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腺苷受体激动剂和拮抗剂对小鼠吗啡镇痛作用的不同影响。

Different influences of adenosine receptor agonists and antagonists on morphine antinociception in mice.

作者信息

Zarrindast M R, Nikfar S

机构信息

Department of Pharmacology, School of Medicine, University of Tehran, Iran.

出版信息

Gen Pharmacol. 1994 Jan;25(1):139-42. doi: 10.1016/0306-3623(94)90023-x.

Abstract
  1. Subcutaneous (s.c.) administration of morphine to mice induced a dose-dependent antinociception. 2. Pretreatment of animals with adenosine receptor antagonists NECA (5'-N-ethylcarboxamide-adenosine) and L-PIA (N6-phenylisopropyladenosine) potentiated, while adenosine agonist CHA (N6-cyclohexyladenosine) decreased the morphine response. 3. Adenosine antagonist theophylline decreased, but adenosine receptor antagonist 8-PT (8-phenyltheophylline) increased the antinociception effect of morphine. Inhibitory effect of CHA on morphine antinociception was also reversed by 8-PT pretreatment. 4. NECA or L-PIA induced a high degree of antinociceptive effect in animals pretreated with 8-PT. 5. Dipyridamole pretreatment did not alter the effect of morphine. 6. It is concluded that A-1 and/or A-2 adenosine receptors are involved in morphine antinociception and the adenosine mechanism(s) may exert a modulatory role in this respect.
摘要
  1. 给小鼠皮下注射吗啡可诱导剂量依赖性的镇痛作用。2. 用腺苷受体拮抗剂NECA(5'-N-乙基羧酰胺-腺苷)和L-PIA(N6-苯基异丙基腺苷)预处理动物可增强吗啡反应,而腺苷激动剂CHA(N6-环己基腺苷)则降低吗啡反应。3. 腺苷拮抗剂茶碱可降低吗啡的镇痛作用,但腺苷受体拮抗剂8-PT(8-苯基茶碱)可增强吗啡的镇痛作用。8-PT预处理也可逆转CHA对吗啡镇痛作用的抑制效应。4. NECA或L-PIA在用8-PT预处理的动物中诱导出高度的镇痛作用。5. 双嘧达莫预处理不改变吗啡的作用。6. 得出结论:A-1和/或A-2腺苷受体参与吗啡的镇痛作用,腺苷机制在这方面可能发挥调节作用。

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