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NMDA受体拮抗剂MK-801对吗啡耐受性和依赖性的抑制作用。

Inhibition of morphine tolerance and dependence by the NMDA receptor antagonist MK-801.

作者信息

Trujillo K A, Akil H

机构信息

Mental Health Research Institute, University of Michigan, Ann Arbor 48109-0720.

出版信息

Science. 1991 Jan 4;251(4989):85-7. doi: 10.1126/science.1824728.

Abstract

The N-methyl-D-aspartate (NMDA) subtype of the glutamate receptor is an important mediator of several forms of neural and behavioral plasticity. The present studies examined whether NMDA receptors might be involved in the development of opiate tolerance and dependence, two examples of behavioral plasticity. The noncompetitive NMDA receptor antagonist MK-801 attenuated the development of tolerance to the analgesic effect of morphine without affecting acute morphine analgesia. In addition, MK-801 attenuated the development of morphine dependence as assessed by naloxone-precipitated withdrawal. These results suggest that NMDA receptors may be important in the development of opiate tolerance and dependence.

摘要

谷氨酸受体的N-甲基-D-天冬氨酸(NMDA)亚型是多种神经和行为可塑性形式的重要介导物。本研究探讨了NMDA受体是否可能参与阿片类药物耐受性和依赖性的形成,这是行为可塑性的两个例子。非竞争性NMDA受体拮抗剂MK-801可减弱对吗啡镇痛作用的耐受性形成,而不影响吗啡的急性镇痛效果。此外,MK-801可减弱由纳洛酮诱发的戒断反应所评估的吗啡依赖性形成。这些结果表明,NMDA受体可能在阿片类药物耐受性和依赖性的形成中起重要作用。

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