内科学
内分泌学
胰岛素抵抗
脂联素
瘦素
胰岛素受体
促炎细胞因子
胰岛素
蛋白激酶B
胰岛素耐受试验
葡萄糖转运蛋白
糖耐量试验
高胰岛素血症
葡萄糖钳夹技术
葡萄糖摄取
化学
医学
磷酸化
胰腺激素
肥胖
生物化学
炎症
胰岛素敏感性
作者
Yang Gou,Bingyang Liu,Mengyao Cheng,Takako Yamada,Takuya Iida,Sixian Wang,Ryoichi Banno,Teruhiko Koike
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2021-10-19
卷期号:26 (20): 6310-6310
被引量:7
标识
DOI:10.3390/molecules26206310
摘要
d-Allulose is a rare sugar with antiobesity and antidiabetic activities. However, its direct effect on insulin sensitivity and the underlying mechanism involved are unknown.This study aimed to investigate the effect of d-allulose on high-fat diet (HFD)-induced insulin resistance using the hyperinsulinemic-euglycemic (HE)-clamp method and intramuscular signaling analysis.Wistar rats were randomly divided into three dietary groups: chow diet, HFD with 5% cellulose (HFC), and HFD with 5% d-allulose (HFA). After four weeks of feeding, the insulin tolerance test (ITT), intraperitoneal glucose tolerance test (IPGTT), and HE-clamp study were performed. The levels of plasma leptin, adiponectin, and tumor necrosis factor (TNF)-α were measured using the enzyme-linked immunosorbent assay. We analyzed the levels of cell signaling pathway components in the skeletal muscle using Western blotting.d-allulose alleviated the increase in HFD-induced body weight and visceral fat and reduced the area under the curve as per ITT and IPGTT. d-Allulose increased the glucose infusion rate in the two-step HE-clamp test. Consistently, the insulin-induced phosphorylation of serine 307 in the insulin receptor substrate-1 and Akt and expression of glucose transporter 4 (Glut-4) in the muscle were higher in the HFA group than HFC group. Furthermore, d-allulose decreased plasma TNF-α concentration and insulin-induced phosphorylation of stress-activated protein kinase/Jun N-terminal kinase in the muscle and inhibited adiponectin secretion in HFD-fed rats.d-allulose improved HFD-induced insulin resistance in Wistar rats. The reduction of the proinflammatory cytokine production, amelioration of adiponectin secretion, and increase in insulin signaling and Glut-4 expression in the muscle contributed to this effect.
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