ETHANOL DRINKING FOLLOWING 6-OHDA LESIONS OF NUCLEUS-ACCUMBENS AND TUBERCULUM OLFACTORIUM OF THE RAT

被引:47
作者
QUARFORDT, SD
KALMUS, GW
MYERS, RD
机构
[1] E CAROLINA UNIV, SCH MED, DEPT PHARMACOL, GREENVILLE, NC 27834 USA
[2] E CAROLINA UNIV, SCH MED, DEPT PSYCHIAT MED, GREENVILLE, NC 27834 USA
[3] E CAROLINA UNIV, DEPT BIOL, GREENVILLE, NC 27834 USA
关键词
ETHANOL DRINKING; ALCOHOL PREFERENCE; DOPAMINE; 6-HYDROXYDOPAMINE; NUCLEUS ACCUMBENS; TUBERCULUM OLFACTORIUM; LESION; REWARD SYSTEM;
D O I
10.1016/0741-8329(91)90854-P
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Previous studies have shown that lesions of the dopaminergic system in the brain produced by an intracerebroventricular injection of the neurotoxin, 6-hydroxydopamine (6-OHDA), evoke significant changes in ethanol drinking. In the present experiments, dopaminergic systems of Sprague-Dawley rats were lesioned by 6-OHDA infused into either the tuberculum olfactorium or nucleus accumbens, two of the structures implicated in drug-related reinforcement. Prior to the lesion and immediately thereafter, tests for ethanol preference were undertaken in which water was offered in a self-selection situation together with ethanol which was increased in concentration from 3-30% over a 10-day interval. Following the circumscribed ablation of dopaminergic neurons within either the N. accumbens or tuberculum olfactorium, preference for ethanol increased significantly with absolute intakes exceeding 4.0 g/kg at the 7% concentration during the first postlesion drinking test. During the second postlesion preference test, the mean consumption of ethanol exceeded 6.0 g/kg at the 11% concentration and 4.0 to 5.0 g/kg at the 20 and 30 percent concentrations offered to the rats. When adjacent areas just dorsal or lateral to these structures were lesioned by 6-OHDA, no significant change in consumption of ethanol occurred. Thus, it is envisaged that one of the functional roles for the dopaminergic neurons of the N. accumbens and tuberculum olfactorium is to regulate the craving for a drug with addictive liability such as ethanol. As a result of an impairment of normal function of dopamine receptors or a perturbation in the release of this catecholaminergic neurotransmitter, ethanol becomes reinforcing upon repeated exposure. Thus, an addictive-like state consequently ensues. Finally, it is envisaged that the control mechanism underlying the function of the dopaminergic neurons in the medial-basal forebrain is functionally disinhibited in individuals that consume ethanol to the point of abuse.
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页码:211 / 217
页数:7
相关论文
共 36 条
[1]   ETHANOL INGESTIVE BEHAVIOR AS A FUNCTION OF CENTRAL NEUROTRANSMISSION [J].
BLUM, K ;
BRIGGS, AH ;
TRACHTENBERG, MC .
EXPERIENTIA, 1989, 45 (05) :444-452
[2]  
Bozarth M A, 1986, NIDA Res Monogr, V67, P190
[3]   EFFECTS OF SELECTIVE CATECHOLAMINE DEPLETIONS BY 6-HYDROXYDOPAMINE ON ETHANOL PREFERENCE IN RATS [J].
BROWN, ZW ;
AMIT, Z .
NEUROSCIENCE LETTERS, 1977, 5 (06) :333-336
[4]   CONDITIONED PLACE PREFERENCE FROM INTRA-ACCUMBENS BUT NOT INTRA-CAUDATE AMPHETAMINE INJECTIONS [J].
CARR, GD ;
WHITE, NM .
LIFE SCIENCES, 1983, 33 (25) :2551-2557
[5]  
COLLINS M, 1985, ALDEHYDE ADDUCTS ALC
[6]   EFFECTS OF TETRAHYDROPAPAVEROLINE IN THE NUCLEUS-ACCUMBENS AND THE VENTRAL TEGMENTAL AREA ON ETHANOL PREFERENCE IN THE RAT [J].
DUNCAN, CC ;
FERNANDO, PW .
ALCOHOL, 1991, 8 (02) :87-90
[7]   LACK OF AN EFFECT OF 6-HYDROYDOPAMINE LESIONS OF THE NUCLEUS ACCUMBENS ON INTRAVENOUS MORPHINE SELF-ADMINISTRATION [J].
DWORKIN, SI ;
GUERIN, GF ;
CO, C ;
GOEDERS, NE ;
SMITH, JE .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1988, 30 (04) :1051-1057
[8]   KAINIC ACID LESIONS OF THE NUCLEUS ACCUMBENS SELECTIVELY ATTENUATE MORPHINE SELF-ADMINISTRATION [J].
DWORKIN, SI ;
GUERIN, GF ;
GOEDERS, NE ;
SMITH, JE .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1988, 29 (01) :175-181
[9]   NEURONAL DEGENERATION IN RAT-BRAIN INDUCED BY 6-HYDROXYDOPAMINE - HISTOLOGICAL AND BIOCHEMICAL STUDY [J].
HEDREEN, JC ;
CHALMERS, JP .
BRAIN RESEARCH, 1972, 47 (01) :1-&
[10]   SELF-INJECTION OF AMPHETAMINE DIRECTLY INTO THE BRAIN [J].
HOEBEL, BG ;
MONACO, AP ;
HERNANDEZ, L ;
AULISI, EF ;
STANLEY, BG ;
LENARD, L .
PSYCHOPHARMACOLOGY, 1983, 81 (02) :158-163