Effects of an ethanolic extract of Berberis vulgaris fruits on hyperglycemia and related gene expression in streptozotocin-induced diabetic rats
© Hemmati et al. 2016
Received: 15 December 2015
Accepted: 22 January 2016
Published: 23 January 2016
Finding a treatment for diabetes that does not have side effects has remained elusive. Among natural agents, much attention has been focused on phenolic compounds. For both their medicinal and nutritional value, barberry plants are of particular interest. Berberis vulgaris is known for its medicinal benefits in Iranian traditional medicine. In this study, we investigated the biological activities of B.vulgaris in a rodent model of experimentally induced diabetes.
The fasting blood glucose (FBG), insulin, malondialdehyde (MDA), and total antioxidant levels were measured in experimental groups of rats, including normoglycemic control, diabetic control, and diabetics treated with B.vulgaris, and the gene expression of the stress proteins HSF-1, HSP27, and HSP70 as well as the enzymes glucokinase (GK) and glucose 6-phosphatase (G6P) were assayed by real-time PCR.
The application of the alcoholic extract of B.vulgaris (25 and 100 mg/kg body mass) significantly increased the total antioxidant levels, decreased MDA and FBG levels, and also increased mRNA level of GK compared with the diabetic control group (P ≤0.05). Our results also showed a reduction in HSP70 gene expression and a significant decrease in G6P gene expression in a dose-dependent manner (P ≤ 0.05). The effect of alcoholic extract of barberry at a higher dose (100 mg/kg) was similar to glibenclamide.
B.vulgaris extract is beneficial in ameliorating oxidative stress and may be useful in the treatment of diabetes. The therapeutic potential of B.vulgaris may be through the modification of the gene expression of key enzymes or stress proteins and requires further investigation.
KeywordsBerberis vulgaris Hyperglycemia Oxidative stress Heat shock protein Glucokinase Glucose 6-phosphatase
Diabetes mellitus (DM) is a major public health concern with numerous clinical manifestations. Of these, hyperglycemia is a major cause of absolute or relative insulin deficiency. According to World Health Organization projections, the diabetic population may increase to ≥300 million by 2050 . Free radical production is stimulated by hyperglycemia, leading to cell damage. In living organisms, oxidation is an essential process during the production of energy for use as fuel for biological processes. However, the increase in the formation of free radicals such as reactive oxygen species (ROS) plays a crucial rule in the pathophysiology of several diseases such as diabetes, cancer, and cardiovascular disease. Oxidative stress may also play a role in metabolic syndrome, which is indicated by the presence of several oxidative biomarkers . In addition, the body’s stress response may result in the progression or acceleration of numerous diseases related to oxidative stress. Heat shock proteins (HSPs) are a highly conserved and ubiquitously expressed family of proteins that respond to a wide variety of physical and metabolic stresses, including during protein refolding and degradation of damaged proteins; moreover, they also protect proteins against aggregation and maintain the overall integrity of cellular components. In summary, HSPs protect against chronically and acutely stressful conditions at the cellular level. Oxidative stress induces a protective HSP response in tissues; however, the protective role of HSP have less well-characterized as antioxidants [3, 4]. Antioxidants can delay or inhibit the oxidation of lipids or other molecules by inhibiting the initiation or progression of oxidizing chain reactions. Previous studies have demonstrated that antioxidants can reduce markers of oxidative stress in both experimental and clinical models of diabetes. The redox status is disrupted in both type 1 and type 2 DM due to hyperglycemia, resulting in stress-mediated cellular injury . Berberis vulgaris (B.vulgaris) Linn, which is commonly known as B.vulgaris, belongs to the family Berberidaceae. B.vulgaris L., a valuable native plant in Iran, has played a prominent role for researchers in herbal healing due to its medicinal benefits and nutritional value. The roots, stems, leaves, and fruits are used in medicine andin the food industry .
