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

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Simar Singh, Kaylin J Ellioff, Michael R Bruchas, Benjamin B Land, Nephi Stella
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引用次数: 0

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 α/β-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 GRABeCB2.0 may be leveraged to enable the discovery of targets modulated by cannabinoids at a circuit-specific level. SIGNIFICANCE STATEMENT: Cannabis 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.

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疗法。
以内源性大麻素(eCB)信号系统为靶点缓解疼痛是一种重要的治疗方法,目前才刚刚开始从机理上对其进行探索。在这篇综述中,我们将重点讨论最近受到关注的两种基于大麻素的靶向策略,即使用大麻二酚 (CBD) 和含 a/b-hydrolase domain containing 6 (ABHD6) 抑制剂进行治疗,这两种药物具有令人兴奋的潜力,可通过不同的作用机制 (MOA) 缓解疼痛,且不会引起中毒。我们回顾了植物源大麻素治疗疼痛的证据,重点是 CBD 及其在疼痛通路中表达的多个分子靶点。我们还讨论了 eCB 信号在调节疼痛反应中的功能,以及针对 ABHD6(一种 2-arachidonoylglycerol (2-AG) 的水解酶)的抑制剂的治疗前景。最后,我们将讨论如何利用新型大麻素生物传感器 GRABeCB2.0,在特定回路水平上发现受大麻素调节的靶点。意义声明 大麻作为一种有效的药物已被人类使用了数千年,包括用于止痛。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 酶抑制剂是通过独特、无毒的作用机制调节疼痛通路中的内源性大麻素信号转导,从而达到止痛目的的有前途的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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