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非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂地佐环平(MK801)真的能阻断与重复给药相关的行为敏化吗?

Does the noncompetitive NMDA receptor antagonist dizocilpine (MK801) really block behavioural sensitization associated with repeated drug administration?

作者信息

Tzschentke T M, Schmidt W J

机构信息

Department of Neuropharmacology, Zoological Institute, University of Tübingen, Germany.

出版信息

Trends Pharmacol Sci. 1998 Nov;19(11):447-51. doi: 10.1016/s0165-6147(98)01255-3.

Abstract

The term 'behavioural sensitization' refers to the progressively augmented behavioural response that is produced by many drugs of abuse upon their repeated administration. From most of the available data, it has been concluded that co-administration of an N-methyl-D-aspartate (NMDA) receptor antagonist [such as dizocilpine (MK801)] together with the sensitizing drug can block the development of behavioural sensitization. However, the picture might not be that simple. Recent experimental evidence suggests that instead of blocking sensitization, co-administration of dizocilpine enhances the effect of the the sensitizing drug or has more complex effects on the development of sensitization. In this article, Thomas Tzschentke and Werner Schmidt present these two different views and emphasize that the conclusions that can be drawn from sensitization experiments about the effects of dizocilpine and related drugs on behavioural plasticity crucially depend on how, when and under what conditions a test for sensitization is conducted.

摘要

术语“行为敏化”指的是许多滥用药物在反复给药后产生的逐渐增强的行为反应。从大多数现有数据来看,已得出结论:将N-甲基-D-天冬氨酸(NMDA)受体拮抗剂[如地佐环平(MK801)]与敏化药物共同给药可阻断行为敏化的发展。然而,情况可能并非那么简单。最近的实验证据表明,地佐环平共同给药非但不会阻断敏化,反而会增强敏化药物的作用,或者对敏化的发展产生更复杂的影响。在本文中,托马斯·茨申特克和维尔纳·施密特提出了这两种不同观点,并强调从敏化实验中得出的关于地佐环平及相关药物对行为可塑性影响的结论,关键取决于敏化测试的进行方式、时间和条件。

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