Adiponectin Receptors in Energy Homeostasis and Obesity Pathogenesis

被引:27
作者
Akingbemi, Benson T. [1 ]
机构
[1] Auburn Univ, Dept Anat Physiol & Pharmacol, Auburn, AL 36849 USA
来源
G PROTEIN-COUPLED RECEPTORS IN ENERGY HOMEOSTASIS AND OBESITY PATHOGENSIS | 2013年 / 114卷
关键词
ACTIVATED PROTEIN-KINASE; FATTY-ACID OXIDATION; BONE-MINERAL DENSITY; INSULIN-RESISTANCE; SKELETAL-MUSCLE; GENE-EXPRESSION; PLASMA-PROTEIN; ADIPOSE-TISSUE; METABOLIC SYNDROME; CELL APOPTOSIS;
D O I
10.1016/B978-0-12-386933-3.00009-1
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
Adipokines, that is factors secreted by adipose tissue, act through a network of autocrine, paracrine, and endocrine pathways to regulate several aspects of physiology, including glucose and lipid metabolism, neuroendocrine function, reproduction, and cardiovascular function. In particular, adiponectin, a 30-kDa protein, is associated with the regulation of insulin sensitivity, and its levels in serum are affected by altered metabolic homeostasis. Adiponectin effects are mediated by adiponectin receptors, which occur as two isoforms (AdipoR1 and AdipoR2). Transcriptional regulation of adiponectin is by the peroxisome proliferator-activated receptor-gamma (PPAR-gamma). However, acting through AdipoR1 and AdipoR2, adiponectin enhances 5' adenosine monophosphate-activated protein kinase (AMPK) and the PPAR alpha-mediated pathways in the liver and skeletal muscles. Adiponectin receptors mediate a wide spectrum of metabolic reactions, including gluconeogenesis and fatty-acid oxidation. Altogether, adiponectin deficiency and/or decreased adiponectin receptor-mediated activity possibly contribute to insulin resistance in metabolic syndromes, coronary heart disease, and liver disease.
引用
收藏
页码:317 / 342
页数:26
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