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麻醉性镇痛药与苯二氮䓬衍生物对小鼠行为的相互作用。

Interactions between narcotic analgesics and benzodiazepine derivatives on behavior in the mouse.

作者信息

Shannon H E, Holtzman S G, Davis D C

出版信息

J Pharmacol Exp Ther. 1976 Nov;199(2):389-99.

PMID:10428
Abstract

Interactions between the benzodiazepine derivatives, diazepam and oxazepam, and the narcotic analgesics, morphine and methadone, were evaluated on locomotor activity and in the tail-flick and hot-plate tests for analgesia in the mouse. The dose-related stimulation of locomotor activity by morphine was reduced by diazepam and oxazepam at doses which alone had no effect on locomotor activity. However, only oxazepam reduced the dose-related stimulation of locomotor activity by methadone. The observed decreases produced by diazepam and oxazepam were comparable in magnitude to those produced by naloxone. Stimulation of locomotor activity by d-amphetamine was not affected by either diazepam or oxazepam. Dose-response curves for locomotor activity were also determined with morphine and methadone administered intraventricularly. As before, diazepam and naloxone given i.p. decreased the stimulation of locomotor activity produced by morphine, but only naloxone affected methadone-stimulated locomotor activity. Neither diazepam, oxazepam nor naloxone reduced the brain or plasma levels of 3H-morphine or 3H-methadone. In contrast to the results on locomotor activity, neither of these benzodiazepines significantly modified the dose-response curves of morphine or methadone in either test for analgesia. The mechanisms involved in the observed interactions on locomotor activity may be related to the influences of benzodiazepines and narcotic analgesics on motor efferent pathways summating in such a manner as to interfere with the ability of the mice to locomote. The present results demonstrate that prominent interactions occur between members of the benzodiazepine and narcotic analgesic classes; these interactions are dependent upon both the specific combination of drugs administered and upon the test procedure.

摘要

研究了苯二氮䓬衍生物地西泮和奥沙西泮与麻醉性镇痛药吗啡和美沙酮之间的相互作用,观察指标包括小鼠的自发活动,以及甩尾试验和热板试验中的镇痛效果。吗啡对自发活动的剂量相关性刺激作用,在单独使用时对地西泮和奥沙西泮的自发活动无影响的剂量下,被地西泮和奥沙西泮减弱。然而,只有奥沙西泮减弱了美沙酮对自发活动的剂量相关性刺激作用。地西泮和奥沙西泮所观察到的自发活动减少程度与纳洛酮所产生的减少程度相当。右旋苯丙胺对自发活动的刺激作用不受地西泮或奥沙西泮的影响。还测定了脑室内注射吗啡和美沙酮后的自发活动剂量-反应曲线。如前所述,腹腔注射地西泮和纳洛酮可减弱吗啡所产生的自发活动刺激作用,但只有纳洛酮影响美沙酮刺激的自发活动。地西泮、奥沙西泮和纳洛酮均未降低脑内或血浆中3H-吗啡或3H-美沙酮的水平。与自发活动的结果相反,这两种苯二氮䓬类药物在任何一种镇痛试验中均未显著改变吗啡或美沙酮的剂量-反应曲线。所观察到的自发活动相互作用的机制可能与苯二氮䓬类药物和麻醉性镇痛药对运动传出通路的影响有关,这些影响以一种干扰小鼠运动能力的方式叠加。目前的结果表明,苯二氮䓬类药物和麻醉性镇痛药之间存在显著的相互作用;这些相互作用取决于所给药药物的具体组合以及试验程序。

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