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腺苷受体激动剂对吗啡镇痛作用的影响。

The effect of adenosine receptor agonists on analgesic effects of morphine.

作者信息

Malec D, Michalska E

机构信息

Department of Pharmacodynamics, Medical Academy, Lublin, Poland.

出版信息

Pol J Pharmacol Pharm. 1990 Jan-Feb;42(1):1-11.

PMID:2281016
Abstract

The effect of adenosine, S-phenylisopropyladenosine (S-PIA) and dipyridamole (an adenosine reuptake inhibitor) on the analgesic action of morphine in mice and rats was investigated in the hot-plate (56 degrees C) and tail immersion (52 degrees C) tests. Adenosine, 50 and 100 mg/kg, induced analgesia in mice and rats in the hot-plate test and potentiated the action of morphine (particularly in mice). The analgesic effects of adenosine were completely abolished by caffeine (10 mg/kg in mice and rats), and partially inhibited by naloxone (1 mg/kg, only in mice). S-PIA given alone (0.6 mg/kg) produced in mice some analgesic effect in the hot-plate test: the effect was abolished by caffeine and partially by naloxone. The effect of S-PIA on the action of morphine depends on the dose and the animal species. Dipyridamole alone did not affect the reactivity of animals in tests for analgesia, but potentiated the action of morphine.

摘要

在热板(56摄氏度)和尾部浸没法(52摄氏度)试验中,研究了腺苷、S-苯异丙基腺苷(S-PIA)和双嘧达莫(一种腺苷再摄取抑制剂)对小鼠和大鼠体内吗啡镇痛作用的影响。在热板试验中,50毫克/千克和100毫克/千克的腺苷可在小鼠和大鼠中诱导镇痛作用,并增强吗啡的作用(尤其是在小鼠中)。咖啡因(小鼠和大鼠均为10毫克/千克)可完全消除腺苷的镇痛作用,纳洛酮(1毫克/千克,仅在小鼠中)可部分抑制其作用。单独给予S-PIA(0.6毫克/千克)可在热板试验中使小鼠产生一定的镇痛作用:该作用可被咖啡因消除,部分可被纳洛酮消除。S-PIA对吗啡作用的影响取决于剂量和动物种类。单独使用双嘧达莫并不影响动物在镇痛试验中的反应性,但可增强吗啡的作用。

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