Yang Jing, Zhao Ping, Wan Dingrong, Zhou Qi, Wang Chao, Shu Guangwen, Mei Zhinan, Yang Xinzhou
College of Pharmacy, South-Central University for Nationalities, 182 Min-Zu Road, Wuhan 430074, China.
College of Life Sciences, South-Central University for Nationalities, 182 Min-Zu Road, Wuhan 430074, China.
Evid Based Complement Alternat Med. 2014;2014:106206. doi: 10.1155/2014/106206. Epub 2014 Sep 2.
We have investigated the antidiabetic effect and mechanism of methanolic extract of Berberis julianae Schneid. (BJSME) in STZ induced Type 2 diabetes mellitus mice. T2DM mice were induced by high fat diet and low dose streptozotocin (STZ). BJSME was orally administrated at the doses of 60, 120, and 240 mg/kg/d, for 21 days. Metformin was used as positive control drug. Food intake, body weight, plasma glucose, oral glucose tolerance test, insulin tolerance test, insulin, and blood-lipid content were measured. The effects of BJSME on the glucose transporter 4 (GLUT4) translocation in L6 myotubes and the GLUT4 protein expression in skeletal muscle as well as phosphorylation of the AMP-activated protein kinase (AMPK) in liver and muscle were examined. In vitro and in vivo results indicate that BJSME increased GLUT4 translocation by 1.8-fold and BJSME significantly improved the oral glucose tolerance and low density lipoprotein cholesterol (LDL-C) of serum and reduced body weight, glucose, and other related blood-lipid contents. The BJSME treatment also stimulated the phosphorylation of AMPK. Thus, BJSME seems to possess promising beneficial effects for the treatment of T2DM with the possible mechanism via stimulating AMPK activity.
我们研究了刺叶小檗甲醇提取物(BJSME)对链脲佐菌素诱导的2型糖尿病小鼠的抗糖尿病作用及其机制。通过高脂饮食和低剂量链脲佐菌素(STZ)诱导建立T2DM小鼠模型。BJSME以60、120和240mg/kg/d的剂量口服给药,持续21天。二甲双胍用作阳性对照药物。测量了食物摄入量、体重、血糖、口服葡萄糖耐量试验、胰岛素耐量试验、胰岛素和血脂含量。检测了BJSME对L6肌管中葡萄糖转运蛋白4(GLUT4)转位、骨骼肌中GLUT4蛋白表达以及肝脏和肌肉中AMP活化蛋白激酶(AMPK)磷酸化的影响。体内外实验结果表明,BJSME使GLUT4转位增加了1.8倍,显著改善了口服葡萄糖耐量以及血清低密度脂蛋白胆固醇(LDL-C)水平,并降低了体重、血糖和其他相关血脂含量。BJSME处理还刺激了AMPK的磷酸化。因此,BJSME似乎对T2DM的治疗具有有前景的有益作用,其可能的机制是通过刺激AMPK活性。