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κ-阿片受体拮抗剂nor-BNI可抑制可卡因和苯丙胺,但不能抑制大麻素(WIN 52212-2)诱导的涡虫戒断反应:一个“药理一致性”的实例。

The kappa-opioid receptor antagonist nor-BNI inhibits cocaine and amphetamine, but not cannabinoid (WIN 52212-2), abstinence-induced withdrawal in planarians: an instance of 'pharmacologic congruence'.

作者信息

Raffa Robert B, Stagliano Gregory W, Ross Geoffrey, Powell Jenay A, Phillips Austin G, Ding Zhe, Rawls Scott M

机构信息

Department of Pharmaceutical Sciences, Temple University School of Pharmacy, 3307 N. Broad Street, Philadelphia, PA 19140, USA.

出版信息

Brain Res. 2008 Feb 8;1193:51-6. doi: 10.1016/j.brainres.2007.12.001. Epub 2007 Dec 8.

DOI:10.1016/j.brainres.2007.12.001
PMID:18178175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2695878/
Abstract

The broad applicability of receptor theory to diverse species, from invertebrates to mammals, provides evidence for the evolution in complexity of pharmacologic receptor diversification and of receptor-effector signal transduction mechanisms. However, pre-mammalian species have less receptor subtype differentiation, and thus, might share signal transduction pathways to a greater extent than do mammals, a phenomenon that we term 'pharmacologic congruence'. We have demonstrated previously that the lowest species considered to have a centralized nervous system, planarians, display both abstinence-induced and antagonist-precipitated withdrawal signs, indicative of the development of physical dependence. We report here: (1) amphetamine abstinence-induced withdrawal, and (2) the attenuation of cocaine and amphetamine, but not cannabinoid agonist (WIN 52212-2), abstinence-induced withdrawal by the opioid receptor antagonist naloxone and by the selective kappa-opioid receptor subtype antagonist nor-BNI (nor-Binaltorphimine), but not by the selective mu-opioid or the delta-opioid receptor subtype antagonists CTAP (D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH(2)) and naltrindole. These results provide evidence that the withdrawal from cocaine and amphetamine, but not cannabinoids, in planarians is mediated through a common nor-BNI-sensitive (kappa-opioid receptor-like) pathway.

摘要

受体理论在从无脊椎动物到哺乳动物等多种物种中的广泛适用性,为药理受体多样化以及受体 - 效应器信号转导机制的复杂性进化提供了证据。然而,哺乳动物之前的物种具有较少的受体亚型分化,因此,与哺乳动物相比,它们可能在更大程度上共享信号转导途径,我们将这种现象称为“药理一致性”。我们之前已经证明,被认为具有集中神经系统的最低等物种涡虫,会表现出禁欲诱导和拮抗剂诱发的戒断症状,这表明身体依赖性的发展。我们在此报告:(1)安非他命禁欲诱导的戒断,以及(2)阿片受体拮抗剂纳洛酮和选择性κ - 阿片受体亚型拮抗剂nor - BNI(诺 - 宾那托啡)可减轻可卡因和安非他命(而非大麻素激动剂WIN 52212 - 2)禁欲诱导的戒断,但选择性μ - 阿片或δ - 阿片受体亚型拮抗剂CTAP(D - Phe - Cys - Tyr - D - Trp - Arg - Thr - Pen - Thr - NH₂)和纳曲吲哚则不能。这些结果提供了证据,表明涡虫中可卡因和安非他命(而非大麻素)的戒断是通过一条共同的对nor - BNI敏感(类κ - 阿片受体)途径介导的。

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