变构调节
烟碱激动剂
精神分裂症(面向对象编程)
烟碱乙酰胆碱受体
变构调节剂
部分激动剂
临床试验
药理学
神经科学
医学
受体
生物信息学
心理学
兴奋剂
精神科
生物
内科学
作者
Kirsten Antonio-Tolentino,Corey R. Hopkins
标识
DOI:10.1080/13543784.2020.1764938
摘要
Alpha 7 nicotinic acetylcholine receptor (α7 nAChR) partial agonists, agonists, and positive allosteric modulators (PAMs) have been in development for over a decade. The initial candidates were in clinical trials for a wide variety of diseases including schizophrenia, but there has yet to be a successful compound to make it to the market for any disorder. Although difficult to assess the cause of all the clinical failures, the lack of efficacy played a major role. The development of more selective compounds, may bring a successful compound to long-suffering schizophrenia patients.This article examines investigational agonists and positive allosteric modulators of the α7 nicotinic receptor in preclinical studies as well as clinical trials. Our search included the use of SciFinder, Google, and clinicaltrials.gov with search dates of 2015 to the present.Researchers must rethink their approach should look more closely at the selectivity of new compounds and how to tackle the translational gap. Perhaps new positive allosteric modulators that can help minimize receptor desensitization and selectivity profiles can be a path forward for α7 nAChRs in schizophrenia.
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