, Y., Zhang, M., Wu, T., Dai, S., Xu, J., and Zhou, Z. (2015). The Anti-obesity Effect of green tea Polysaccharides, Polyphenols and Caffeine in Rats Fed with a High-Fat Diet. Food Funct. 6 (1), 297–304. doi:10.1039/c4fo00970c
Yang, Q. Q., Shao, D., Li, J., Yang, C. L., Fan, M. H., and Cao, F. L. (2020). Positive Association between Serum Levels of High-Sensitivity C-Reactive Protein and Depression/anxiety in Female, but Not Male, Patients with Type 2 Diabetes Mellitus. Biol. Res. Nurs. 22 (2), 178–187. doi:10.1177/1099800419894641
Yang, Z., Zhu, M. Z., Zhang, Y. B., Wen, B. B., An, H. M., Ou, X. C., et al. (2019). Coadministration of Epigallocatechin-3-Gallate (EGCG) and Caffeine in Low Dose Ameliorates Obesity and Nonalcoholic Fatty Liver Disease in Obese Rats. Phytother Res. 33 (4), 1019–1026. doi:10.1002/ptr.6295
Yi, M., Wu, X., Zhuang, W., Xia, L., Chen, Y., Zhao, R., et al. (2019). Tea Consumption and Health Outcomes: Umbrella Review of Meta‐Analyses of Observational Studies in Humans. Mol. Nutr. Food Res. 63 (16), 1900389. doi:10.1002/mnfr.201900389
Yimer, E. M., Tuem, K. B., Karim, A., Ur-Rehman, N., and Anwar, F. (2019). Nigella Sativa L.(Black Cumin): A Promising Natural Remedy for Wide Range of Illnesses. Evidence-Based Complement. Altern. Med. 2019, 1–16. doi:10.1155/2019/1528635
Zhang, H. Y., Tian, J. X., Lian, F. M., Li, M., Liu, W. K., Zhen, Z., et al. (2020). Therapeutic Mechanisms of Traditional Chinese Medicine to Improve Metabolic Diseases via the Gut Microbiota. Biomed. Pharmacother. 133, 110857. doi:10.1016/j.biopha.2020.110857
Keywords: metabolic disorders, Nigella sativa L., white tea, Garlic, anti-obesity effects, anti-diabetic effects, anti-inflammatory effects
Citation: Anaeigoudari A, Safari H and Khazdair MR (2021) Effects of Nigella sativa, Camellia sinensis, and Allium sativum as Food Additives on Metabolic Disorders, a Literature Review. Front. Pharmacol. 12:762182. doi: 10.3389/fphar.2021.762182
Received: 21 August 2021; Accepted: 25 October 2021;
Published: 17 November 2021.
Edited by:Ilaria Peluso, Council for Agricultural and Economics Research (CREA), Italy
Reviewed by:Mohamed Fawzy Ramadan Hassanien, Zagazig University, Egypt
Claudio Ferrante, University of Studies G. d'Annunzio Chieti and Pescara, Italy
Ren-You Gan, Institute of Urban Agriculture (CAAS), China
Copyright © 2021 Anaeigoudari, Safari and Khazdair. 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.