Electrolytic lesions of the medial nucleus accumbens shell selectively decrease ethanol consumption without altering preference in a limited access procedure in C57BL/6J mice

被引:15
作者
Dhaher, Ronnie [1 ]
Finn, Deborah A. [1 ,2 ]
Oberbeck, Denesa L. [1 ]
Yoneyama, Naomi [1 ]
Snelling, Christopher C. [1 ]
Wu, Weiran [1 ]
Hitzemann, Robert J. [1 ,2 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Behav Neurosci, Portland, OR 97239 USA
[2] Vet Affairs Med Ctr, Res Serv, Portland, OR 97239 USA
关键词
Extended amygdala; Electrolytic lesions; C57BL/6J; Ethanol consumption; Sucrose consumption; Nucleus accumbens; CONDITIONED PLACE PREFERENCE; MESOLIMBIC DOPAMINE SYSTEM; 5-HT1B RECEPTORS; 6-HYDROXYDOPAMINE LESIONS; EXTENDED AMYGDALA; DEPENDENT RATS; 6-OHDA LESIONS; ALCOHOL INTAKE; GENE-TRANSFER; DRINKING;
D O I
10.1016/j.pbb.2008.12.024
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
The central extended amygdala (cExtA) is a limbic region proposed to play a key role in drug and alcohol addiction and to contain the medial nucleus accumbens shell (MNAc shell). The aim of this study was to examine the involvement of the MNAc shell in ethanol and sucrose consumption in a limited and free access procedure in the C57BL/6J (B6) mouse. Separate groups of mice received bilateral electrolytic lesions of the MNAc shell or sham Surgery, and following recovery from Surgery, were allowed to Voluntarily consume ethanol (15% v/v) in a 2 h limited access 2-bottle-choice procedure. Following 1 week of limited access ethanol Consumption, mice were given I week of limited access Sucrose consumption. A separate group of lesioned and sham mice were given free access (24 h) to ethanol in a 2-bottle choice procedure and were run in parallel to the mice receiving limited access Consumption. Electrolytic lesions of the MNAc shell decreased ethanol (but not sucrose) consumption in a limited access procedure, but did not alter free access ethanol consumption. These results suggest that the MNAc shell is a component of the underlying neural circuitry contributing to limited access alcohol consumption in the B6 Mouse. (C) Published by Elsevier Inc.
引用
收藏
页码:335 / 342
页数:8
相关论文
共 58 条
[1]   5-HT1B receptors in nucleus accumbens efferents enhance both rewarding and aversive effects of cocaine [J].
Barot, Sabiha K. ;
Ferguson, Susan M. ;
Neumaier, John F. .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2007, 25 (10) :3125-3131
[2]   Differential expression of motivational stimulus properties by dopamine in nucleus accumbens shell versus core and prefrontal cortex [J].
Bassareo, V ;
De Luca, MA ;
Di Chiar, G .
JOURNAL OF NEUROSCIENCE, 2002, 22 (11) :4709-4719
[3]   SEROTONIN 5-HT3 ANTAGONISTS FAIL TO AFFECT ETHANOL SELF-ADMINISTRATION OF RATS [J].
BEARDSLEY, PM ;
LOPEZ, OT ;
GULLIKSON, G ;
FLYNN, D .
ALCOHOL, 1994, 11 (05) :389-395
[4]   VOLUNTARY CONSUMPTION OF ETHANOL IN 15 INBRED MOUSE STRAINS [J].
BELKNAP, JK ;
CRABBE, JC ;
YOUNG, ER .
PSYCHOPHARMACOLOGY, 1993, 112 (04) :503-510
[5]   Differential effects of blockade of dopamine D1-family receptors in nucleus Accumbens core or shell on reinstatement of heroin seeking induced by contextual and discrete cues [J].
Bossert, Jennifer M. ;
Poles, Gabriela C. ;
Wihbey, Kristina A. ;
Koya, Eisuke ;
Shaham, Yavin .
JOURNAL OF NEUROSCIENCE, 2007, 27 (46) :12655-12663
[6]   Lesions of the extended amygdala in C57BL/6J mice do not block the intermittent ethanol vapor-induced increase in ethanol consumption [J].
Dhaher, Ronnie ;
Finn, Deborah ;
Snelling, Christopher ;
Hitzemann, Robert .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2008, 32 (02) :197-208
[7]   Nucleus accumbens shell and core dopamine: differential role in behavior and addiction [J].
Di Chiara, G .
BEHAVIOURAL BRAIN RESEARCH, 2002, 137 (1-2) :75-114
[8]   Effect of operant self-administration of 10% ethanol plus 10% sucrose on dopamine and ethanol concentrations in the nucleus accumbens [J].
Doyon, WM ;
Anders, SK ;
Ramachandra, VS ;
Czachowski, CL ;
Gonzales, RA .
JOURNAL OF NEUROCHEMISTRY, 2005, 93 (06) :1469-1481
[9]   D1 dopamine receptor regulates alcohol-motivated behaviors in the bed nucleus of the stria terminalis in alcohol-preferring (P) rats [J].
Eiler, WJA ;
Seyoum, R ;
Foster, KL ;
Mailey, C ;
June, HL .
SYNAPSE, 2003, 48 (01) :45-56
[10]   MDL 72222, A SELECTIVE 5-HT3 RECEPTOR ANTAGONIST, SUPPRESSES VOLUNTARY ETHANOL-CONSUMPTION IN ALCOHOL-PREFERRING RATS [J].
FADDA, F ;
GARAU, B ;
MARCHEI, F ;
COLOMBO, G ;
GESSA, GL .
ALCOHOL AND ALCOHOLISM, 1991, 26 (02) :107-110