Emerging drugs for panic disorder

被引:22
|
作者
Perna, Giampaolo [1 ,2 ,3 ]
Guerriero, Giuseppe [1 ]
Caldirola, Daniela [1 ]
机构
[1] Hermanas Hosp, San Benedetto Hosp, Dept Clin Neurosci, Albese Con Cassano, Como, Italy
[2] Univ Maastricht, Dept Psychiat & Neuropsychol, Fac Hlth Med & Life Sci, Maastricht, Netherlands
[3] Univ Miami, Leonard M Miller Sch Med, Dept Psychiat & Behav Sci, Coral Gables, FL 33124 USA
关键词
anticonvulsants; atypical antipsychotics; cholinergic system; D-cycloserine; drug development; glutamate receptor; orexin; panic disorder; treatment; 35-PERCENT CO2 HYPERREACTIVITY; MGLU2/3 RECEPTOR AGONIST; CARBON-DIOXIDE HYPERSENSITIVITY; CORTICOTROPIN-RELEASING-FACTOR; COGNITIVE-BEHAVIORAL THERAPY; LOW-DOSE RISPERIDONE; DOUBLE-BLIND; BENZODIAZEPINE-RECEPTOR; ANXIETY DISORDERS; OPEN-LABEL;
D O I
10.1517/14728214.2011.628313
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Panic disorder (PD) is a common anxiety disorder impairing strongly quality of life with high social costs. Effective anti-panic medications exist but a substantial proportion of patients do not fully respond, the available drugs have several side effects and most medications have a delayed onset of their therapeutic effect. Thus, further advances are needed. Areas covered: We review available data on emerging drugs for the treatment of PD including those in development, such as metabotropic glutamate II receptor agonists, D-cycloserine and levetiracetam, and new compounds with potential efficacy that may be relevant for future developments, such as modulators of cholinergic and orexin systems. Expert opinion: To date, the pharmacological research on PD appears to be relatively limited and probably still needs more time before making available new advances beyond the currently used medications. Many reasons may explain these difficulties, including the heterogeneity of the disorder, the incomplete understanding of its underlying pathophysiological mechanisms and difficulties in the selection of appropriate animal models in preclinical studies. Defining biomarkers and endophenotypes in PD may offer advantages in both understanding the pathophysiology of the disorder and selecting appropriate targets and outcomes for planning future pharmacological research.
引用
收藏
页码:631 / 645
页数:15
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