Department of Pharmacology of Rio de Janeiro State University, Brazil.
J Pharm Pharmacol. 2012 Feb;64(2):268-76. doi: 10.1111/j.2042-7158.2011.01395.x. Epub 2011 Nov 18.
This study examined the effect of Vitis vinifera grape skin extract (ACH09) on hyperglycaemia and the insulin-signalling cascade in alloxan-treated mice.
Glycaemia, serum insulin and Western blot analysis of insulin cascade proteins were evaluated in the gastrocnemius muscles of four groups of adult mice: control, ACH09 (200 mg/kg per day, p.o.), alloxan (300 mg/kg, i.p.) and alloxan + ACH09. Insulin secretion in isolated pancreatic islets was also studied.
Glycaemia values in the alloxan + ACH09 and ACH09 groups were significantly lower than in the alloxan-treated and control groups, respectively. Increased insulin resistance (HOMA index) was observed in the alloxan-treated group but not in the alloxan + ACH09 group. Insulin receptor content and Akt phosphorylation were significantly greater in the alloxan + ACH09 group compared with the alloxan-treated group. The glucose transporter (GLUT-4) content was reduced in alloxan-treated mice compared with the control group, while alloxan + ACH09 and ACH09-treated mice showed a significant increase in GLUT-4 content. ACH09 treatment did not change glucose-induced insulin secretion in isolated pancreatic islets.
The results suggest that ACH09 has hypoglycaemic and antihyperglycaemic effects that are independent of an increase in insulin release but are probably dependent on an increase in insulin sensitivity resulting from an activation of the insulin-signalling cascade in skeletal muscle.
本研究旨在探讨葡萄皮提取物(ACH09)对葡聚糖诱导的糖尿病小鼠高血糖和胰岛素信号级联的影响。
在四组成年小鼠的腓肠肌中评估血糖、血清胰岛素和胰岛素信号级联蛋白的 Western blot 分析:对照组、ACH09(200mg/kg/天,po)组、葡聚糖(300mg/kg,ip)组和葡聚糖+ACH09 组。还研究了分离的胰岛中胰岛素的分泌情况。
葡聚糖+ACH09 组和 ACH09 组的血糖值明显低于葡聚糖处理组和对照组。葡聚糖处理组的胰岛素抵抗(HOMA 指数)增加,但葡聚糖+ACH09 组没有。与葡聚糖处理组相比,ACH09 处理组的胰岛素受体含量和 Akt 磷酸化显著增加。与对照组相比,葡聚糖处理组的葡萄糖转运蛋白(GLUT-4)含量降低,而葡聚糖+ACH09 组和 ACH09 组的 GLUT-4 含量显著增加。ACH09 处理对分离的胰岛中葡萄糖诱导的胰岛素分泌没有影响。
结果表明,ACH09 具有降血糖和抗高血糖作用,不依赖于胰岛素释放的增加,而可能依赖于胰岛素信号级联在骨骼肌中的激活导致的胰岛素敏感性的增加。