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[长期给大鼠服用麻醉性镇痛药期间的戒断综合征与脂质过氧化作用]

[The withdrawal syndrome and lipid peroxidation during the chronic administration of narcotic analgesics to rats].

作者信息

Konstantinopol'skiĭ M A, Pirozhkov S V, Solov'eva A G, Panchenko L F, Barkov N K

出版信息

Eksp Klin Farmakol. 1992 Jan-Feb;55(1):21-4.

PMID:1363943
Abstract

Diverse behavioral disorders and the intensity of lipid peroxidation (LPO) of biological membranes were estimated in different rat tissues after the 7-day administration and subsequent withdrawal of morphine or promedol. 24 hours after the withdrawal of the analgetics the demonstrated a high initial level of motor activity in the open field. Naloxone, an antagonist of opiate receptors, potentiated motor activity and the intensity of withdrawal syndrome (by 160%) in rats with morphine rather than promedol dependence. The behavioral disorders in dependent animals were accompanied by LPO activation in liver and brain membranes.

摘要

在给予吗啡或异丙嗪7天并随后停药后,对不同大鼠组织中的多种行为障碍和生物膜脂质过氧化(LPO)强度进行了评估。镇痛药停药24小时后,在旷场试验中表现出较高的初始运动活动水平。阿片受体拮抗剂纳洛酮增强了吗啡依赖而非异丙嗪依赖大鼠的运动活动和戒断综合征强度(提高了160%)。依赖动物的行为障碍伴随着肝膜和脑膜中LPO的激活。

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