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μ-阿片受体对于[D-青霉胺2,D-青霉胺5]脑啡肽诱导的镇痛作用是必需的。

The mu-opioid receptor is necessary for [D-Pen2,D-Pen5]enkephalin-induced analgesia.

作者信息

Sora I, Funada M, Uhl G R

机构信息

Molecular Neurobiology Branch, National Institute on Drug Abuse-IRP, Baltimore, MD 21224, USA.

出版信息

Eur J Pharmacol. 1997 Apr 18;324(2-3):R1-2. doi: 10.1016/s0014-2999(97)10016-4.

Abstract

Interactions between delta-opioid receptors and morphine-preferring mu-opioid receptor subtypes have been suggested. Availability of transgenic mu-opioid receptor knockout mice allows assessment of mu-opioid receptor roles in the analgesia produced by the classical delta-opioid receptor agonist [D-Pen2,D-Pen5]enkephalin (DPDPE) in hot-plate and tail-flick tests. DPDPE analgesia was dramatically reduced in mu-opioid receptor knockout mice in a gene-dose-dependent fashion. The analgesia induced by this classic delta-opioid receptor agonist depends on intact mu-opioid receptors, suggesting that selective delta-opioid receptor drugs may require mu-opioid receptor occupancies for full efficacy.

摘要

已有人提出δ-阿片受体与偏好吗啡的μ-阿片受体亚型之间存在相互作用。转基因μ-阿片受体基因敲除小鼠的可得性,使得在热板和甩尾试验中,能够评估μ-阿片受体在经典δ-阿片受体激动剂[D-青霉胺2,D-青霉胺5]脑啡肽(DPDPE)产生的镇痛作用中的作用。在μ-阿片受体基因敲除小鼠中,DPDPE的镇痛作用以基因剂量依赖的方式显著降低。这种经典δ-阿片受体激动剂诱导的镇痛作用依赖于完整的μ-阿片受体,这表明选择性δ-阿片受体药物可能需要占据μ-阿片受体才能发挥完全疗效。

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