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乙醇与氯氮卓之间的交叉耐受性。

Cross-tolerance between ethanol and chlordiazepoxide.

作者信息

Chan A W, Schanley D L, Aleo M D, Leong F W

出版信息

Alcohol. 1985 Mar-Apr;2(2):209-13. doi: 10.1016/0741-8329(85)90047-3.

DOI:10.1016/0741-8329(85)90047-3
PMID:4015844
Abstract

Drug-induced hypothermia was used to investigate drug tolerance and cross-tolerance. C57BL/6J mice, which were injected with a single dose of chlordiazepoxide (CDP; 30 mg/kg) one day before and reinjected with an equivalent dose of CDP the next day, did not develop tolerance to the drug. However, ethanol-pretreated (3.5 g/kg, 24 hr earlier) mice, when injected with CDP (30 mg/kg), showed cross-tolerance to CDP. The cross-tolerance was short-lived (less than 48 hr). On the other hand, CDP-pretreated mice (30 mg/kg, 24 hr earlier) did not show cross-tolerance to ethanol. The lack of a reciprocating effect of CDP-pretreatment was not likely to be due to the difference in initial dosage between ethanol and CDP. It may be due to different rates of tolerance development or different mechanisms of actions between CDP and ethanol. Mice chronically treated with ethanol also showed a similar degree of cross-tolerance to CDP compared to those exposed to an acute dose of ethanol.

摘要

药物诱导的体温过低被用于研究药物耐受性和交叉耐受性。C57BL/6J小鼠,在一天前注射单剂量的氯氮卓(CDP;30毫克/千克),并在第二天再次注射等量的CDP,对该药物未产生耐受性。然而,乙醇预处理(3.5克/千克,提前24小时)的小鼠,在注射CDP(30毫克/千克)时,对CDP表现出交叉耐受性。这种交叉耐受性是短暂的(小于48小时)。另一方面,CDP预处理的小鼠(30毫克/千克,提前24小时)对乙醇未表现出交叉耐受性。CDP预处理缺乏相互作用的效应不太可能是由于乙醇和CDP初始剂量的差异。这可能是由于耐受性发展的速率不同或CDP与乙醇之间的作用机制不同。与急性剂量乙醇处理的小鼠相比,长期用乙醇处理的小鼠对CDP也表现出相似程度的交叉耐受性。

相似文献

1
Cross-tolerance between ethanol and chlordiazepoxide.乙醇与氯氮卓之间的交叉耐受性。
Alcohol. 1985 Mar-Apr;2(2):209-13. doi: 10.1016/0741-8329(85)90047-3.
2
Does chronic ethanol intake confer full cross-tolerance to chlordiazepoxide?长期摄入乙醇是否会对氯氮卓产生完全交叉耐受性?
Pharmacol Biochem Behav. 1988 Jun;30(2):385-9. doi: 10.1016/0091-3057(88)90472-8.
3
The ability of chlordiazepoxide to maintain ethanol tolerance and dependence.氯氮䓬维持乙醇耐受性和依赖性的能力。
Pharmacol Biochem Behav. 1991 Feb;38(2):433-9. doi: 10.1016/0091-3057(91)90303-j.
4
Chronic treatment with ethanol or chlordiazepoxide alters the metabolism of chlordiazepoxide.长期用乙醇或氯氮䓬治疗会改变氯氮䓬的代谢。
Pharmacol Biochem Behav. 1990 Feb;35(2):363-6. doi: 10.1016/0091-3057(90)90170-m.
5
Partial cross-dependence on ethanol in mice dependent on chlordiazepoxide.对氯氮卓依赖的小鼠对乙醇存在部分交叉依赖性。
Pharmacol Biochem Behav. 1990 Feb;35(2):379-84. doi: 10.1016/0091-3057(90)90173-f.
6
Alcohol-chlordiazepoxide interaction.酒精与氯氮卓的相互作用。
Pharmacol Biochem Behav. 1982 Jul;17(1):141-5. doi: 10.1016/0091-3057(82)90276-3.
7
Differential effects of Ro15-1788 in actions of chlordiazepoxide and ethanol.Ro15 - 1788对氯氮卓和乙醇作用的差异效应。
Pharmacol Biochem Behav. 1988 Feb;29(2):315-20. doi: 10.1016/0091-3057(88)90162-1.
8
Long-lasting reduction in ethanol selection after involuntary intake of ethanol/chlordiazepoxide.在非自愿摄入乙醇/氯氮卓后,乙醇选择的持久减少。
Pharmacol Biochem Behav. 1983 Aug;19(2):275-80. doi: 10.1016/0091-3057(83)90052-7.
9
Relationship of brain cyclic nucleotide levels and the interaction of ethanol with chlordiazepoxide.脑环核苷酸水平与乙醇和氯氮卓相互作用的关系
Biochem Pharmacol. 1982 Jan 1;31(1):85-9. doi: 10.1016/0006-2952(82)90241-6.
10
Chlordiazepoxide-induced expression of c-Fos in the central extended amygdala and other brain regions of the C57BL/6J and DBA/2J inbred mouse strains: relationships to mechanisms of ethanol action.氯氮卓诱导C57BL/6J和DBA/2J近交系小鼠中枢扩展杏仁核及其他脑区c-Fos的表达:与乙醇作用机制的关系
Alcohol Clin Exp Res. 1999 Jul;23(7):1158-72.

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