Enhanced ethanol, but not cocaine-induced, conditioned place preference in Apoe-/- mice

被引:18
作者
Bechtholt, AJ
Smith, R
Raber, J
Cunningham, CL
机构
[1] Oregon Hlth Sci Univ, Dept Behav Neurosci, Portland, OR 97239 USA
[2] Oregon Hlth Sci Univ, ONPRC, Dept Neurol, Portland, OR 97239 USA
[3] Oregon Hlth Sci Univ, ONPRC, Div Neurosci, Portland, OR 97239 USA
[4] Oregon Hlth Sci Univ, Portland Alchol Res Ctr, Portland, OR 97239 USA
关键词
conditioned place preference; place conditioning; ethanol; cocaine; apolipoprotein E; apoE; locomotor activity; knockout mice; C57BL/6J;
D O I
10.1016/j.pbb.2004.02.002
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
Apolipoprotein (apo) E is a glycoprotein that is most commonly associated with cardiovascular and Alzheimer's disease risk. Recent data showing that apoE mRNA expression is reduced in the frontal cortex of alcoholics raise the possibility that apoE may also be related to the rewarding properties of ethanol. In this study, we examined whether Apoe deletion affects the rewarding properties of ethanol in mice. Male and female wild-type (WT; C57BL/6J) and apoE knockout (Apoe(-/-); C57BL/6J-Apoe(tul) (Unc)) mice underwent an unbiased place conditioning procedure with ethanol (2 g/kg) or cocaine (5 mg/kg). Female mice were also tested for ethanol intake in a two-bottle choice procedure. Apoe(-/-) mice showed greater ethanol-induced conditioned place preference (CPP). In contrast, cocaine-induced CPP and ethanol intake were similar between the genotypes. These findings suggest that apoE normally reduces the conditioned rewarding properties of ethanol but not of cocaine. While the exact mechanisms underlying these effects of apoE are unknown, these data support a possible role for apoE in modulating the conditioned rewarding properties of ethanol. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:783 / 792
页数:10
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