In Iran, two important B.vulgaris species are B.Integerrima (abi) and B.vulgaris (poloei). B.vulgaris has been shown to have anti-microbial and anti-fungal effects, to stimulate the immune system, and to have hypotensive properties that are attributable to berberine and other isoquinoline alkaloids, the main active ingredients of B.vulgaris. The secondary metabolites of B.vulgaris, which are used in the pharmaceutical industry, include berberin, berlambine, oxyberberine, oxycanthine, chlorumamine, anthocyanine, bervulcine, lambertine, and magniflorine . Insulin and oral anti-diabetic agents such as sulfonylureas, biguanides, glycosidase inhibitors, and glinides are present available therapies for diabetes, which are used as mono-therapy or in combination to achieve better glycemic regulation. Many of these anti-diabetic agents have numerous serious side effects. Thus, finding a treatment for diabetes that does not have adverse side effects remains a challenge. Approximately 80 % of the world population use traditional medicines. More than 150 plant extracts are used to treat diabetes, and the potential uses of several plants are known at present. However, there is much we do not know about plants with hypoglycemic properties. Hypoglycemic activity could be related to the existence of saponins, polyphenols, or alkaloids. The root bark of B.vulgaris is recommended in the management of diabetes. However, the mechanisms action of the plant remains unknown, and in addition, the use of antioxidants for disease therapy remains debatable . Some natural compounds such as antioxidants are effective in protecting the human body against damage caused by ROS. Among natural antioxidants, a great deal of research has focused on phenolic compounds because of their wide distribution. All phenolic classes are free radical scavengers due to their redox properties, which act as reducing agents, hydrogen donors, and single oxygen quencher agents. Phenols particularly flavonoids, can also have additional properties including anti-inflammatory, anti-bacterial, anti-fungal, and anti-cancer effects [2, 8]. B.vulgaris fruits contain phenolic compounds with beneficial antioxidant activity that can reduce damage due to free radicals and prevent chronic disease . This study was conducted to investigate the effect of B.vulgaris against oxidative stress in experimentally induced diabetes in a rodent model. The most common substance inducing type 1diabetes in the rat is streptozocin (streptozotocin, STZ). STZ is taken up by pancreatic β-cells via glucose transporter GLUT2. The main cause of STZ-induced β-cell death is alkylation of DNA by the nitrosourea moiety of this compound. However, production of NOo and ROS may also be involved in DNA fragmentation and other deleterious effects of STZ . ROS plays an important role in pathogenesis of diabetes, so natural antioxidants could help us in managing diabetes.
Plant materials and preparation of ethanolic extracts
Fresh-ripened fruits of the B.vulgaris plant were collected from South Khorasan from August to October, 2013. The fresh fruits were washed, air dried, powdered, and extracted using 2 L of ethanol by refluxing for 48 h. The extract obtained was vacuum-evaporated to obtain the crude extract, which was dissolved in distilled water just prior to oral administration. Each extract was administered in two doses equal to 25 and 100 mg/kg . A voucher specimen for B.vulgaris (H, No. 769) was preserved in the Herbarium of the School of Agriculture, Ferdowsi University of Mashhad, Iran.
Wistar-derived male rats (6–8-week-old; 200 ± 20 g, purchased from the Pasteur Institute, Tehran, Iran) were raised at the university animal quarters and housed in a thermally controlled (25 ± 2 °C) room free from any sources of chemical contamination. Light was maintained on a 12 h dark–light cycle, and rats were fed a standard laboratory diet of rat chow (Pars Dam Co., Tehran, Iran) at the Animal House Lab research center, Birjand.
List of animal groups with different treatments
Status and treatment
Healthy, treated with saline in equivalent volume to the test treatments
Diabetic, treated with saline in equivalent volume to the test treatments
Diabetic, treated with ethanolic extract of B.vulgaris (25 mg/kg)
Diabetic, treated with ethanolic extract of B.vulgaris (100 mg/kg)
Diabetic, treated with glibenclamide (0. 6 mg/kg)
Normal and diabetic rats were anesthetized with ether. Blood was collected from the rats in order to measure glucose, insulin, and other biochemical factors. For gene expression analysis, liver biopsies of normal and diabetic rats were performed, and the samples were placed in liquid nitrogen.
