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靶向α4β2-烟碱型乙酰胆碱受体的新型抗抑郁药的最新进展。

Recent developments in novel antidepressants targeting α4β2-nicotinic acetylcholine receptors.

作者信息

Yu Li-Fang, Zhang Han-Kun, Caldarone Barbara J, Eaton J Brek, Lukas Ronald J, Kozikowski Alan P

机构信息

Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago , 833 South Wood Street, Chicago, Illinois 60612, United States.

出版信息

J Med Chem. 2014 Oct 23;57(20):8204-23. doi: 10.1021/jm401937a. Epub 2014 Jul 2.

Abstract

Nicotinic acetylcholine receptors (nAChRs) have been investigated for developing drugs that can potentially treat various central nervous system disorders. Considerable evidence supports the hypothesis that modulation of the cholinergic system through activation and/or desensitization/inactivation of nAChR holds promise for the development of new antidepressants. The introductory portion of this Miniperspective discusses the basic pharmacology that underpins the involvement of α4β2-nAChRs in depression, along with the structural features that are essential to ligand recognition by the α4β2-nAChRs. The remainder of this Miniperspective analyzes reported nicotinic ligands in terms of drug design considerations and their potency and selectivity, with a particular focus on compounds exhibiting antidepressant-like effects in preclinical or clinical studies. This Miniperspective aims to provide an in-depth analysis of the potential for using nicotinic ligands in the treatment of depression, which may hold some promise in addressing an unmet clinical need by providing relief from depressive symptoms in refractory patients.

摘要

烟碱型乙酰胆碱受体(nAChRs)已被用于研发可能治疗各种中枢神经系统疾病的药物。大量证据支持这样的假说,即通过激活和/或使nAChR脱敏/失活来调节胆碱能系统有望开发出新的抗抑郁药。本微型综述的引言部分讨论了α4β2-nAChRs参与抑郁症的基础药理学,以及α4β2-nAChRs识别配体所必需的结构特征。本微型综述的其余部分从药物设计考虑因素及其效力和选择性方面分析了已报道的烟碱配体,特别关注在临床前或临床研究中表现出抗抑郁样作用的化合物。本微型综述旨在深入分析使用烟碱配体治疗抑郁症的潜力,这可能有望通过缓解难治性患者的抑郁症状来满足未满足的临床需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/019c/4207546/a8c50a2635bf/jm-2013-01937a_0001.jpg

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