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布托啡诺与单胺氧化酶抑制剂反苯环丙胺的相互作用。

Interaction of butorphanol, with monoamine oxidase inhibitor, tranylcypromine.

作者信息

Gomaa A A, Mohammed L H, Ahmed H N, Farghaly A M

机构信息

Department of Pharmacology, Faculty of Medicine, Assiut University, Egypt.

出版信息

Forensic Sci Int. 1991 Mar;49(2):185-92. doi: 10.1016/0379-0738(91)90078-w.

Abstract

This investigation examines the possibility of interaction between tranylcypromine and butorphanol in comparison to pethidine. The LD50 of pethidine and butorphanol were determined in mice pretreated with the non-selective monoamine oxidase (MAO) inhibitor, tranylcypromine orally for 8 days or with oral saline solution. Tranylcypromine decreased the LD50 of both pethidine and butorphanol by 78% and 41%, respectively. Anesthetized rabbits with halothane pretreated with tranylcypromine or saline were given pethidine (5 mg/kg i.v.) or butorphanol (0.5, 1 and 2 mg/kg i.v.). Pethidine produced a marked increase in blood pressure in rabbits pretreated with tranylcypromine and did not affect significantly the heart rate. Butorphanol did not affect either blood pressure or heart rate at doses of 0.5 or 1 mg/kg. However, the largest dose of butorphanol (2 mg/kg) produced hypotension and tachycardia in rabbits pretreated with tranylcypromine. Neither pethidine nor butorphanol affected the temperature of anesthetized rabbits pretreated with tranylcypromine or saline.

摘要

本研究考察了反苯环丙胺与布托啡诺之间相互作用的可能性,并与哌替啶进行比较。在经非选择性单胺氧化酶(MAO)抑制剂反苯环丙胺口服预处理8天的小鼠或经口服生理盐水溶液预处理的小鼠中,测定了哌替啶和布托啡诺的半数致死量(LD50)。反苯环丙胺分别使哌替啶和布托啡诺的LD50降低了78%和41%。用氟烷麻醉并经反苯环丙胺或生理盐水预处理的家兔,静脉注射哌替啶(5mg/kg)或布托啡诺(0.5、1和2mg/kg)。哌替啶使经反苯环丙胺预处理的家兔血压显著升高,对心率无明显影响。布托啡诺剂量为0.5或1mg/kg时,对血压和心率均无影响。然而,最大剂量的布托啡诺(2mg/kg)使经反苯环丙胺预处理的家兔出现低血压和心动过速。哌替啶和布托啡诺对经反苯环丙胺或生理盐水预处理的麻醉家兔的体温均无影响。

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