Ferric reducing antioxidant power (FRAP) assay
Total antioxidant power in the serum of the five groups mentioned above was evaluated by the FRAP assay according to the procedures of Benzie & Strain . Ferric iron was reduced to its ferrous state due to the presence of antioxidant activity and low pH levels in the samples, which led to the formation of an intensive blue ferrous-tripyridyltriazine complex. This complex could be monitored at a maximum absorption of 593 nm. In total, 2 ml of FRAP reagent consisting of 300 mM sodium acetate buffer (pH 3.6), 10 mM 2,4,6-tris (2-pyridyl)-S-triazine (TPTZ) solution in HCl, and 20 mM FeCl3.6H2O solution in a proportion of 10:1:1 (v/v) was added to 50 μl of sample. After 15 min, the absorbance was measured at 593 nm .
Measurement of thiobarbituric acid reactive substances (TBARS)
The TBARS assay measures the amount of malondialdehyde (MDA) present in the sample. At the end of the treatment period, blood was collected from the hearts of the rats in order to measure the MDA levels. Plasma samples (300 μl) were added to 3 ml TBARS reagent (7.5 g trichloroacetic acid, 187 mg TBA, and 6.25 ml chloridric acid). Next, the mixture was warmed for 20 min in a boiling water bath. Finally, the absorbance of the samples was determined at 532 nm .
RNA extraction and quantitative reverse transcription polymerase chain reaction (qRT-PCR)
Real-time primer sequences
G6P (glucose 6-phosphatase)
For the evaluation of pancreatic β cell regeneration in response to B.vulgaris, the number of pancreatic islets was calculated. For this analysis, the pancreatic tissue was removed and immediately fixed in 10 % formalin. After fixation, paraffin blocks were cut into 5 μm thick sections and stained with hematoxylin and eosin. Next, the stained sections of pancreatic tissue were examined under a light microscope. The total number of islet cells in each section was counted, the total area of each stained section was characterized, and the average number of pancreatic islets per cm2 was calculated.
Using SPSS version 16, the data were statistically computed by one-way ANOVA, and the means were compared using Student’s t test. P < 0.05 was considered statistically significant. The data are expressed as mean ± SD.
Effects of B.vulgaris on biochemical parameters and oxidative stress markers
Effects of B.Vulgaris on biochemical parameters of normoglycemic and STZ-induced diabetic rats
Fasting Blood Glucose (FBG) (mmol/L)
Malondialdehyde (MDA) (μmol/L)
Total antioxidant (FRAP) (μmol/L)
Number of pancreatic islets (cm−2)
7.6 ± 0.4b*
15.2 ± 0.7*
1.27 ± 0.5*
780 ± 14*
43 ± 3.5*
25 ± 1.2
7.4 ± 0.3
4.3 ± 0.7
550 ± 21
13 ± 1.8
Diabetic + B.vulgaris (25 mg/kg body mass)
12.9 ± 0.7*
9.2 ± 0.5
2.9 ± 0.3*
655 ± 18*
18 ± 1.9*
Diabetic + B.vulgaris (100 mg/kg body mass)
8.2 ± 0.4*
11.9 ± 0.6*
2.1 ± 0.2*
760 ± 16*
29 ± 2.6*
Diabetic + Glibenclamide (0.6 mg/kg body mass)
7.8 ± 0.8*
13.4 ± 0.4*
1.85 ± 0.1*
810 ± 15*
34 ± 0.4*
Effect of B.vulgaris on the gene expression of HSP70, HSP27, and HSF1
Effects of B.vulgaris on the gene expression of glucokinase (GK) and glucose 6-phosphatase (G6P)
The data presented here shows that B.vulgaris hydroalcoholic extract ameliorates the hyperglycemia-mediated oxidative stress and related gene expression. DM is a major illness characterized by hyperglycemia due to absolute or relative deficiency of insulin . In this study, we have demonstrated that an alcoholic extract of the B.vulgaris plant is able to normalize blood glucose levels and reduce stress protein expression in rats with streptozotocin-induced diabetes.
