Long-term orexigenic effects of AgRP-(83-132) involve mechanisms other than melanocortin receptor blockade

被引:256
作者
Hagan, MM
Rushing, PA
Pritchard, LM
Schwartz, MW
Strack, AM
Van der Ploeg, LHT
Woods, SC
Seeley, RJ
机构
[1] Univ Cincinnati, Med Ctr, Dept Psychiat, Cincinnati, OH 45267 USA
[2] Univ Washington, Harborview Med Ctr, Dept Med, Seattle, WA 98195 USA
[3] Univ Washington, Harborview Med Ctr, Puget Sound Vet Affairs Hlth Care Syst, Seattle, WA 98195 USA
[4] Merck Res Labs, Dept Anim Pharmacol, Rahway, NJ 07065 USA
[5] Merck Res Labs, Dept Obes Res, Rahway, NJ 07065 USA
关键词
MTII; obesity; arcuate nucleus; hyperphagia; hypothalamus; alpha-melanocyte-stimulating hormone;
D O I
10.1152/ajpregu.2000.279.1.R47
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Overexpression of agouti-related peptide (AgRP), an endogenous melanocortin (MC) 3 and 4 receptor antagonist (MC3/4-R), causes obesity. Exogenous AgRP(83-132) increases food intake, but its duration and mode of action are unknown. We report herein that doses as low as 10 pmol can have a potent effect on food intake of rats over a 24-h period after intracerebroventricular injection. Additionally, a single third ventricular dose as low as 100 pmol in rats produces a robust increase in food intake that persists for an entire week. AgRP-(83-132) completely blocks the anorectic effect of MTII (MC3/4-R agonist), given simultaneously, consistent with a competitive antagonist action. However, when given 24 h prior to MTII, AgRP-(83-132) is ineffective at reversing the anorectic effects of the agonist. These results support a critical role of MC tone in limiting food intake and indicate that the orexigenic effects of AgRP-(83-132) are initially mediated by competitive antagonism at MC receptors but are sustained by alternate mechanisms.
引用
收藏
页码:R47 / R52
页数:6
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