Amaral Olavo B, Roesler Rafael
Cellular and Molecular Neuropharmacology Research Group, Department of Pharmacology, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, 90046-900 Porto Alegre, RS, Brazil.
Recent Pat CNS Drug Discov. 2008 Nov;3(3):166-78. doi: 10.2174/157488908786242470.
The gap between basic neuroscience and clinical psychiatry in the treatment of anxiety disorders has been steadily diminishing over recent years. Among the leading advances in this field of translation research is the application of knowledge on the neurobiology of fear memory to the treatment of anxiety disorders in humans. Animal studies have identified N-methyl-D-aspartate (NMDA) receptors as crucial in fear memory acquisition and consolidation, as well as in its extinction and reconsolidation. Based on this, the NMDA receptor partial agonist D-cycloserine, which facilitates fear extinction in rodents, has been shown to increase the effect of exposure therapy in psychiatric patients for conditions such as phobias, social anxiety and obsessive-compulsive disorder. In this article, we review current strategies for targeting the NMDA receptor in the treatment of fear-related disorders, analyzing experimental results, clinical data, and recent patents in the field, while also addressing potential new approaches to explore this field of drug discovery.
近年来,基础神经科学与临床精神病学在焦虑症治疗方面的差距一直在稳步缩小。该转化研究领域的主要进展之一是将恐惧记忆神经生物学知识应用于人类焦虑症的治疗。动物研究已确定N-甲基-D-天冬氨酸(NMDA)受体在恐惧记忆的获取、巩固以及消退和重新巩固中起着关键作用。基于此,NMDA受体部分激动剂D-环丝氨酸在啮齿动物中可促进恐惧消退,已被证明可增强暴露疗法对恐惧症、社交焦虑症和强迫症等疾病的精神病患者的治疗效果。在本文中,我们综述了目前在恐惧相关疾病治疗中靶向NMDA受体的策略,分析了该领域的实验结果、临床数据和近期专利,同时还探讨了该药物发现领域潜在的新方法。