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μ和κ阿片类药物对鸽子的辨别性刺激作用:μ和κ完全激动剂与部分激动剂作用的分析

Discriminative stimulus effects of mu and kappa opioids in the pigeon: analysis of the effects of full and partial mu and kappa agonists.

作者信息

Picker M J, Dykstra L A

机构信息

Department of Psychology, University of North Carolina, Chapel Hill.

出版信息

J Pharmacol Exp Ther. 1989 May;249(2):557-66.

PMID:2566680
Abstract

Pigeons were trained to discriminate a dose of either 0.01 mg/kg of bremazocine or 0.05 mg/kg of fentanyl from water using a two-key drug discrimination procedure. During tests of substitution, the selective kappa-opioid agonists bremazocine, U50, 488 and tifluadom substituted for the bremazocine stimulus, whereas the less selective kappa-opioid agonists ethylketocyclazocine, levallorphan, proxorphan and nalorphine substituted for the fentanyl stimulus. The full mu-opioid agonists fentanyl, morphine, I-methadone and levorphanol, as well as the partial agonists nalbuphine, butorphanol and buprenorphine, substituted for the fentanyl stimulus. Compounds with partial-opioid agonist effects, namely nalbuphine, butorphanol, buprenorphine, proxorphan, levallorphan and nalorphine, produced 50% fentanyl-appropriate responding at doses 25 to 369.2 times smaller than the doses required to decrease response rates to 50% of control values. In contrast, the full mu-opioid agonists fentanyl, morphine, I-methadone and levorphanol produced 50% fentanyl-appropriate responding at doses only 1.3 to 10.9 times smaller than those required to decrease response rates by 50%. During tests of antagonism, both naloxone and Mr2266 produced a dose-dependent attenuation of the stimulus effects of bremazocine and fentanyl, whereas beta-funaltrexamine antagonized the stimulus effects of fentanyl but not bremazocine. Although bremazocine has been reported to have mu-opioid antagonist effects, it failed to antagonize the stimulus effects of the training dose of fentanyl. The present investigation establishes further that pigeons can discriminate selective kappa-opioid agonists from mu-opioid agonists and that in pigeons the classification of numerous opioid compounds on the basis of their kappa-like or mu-like stimulus effects differ from those in rat and monkey. In addition, under the drug discrimination procedure the actions of compounds classified as partial-opioid agonists can be differentiated from those of full mu-opioid agonists on the basis of the ratio of the dose required to engender fentanyl-like stimulus effects to the dose required to reduce response rates.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

使用双键药物辨别程序训练鸽子从水中辨别出剂量为0.01mg/kg的布马佐辛或0.05mg/kg的芬太尼。在替代测试中,选择性κ-阿片受体激动剂布马佐辛、U50,488和替氟杜姆替代了布马佐辛刺激,而选择性较低的κ-阿片受体激动剂乙基酮环唑辛、左洛啡烷、丙氧芬和烯丙吗啡替代了芬太尼刺激。完全μ-阿片受体激动剂芬太尼、吗啡、1-美沙酮和左啡诺,以及部分激动剂纳布啡、布托啡诺和丁丙诺啡替代了芬太尼刺激。具有部分阿片受体激动作用的化合物,即纳布啡、布托啡诺、丁丙诺啡、丙氧芬、左洛啡烷和烯丙吗啡,产生50%芬太尼样反应的剂量比降低反应率至对照值50%所需剂量小25至369.2倍。相比之下,完全μ-阿片受体激动剂芬太尼、吗啡、1-美沙酮和左啡诺产生50%芬太尼样反应的剂量仅比降低反应率50%所需剂量小1.3至10.9倍。在拮抗测试中,纳洛酮和Mr2266均产生了剂量依赖性的布马佐辛和芬太尼刺激作用减弱,而β-氟奈曲明拮抗了芬太尼的刺激作用,但不拮抗布马佐辛的刺激作用。尽管据报道布马佐辛具有μ-阿片受体拮抗作用,但它未能拮抗训练剂量芬太尼的刺激作用。本研究进一步证实,鸽子可以区分选择性κ-阿片受体激动剂和μ-阿片受体激动剂,并且在鸽子中,许多阿片类化合物根据其κ样或μ样刺激作用的分类与大鼠和猴子中的不同。此外,在药物辨别程序下,根据产生芬太尼样刺激作用所需剂量与降低反应率所需剂量的比值,可以区分分类为部分阿片受体激动剂的化合物和完全μ-阿片受体激动剂的作用。(摘要截至于250字)

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