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急性给予氯氮平不会改变纳洛酮诱导的吗啡依赖小鼠的戒断跳跃行为。

Acutely administered clozapine does not modify naloxone-induced withdrawal jumping in morphine-dependent mice.

作者信息

Ballard T M, McAllister K H

机构信息

Novartis Pharma Inc., Basel, Switzerland.

出版信息

Pharmacol Biochem Behav. 1999 Feb;62(2):285-90. doi: 10.1016/s0091-3057(98)00141-5.

Abstract

A direct comparison of the effects of clozapine and haloperidol upon naloxone-induced withdrawal jumping was investigated in morphine-dependent mice, as this syndrome may provide a behavioral baseline to differentiate between the two neuroleptics. Neither clozapine ((0.03-3.0 mg/kg s.c., n=9-10) nor haloperidol (0.01-04).1 mg/kg s.c., n=9-10) affected withdrawal jumping precipitated by 0.1 or 15.0 mg/kg i.p. naloxone in morphine-dependent mice. Measurement of locomotor activity immediately prior to naloxone administration revealed a dose-dependent reduction in activity by both compounds, indicating pharmacological effects at the time of naloxone-induced withdrawal. Clonidine (0.02-0.5 mg/kg s.c., n=9-10) also had no affect upon withdrawal jumping, although reductions in locomotor activity prior to naloxone administration were detected. There is no difference in the effects of acutely administered clozapine and haloperidol upon naloxone-precipitated withdrawal jumping in morphine-dependent mice.

摘要

在吗啡依赖的小鼠中研究了氯氮平和氟哌啶醇对纳洛酮诱发的戒断跳跃效应的直接比较,因为这种综合征可能为区分这两种抗精神病药物提供行为基线。氯氮平(0.03 - 3.0毫克/千克皮下注射,n = 9 - 10)和氟哌啶醇(0.01 - 0.4毫克/千克皮下注射,n = 9 - 10)均未影响吗啡依赖小鼠腹腔注射0.1或15.0毫克/千克纳洛酮诱发的戒断跳跃。在给予纳洛酮之前立即测量运动活性发现,两种化合物均使活性呈剂量依赖性降低,表明在纳洛酮诱发戒断时存在药理作用。可乐定(0.02 - 0.5毫克/千克皮下注射,n = 9 - 10)对戒断跳跃也没有影响,尽管在给予纳洛酮之前检测到运动活性降低。急性给予氯氮平和氟哌啶醇对吗啡依赖小鼠中纳洛酮诱发的戒断跳跃的影响没有差异。

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