Collins A C, Burch J B, de Fiebre C M, Marks M J
School of Pharmacy, University of Colorado, Boulder 80309.
Pharmacol Biochem Behav. 1988 Feb;29(2):365-73. doi: 10.1016/0091-3057(88)90170-0.
Female DBA mice were subjected to one of four treatments: ethanol-containing or control diets, nicotine (0.2, 1.0, 5.0 mg/kg/hr) infusion or saline infusion. After removal from the liquid diets or cessation of infusion, the animals were challenged with an acute dose of ethanol or nicotine. Chronic ethanol-fed mice were tolerant to the effects of ethanol on body temperature and open field activity and were cross tolerant to the effects of nicotine on body temperature and heart rate. Nicotine infused animals were tolerant to the effects of nicotine on body temperature and rotarod performance and were cross tolerant to the effects of ethanol on body temperature. Ethanol-induced sleep time was decreased in chronic ethanol- but not chronic nicotine-treated mice. Chronic drug treatment did not alter the elimination rate of either drug. Chronic ethanol treatment did not alter the number or affinity of brain nicotinic receptors whereas chronic nicotine treatment elicited an increase in the number of [3H]-nicotine binding sites. Tolerance and cross tolerance between ethanol and nicotine is discussed in terms of potential effects on desensitization of brain nicotinic receptors.
雌性DBA小鼠接受以下四种处理之一:含乙醇或对照饮食、尼古丁(0.2、1.0、5.0毫克/千克/小时)输注或生理盐水输注。从液体饮食中取出或停止输注后,对动物给予急性剂量的乙醇或尼古丁。长期喂食乙醇的小鼠对乙醇对体温和旷场活动的影响产生耐受,并对尼古丁对体温和心率的影响产生交叉耐受。输注尼古丁的动物对尼古丁对体温和转棒试验表现的影响产生耐受,并对乙醇对体温的影响产生交叉耐受。在长期接受乙醇而非尼古丁处理的小鼠中,乙醇诱导的睡眠时间缩短。长期药物处理未改变任何一种药物的消除率。长期乙醇处理未改变脑烟碱受体的数量或亲和力,而长期尼古丁处理导致[3H]-尼古丁结合位点数量增加。从对脑烟碱受体脱敏的潜在影响方面讨论了乙醇和尼古丁之间的耐受和交叉耐受。