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Kappa opiate receptors localized by autoradiography to deep layers of cerebral cortex: relation to sedative effects.

机译:放射自显影定位于大脑皮质深层的阿片受体阿片受体:与镇静作用有关。

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摘要

Kappa opiate drugs differ from other opiates in their unique sedative actions and lack of cross-tolerance. We have visualized kappa opiate receptors by in vitro autoradiography using the kappa drugs [3H]ethylketazocine ([3H]EKC) and [3H]bremazocine. Though these ligands also label mu and delta opiate receptors, their binding is rendered kappa specific by coincubation with morphine and [D-Ala2, D-Leu5]enkephalin (DADL-Enk) to displace mu and delta interactions, respectively. Labeling patterns with [3H]EKC and [3H]bremazocine are the same and differ markedly from localizations of mu and delta opiate receptors visualized with [3H]dihydromorphine and [3H]DADL-Enk, respectively. The highest density and most selective localization of putative kappa receptors occurs in layers V and VI of the cerebral cortex. In these layers cells are localized which project to the thalamus regulating sensory input to the cortex. Receptors in these layers could account for the unique sedative and possibly analgesic effects of kappa opiates.
机译:Kappa阿片类药物与其他阿片类药物的不同之处在于其独特的镇静作用和缺乏交叉耐受性。我们已经通过体外放射自显影术使用Kappa药物[3H]乙基酮唑嗪([3H] EKC)和[3H]溴唑嗪来可视化了阿片受体。尽管这些配体还标记了mu和delta鸦片受体,但它们的结合通过与吗啡和[D-Ala2,D-Leu5]脑啡肽(DADL-Enk)共温育分别取代了mu和delta相互作用而赋予了kappa特异性。用[3H] EKC和[3H]溴唑胺标记的模式是相同的,并且与分别用[3H] dihydromorphine和[3H] DADL-Enk显现的mu和阿片类鸦片受体的定位显着不同。假定的κ受体的最高密度和最有选择性的定位发生在大脑皮层的V和VI层。在这些层中,细胞定位于丘脑,调节对皮质的感觉输入。这些层中的受体可以解释κ鸦片鸦片的独特镇静作用和可能的镇痛作用。

著录项

  • 作者

    Goodman, R R; Snyder, S H;

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  • 年度 1982
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  • 原文格式 PDF
  • 正文语种 en
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