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μ和κ阿片类药物对鸽子心率降低作用的药理学分析

Pharmacological analysis of the rate-decreasing effects of mu and kappa opioids in pigeons.

作者信息

Mattox A J, Picker M J, Dykstra L A

机构信息

Department of Psychology, University of North Carolina at Chapel Hill 27599-3270.

出版信息

Psychopharmacology (Berl). 1994 Jan;113(3-4):457-62. doi: 10.1007/BF02245223.

Abstract

The present study investigated the rate-decreasing effects of several mu (morphine and l-methadone) and kappa (bremazocine, U69,593 and U50,488) opioid agonists in pigeons. Mu and kappa agonists were examined alone, in combination with naltrexone or the mu-selective opioid antagonist, beta-funaltrexamine (beta-FNA), and in pigeons treated chronically with U50,488. Naltrexone was equipotent in shifting the morphine, l-methadone and bremazocine dose-effect curves to the right, but was less potent in shifting the U69,593 dose-effect curve and did not shift the U50,488 dose-effect curve. Beta-FNA shifted the l-methadone dose-effect curve to the right but did not shift the bremazocine, U69,593 or U50,488 dose-effect curves. Pigeons that developed tolerance to U50,488 following daily administration were cross-tolerant to bremazocine but not to l-methadone. Taken together, these experiments indicate that the rate-decreasing effects of morphine and l-methadone are mediated by mu opioid receptors, whereas the rate-decreasing effects of bremazocine, U69,593 and U50,488 in pigeons differ depending on the pharmacological procedures used to assess their effects.

摘要

本研究调查了几种μ(吗啡和左旋美沙酮)和κ(布瑞马唑辛、U69,593和U50,488)阿片类激动剂对鸽子的减率作用。单独检测μ和κ激动剂,检测其与纳曲酮或μ选择性阿片拮抗剂β-氟纳曲胺(β-FNA)联合使用时的情况,以及在长期接受U50,488治疗的鸽子中的情况。纳曲酮在将吗啡、左旋美沙酮和布瑞马唑辛的剂量-效应曲线右移方面效力相当,但在将U69,593剂量-效应曲线右移方面效力较弱,且未使U50,488剂量-效应曲线右移。β-FNA使左旋美沙酮剂量-效应曲线右移,但未使布瑞马唑辛、U69,593或U50,488剂量-效应曲线右移。每日给药后对U50,488产生耐受性的鸽子对布瑞马唑辛有交叉耐受性,但对左旋美沙酮没有。综上所述,这些实验表明,吗啡和左旋美沙酮的减率作用由μ阿片受体介导,而布瑞马唑辛、U69,593和U50,488对鸽子的减率作用则因用于评估其作用的药理学方法而异。

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