The PI3K/AKT pathway in obesity and type 2 diabetes

被引:1157
|
作者
Huang, Xingjun [1 ,2 ]
Liu, Guihua [3 ]
Guo, Jiao [2 ]
Su, Zhengquan [1 ,2 ]
机构
[1] Guangdong Pharmaceut Univ, Guangdong Engn Res Ctr Nat Prod & New Drugs, Guangdong Prov Univ Engn Technol Res Ctr Nat Prod, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangdong Pharmaceut Univ, Guangdong Metab Dis Res Ctr Integrated Chinese &, Guangzhou 510006, Guangdong, Peoples R China
[3] Shenzhen Ctr Dis Control & Prevent, 8 Longyuan Rd, Shenzhen 518055, Peoples R China
来源
基金
美国国家科学基金会;
关键词
PROTEIN-KINASE-B; HEPATIC GLUCOSE-PRODUCTION; HYPOTHALAMIC INSULIN-RESISTANCE; RECEPTOR SUBSTRATE 2; FATTY LIVER-DISEASE; BETA-CELL MASS; MTOR COMPLEX 1; P70; S6; KINASE; SKELETAL-MUSCLE; AGRP NEURONS;
D O I
10.7150/ijbs.27173
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Obesity and type 2 diabetes mellitus are complicated metabolic diseases that affect multiple organs and are characterized by hyperglycaemia. Currently, stable and effective treatments for obesity and type 2 diabetes mellitus are not available. Therefore, the mechanisms leading to obesity and diabetes and more effective ways to treat obesity and diabetes should be identified. Based on accumulated evidences, the PI3K/AKT signalling pathway is required for normal metabolism due to its characteristics, and its imbalance leads to the development of obesity and type 2 diabetes mellitus. This review focuses on the role of PI3K/AKT signalling in the skeletal muscle, adipose tissue, liver, brain and pancreas, and discusses how this signalling pathway affects the development of the aforementioned diseases. We also summarize evidences for recently identified therapeutic targets of the PI3K/AKT pathway as treatments for obesity and type 2 diabetes mellitus. PI3K/AKT pathway damaged in various tissues of the body leads to obesity and type 2 diabetes as the result of insulin resistance, and in turn, insulin resistance exacerbates the PI3K/AKT pathway, forming a vicious circle.
引用
收藏
页码:1483 / 1496
页数:14
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