The mesolimbic dopamine system: The final common pathway for the reinforcing effect of drugs of abuse?

被引:607
作者
Pierce, RC
Kumaresan, V
机构
[1] Boston Univ, Sch Med, Dept Pharmacol, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Dept Psychiat, Boston, MA 02118 USA
[3] Brown Univ, Dept Mol Pharmacol Physiol & Biotechnol, Providence, RI 02912 USA
关键词
amphetamine; cocaine; heroin; morphine nicotine; alcohol; nucleus; accumbens; ventral tegemental area; self administration;
D O I
10.1016/j.neubiorev.2005.04.016
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
In this review we will critically assess the hypothesis that the reinforcing effect of virtually all drugs of abuse is primarily dependent on activation of the mesolimbic dopamine system. The focus is on five classes of abused drugs: psychostimulants, opiates, ethanol, cannabinoids and nicotine. For each of these drug classes, the pharmacological and physiological mechanisms underlying the direct or indirect influence on mesolimbic dopamine transmission will be reviewed. Next, we evaluate behavioral pharmacological experiments that specifically assess the influence of activation of the mesolimbic dopamine system on drug reinforcement, with particular emphasis on animal experiments using drug self-administration paradigms. There is overwhelming evidence that all five classes of abused drugs increase dopamine transmission in limbic regions of the brain through interactions with a variety of transporters, ionotropic receptors and metabotropic receptors. Behavioral pharmacological experiments indicate that increased dopamine transmission is clearly both necessary and sufficient to promote psychostimulant reinforcement. For the other four classes of abused substances, self-administration experiments Suggest that although increasing mesolimbic dopamine transmission plays an important role in the reinforcing effects of opiates. ethanol, cannabinoids and nicotine, there are also dopamine-independent processes that contribute significantly to the reinforcing effects of these compounds. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:215 / 238
页数:24
相关论文
共 365 条
[1]  
ALEXANDER GE, 1990, PROG BRAIN RES, V85, P119
[2]   The effects of cannabinoids on the brain [J].
Ameri, A .
PROGRESS IN NEUROBIOLOGY, 1999, 58 (04) :315-348
[3]   REMOXIPRIDE, A SPECIFIC D2-DOPAMINE ANTAGONIST - AN EXAMINATION OF ITS SELF-ADMINISTRATION LIABILITY AND ITS EFFECTS ON D-AMPHETAMINE SELF-ADMINISTRATION [J].
AMIT, Z ;
SMITH, BR .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1992, 41 (01) :259-261
[4]   ACTIONS OF DRUGS OF ABUSE ON BRAIN REWARD SYSTEMS - A RECONSIDERATION WITH SPECIFIC ATTENTION TO ALCOHOL [J].
AMIT, Z ;
BROWN, ZW .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1982, 17 (02) :233-238
[5]  
[Anonymous], 2001, Goodman Gilman's
[6]   Ethanol excitation of dopaminergic ventral tegmental area neurons is blocked by quinidine [J].
Appel, SB ;
Liu, ZP ;
McElvain, MA ;
Brodie, MS .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 306 (02) :437-446
[7]   INFLUENCE OF TETRODOTOXIN AND CALCIUM ON CHANGES IN EXTRACELLULAR DOPAMINE LEVELS EVOKED BY SYSTEMIC NICOTINE [J].
BENWELL, MEM ;
BALFOUR, DJK ;
LUCCHI, HM .
PSYCHOPHARMACOLOGY, 1993, 112 (04) :467-474
[8]  
Bergman J., 1990, Behav Pharmacol, V1, P355
[9]  
BERGMAN J, 1989, J PHARMACOL EXP THER, V251, P150
[10]  
Berridge CW, 1997, SYNAPSE, V27, P230, DOI 10.1002/(SICI)1098-2396(199711)27:3<230::AID-SYN8>3.0.CO