Phillips T J, Feller D J, Crabbe J C
VA Medical Center, Research Service, Portland, Oregon 97201.
Experientia. 1989 Sep 15;45(9):805-27. doi: 10.1007/BF01954056.
The technique of selective breeding has been employed to develop a number of mouse lines differing in genetic sensitivity to specific effects of ethanol. Genetic animal models for sensitivity to the hypnotic, thermoregulatory, excitatory, and dependence-producing effects of alcohol have been developed. These genetic animal models have been utilized in numerous studies to assess the bases for those genetic differences, and to determine the specific neurochemical and neurophysiological bases for ethanol's actions. Work with these lines has challenged some long-held beliefs about ethanol's mechanisms of action. For example, lines genetically sensitive to one effect of ethanol are not necessarily sensitive to others, which demonstrates that no single set of genes modulates all ethanol effects. LS mice, selected for sensitivity to ethanol anesthesia, are not similarly sensitive to all anesthetic drugs, which demonstrates that all such drugs cannot have a common mechanism of action. On the other hand, WSP mice, genetically susceptible to the development of severe ethanol withdrawal, show a similar predisposition to diazepam and phenobarbital withdrawal, which suggests that there may be a common set of genes underlying drug dependencies. Studies with these models have also revealed important new directions for future mechanism-oriented research. Several studies implicate brain gamma-aminobutyric acid and dopamine systems as potentially important mediators of susceptibility to alcohol intoxication. The stability of the genetic animal models across laboratories and generations will continue to increase their power as analytic tools.
选择性育种技术已被用于培育一些对乙醇特定作用的遗传敏感性不同的小鼠品系。已经建立了对酒精的催眠、体温调节、兴奋和产生依赖性作用敏感的遗传动物模型。这些遗传动物模型已被用于众多研究中,以评估这些遗传差异的基础,并确定乙醇作用的特定神经化学和神经生理基础。对这些品系的研究挑战了一些关于乙醇作用机制的长期观点。例如,对乙醇一种作用遗传敏感的品系不一定对其他作用敏感,这表明没有一组单一的基因调节所有乙醇作用。为对乙醇麻醉敏感而选择的LS小鼠对所有麻醉药物并非同样敏感,这表明所有此类药物不可能有共同的作用机制。另一方面,对严重乙醇戒断发展遗传易感的WSP小鼠对安定和苯巴比妥戒断也有类似的易感性,这表明药物依赖性可能有一组共同的基因基础。对这些模型的研究也揭示了未来面向机制研究的重要新方向。几项研究表明,脑γ-氨基丁酸和多巴胺系统可能是酒精中毒易感性的重要潜在介质。遗传动物模型在不同实验室和不同世代间的稳定性将继续增强其作为分析工具的效力。