Asadi Soheila, Goodarzi Mohammad Taghi, Saidijam Massoud, Karimi Jamshid, Azari Reza Yadgar, Farimani Azam Rezaei, Salehi Iraj
Department of Clinical Biochemistry, Medical School, Hamadan University of Medical Sciences, Hamadan, Iran.
Research Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Iran J Basic Med Sci. 2015 Jun;18(6):537-43.
Visfatin and vaspin are secreted by adipose tissue and play key roles in glucose homeostasis and subsequently are potential targets for diabetes treatment. Resveratrol (RVS) corrects insulin secretion and improves insulin sensitivity. We investigated the RVS effects on serum antioxidants, insulin and glucose levels, also visfatin and vaspin genes expression in adipose tissue of streptozotocin-nicotinamide (STZ-NA) induced type 2 diabetic rats.
Diabetes was induced in Wistar rats (n=32) using STZ (60 mg/kg body weight) and NA (120 mg/kg body weight); rats were divided into 4 groups (n=8). Eight untreated normal rats were used as control group; four diabetic rat groups (2-5) were treated with 0, 1, 5 and 10 mg/kg body weight of RVS, respectively for 30 days. After treatment blood and adipose tissue were prepared from all animals. Serum glucose, insulin, HOMA index, total antioxidant capacity (TAC), and malondialdehyde (MDA) were measured. Visfatin and vaspin genes expression in adipose tissue were evaluated using real-time PCR.
RVS reduced blood glucose significantly and increased insulin level, resulting in insulin sensitivity improvement. Furthermore RVS increased weight and TAC, while reducing serum MDA in the diabetic groups. Visfatin gene expression increased in the diabetic group, and RVS treatment reduced it. Vaspin gene expression was reduced in RVS receiving diabetic groups.
The results indicated that RVS has potential hypoglycemic effect, probably by increasing insulin level and changing gene expression of visfatin and vaspin. Moreover RVS showed antioxidant effects through reduction in peroxidiation products and augmented antioxidant capacity.
内脂素和内脏脂肪素由脂肪组织分泌,在葡萄糖稳态中起关键作用,因此是糖尿病治疗的潜在靶点。白藜芦醇(RVS)可纠正胰岛素分泌并改善胰岛素敏感性。我们研究了RVS对链脲佐菌素 - 烟酰胺(STZ - NA)诱导的2型糖尿病大鼠血清抗氧化剂、胰岛素和葡萄糖水平以及脂肪组织中内脂素和内脏脂肪素基因表达的影响。
使用STZ(60 mg/kg体重)和NA(120 mg/kg体重)诱导Wistar大鼠(n = 32)患糖尿病;大鼠分为4组(n = 8)。八只未治疗的正常大鼠作为对照组;四个糖尿病大鼠组(2 - 5组)分别用0、1、5和10 mg/kg体重的RVS治疗30天。治疗后,从所有动物身上采集血液和脂肪组织。测量血清葡萄糖、胰岛素、HOMA指数、总抗氧化能力(TAC)和丙二醛(MDA)。使用实时PCR评估脂肪组织中内脂素和内脏脂肪素基因的表达。
RVS显著降低血糖并提高胰岛素水平,从而改善胰岛素敏感性。此外,RVS增加了糖尿病组的体重和TAC,同时降低了血清MDA。糖尿病组内脂素基因表达增加,而RVS治疗使其降低。接受RVS治疗的糖尿病组内脏脂肪素基因表达降低。
结果表明,RVS可能通过提高胰岛素水平以及改变内脂素和内脏脂肪素的基因表达而具有潜在的降血糖作用。此外,RVS通过减少过氧化产物和增强抗氧化能力显示出抗氧化作用。