Hofmann Stefan G, Wu Jade Q, Boettcher Hannah
Department of Psychology, Boston University, Boston, MA, 02215-2002, USA.
Biol Mood Anxiety Disord. 2013 Jun 15;3(1):11. doi: 10.1186/2045-5380-3-11.
The goal of this review is to examine the clinical studies on d-cycloserine, a partial glutamatergic N-methyl-D-aspartate agonist, as an augmentation strategy for exposure procedures during cognitive behavioral therapy for anxiety disorders. Although cognitive behavioral therapy and anxiolytic medications are more effective than placebo for treating anxiety disorders, there is still considerable room for further improvement. Traditional combination strategies typically yield disappointing results. However, recent studies based on translational research have shown promise to augment the neural circuitry underlying fear extinction with pharmacological means. We discuss the current state of the literature, including inconsistencies of findings and issues concerning the drug mechanism, dosing, and dose timing. D-cycloserine is a promising combination strategy for cognitive behavioral therapy of anxiety disorders by augmenting extinction learning. However, there is also evidence to suggest that d-cycloserine can facilitate reconsolidation of fear memory when exposure procedures are unsuccessful.
本综述的目的是考察关于D-环丝氨酸(一种部分谷氨酸能N-甲基-D-天冬氨酸受体激动剂)作为焦虑症认知行为疗法中暴露程序强化策略的临床研究。尽管认知行为疗法和抗焦虑药物在治疗焦虑症方面比安慰剂更有效,但仍有很大的进一步改善空间。传统的联合策略通常产生令人失望的结果。然而,基于转化研究的近期研究显示,有望通过药理学手段强化恐惧消退背后的神经回路。我们讨论了文献的现状,包括研究结果的不一致性以及有关药物机制、给药剂量和给药时间的问题。通过强化消退学习,D-环丝氨酸是一种有前景的焦虑症认知行为疗法联合策略。然而,也有证据表明,当暴露程序不成功时,D-环丝氨酸可促进恐惧记忆的重新巩固。