Faculty of Military Health Sciences, University of Defense, Trebesska 1575, Hradec Kralove CZ-50001, Czech Republic.
Mini Rev Med Chem. 2021;21(6):660-669. doi: 10.2174/1389557520666201117111715.
The cholinergic anti-inflammatory pathway is a part of the parasympathetic nervous system and it can also be entitled as an anti-inflammatory reflex. It consists of terminations of the vagal nerve into blood, acetylcholine released from the terminations, macrophages and other cells having α7 nicotinic acetylcholine receptor (α7 nAChR), calcium ions crossing through the receptor and interacting with nuclear factors, and erythrocytes with acetylcholinesterase (AChE) terminating the neurotransmission. Stopping of inflammatory cytokines production is the major task for the cholinergic antiinflammatory pathway. The cholinergic anti-inflammatory pathway can be stimulated or suppressed by agonizing or antagonizing α7 nAChR or by inhibition of AChE. This review is focused on cholinergic anti-inflammatory pathway regulation by drugs. Compounds that inhibit cholinesterases (for instance, huperzine, rivastigmine, galantamine), and their impact on the cholinergic anti-inflammatory pathway are discussed here and a survey of actual literature is provided.
胆碱能抗炎途径是副交感神经系统的一部分,也可以称为抗炎反射。它由迷走神经末梢进入血液、从末梢释放的乙酰胆碱、具有α7 烟碱型乙酰胆碱受体 (α7 nAChR) 的巨噬细胞和其他细胞、钙离子穿过受体并与核因子相互作用以及具有乙酰胆碱酯酶 (AChE) 的红细胞终止神经传递组成。抑制炎症细胞因子的产生是胆碱能抗炎途径的主要任务。通过激动或拮抗α7 nAChR 或抑制 AChE 可以刺激或抑制胆碱能抗炎途径。这篇综述主要关注药物对胆碱能抗炎途径的调节。本文讨论了抑制胆碱酯酶的化合物(例如,石杉碱甲、利斯的明、加兰他敏)及其对胆碱能抗炎途径的影响,并提供了对现有文献的调查。