Anandamide induces overeating: mediation by central cannabinoid (CB1) receptors

被引:359
作者
Williams, CM [1 ]
Kirkham, TC [1 ]
机构
[1] Univ Reading, Dept Psychol, Reading RG6 6AL, Berks, England
基金
英国生物技术与生命科学研究理事会;
关键词
SR141716; hyperphagia; rat; pre-feed; eating; appetite;
D O I
10.1007/s002130050953
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale: Central cannabinoid systems have been implicated in appetite regulation by the respective hyperphagic actions of exogenous cannabinoids, such as Delta 9-THC, and hypophagic effects of selective cannabinoid receptor antagonists. Objective: This study examined whether an endogenous cannabinoid, anandamide, could induce overeating, via a specific action at central (CB1) cannabinoid receptors. Methods: Pre-satiated male rats (n=18), received subcutaneous injections of anandamide (0.5, 1.0, 5.0, 10.0 mg/kg) before 3-h, nocturnal food intake tests. In a second series of intake tests (n=8), anandamide injection (1.0 mg/kg) was preceded by injection of the specific CBI receptor antagonist, SR141716 (0.1, 0.5, 1.0 mg/kg SC). Results: All doses of anandamide induced significant overeating, with 1.0 mg/kg being most potent. Additionally, hyperphagia induced by 1.0 mg/kg anandamide was dose-dependently attenuated by SR141716 pretreatment. Conclusion: This first demonstration of anandamide-induced, CB1-mediated, overeating provides important evidence for the involvement of a central cannabinoid system in the normal control of eating.
引用
收藏
页码:315 / 317
页数:3
相关论文
共 16 条
[1]   Selective inhibition of sucrose and ethanol intake by SR 141716, an antagonist of central cannabinoid (CB1) receptors [J].
Arnone, M ;
Maruani, J ;
Chaperon, F ;
Thiebot, MH ;
Poncelet, M ;
Soubrie, P ;
LeFur, G .
PSYCHOPHARMACOLOGY, 1997, 132 (01) :104-106
[2]   KINETIC STUDIES OF FOOD-INTAKE AND SUCROSE SOLUTION PREFERENCE BY RATS TREATED WITH LOW-DOSES OF DELTA-9-TETRAHYDROCANNABINOL [J].
BROWN, JE ;
KASSOUNY, M ;
CROSS, JK .
BEHAVIORAL BIOLOGY, 1977, 20 (01) :104-110
[3]  
COLOMBO G, 1998, LIFE SCI, V63, pL113
[4]   ANANDAMIDE, AN ENDOGENOUS LIGAND OF THE CANNABINOID RECEPTOR, INDUCES HYPOMOTILITY AND HYPOTHERMIA IN-VIVO IN RODENTS [J].
CRAWLEY, JN ;
CORWIN, RL ;
ROBINSON, JK ;
FELDER, CC ;
DEVANE, WA ;
AXELROD, J .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1993, 46 (04) :967-972
[5]   ISOLATION AND STRUCTURE OF A BRAIN CONSTITUENT THAT BINDS TO THE CANNABINOID RECEPTOR [J].
DEVANE, WA ;
HANUS, L ;
BREUER, A ;
PERTWEE, RG ;
STEVENSON, LA ;
GRIFFIN, G ;
GIBSON, D ;
MANDELBAUM, A ;
ETINGER, A ;
MECHOULAM, R .
SCIENCE, 1992, 258 (5090) :1946-1949
[6]   PHARMACOLOGICAL ACTIVITY OF THE CANNABINOID RECEPTOR AGONIST, ANANDAMIDE, A BRAIN CONSTITUENT [J].
FRIDE, E ;
MECHOULAM, R .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 231 (02) :313-314
[7]  
HERKENHAM M, 1995, CANNABINOID RECEPTOR, P145
[8]   PREFEEDING POTENTIATES ANORECTIC ACTIONS OF NEUROMEDIN-B AND GASTRIN-RELEASING PEPTIDE [J].
KIRKHAM, TC ;
PEREZ, S ;
GIBBS, J .
PHYSIOLOGY & BEHAVIOR, 1995, 58 (06) :1175-1179
[9]   The cannabinoid CB1 receptor antagonist SR141716A attenuates the memory impairment produced by Δ9-tetrahydrocannabinol or anandamide [J].
Mallet, PE ;
Beninger, RJ .
PSYCHOPHARMACOLOGY, 1998, 140 (01) :11-19
[10]   STRUCTURE OF A CANNABINOID RECEPTOR AND FUNCTIONAL EXPRESSION OF THE CLONED CDNA [J].
MATSUDA, LA ;
LOLAIT, SJ ;
BROWNSTEIN, MJ ;
YOUNG, AC ;
BONNER, TI .
NATURE, 1990, 346 (6284) :561-564