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μ-阿片受体拮抗剂和δ-阿片受体拮抗剂对应激小鼠血浆皮质酮水平影响的差异。

Differences in the effects of mu- and delta-opioid receptor antagonists upon plasma corticosterone levels in stressed mice.

作者信息

Kitchen I, Rowan K M

出版信息

Eur J Pharmacol. 1984 May 18;101(1-2):153-6. doi: 10.1016/0014-2999(84)90042-6.

Abstract

The effects of intraperitoneal injections of two opioid antagonists on plasma corticosterone levels in stressed mice was investigated. The effects of the mu-opioid receptor antagonist naloxone was dependent on the dose used. Low doses (0.5 and 1 mg/kg) potentiated the elevation of plasma corticosterone observed in saline treated or ether stressed mice, whereas a higher dose (10 mg/kg) produced the opposite effect. The delta-opioid receptor antagonist ICI 154,129 had no significant effect on corticosterone levels. The findings suggest that mu- rather than delta-opioid receptors are important in modifying corticosterone responses to stress and raise the question as to specificity of naloxone at doses above 1 mg/kg.

摘要

研究了腹腔注射两种阿片类拮抗剂对应激小鼠血浆皮质酮水平的影响。μ-阿片受体拮抗剂纳洛酮的作用取决于所用剂量。低剂量(0.5和1毫克/千克)增强了在生理盐水处理或乙醚应激小鼠中观察到的血浆皮质酮升高,而高剂量(10毫克/千克)则产生相反的效果。δ-阿片受体拮抗剂ICI 154,129对皮质酮水平没有显著影响。这些发现表明,在调节皮质酮对应激的反应中,μ-阿片受体而非δ-阿片受体起重要作用,并提出了纳洛酮在剂量高于1毫克/千克时的特异性问题。

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