de Fiebre C M, Marks M J, Collins A C
Institute for Behavioral Genetics, School of Pharmacy, University of Colorado, Boulder 80309.
Alcohol. 1990 May-Jun;7(3):249-57. doi: 10.1016/0741-8329(90)90014-4.
The possibility that common genetic factors regulate initial sensitivities to ethanol and nicotine as well as the development of cross-tolerance between these agents was explored using the long-sleep (LS) and short-sleep (SS) mice. The LS mice proved to be more sensitive to an acute challenge with nicotine than were the SS mice. Segregation analysis (F1, F2, backcross) indicated that ethanol sensitivity and nicotine sensitivity segregate together. Acute pretreatment with nicotine did not significantly affect sensitivity to ethanol, but ethanol pretreatment altered nicotine responsiveness. The LS mice develop more tolerance to nicotine and ethanol than do the SS and they also develop more cross-tolerance. These genetically determined differences in initial sensitivities, and tolerance and cross-tolerance development are not readily explained by differences in brain nicotinic receptor numbers.
利用长睡眠(LS)和短睡眠(SS)小鼠,探讨了常见遗传因素调节对乙醇和尼古丁的初始敏感性以及这些药物之间交叉耐受性发展的可能性。结果表明,LS小鼠对尼古丁急性刺激的敏感性高于SS小鼠。分离分析(F1、F2、回交)表明,乙醇敏感性和尼古丁敏感性是共同分离的。尼古丁急性预处理对乙醇敏感性无显著影响,但乙醇预处理会改变尼古丁反应性。与SS小鼠相比,LS小鼠对尼古丁和乙醇产生的耐受性更强,并且它们也产生了更多的交叉耐受性。这些在初始敏感性、耐受性和交叉耐受性发展方面由基因决定的差异,不能轻易地用脑烟碱受体数量的差异来解释。