Apelin/APJ system as a therapeutic target in diabetes and its complications

被引:72
作者
Hu, Haoliang [1 ]
He, Lu [1 ,2 ]
Li, Lanfang [1 ]
Chen, Linxi [1 ]
机构
[1] Univ South China, Inst Pharm & Pharmacol, Hunan Prov Cooperat Innovat Ctr Mol Target New Dr, Hengyang 421001, Peoples R China
[2] Univ South China, Affiliated Hosp 1, Dept Neurosurg, Hengyang 421001, Peoples R China
基金
中国国家自然科学基金;
关键词
Apelin; APJ; ELABELA; Diabetes; Obesity; Insulin resistance; Cardiopathy; Retinopathy; Nephropathy; SIGNALING TRANSDUCTION PATHWAY; FATTY-ACID OXIDATION; DIET-INDUCED OBESITY; GLUCOSE-HOMEOSTASIS; CARDIOMYOCYTE HYPERTROPHY; MITOCHONDRIAL BIOGENESIS; ENDOGENOUS LIGAND; UP-REGULATION; APJ RECEPTOR; IN-VITRO;
D O I
10.1016/j.ymgme.2016.07.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The G-protein-coupled receptor APJ and its endogenous ligand apelin are widely expressed in many peripheral tissues and central nervous system, including adipose tissue, skeletal muscles and hypothalamus. Apelin/APJ system, involved in numerous physiological functions like angiogenesis, fluid homeostasis and energy metabolism regulation, is notably implicated in the development of different pathologies such as diabetes and its complications. Increasing evidence suggests that apelin regulates insulin sensitivity, stimulates glucose utilization and enhances brown adipogenesis in different tissues associated with diabetes. Moreover, apelin is also involved in the regulation of diabetic complications via binding to APJ receptor. Apelin improves diabetes-induced kidney hypertrophia, normalizes obesity-associated cardiac hypertrophy and negatively promotes retinal angiogenesis in diabetic retinopathy. In this review, we provide a comprehensive overview about the role of apelin/APJ system in different tissues related with diabetes. Furthermore, we describe the pathogenesis of diabetic complications associated with apelin/APJ system. Finally, agonists and antagonists targeted to APJ receptor are described in the literature. Thus, we highlight apelin/APJ system as a novel therapeutic target for pharmacological intervention in treating diabetes and its complications. (C) 2016 Published by Elsevier Inc.
引用
收藏
页码:20 / 27
页数:8
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