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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Enhanced ethanol-, but not cocaine-induced, conditioned place preference in Apoe(-/-) mice.
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Enhanced ethanol-, but not cocaine-induced, conditioned place preference in Apoe(-/-) mice.

机译:在Apoe(-/-)小鼠中增强的乙醇诱导但不是可卡因诱导的条件位置偏爱。

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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(tm1Unc)) 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.
机译:载脂蛋白(apo)E是一种糖蛋白,最常与心血管疾病和阿尔茨海默氏病风险相关。最近的数据表明,酗酒者的额叶皮质中apoE mRNA表达降低,这增加了apoE也可能与乙醇的有益特性有关的可能性。在这项研究中,我们检查了Apoe缺失是否影响小鼠乙醇的奖励特性。雄性和雌性野生型(WT; C57BL / 6J)和apoE基因敲除(Apoe(-/-); C57BL / 6J-Apoe(tm1Unc))小鼠经过无偏位处理,使用乙醇(2 g / kg)或可卡因(5 mg / kg)。还通过两瓶选择程序测试了雌性小鼠的乙醇摄入量。 Apoe(-/-)小鼠表现出更高的乙醇诱导条件性位置偏爱(CPP)。相比之下,可卡因诱导的CPP和乙醇摄入在基因型之间相似。这些发现表明,apoE通常会降低乙醇的条件性奖励特性,但不会降低可卡因的条件奖励特性。尽管尚不清楚apoE产生这些作用的确切机制,但这些数据支持apoE在调节乙醇的条件性奖励特性中的可能作用。

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