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大麻素受体配体与烟碱型乙酰胆碱受体相互作用的细胞研究方法

Cellular approaches to the interaction between cannabinoid receptor ligands and nicotinic acetylcholine receptors.

作者信息

Oz Murat, Al Kury Lina, Keun-Hang Susan Yang, Mahgoub Mohamed, Galadari Sehamuddin

机构信息

Functional Lipidomics Branch, Department of Pharmacology, Faculty of Medicine and Health Sciences, UAE University, P.O. Box 17666, Al Ain, Abu Dhabi, UAE.

Functional Lipidomics Branch, Department of Pharmacology, Faculty of Medicine and Health Sciences, UAE University, P.O. Box 17666, Al Ain, Abu Dhabi, UAE.

出版信息

Eur J Pharmacol. 2014 May 15;731:100-5. doi: 10.1016/j.ejphar.2014.03.010. Epub 2014 Mar 16.

Abstract

Cannabinoids are among the earliest known drugs to humanity. Cannabis plant contains various phytochemicals that bind to cannabinoid receptors. In addition, synthetic and endogenously produced cannabinoids (endocannabinoids) constitute other classes of cannabinoid receptor ligands. Although many pharmacological effects of these cannabinoids are mediated by the activation of cannabinoid receptors, recent studies indicate that cannabinoids also modulate the functions of various integral membrane proteins including ion channels, receptors, neurotransmitter transporters, and enzymes by mechanism(s) not involving the activation of known cannabinoid receptors. Currently, the mechanisms of these effects were not fully understood. However, it is likely that direct actions of cannabinoids are closely linked to their lipophilic structures. This report will focus on the actions of cannabinoids on nicotinic acetylcholine receptors and will examine the results of recent studies in this field. In addition some mechanistic approaches will be provided. The results discussed in this review indicate that, besides cannabinoid receptors, further molecular targets for cannabinoids exist and that these targets may represent important novel sites to alter neuronal excitability.

摘要

大麻素是人类已知最早的药物之一。大麻植物含有多种可与大麻素受体结合的植物化学物质。此外,合成的和内源性产生的大麻素(内源性大麻素)构成了其他类别的大麻素受体配体。尽管这些大麻素的许多药理作用是通过大麻素受体的激活介导的,但最近的研究表明,大麻素还通过不涉及已知大麻素受体激活的机制来调节各种整合膜蛋白的功能,包括离子通道、受体、神经递质转运体和酶。目前,这些作用的机制尚未完全了解。然而,大麻素的直接作用可能与其亲脂性结构密切相关。本报告将重点关注大麻素对烟碱型乙酰胆碱受体的作用,并将审视该领域最近的研究结果。此外,还将提供一些作用机制方面的探讨。本综述中讨论的结果表明,除了大麻素受体外,大麻素还存在其他分子靶点,这些靶点可能代表改变神经元兴奋性的重要新位点。

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