The alcoholic extract from B.vulgaris is recommended for the management of diabetes. Considering the wide use of this plant, in this study, we investigated the plasma glucose and insulin levels as well as oxidative stress markers under treatment with B.vulgaris in diabetic rats. The MDA and FBG levels were increased, in contrast to insulin and total antioxidants, which were decreased in rats with streptozotocin-induced diabetes (Table 3). The results shown in Table 3 clearly indicate that B.vulgaris significantly increase insulin, pancreatic β cell numbers and total antioxidants and spontaneously reduce blood FBG and MDA levels. The findings of the current study are in close agreement with the results of other studies [14, 15]. Several studies have demonstrated the beneficial effects of B.vulgaris on oxidative stress parameters in diabetic rats, which are consistent with our results [6, 16]. In diabetes, the pancreas is considered to be the principal target organ susceptible to oxidative stress and damage produced by free radicals. Therefore, agents with antioxidant properties are quite useful and reasonable in the treatment of pancreatic oxidative stress [15, 17]. The antioxidant properties of different varieties of B.vulgaris from various countries have been demonstrated . Furthermore, B.vulgaris contains phenolic compounds with beneficial antioxidant activities that can prevent chronic diseases and cancers .
In the present study, we found that treatment with B.vulgaris led to a significant decrease in the blood glucose level by decreasing the gene expression of G6P (Fig. 2). These results suggest that B.vulgaris downregulates the gluconeogenesis pathway in diabetic rats. There was also a significant decrease in GK mRNA level in diabetic rats when compared with the normal group. Treating diabetic rats with B.vulgaris resulted in a significant improvement in the gene expression of GK compared with the diabetic control group (P < 0.05; Fig. 2). Furthermore, it was established that the expression of stress genes such as HSP70, HSP27, and HSF1 increased significantly in the pancreas tissue of diabetic rats. These results support the hypothesis that there is a significant correlation between oxidative stress and the gene expression of HSPs. We also demonstrated that B.vulgaris ameliorated oxidative stress due to a reduction in HSP70 and HSP27 gene expression (Fig. 1). β Cell regeneration observed in B.vulgaris treating groups confirms protective effects of B.vulgaris in pancreas (Table 3). These observations revealed that B.vulgaris in a dose-dependent manner and tissue specifically improved hyperglycemia-mediated oxidative stress in diabetic rats. B.vulgaris in high doses showed the same effect as glibenclamide that can be considered for use in pharmaceutical industry. In the present study, the biochemical, gene expression, and histological results collectively revealed that B.vulgaris has protective effects against oxidative stress in diabetic rats. Moreover, the hypoglycemic effect of B.vulgaris could be through an increase in insulin level, resulting in the regulation of the glycolysis and gluconeogenesis pathways, and, in this case, the effect on glycolysis is notable. To better understand the exact mechanism of the effects of B.vulgaris and to develop its application in clinical trials, additional genes involved in glucose and lipid metabolism and related signaling pathways should be investigated.
B.vulgaris ameliorated oxidative stress in diabetic rats by increasing total antioxidant capacity accompanied by a decrease in lipid peroxidation. Reduced level of stress genes in treated diabetic groups confirm the ability of B.vulgaris to decrease pancreatic oxidative stress and resulting regeneration in β cells. Moreover, the mechanism of the hypoglycemic effect of this plant may be through modification in the gene expression of hepatic GK and G6P. To uncover exact mechanism action of B.vulgaris, its needed to understand the specific role of stress proteins in pancreatic β cells regeneration.
fasting blood glucose
Ferric reducing antioxidant power assay
Heat shock factor
Heat shock protein
Reactive oxygen species
The authors would like to thank personnel of research laboratory in Birjand University of Medical Sciences. This investigation was supported by Grant No. 711 from the office of Vice Chancellor for Research, Birjand University of Medical Sciences.
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