Traditional Chinese Medicine College, Chongqing Medical University, Chongqing 400016, P.R. China.
Mol Med Rep. 2019 Dec;20(6):5152-5162. doi: 10.3892/mmr.2019.10783. Epub 2019 Oct 30.
Insulin resistance (IR) is the impaired insulin response that causes decreased glucose tolerance. Electrical stimulation (ES) can improve insulin sensitivity in the skeletal muscle. However, the underlying molecular mechanisms remain to be elucidated. In the present study, the effect of ES and diet therapy on IR and the role of the mammalian target of rapamycin (mTOR) pathway in the improvement of IR by ES were investigated. A total of 70 Sprague‑Dawley male rats were divided into five groups: Normal (n=10), IR control (n=15), diet (n=15), ES (n=15) and ES + diet (n=15) groups. An IR rat model was established by high‑fat and high‑carbohydrate diet for 5 weeks and confirmed by measurement of fasting plasma glucose (FPG), insulin, insulin sensitivity index (ISI) and IR index. ES on the Zusanli (ST36), Sanyinjiao (SP 6) and Weiwanxiashu (EX‑B3) acupoints and the low‑fat and low‑carbohydrate diet demonstrated protective effects. The body weight, concentrations of FPG, insulin, triglycerides (TG), free fatty acids (FFA) and total cholesterol (TC) of the rats were detected. Pathologic changes in the liver and pancreatic tissues were assessed. Western blotting and immunohistochemistry were performed to determine the role of PI3K/Akt/mTOR signaling. Results demonstrated that ES and diet therapy significantly increased ISI and reduced FPG, IR index, FFA, TG, TC and weight. Inflammatory cell infiltration in the liver and pancreatic tissues was ameliorated and lipid droplets and cavitation in hepatocyte were decreased after ES and diet therapy. The administration of ES and diet therapy also enhanced glucose transport by the upregulation of glucose transporter 4 and accelerated glycogen synthesis through the suppression of glycogen synthase kinase 3α/β via PI3K/Akt/mTOR signaling. Hence, the present results demonstrated that ES combined with diet therapy improved IR through PI3K/Akt/mTOR signaling. The proposed therapy was superior to the method of diet alone.
胰岛素抵抗(IR)是一种胰岛素反应受损的疾病,导致葡萄糖耐量降低。电刺激(ES)可以改善骨骼肌的胰岛素敏感性。然而,其潜在的分子机制仍有待阐明。在本研究中,研究了 ES 对 IR 的影响以及哺乳动物雷帕霉素靶蛋白(mTOR)通路在 ES 改善 IR 中的作用。将 70 只雄性 Sprague-Dawley 大鼠分为五组:正常组(n=10)、IR 对照组(n=15)、饮食组(n=15)、ES 组(n=15)和 ES+饮食组(n=15)。通过高脂高糖饮食喂养 5 周建立 IR 大鼠模型,并通过测量空腹血糖(FPG)、胰岛素、胰岛素敏感指数(ISI)和 IR 指数来验证模型。ES 对足三里(ST36)、三阴交(SP 6)和外关下(EX-B3)穴位的刺激以及低脂低糖饮食均表现出保护作用。检测大鼠的体重、FPG、胰岛素、三酰甘油(TG)、游离脂肪酸(FFA)和总胆固醇(TC)浓度。评估肝和胰腺组织的病理变化。采用 Western blot 法和免疫组化法检测 PI3K/Akt/mTOR 信号通路的作用。结果表明,ES 和饮食治疗可显著增加 ISI,降低 FPG、IR 指数、FFA、TG、TC 和体重。ES 和饮食治疗后,肝和胰腺组织的炎症细胞浸润减轻,肝细胞内的脂质滴和空泡减少。ES 和饮食治疗还通过上调葡萄糖转运蛋白 4 促进葡萄糖转运,并通过抑制糖原合酶激酶 3α/β 加速糖原合成,从而增强葡萄糖的摄取。因此,本研究结果表明,ES 联合饮食治疗通过 PI3K/Akt/mTOR 信号通路改善 IR。与单纯饮食治疗相比,该治疗方法具有优越性。