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下一代内源性大麻素信号调节剂的镇痛特性:利用现代工具开发新型治疗药物。

Analgesic Properties of Next-Generation Modulators of Endocannabinoid Signaling: Leveraging Modern Tools for the Development of Novel Therapeutics.

机构信息

Departments of Pharmacology (S.S., K.J.E., M.R.B., B.B.L., N.S.), Anesthesiology and Pain Medicine (M.R.B.), and Psychiatry and Behavioral Sciences (N.S.), and Center of Excellence in Neuroscience of Addiction, Pain, and Emotion (S.S., K.J.E., M.R.B., B.B.L., N.S.), University of Washington, Seattle, Washington.

Departments of Pharmacology (S.S., K.J.E., M.R.B., B.B.L., N.S.), Anesthesiology and Pain Medicine (M.R.B.), and Psychiatry and Behavioral Sciences (N.S.), and Center of Excellence in Neuroscience of Addiction, Pain, and Emotion (S.S., K.J.E., M.R.B., B.B.L., N.S.), University of Washington, Seattle, Washington

出版信息

J Pharmacol Exp Ther. 2024 Oct 18;391(2):162-173. doi: 10.1124/jpet.124.002119.

Abstract

Targeting the endocannabinoid (eCB) signaling system for pain relief is an important treatment option that is only now beginning to be mechanistically explored. In this review, we focus on two recently appreciated cannabinoid-based targeting strategies, treatments with cannabidiol (CBD) and /-hydrolase domain containing 6 (ABHD6) inhibitors, which have the exciting potential to produce pain relief through distinct mechanisms of action and without intoxication. We review evidence on plant-derived cannabinoids for pain, with an emphasis on CBD and its multiple molecular targets expressed in pain pathways. We also discuss the function of eCB signaling in regulating pain responses and the therapeutic promises of inhibitors targeting ABHD6, a 2-arachidonoylglycerol (2-AG)-hydrolyzing enzyme. Finally, we discuss how the novel cannabinoid biosensor GRAB may be leveraged to enable the discovery of targets modulated by cannabinoids at a circuit-specific level. SIGNIFICANCE STATEMENT: has been used by humans as an effective medicine for millennia, including for pain management. Recent evidence emphasizes the therapeutic potential of compounds that modulate endocannabinoid signaling. Specifically, cannabidiol and inhibitors of the enzyme ABHD6 represent promising strategies to achieve pain relief by modulating endocannabinoid signaling in pain pathways via distinct, nonintoxicating mechanisms of action.

摘要

针对内源性大麻素(eCB)信号系统的止痛治疗是一种重要的治疗选择,目前才刚刚开始从机制上进行探索。在这篇综述中,我们专注于两种最近被认可的基于大麻素的靶向策略,即使用大麻二酚(CBD)和/或水解酶域包含 6(ABHD6)抑制剂的治疗方法,它们具有通过不同的作用机制产生止痛效果而不产生中毒的令人兴奋的潜力。我们回顾了植物源性大麻素在疼痛中的应用证据,重点介绍了 CBD 及其在疼痛途径中表达的多种分子靶点。我们还讨论了 eCB 信号在调节疼痛反应中的作用,以及靶向 ABHD6 的抑制剂的治疗潜力,ABHD6 是一种 2-花生四烯酸甘油(2-AG)水解酶。最后,我们讨论了新型大麻素生物传感器 GRAB 如何被利用来实现对大麻素在特定回路水平上调节的目标的发现。

意义陈述

大麻素已被人类用作有效的药物数千年,包括用于治疗疼痛。最近的证据强调了调节内源性大麻素信号的化合物的治疗潜力。具体来说,大麻二酚和 ABHD6 酶抑制剂代表了通过不同的非成瘾作用机制调节疼痛途径中的内源性大麻素信号以实现止痛的有前途的策略。

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