Acta Pharmaceutica Sinica B (Nov 2017)

The current agonists and positive allosteric modulators of α7 nAChR for CNS indications in clinical trials

  • Taoyi Yang,
  • Ting Xiao,
  • Qi Sun,
  • Kewei Wang

DOI
https://doi.org/10.1016/j.apsb.2017.09.001
Journal volume & issue
Vol. 7, no. 6
pp. 611 – 622

Abstract

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The alpha-7 nicotinic acetylcholine receptor (α7 nAChR), consisting of homomeric α7 subunits, is a ligand-gated Ca2+-permeable ion channel implicated in cognition and neuropsychiatric disorders. Enhancement of α7 nAChR function is considered to be a potential therapeutic strategy aiming at ameliorating cognitive deficits of neuropsychiatric disorders such as Alzheimer's disease (AD) and schizophrenia. Currently, a number of α7 nAChR modulators have been reported and several of them have advanced into clinical trials. In this brief review, we outline recent progress made in understanding the role of the α7 nAChR in multiple neuropsychiatric disorders and the pharmacological effects of α7 nAChR modulators used in clinical trials.

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