Stefan G. Hofmann, Mark H. Pollack, Michael W. Otto
{"title":"Augmentation Treatment of Psychotherapy for Anxiety Disorders with D-Cycloserine","authors":"Stefan G. Hofmann, Mark H. Pollack, Michael W. Otto","doi":"10.1111/j.1527-3458.2006.00208.x","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Anxiety disorders are among the most common mental disorders. One of the most effective strategies to treat anxiety disorders is exposure therapy with or without cognitive intervention. Fear reduction in exposure therapy is similar to extinction learning. Preclinical studies suggest that extinction learning can be blocked by antagonists at the glutamatergic N-methyl-D-aspartate (NMDA) receptor, and facilitated with D-cycloserine (DCS), a partial agonist at the glycine recognition site of the NMDA receptor in the amygdala. DCS is an established antibiotic drug for the chronic treatment of tuberculosis in humans, but has only recently been investigated as an augmentation therapy for psychological treatment procedures. The review of the literature provides preliminary support for the use of acute dosing of DCS as an adjunctive intervention to exposure therapy for anxiety disorders, including specific phobia and social anxiety disorder. Negative results have recently been reported in the treatment of subclinical fears of animals. These studies suggest that DCS needs to be administered on an acute rather than a chronic dosing schedule, include sufficient time for memory consolidation, and be administered together with psychological treatment that leaves sufficient room for further improvement. It remains to be seen whether these highly promising findings represent reliable pharmacological strategies to enhance exposure therapy of anxiety disorders.</p>\n </div>","PeriodicalId":94307,"journal":{"name":"CNS drug reviews","volume":"12 3-4","pages":"208-217"},"PeriodicalIF":0.0000,"publicationDate":"2007-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1527-3458.2006.00208.x","citationCount":"116","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"CNS drug reviews","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/j.1527-3458.2006.00208.x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 116
Abstract
Anxiety disorders are among the most common mental disorders. One of the most effective strategies to treat anxiety disorders is exposure therapy with or without cognitive intervention. Fear reduction in exposure therapy is similar to extinction learning. Preclinical studies suggest that extinction learning can be blocked by antagonists at the glutamatergic N-methyl-D-aspartate (NMDA) receptor, and facilitated with D-cycloserine (DCS), a partial agonist at the glycine recognition site of the NMDA receptor in the amygdala. DCS is an established antibiotic drug for the chronic treatment of tuberculosis in humans, but has only recently been investigated as an augmentation therapy for psychological treatment procedures. The review of the literature provides preliminary support for the use of acute dosing of DCS as an adjunctive intervention to exposure therapy for anxiety disorders, including specific phobia and social anxiety disorder. Negative results have recently been reported in the treatment of subclinical fears of animals. These studies suggest that DCS needs to be administered on an acute rather than a chronic dosing schedule, include sufficient time for memory consolidation, and be administered together with psychological treatment that leaves sufficient room for further improvement. It remains to be seen whether these highly promising findings represent reliable pharmacological strategies to enhance exposure therapy of anxiety disorders.
焦虑症是最常见的精神障碍之一。治疗焦虑症最有效的策略之一是有或没有认知干预的暴露疗法。暴露疗法中减少恐惧类似于灭绝学习。临床前研究表明,消除学习可以被谷氨酸能n -甲基- d -天冬氨酸(NMDA)受体的拮抗剂阻断,并与d -环丝氨酸(DCS)一起促进,DCS是杏仁核中NMDA受体的甘氨酸识别位点的部分激动剂。DCS是一种用于人类结核病慢性治疗的抗生素药物,但直到最近才被研究作为心理治疗程序的增强疗法。文献综述初步支持使用急性剂量DCS作为焦虑障碍暴露治疗的辅助干预,包括特定恐惧症和社交焦虑障碍。最近在治疗动物的亚临床恐惧方面有负面结果的报道。这些研究表明,DCS需要急性给药,而不是慢性给药,要有足够的时间巩固记忆,并与心理治疗一起给药,以留下足够的空间进一步改善。这些非常有希望的发现是否代表可靠的药理学策略来加强焦虑障碍的暴露治疗还有待观察。