Serotonin and drug reward:: focus on 5-HT2C receptors

被引:126
作者
Higgins, GA
Fletcher, PJ
机构
[1] Schering Plough Res Inst, Kenilworth, NJ 07033 USA
[2] Ctr Addict & Mental Hlth, Toronto, ON M5T 1R8, Canada
关键词
cocaine; 5-HT; (5-hydroxytryptamine; serotonin); 5-HT2C receptor knockout mouse; drug self-administration; feeding behaviour; RNA editing;
D O I
10.1016/j.ejphar.2003.08.102
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pharmacological manipulation of the 5-hydroxytryptamine (5-HT; serotonin) system has long been associated with a regulation of feeding behaviour, however, the initial part of this article reviews evidence that central 5-HT systems similarly modulate reward-related behaviours, particularly drug reward. The second part of this article considers what we believe to be strong emerging pharmacological and genetic evidence that many of these effects are mediated through 5-HT2C receptor signalling mechanisms. Finally, we consider the potential for selective 5-HT2C agonists as therapies for substance abuse disorders and the medical implications for different 5-HT2C receptor isoforms generated by RNA editing. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:151 / 162
页数:12
相关论文
共 115 条
[61]   Activation of mesolimbic dopamine function by phencyclidine is enhanced by 5-HT2C/2B receptor antagonists:: neurochemical and behavioural studies [J].
Hutson, PH ;
Barton, CL ;
Jay, M ;
Blurton, P ;
Burkamp, F ;
Clarkson, R ;
Bristow, LJ .
NEUROPHARMACOLOGY, 2000, 39 (12) :2318-2328
[62]   5-HT3 receptor antagonist MDL 72222 attenuates cocaine- and mazindol-, but not methylphenidate-induced neurochemical and behavioral effects in the rat [J].
Kankaanpää, A ;
Meririnne, E ;
Seppälä, T .
PSYCHOPHARMACOLOGY, 2002, 159 (04) :341-350
[63]   EVIDENCE THAT MCPP MAY HAVE BEHAVIORAL-EFFECTS MEDIATED BY CENTRAL 5-HT1C RECEPTORS [J].
KENNETT, GA ;
CURZON, G .
BRITISH JOURNAL OF PHARMACOLOGY, 1988, 94 (01) :137-147
[64]   SB 242084, a selective and brain penetrant 5-HT2C receptor antagonist [J].
Kennett, GA ;
Wood, MD ;
Bright, F ;
Trail, B ;
Riley, G ;
Holland, V ;
Avenell, KY ;
Stean, T ;
Upton, N ;
Bromidge, S ;
Forbes, IT ;
Brown, AM ;
Middlemiss, DN ;
Blackburn, TP .
NEUROPHARMACOLOGY, 1997, 36 (4-5) :609-620
[65]   MDL-72222, KETANSERIN, AND METHYSERGIDE PRETREATMENTS FAIL TO ALTER BREAKING POINTS ON A PROGRESSIVE RATIO SCHEDULE REINFORCED BY INTRAVENOUS COCAINE [J].
LACOSTA, S ;
ROBERTS, DCS .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1993, 44 (01) :161-165
[66]   GABAA receptors in the ventral tegmental area control bidirectional reward signalling between dopaminergic and non-dopaminergic neural motivational systems [J].
Laviolette, SR ;
van der Kooy, D .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 13 (05) :1009-1015
[67]   Effects of naltrexone and fluoxetine on alcohol self-administration and reinstatement of alcohol seeking induced by priming injections of alcohol and exposure to stress [J].
Lê, AD ;
Poulos, CX ;
Harding, S ;
Watchus, J ;
Juzytsch, W ;
Shaham, Y .
NEUROPSYCHOPHARMACOLOGY, 1999, 21 (03) :435-444
[68]   THE EFFECTS OF PUTATIVE 5-HYDROXYTRYPTAMINE RECEPTOR ACTIVE AGENTS ON D-AMPHETAMINE SELF-ADMINISTRATION IN CONTROLS AND RATS WITH 5,7-DIHYDROXYTRYPTAMINE MEDIAN FOREBRAIN-BUNDLE LESIONS [J].
LECCESE, AP ;
LYNESS, WH .
BRAIN RESEARCH, 1984, 303 (01) :153-162
[69]   BREAK-POINTS ON A PROGRESSIVE RATIO SCHEDULE REINFORCED BY INTRAVENOUS COCAINE INCREASE FOLLOWING DEPLETION OF FOREBRAIN SEROTONIN [J].
LOH, EA ;
ROBERTS, DCS .
PSYCHOPHARMACOLOGY, 1990, 101 (02) :262-266
[70]   INCREASED SELF-ADMINISTRATION OF D-AMPHETAMINE BY RATS PRETREATED WITH METERGOLINE [J].
LYNESS, WH ;
MOORE, KE .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1983, 18 (05) :721-724