Raffa Robert B, Stagliano Gregory W, Ross Geoffrey, Powell Jenay A, Phillips Austin G, Ding Zhe, Rawls Scott M
Department of Pharmaceutical Sciences, Temple University School of Pharmacy, 3307 N. Broad Street, Philadelphia, PA 19140, USA.
Brain Res. 2008 Feb 8;1193:51-6. doi: 10.1016/j.brainres.2007.12.001. Epub 2007 Dec 8.
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.
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。