Opioid receptor involvement in the effect of AgRP-(83-132) on food intake and food selection

被引:115
作者
Hagan, MM
Rushing, PA
Benoit, SC
Woods, SC
Seeley, RJ
机构
[1] Univ Alabama, Dept Psychol, Birmingham, AL 35294 USA
[2] Univ Cincinnati, Med Ctr, Dept Psychiat, Cincinnati, OH 45267 USA
关键词
melanocortin; obesity; hyperphagia; enkephalin; naloxone;
D O I
10.1152/ajpregu.2001.280.3.R814
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Agouti-related peptide (AgRP) is a receptor antagonist of central nervous system (CNS) melanocortin receptors and appears to have an important role in the control of food intake since exogenous CNS administration in rats and overexpression in mice result in profound hyperphagia and weight gain. Given that AgRP is heavily colocalized with neuropeptide Y (NPY) and that orexigenic effects of NPY depend on activity at opioid receptors, we hypothesized that AgRP's food-intake effects are also mediated by opioid receptors. Subthreshold doses of the opioid receptor antagonist naloxone blocked AgRP-induced intake when given simultaneously but not 24 h after AgRP injection. Opioids not only influence food intake but food selection as well. Hence, we tested AgRP's effect to alter food choice between matched diets with differing dietary fat content. AgRP selectively enhanced intake of the high-fat but not the low-fat diet. Additionally, AgRP selectively increased chow intake in rats given ad libitum access to a 20% sucrose solution and standard rat chow. The current results indicate that AgRP influences not only caloric intake but food selection as well and that the early effects of AgRP depend critically on an interaction with opioid receptors.
引用
收藏
页码:R814 / R821
页数:8
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