The metabotropic glutamate mGluR5 receptor agonist CHPG stimulates food intake.

NEUROREPORT(2010)

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摘要
The metabotropic glutamate receptor 5 (mGluR5) has been suggested to modulate energy balance. For example, mGluR5 antagonists inhibit food intake in rodents and mGluR5 knockout mice resist diet-induced obesity. However, nonspecific effects can reduce food intake. Thus, to further support the role of mGluR5 in feeding behaviour, we evaluated if the mGluR5 agonist (R, S)-2-chloro-5-hydroxyphenylglycine (CHPG) would induce the opposite effect, i.e. increased food intake in rats. Intracerebroventricularly injected CHPG (0.5-1.5 mu mol) induced a dose-dependent stimulation of food intake (349% increase at 2 h with 1.5 mu mol). The mGluR5 antagonist 3-[(2-methyl-1,3-thiazol-4-yl)ethynyl]-pyridine (10 mg/kg intraperitoneally) reduced 24 h food intake, without altering CHPG-induced feeding. These findings further support a physiologically relevant role of mGluR5 in appetite regulation. NeuroReport 21:704-708 (C) 2010 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
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food intake,intracerebroventricular,3-[(2-methyl-1,3-thiazol-4-yl)ethynyl]-pyridine,mGluR5,obesity,rat,[R,S]-2-chloro-5-hydroxyphenylglycine
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