Effect of metformin on the expression of SNAER proteins in the skeletal muscle of rats with type 2 diabetes

Y. Mohammadi, A. Farimani
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Abstract

Background and Aims: SNARE proteins are composed of a combination of SNAP-23, Stx-4, and VAMP-2 isoforms that are significantly expressed in skeletal muscle. These proteins control the transport of GLUT4 to the cell membranes. The modifications in the expression of SNARE proteins can cause Type 2 diabetes. The present study aimed to assess the effect of metformin on the expression of these proteins in rats. Materials and Methods: For the purpose of the study, 40 male Wistar rats were randomly selected. Streptozotocin and Nicotinamide were used for the induction of type 2 diabetes. The animals were assigned to five groups (n=8), including healthy and diabetic groups as control, as well as three experimental groups which were treated with different doses of metformin (100, 150, and 200 mg/kg body weight) for 30 days. The quantitative reverse transcription PCR (RT-qPCR) method was applied to evaluate the expression of SNARE complex proteins.. Results: Based on the results, metformin (100, 150, and 200 mg/kg body weight) decreased serum glucose levels and increased serum insulin levels. This difference in dose of 200 mg/kg body weight was statistically significant (P<0.05). Moreover, all three doses of metformin increased the expression of SNAP- 23, syntaxin-4, and VAMP-2 proteins in skeletal muscle tissue. Metformin at a dose of 200 mg/kg body weight demonstrated the most significant effects (P<0.05). Conclusion: As evidenced by the results of the current study, another anti-diabetic mechanism of metformin is to increase the expression of SNARE proteins, which effectively improves insulin resistance and lowers blood glucose.
二甲双胍对2型糖尿病大鼠骨骼肌SNAER蛋白表达的影响
背景和目的:SNARE蛋白由SNAP-23、Stx-4和VAMP-2亚型的组合组成,这些亚型在骨骼肌中显著表达。这些蛋白控制GLUT4向细胞膜的转运。SNARE蛋白表达的改变可导致2型糖尿病。本研究旨在评估二甲双胍对大鼠这些蛋白表达的影响。材料与方法:以雄性Wistar大鼠为研究对象,随机选取40只。采用链脲佐菌素和烟酰胺诱导2型糖尿病。将实验动物分为5组(n=8),其中健康组和糖尿病组为对照组,另外3个实验组分别给予不同剂量的二甲双胍(100、150和200 mg/kg体重)治疗30 d。结果:二甲双胍(100、150和200 mg/kg体重)可降低小鼠血清葡萄糖水平,升高血清胰岛素水平。200 mg/kg体重组的剂量差异有统计学意义(P<0.05)。此外,三种剂量的二甲双胍均增加了骨骼肌组织中SNAP- 23、syntaxin-4和VAMP-2蛋白的表达。二甲双胍剂量为200 mg/kg体重时效果最显著(P<0.05)。结论:本研究结果表明,二甲双胍的另一个抗糖尿病机制是增加SNARE蛋白的表达,有效改善胰岛素抵抗,降低血糖。
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