Evidence that α-calcitonin gene-related peptide is a neurohormone that controls systemic lipid availability and utilization

被引:35
作者
Danaher, Rachel N. [1 ]
Loomes, Kerry M. [1 ]
Leonard, Bridget L. [1 ]
Whiting, Lynda [1 ]
Hay, Debbie L. [1 ]
Xu, Lance Yi [1 ]
Kraegen, Edward W. [2 ]
Phillips, Anthony R. J. [1 ]
Cooper, Garth J. S. [1 ,3 ]
机构
[1] Univ Auckland, Sch Biol Sci, Maurice Wilkins Ctr Res Excellence Mol Biodiscove, Auckland 1142, New Zealand
[2] Garvan Inst Med Res, Diabet & Obes Res Program, Darlinghurst, NSW 2010, Australia
[3] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
关键词
D O I
10.1210/en.2007-0583
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
alpha-Calcitonin gene-related peptide (alpha CGRP) is released mainly from sensory and motor nerves in response to physiological stimuli. Despite well-documented pharmacological effects, its primary physiological role has thus far remained obscure. Increased lipid content, particularly in skeletal muscle and liver, is strongly implicated in the pathogenesis of insulin resistance, but the physiological regulation of organ lipid is imperfectly understood. Here we report our systematic investigations of the effects of alpha CGRP on in vitro and in vivo indices of lipid metabolism. In rodents, levels of alpha CGRP similar to those in the blood markedly stimulated fatty acid beta-oxidation and evoked concomitant mobilization of muscle lipid via receptor-mediated activation of muscle lipolysis. alpha CGRP exerted potent in vivo effects on lipid metabolism in muscle, liver, and the blood via receptor-mediated pathways. Studies with receptor antagonists were consistent with tonic regulation of lipid metabolism by an endogenous CGRP agonist. These data reveal that alpha CGRP is a newly recognized regulator of lipid availability and utilization in key tissues and that it may elevate the availability of intramyocellular free fatty acids to meet muscle energy requirements generated by contraction by evoking their release from endogenous triglyceride.
引用
收藏
页码:154 / 160
页数:7
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