Selective modulation of the cannabinoid type 1 (CB1) receptor as an emerging platform for the treatment of neuropathic pain.

IF 3.597 Q2 Pharmacology, Toxicology and Pharmaceutics
MedChemComm Pub Date : 2019-03-18 eCollection Date: 2019-05-01 DOI:10.1039/c8md00595h
Samuel D Banister, Kaavya Krishna Kumar, Vineet Kumar, Brian K Kobilka, Sanjay V Malhotra
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引用次数: 0

Abstract

Neuropathic pain is caused by a lesion or dysfunction in the nervous system, and it may arise from illness, be drug-induced or caused by toxin exposure. Since the discovery of two G-protein-coupled cannabinoid receptors (CB1 and CB2) nearly three decades ago, there has been a rapid expansion in our understanding of cannabinoid pharmacology. This is currently one of the most active fields of neuropharmacology, and interest has emerged in developing cannabinoids and other small molecule modulators of CB1 and CB2 as therapeutics for neuropathic pain. This short review article provides an overview of the chemotypes currently under investigation for the development of novel neuropathic pain treatments targeting CB1 receptors.

Abstract Image

Abstract Image

选择性调节 1 型大麻素 (CB1) 受体作为治疗神经性疼痛的新兴平台。
神经病理性疼痛是由神经系统的病变或功能障碍引起的,它可能源于疾病、药物诱发或毒素暴露。自近三十年前发现两种 G 蛋白偶联大麻素受体(CB1 和 CB2)以来,我们对大麻素药理学的了解迅速加深。这是目前神经药理学最活跃的领域之一,人们开始关注开发大麻素和其他 CB1 和 CB2 小分子调节剂作为神经病理性疼痛的治疗药物。这篇简短的综述文章概述了目前正在研究的以 CB1 受体为靶点开发新型神经病理性疼痛治疗药物的化学类型。
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
MedChemComm
MedChemComm BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
2.2 months
期刊介绍: Research and review articles in medicinal chemistry and related drug discovery science; the official journal of the European Federation for Medicinal Chemistry. In 2020, MedChemComm will change its name to RSC Medicinal Chemistry. Issue 12, 2019 will be the last issue as MedChemComm.
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