Montigné Edouard, Balayssac David
INSERM, U1107, NEURO-DOL, Université Clermont Auvergne, F-63000 Clermont-Ferrand, France.
INSERM, U1107, NEURO-DOL, Université Clermont Auvergne, Direction de la Recherche Clinique et de l'Innovation, CHU Clermont-Ferrand, F-63000 Clermont-Ferrand, France.
Pharmaceuticals (Basel). 2023 Sep 27;16(10):1363. doi: 10.3390/ph16101363.
Neuropathic pain affects about 7-8% of the population, and its management still poses challenges with unmet needs. Over the past decades, researchers have explored the cholinergic system (muscarinic and nicotinic acetylcholine receptors: mAChR and nAChR) and compounds targeting these receptors as potential analgesics for neuropathic pain management. This scoping review aims to provide an overview of studies on peripheral neuropathic pain (PNP) in rodent models, exploring compounds targeting cholinergic neurotransmission. The inclusion criteria were original articles on PNP in rodent models that explored the use of compounds directly targeting cholinergic neurotransmission and reported results of nociceptive behavioral assays. The literature search was performed in the PubMed and Web of Science databases (1 January 2000-22 April 2023). The selection process yielded 82 publications, encompassing 62 compounds. The most studied compounds were agonists of α4β2 nAChR and α7 nAChR, and antagonists of α9/α10 nAChR, along with those increasing acetylcholine and targeting mAChRs. Studies mainly reported antinociceptive effects in traumatic PNP models, and to a lesser extent, chemotherapy-induced neuropathy or diabetic models. These preclinical studies underscore the considerable potential of cholinergic compounds in the management of PNP, warranting the initiation of clinical trials.
神经性疼痛影响着约7%-8%的人口,其治疗仍然面临挑战,存在未满足的需求。在过去几十年里,研究人员探索了胆碱能系统(毒蕈碱型和烟碱型乙酰胆碱受体:M型乙酰胆碱受体和N型乙酰胆碱受体)以及靶向这些受体的化合物,将其作为治疗神经性疼痛的潜在镇痛药。本综述旨在概述啮齿动物模型中关于周围神经性疼痛(PNP)的研究,探索靶向胆碱能神经传递的化合物。纳入标准为关于啮齿动物模型中PNP的原始文章,这些文章探索了直接靶向胆碱能神经传递的化合物的使用,并报告了伤害性行为测定的结果。文献检索在PubMed和Web of Science数据库中进行(2000年1月1日至2023年4月22日)。筛选过程产生了82篇出版物,涵盖62种化合物。研究最多的化合物是α4β2 N型乙酰胆碱受体和α7 N型乙酰胆碱受体的激动剂,α9/α10 N型乙酰胆碱受体的拮抗剂,以及那些增加乙酰胆碱和靶向M型乙酰胆碱受体的化合物。研究主要报告了在创伤性PNP模型中的镇痛作用,在较小程度上,也报告了化疗引起的神经病变或糖尿病模型中的镇痛作用。这些临床前研究强调了胆碱能化合物在PNP治疗中的巨大潜力,值得开展临床试验。