腺苷类似物与吗啡在镇痛试验中的相互作用。

D Malec, E Michalska
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引用次数: 0

摘要

研究了选择性腺苷受体激动剂对小鼠和大鼠痛觉反应及吗啡镇痛的影响。所有使用的化合物:苯异丙基腺苷(R-PIA),腺苷乙基羧酰胺(NECA),环己基腺苷(CHA)和2-氯腺苷(2-CADO)在热板(56℃)和尾浸(52℃)试验中对小鼠和大鼠表现出抗伤感受作用。R-PIA、CHA和NECA能增强吗啡在小鼠中的抗伤害感受作用,R-PIA和NECA在大鼠中的抗伤害感受作用。2-CADO对吗啡的作用无明显影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interaction of adenosine analogs with morphine in analgesic tests.

The effect of selective adenosine receptor agonists on nociceptive responses of mice and rats and on morphine analgesia was investigated. All compounds used: phenylisopropyladenosine (R-PIA), adenosine ethylcarboxamide (NECA), cyclohexyladenosine (CHA) and 2-chloroadenosine (2-CADO) exhibited antinociceptive action in mice and rats in the hot-plate (56 degrees C) and tail-immersion (52 degrees C) tests. R-PIA, CHA and NECA potentiated the antinociceptive action of morphine in mice, and R-PIA and NECA--in rats. 2-CADO did not affect the morphine action in the tests.

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