Palmer Abraham A, Moyer Michelle R, Crabbe John C, Phillips Tamara J
Portland Alcohol Research Center, Portland, OR 97201, USA.
Psychopharmacology (Berl). 2002 Jul;162(3):313-22. doi: 10.1007/s00213-002-1106-2. Epub 2002 May 14.
Acute ethanol administration induces hypothermia in genetically susceptible animals. Tolerance to this effect may develop with repeated administration. Allopregnanolone is an endogenously produced neuroactive steroid that acts at the GABA-A receptor. We postulated that allopregnanolone would induce hypothermia, and that lines of mice selectively bred for high (COLD-1 and COLD-2) or low (HOT-1 and HOT-2) sensitivity to ethanol's hypothermic effects would also be differentially sensitive to allopregnanolone-induced hypothermia. We also postulated that tolerance would develop to these two drugs by similar mechanisms, such that tolerance to one would impart cross-tolerance to the other.
To assess sensitivity, tolerance and cross-tolerance to allopregnanolone's and ethanol's hypothermic effects in HOT-1 and 2, and COLD-1 and 2 mice.
Mice were administered one of several doses of allopregnanolone each day, for 4 days, and initial sensitivity and tolerance to allopregnanolone-induced hypothermia were assessed. On day 5, ethanol was administered to assess cross-tolerance. In a separate experiment, COLD-1 and 2 mice were made tolerant to ethanol's hypothermic effects, and challenged with allopregnanolone to assess cross-tolerance.
COLD mice exhibited greater initial sensitivity to the hypothermic effect of allopregnanolone, as compared to HOT mice. Tolerance to allopregnanolone-induced hypothermia was greater in COLD mice than in HOT mice, but only COLD-1 mice showed cross-tolerance to ethanol. Both replicate lines of COLD mice developed tolerance following repeated administration of ethanol, but only COLD-2 mice showed cross-tolerance to allopregnanolone.
These results demonstrate shared genetic influence over allopregnanolone and ethanol's initial hypothermic effects. They also suggest genotype-dependent differences in the mechanisms for tolerance to these two compounds.
急性给予乙醇会在基因易感性动物中诱发体温过低。反复给药可能会产生对此效应的耐受性。别孕烯醇酮是一种内源性产生的神经活性类固醇,作用于GABA - A受体。我们推测别孕烯醇酮会诱发体温过低,并且对乙醇体温过低效应具有高敏感性(COLD - 1和COLD - 2)或低敏感性(HOT - 1和HOT - 2)的品系小鼠对别孕烯醇酮诱发的体温过低也会有不同的敏感性。我们还推测对这两种药物的耐受性会通过相似的机制产生,以至于对一种药物的耐受性会赋予对另一种药物的交叉耐受性。
评估HOT - 1和2以及COLD - 1和2小鼠对别孕烯醇酮和乙醇体温过低效应的敏感性、耐受性和交叉耐受性。
每天给小鼠给予几种剂量的别孕烯醇酮之一,持续4天,并评估对别孕烯醇酮诱发体温过低的初始敏感性和耐受性。在第5天,给予乙醇以评估交叉耐受性。在另一个实验中,使COLD - 1和2小鼠对乙醇的体温过低效应产生耐受性,并用别孕烯醇酮进行挑战以评估交叉耐受性。
与HOT小鼠相比,COLD小鼠对别孕烯醇酮的体温过低效应表现出更高的初始敏感性。COLD小鼠对别孕烯醇酮诱发体温过低的耐受性高于HOT小鼠,但只有COLD - 1小鼠表现出对乙醇的交叉耐受性。两个COLD小鼠重复品系在反复给予乙醇后都产生了耐受性,但只有COLD - 2小鼠表现出对别孕烯醇酮的交叉耐受性。
这些结果表明对别孕烯醇酮和乙醇的初始体温过低效应存在共同的遗传影响。它们还表明对这两种化合物耐受性机制存在基因型依赖性差异。