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[脑啡肽类似物EK-399对大鼠辨别刺激效应的评估]

[Evaluation of the discriminative stimulus effect of an enkephalin analog, EK-399, in the rat].

作者信息

Nishida N, Yasuhara Y, Chiba S

机构信息

Drug Safety Research Laboratories, Takeda Chemical Industries, Ltd., Osaka, Japan.

出版信息

Nihon Yakurigaku Zasshi. 1991 Jun;97(6):361-9. doi: 10.1254/fpj.97.6_361.

DOI:10.1254/fpj.97.6_361
PMID:1651892
Abstract

Four groups of rats were trained to discriminate between the no-drug conditions (saline, s.c.) and the effect of s.c. injection of the novel enkephalin analog Tyr-D-Met (O)-Gly-EtPhe-NHNHCOCH3.AcOH (EK-399, 1 mg/kg), morphine (3 mg/kg), ethylketocyclazocine (EKC, 0.3 mg/kg) or N-allylnormetazocine (NANM, 3 mg/kg) in a two-lever choice, water reinforced procedure. All groups of animals acquired the ability to discriminate EK-399, morphine, EKC or NANM from saline. Naloxone (0.03-0.3 mg/kg, s.c.) completely antagonized the discriminative stimulus effects of EK-399, morphine and EKC, but not that of NANM. In stimulus generalization tests, morphine (10 mg/kg) and buprenorphine (0.03 mg/kg), mu-opioid receptor agonists, completely substituted for EK-399 in groups trained with EK-399, whereas EK-399 (0.1-3 mg/kg) only partially substituted for morphine in rats trained with morphine. EKC (0.01-0.1 mg/kg), a kappa-opioid receptor agonist, partially substituted for EK-399, and EK-399 (0.1-3 mg/kg) partially substituted for EKC. NANM (0.3-10 mg/kg), a sigma-receptor agonist, partially substituted for EK-399, but EK-399 (0.1-3 mg/kg) did not substitute for NANM. These results suggest that the discriminative stimulus effect of EK-399 in rats mainly involves mu-opioid receptor-mediating action and also involves, to a lesser extent, other receptor (probably delta-opioid receptor)-mediating actions.

摘要

将四组大鼠训练至能在无药物状态(皮下注射生理盐水)与皮下注射新型脑啡肽类似物Tyr-D-Met(O)-Gly-EtPhe-NHNHCOCH3.AcOH(EK-399,1毫克/千克)、吗啡(3毫克/千克)、乙基酮环唑辛(EKC,0.3毫克/千克)或烯丙基去甲左啡诺(NANM,3毫克/千克)的效果之间进行辨别,采用双杠杆选择、水强化程序。所有动物组均获得了从盐水中辨别出EK-399、吗啡、EKC或NANM的能力。纳洛酮(0.03 - 0.3毫克/千克,皮下注射)完全拮抗了EK-399、吗啡和EKC的辨别性刺激效应,但对NANM无效。在刺激泛化试验中,吗啡(10毫克/千克)和丁丙诺啡(0.03毫克/千克),μ-阿片受体激动剂,在以EK-399训练的组中完全替代了EK-399,而EK-399(0.1 - 3毫克/千克)在以吗啡训练的大鼠中仅部分替代了吗啡。EKC(0.01 - 0.1毫克/千克),一种κ-阿片受体激动剂,部分替代了EK-399,且EK-399(0.1 - 3毫克/千克)部分替代了EKC。NANM(0.3 - 10毫克/千克),一种σ-受体激动剂,部分替代了EK-399,但EK-399(0.1 - 3毫克/千克)未替代NANM。这些结果表明,EK-399在大鼠中的辨别性刺激效应主要涉及μ-阿片受体介导的作用,在较小程度上还涉及其他受体(可能是δ-阿片受体)介导的作用。

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