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使用阿片类拮抗剂16-甲基环丙羟丙吗啡的体内研究。

In-vivo studies with the opioid antagonist, 16-methylcyprenorphine.

作者信息

Birch P J, Hayes A G, Sheehan M J, Tyers M B

机构信息

Department of Neuropharmacology, Glaxo Group Research Ltd., Ware, Herts, UK.

出版信息

J Pharm Pharmacol. 1988 Mar;40(3):213-4. doi: 10.1111/j.2042-7158.1988.tb05224.x.

Abstract

The effect of the opioid antagonist, 16-methylcyprenorphine (RX8008M), on the antinociceptive action of the mu-selective agonist, morphine, and the kappa-selective agonist, U50488H, has been investigated in the mouse abdominal constriction test. RX8008M produced a dose-dependent antagonism of the antinociceptive effect of morphine, but did not antagonize the response to U50488H. RX8008M should prove a useful probe for the in-vivo characterization of the receptor selectivity of opioid drugs.

摘要

在小鼠腹部收缩试验中,研究了阿片类拮抗剂16-甲基环丙诺啡(RX8008M)对μ选择性激动剂吗啡和κ选择性激动剂U50488H的抗伤害感受作用的影响。RX8008M对吗啡的抗伤害感受作用产生剂量依赖性拮抗,但不拮抗对U50488H的反应。RX8008M应可成为用于阿片类药物受体选择性体内表征的有用探针。

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