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利用基因不同的小鼠群体探索乙醇强化作用。

Use of genetically distinct mouse populations to explore ethanol reinforcement.

作者信息

Phillips T J

机构信息

Veterans Affairs Medical Center, Portland, OR, USA.

出版信息

Alcohol Alcohol Suppl. 1993;2:451-5.

PMID:7748338
Abstract

Alcohol-induced locomotor stimulation in mice may provide an animal model of human euphoric responses to moderate alcohol (ethanol) doses. If a common mechanism mediates sensitivity to both drug reward (reinforcement) and drug stimulation, rodent models of drug stimulation would provide powerful tools for investigating drug reinforcement. In addition, stimulant sensitivity might provide a simple marker for susceptibility to ethanol reward, and perhaps addiction (e.g., Newlin and Thomson, 1991). This short report describes the use of three genetic mouse models, (1) FAST and SLOW selectively bred lines, (2) BXD Recombinant Inbred Strains, and (3) a panel of inbred strains of diverse genetic origin, to explore mechanisms mediating ethanol stimulation and reinforcement.

摘要

酒精诱导的小鼠运动兴奋可能为人类对适度酒精(乙醇)剂量产生欣快感反应提供一种动物模型。如果存在一种共同机制介导对药物奖赏(强化)和药物刺激的敏感性,那么药物刺激的啮齿动物模型将为研究药物强化提供强大工具。此外,兴奋剂敏感性可能为乙醇奖赏易感性,甚至成瘾性(例如,纽林和汤姆森,1991年)提供一个简单的标志物。本简短报告描述了使用三种基因小鼠模型,(1)快速和慢速选择性培育品系,(2)BXD重组近交系,以及(3)一组具有不同遗传起源的近交系,来探索介导乙醇刺激和强化的机制。

相似文献

1
Use of genetically distinct mouse populations to explore ethanol reinforcement.利用基因不同的小鼠群体探索乙醇强化作用。
Alcohol Alcohol Suppl. 1993;2:451-5.
2
Locomotor activity response to chronic ethanol treatment in selectively bred FAST and SLOW mice.选择性培育的快速和慢速小鼠对慢性乙醇处理的运动活动反应。
Alcohol Alcohol Suppl. 1991;1:109-13.
3
Approaches to understanding the neurobiological regulation of ethanol self-administration: a young investigators forum.理解乙醇自我给药神经生物学调节的方法:青年研究者论坛
Alcohol Clin Exp Res. 2001 Feb;25(2):293-8.
4
Ethanol preexposure increases ethanol self-administration in C57BL/6J and DBA/2J mice.乙醇预暴露会增加C57BL/6J和DBA/2J小鼠的乙醇自我给药量。
Pharmacol Biochem Behav. 2004 Dec;79(4):623-32. doi: 10.1016/j.pbb.2004.09.012.
5
Selectively bred lines of mice show response and drug specificity for genetic regulation of acute functional tolerance to ethanol and pentobarbital.经过选择性培育的小鼠品系对乙醇和戊巴比妥急性功能耐受性的遗传调控表现出反应和药物特异性。
J Pharmacol Exp Ther. 2000 Apr;293(1):188-95.
6
MK-801-induced locomotor activity in long-sleep x short-sleep recombinant inbred mouse strains: correlational analysis with low-dose ethanol and provisional quantitative trait loci.MK-801诱导的长睡眠×短睡眠重组近交小鼠品系的自发活动:与低剂量乙醇的相关性分析及初步数量性状基因座
Alcohol Clin Exp Res. 1999 Nov;23(11):1721-9.
7
Acute sensitivity of FAST and SLOW mice to the effects of abused drugs on locomotor activity.快速代谢型和慢速代谢型小鼠对滥用药物对运动活动影响的急性敏感性。
J Pharmacol Exp Ther. 1992 May;261(2):525-33.
8
Evidence that the Lore-1 region specifies ethanol-induced activation in addition to sedative/hypnotic sensitivity to ethanol.有证据表明,Lore-1区域除了对乙醇的镇静/催眠敏感性外,还决定乙醇诱导的激活作用。
Alcohol Clin Exp Res. 2001 Nov;25(11):1551-7.
9
Locomotor effects of ethanol and acetaldehyde after peripheral and intraventricular injections in Swiss and C57BL/6J mice.乙醇和乙醛经外周及脑室内注射后对瑞士小鼠和C57BL/6J小鼠运动功能的影响。
Behav Brain Res. 2006 Sep 15;172(1):145-54. doi: 10.1016/j.bbr.2006.05.010. Epub 2006 Jun 9.
10
Ethanol self-administration is genetically independent of locomotor stimulation in fast and slow mice.在快速和慢速小鼠中,乙醇自我给药在基因上独立于运动刺激。
Alcohol. 1996 Jan-Feb;13(1):79-84. doi: 10.1016/0741-8329(95)02017-9.

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