Potassium channel modulators and schizophrenia: an overview of investigational drugs

被引:7
|
作者
Musselman, Meghan [1 ]
Huynh, Eric [1 ]
Kelshikar, Rachana [1 ]
Lee, Eric [1 ]
Malik, Mohammed [1 ]
Faden, Justin [1 ,2 ]
机构
[1] Temple Univ, Dept Psychiat, Lewis Katz Sch Med, Philadelphia, PA USA
[2] Temple Univ, Dept Psychiat, Lewis Katz Sch Med, 100 E Lehigh Ave, Suite 305B, Philadelphia, PA 19122 USA
关键词
Schizophrenia; psychopharmacology; potassium channel modulators; AUT00206; gamma oscillations; NMDA receptor; glutamate; DOPAMINE SYNTHESIS CAPACITY; NEURAL-NETWORKS; K+ CHANNELS; PSYCHOSIS; EFFICACY; AUT00206; SYSTEM; REWARD; MODEL; ANTIPSYCHOTICS;
D O I
10.1080/13543784.2023.2219385
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Schizophrenia is a severe mental illness comprising positive, negative, and cognitive symptoms. Existing pharmacologic options exert their actions on the dopamine receptor but are largely ineffective at treating negative and cognitive symptoms. Alternative pharmacologic options that do not act directly on the dopamine receptor are being investigated, including potassium channel modulators. It has been hypothesized that dysfunctional fast-spiking parvalbumin-positive GABA interneurons, regulated by Kv3.1 and Kv3.2 potassium channels, contribute to the symptoms of schizophrenia, making potassium channels an area of clinical interest.Areas covered: This review will highlight potassium channel modulators for the treatment of schizophrenia, with a focus on AUT00206. Background on Kv3.1 and Kv3.2 potassium channels will be explored. Our search strategy included a literature review utilizing PubMed, Clinicaltrials.gov, and sources available on the manufacturer's website.Expert opinion: Initial data on potassium channel modulators is promising; however, further study is needed, and existing evidence is limited. Early data suggests that dysfunctional GABA interneurons can be ameliorated through modulators of Kv3.1 and Kv3.2 channels. AUT00206 has been shown to improve dopaminergic dysfunction induced by ketamine and PCP, improve resting gamma power in patients with schizophrenia, impact dopamine synthesis capacity in a subgroup of individuals with schizophrenia, and affect reward anticipation-related neural activation.
引用
收藏
页码:471 / 477
页数:7
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