Feller D J, Crabbe J C
Research Service, Veteran's Administration Medical Center, Portland, Oregon.
J Pharmacol Exp Ther. 1991 Mar;256(3):954-8.
Mice selectively bred for resistance (HOT) and sensitivity (COLD) to the hypothermic effect of EtOH were tested for their hypothermic response to neurotransmitter-specific drugs and for the effect of such drugs on EtOH induced hypothermia (HT). The drugs administered were the opiate drugs morphine, levorphanol and U50488H, the dopamine agonists apomorphine, LY171535 and SKF38393, the dopamine antagonist chlorpromazine, the alpha adrenergic agonist St587, the cholinergic agonist nicotine and amphetamine, which increases the release of catecholamines. All of the drugs tested, with the exception of SKF38393 and amphetamine, induced a hypothermic response in HOT and COLD mice. SKF38393 had no effect on body temperature or HT produced by EtOH. Amphetamine caused HT at low doses and hyperthermia at high doses. COLD mice were more sensitive than HOT mice to the hypothermic effect of morphine and levorphanol, mu-opiate agonists, and U50488H, a relatively specific kappa agonist. All of the other drugs tested were approximately equally potent in HOT and COLD mice. These results suggest that the differential sensitivity of HOT and COLD mice to EtOH-induced HT may be partially mediated through genetic changes in opiate mechanisms.
对经选择性培育而分别具有对乙醇低温效应抗性(HOT)和敏感性(COLD)的小鼠,测试它们对神经递质特异性药物的低温反应以及此类药物对乙醇诱导的低温(HT)的影响。所施用的药物有阿片类药物吗啡、左啡诺和U50488H,多巴胺激动剂阿扑吗啡、LY171535和SKF38393,多巴胺拮抗剂氯丙嗪,α肾上腺素能激动剂St587,胆碱能激动剂尼古丁以及可增加儿茶酚胺释放的苯丙胺。除SKF38393和苯丙胺外,所有测试药物均在HOT和COLD小鼠中诱导出低温反应。SKF38393对乙醇产生的体温或低温没有影响。苯丙胺在低剂量时引起低温,在高剂量时引起体温过高。COLD小鼠比HOT小鼠对吗啡、左啡诺(μ阿片类激动剂)和U50488H(一种相对特异性的κ激动剂)的低温效应更敏感。所有其他测试药物在HOT和COLD小鼠中的效力大致相同。这些结果表明,HOT和COLD小鼠对乙醇诱导的低温的差异敏感性可能部分通过阿片类机制的基因变化介导。