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μ和κ阿片受体激动剂对大鼠血浆皮质酮水平的影响。

Effect of mu and kappa opioid receptor agonists on rat plasma corticosterone levels.

作者信息

Hayes A G, Stewart B R

出版信息

Eur J Pharmacol. 1985 Oct 8;116(1-2):75-9. doi: 10.1016/0014-2999(85)90186-4.

Abstract

The effect of several mu and kappa opioid receptor agonists on rat plasma corticosterone levels, measured using radioimmunoassay, was investigated. The mu agonists, morphine and fentanyl, and the kappa agonists, U-50,488, tifluadom and bremazocine, all produced dose-related increases in rat plasma corticosterone levels. The effects of both fentanyl and U-50,488 were reversed by naloxone, indicating an action at opioid receptors. Pretreatment of the rats with the irreversible, mu-selective antagonist, beta-funaltrexamine, reduced the effect of fentanyl, but not that of U-50,488, indicating that both mu and kappa opioid receptors are involved in mediating this effect.

摘要

研究了几种μ和κ阿片受体激动剂对大鼠血浆皮质酮水平的影响,采用放射免疫分析法进行测定。μ激动剂吗啡和芬太尼,以及κ激动剂U-50,488、替氟朵和布瑞马佐辛,均使大鼠血浆皮质酮水平呈剂量相关升高。芬太尼和U-50,488的作用均被纳洛酮逆转,表明其作用于阿片受体。用不可逆的μ选择性拮抗剂β-氟纳曲胺对大鼠进行预处理,可降低芬太尼的作用,但不影响U-50,488的作用,表明μ和κ阿片受体均参与介导此效应。

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