BNC210: an investigational α7-nicotinic acetylcholine receptor modulator for the treatment of anxiety disorders

被引:3
作者
Hampsey, Elliot [1 ,3 ]
Perkins, Adam [1 ]
Young, Allan H. [1 ,2 ]
机构
[1] Kings Coll London, Ctr Affect Disorders, London, England
[2] South London & Maudsley NHS Fdn Trust, London, England
[3] Inst Psychiat Psychol & Neurosci, 16 Crespigny Pk, London SE5 8AB, England
基金
英国医学研究理事会; 英国惠康基金; 加拿大健康研究院;
关键词
Anxiety disorders; social anxiety disorder; anxiolytic; nicotinic acetylcholine receptor; BNC210; non-sedating; AGE-OF-ONSET; ANTERIOR CINGULATE; AMYGDALA; PREVALENCE; ACTIVATION; COMPOUND; LIFETIME;
D O I
10.1080/13543784.2023.2192922
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionAnxiety disorders are common, disabling psychiatric conditions associated with excessive worry, irritability, and physiological symptoms of stress. Following insufficient response to psychological therapies, first-line pharmacological treatments for anxiety disorders suffer from inconsistent efficacy, addiction, and intolerable side-effect profiles (e.g. sedation), especially when used inappropriately or contrary to evidence-based guidelines. Developing anxiolytics acting via cholinergic modulation may provide novel options for the treatment of anxiety disorders, without the drawbacks of existing anxiolytics.Areas coveredWe review pharmacological treatment of anxiety disorders and proposed mechanisms of action in relation to the associated neural circuitry. We then consider the mechanism of action, pharmacodynamics, and pharmacokinetics of the negative-allosteric modulator of the alpha7 nicotinic receptor BNC210, an investigational anxiolytic so far employed in studies of those with social anxiety disorder, post-traumatic stress disorder, and agitation in hospitalized elderly. Lastly, we consider the environment of competitor compounds for this indication, and BNC210MODIFIER LETTER PRIMEs place within it, in both the present and near-future.Expert opinion: There is a relative paucity of data regarding BNC210, albeit the small amount of mostly non-peer reviewed data indicate it is a well-tolerated, effective anxiolytic. Phase III trials are required for proper appraisal of its utility.
引用
收藏
页码:277 / 282
页数:6
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