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可卡因致敏与耐受的遗传分析。

Genetic analysis of sensitization and tolerance to cocaine.

作者信息

Tolliver B K, Belknap J K, Woods W E, Carney J M

机构信息

Department of Pharmacology, University of Kentucky College of Medicine, Lexington.

出版信息

J Pharmacol Exp Ther. 1994 Sep;270(3):1230-8.

PMID:7932176
Abstract

The present study investigated the effects of acute and repeated administration of cocaine (1.0-56.0 mg/kg) on locomotor activity in the genetically distinct DBA/2J and C57BL/6J inbred strains of mice. In addition, quantitative trait loci analysis of the effects of acute and repeated cocaine in 16 BXD recombinant inbred strains was used to provisionally detect and map minor gene loci which associate with cocaine responsiveness. Whereas locomotor activity was elevated maximally in both strains by 32 mg/kg of cocaine, DBA/2J mice were stimulated to a much greater extent than C57BL/6J mice. The stimulant effects of cocaine were diminished to control levels in DBA/2J mice after repeated daily injections, whereas cocaine-induced locomotion remained consistent in C57BL/6J mice throughout the 7-day testing period. Emergence of stereotyped behavior with repeated daily injections of 32 mg/kg of cocaine was observed in DBA/2J but not C57BL/6J mice. No differences in brain cocaine levels were found between the DBA/2J and C57BL/6J strains after acute or repeated injections. Quantitative trait loci analysis indicated significant associations of differences in cocaine responsiveness with marker loci on several chromosomes in the BXD recombinant inbred series. Those marker loci associated with the acute cocaine response were in most cases different from those markers associated with long-term responses. The current results demonstrate that genotype-dependent variation exists in behavioral responsiveness to cocaine in mice and suggest that the acute and long-term responses to cocaine may be under the control of separate sets of genes.

摘要

本研究调查了急性和重复给予可卡因(1.0 - 56.0毫克/千克)对基因不同的DBA/2J和C57BL/6J近交系小鼠运动活性的影响。此外,利用对16个BXD重组近交系小鼠急性和重复给予可卡因效应的数量性状位点分析,初步检测并定位了与可卡因反应性相关的微基因座。虽然两种品系小鼠的运动活性在给予32毫克/千克可卡因时均达到最大升高,但DBA/2J小鼠受到的刺激程度远大于C57BL/6J小鼠。在DBA/2J小鼠中,每日重复注射后,可卡因的刺激作用减弱至对照水平,而在整个7天的测试期内,可卡因诱导的运动在C57BL/6J小鼠中保持一致。在DBA/2J小鼠中观察到每日重复注射32毫克/千克可卡因会出现刻板行为,而C57BL/6J小鼠未出现。急性或重复注射后,DBA/2J和C57BL/6J品系小鼠的脑可卡因水平未发现差异。数量性状位点分析表明,在BXD重组近交系中,可卡因反应性差异与几条染色体上的标记基因座存在显著关联。那些与急性可卡因反应相关的标记基因座在大多数情况下与那些与长期反应相关的标记不同。目前的结果表明,小鼠对可卡因的行为反应存在基因型依赖性差异,并提示对可卡因的急性和长期反应可能受不同基因集的控制。

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