Khanna J M, Mayer J M, Lê D A, Kalant H
Alcohol. 1984 Jan-Feb;1(1):3-7. doi: 10.1016/0741-8329(84)90029-6.
Males of two lines of mice, long sleep (LS) and short sleep (SS), that had been selectively bred for their differential sensitivity to ethanol-induced sleep, were examined for their responses to the hypothermic and analgesic effects of ethanol, pentobarbital and morphine, and to the cataleptic effect of morphine. SS mice were found to be less sensitive than the LS animals to ethanol but not pentobarbital-induced analgesia and hypothermia. The SS animals were also less sensitive to morphine-induced hypothermia, but were, by contrast, more sensitive than their LS counterparts to morphine-induced analgesia, while no line differences existed with respect to catalepsy. The rate of morphine disappearance from the blood was somewhat higher in the LS animals but this difference is probably too small to account for the observed differential responses to morphine.
对经过选择性培育、对乙醇诱导睡眠具有不同敏感性的两系小鼠(长睡眠[LS]和短睡眠[SS])的雄性小鼠进行了研究,观察它们对乙醇、戊巴比妥和吗啡的低温及镇痛作用以及吗啡的僵住作用的反应。发现SS小鼠对乙醇诱导的镇痛和低温作用的敏感性低于LS小鼠,但对戊巴比妥诱导的镇痛和低温作用并非如此。SS小鼠对吗啡诱导的低温作用也较不敏感,但相比之下,它们对吗啡诱导的镇痛作用比LS小鼠更敏感,而在僵住作用方面两系小鼠没有差异。LS小鼠血液中吗啡消失的速率略高,但这种差异可能太小,无法解释观察到的对吗啡的不同反应。