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

被引:2
|
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; 加拿大健康研究院; 英国惠康基金;
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
相关论文
共 50 条
  • [41] Synthesis and biological evaluation of 9-fluorenone derivatives for SPECT imaging of α7-nicotinic acetylcholine receptor
    Gao, Hang
    Wang, Shuxia
    Qi, Yueheng
    He, Guoxue
    Qiang, Bingchao
    Wang, Sixuan
    Zhang, Huabei
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2019, 29 (23)
  • [42] Pharmacological Activation of α7-Nicotinic Acetylcholine Receptor (α7AChR) Attenuates Cytokine-Mediated Islet Inflammation
    Gupta, Dhananjay
    Satish, Basanthi
    Leahy, Jack L.
    Jetton, Thomas
    DIABETES, 2013, 62 : A584 - A584
  • [43] Inducible, heterologous expression of human α7-nicotinic acetylcholine receptors in a native nicotinic receptor-null human clonal line
    Peng, JH
    Lucero, L
    Flyer, J
    Herl, J
    Leonard, SS
    Lukas, RJ
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1998, 358 (01) : R87 - R87
  • [44] The α7-nicotinic acetylcholine receptor gene (CHRNA7) in schizophrenia:: Are gene variants in the 5′-flanking region implicated?
    Morris, A
    Ftouh, S
    Tyson, P
    Mortimer, A
    Hunt, D
    Hirsch, S
    deBelleroche, J
    SCHIZOPHRENIA RESEARCH, 2002, 53 (03) : 71 - 71
  • [45] The efficacy of an allosteric modulator of the alpha 7 nicotinic acetylcholine receptor in a murine model of stroke
    Hernandez, Katherine
    Jones, Nathan
    Ortega, Sterling B.
    FRONTIERS IN NEUROSCIENCE, 2025, 19
  • [46] The alpha7 nicotinic acetylcholine receptor - a crucial modulator of cutaneous and extracutaneous fibrosis?
    Stegemann, A.
    Sindrilaru, A.
    Eckes, B.
    del Rey, A.
    Grando, S.
    Fiebich, B. L.
    Scharffetter-Kochanek, K.
    Luger, T. A.
    Boehm, M.
    EXPERIMENTAL DERMATOLOGY, 2018, 27 (03) : E28 - E28
  • [47] An allosteric modulator of the α7 nicotinic acetylcholine receptor possessing cognition enhancing properties in vivo
    Timmermann, Daniel B.
    Gronlien, Jens Halvard
    Kohlhaas, Kathy L.
    Nielsen, Elsebet O.
    Dam, Eva
    Jorgensen, Tino D.
    Ahring, Philip K.
    Peters, Dan
    Holst, Dorte
    Christensen, Jeppe K.
    Malysz, John
    Briggs, Clark A.
    Gopalakrishnan, Murali
    Olsen, Gunnar M.
    BIOCHEMICAL PHARMACOLOGY, 2007, 74 (08) : SMA33 - SMA34
  • [48] Microwave-assisted radiosynthesis of [18F] ASEM, a radiolabeled α7-nicotinic acetylcholine receptor antagonist
    Ravert, Hayden T.
    Holt, Daniel P.
    Gao, Yongjun
    Horti, Andrew G.
    Dannals, Robert F.
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2015, 58 (04): : 180 - 182
  • [49] Characterization of a novel nicotinic acetylcholine receptor α7 (α7 nAChR) positive modulator in recombinant and native systems
    Hirakawa, Ryoko
    Maag, Hans
    Misner, Dinah
    Milla, Marcos
    Button, Donald
    Sahdeo, Sunil
    BIOCHEMICAL PHARMACOLOGY, 2007, 74 (08) : SMA35 - SMA35
  • [50] Differential effects of endogenous and synthetic cannabinoids on α7-nicotinic acetylcholine receptor-mediated responses in Xenopus oocytes
    Oz, M
    Zhang, L
    Ravindran, A
    Morales, M
    Lupica, CR
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2004, 310 (03): : 1152 - 1160