Cortese Bernadette M, Phan K Luan
Department of Psychiatry, Pennsylvania State University College of Medicine, Hershey, PA, USA.
CNS Spectr. 2005 Oct;10(10):820-30. doi: 10.1017/s1092852900010427.
Anxiety, stress, and trauma-related disorders are a major public health concern in the United States. Drugs that target the gamma-aminobutyric acid or serotonergic system, such as benzodiazepines and selective serotonin reuptake inhibitors, respectively, are the most widely prescribed treatments for these disorders. However, the role of glutamate in anxiety disorders is becoming more recognized with the belief that drugs that modulate glutamatergic function through either ionotropic or metabotropic glutamate receptors have the potential to improve the current treatment of these severe and disabling illnesses. Animal models of fear and anxiety have provided a method to study the role of glutamate in anxiety. This research has demonstrated that drugs that alter glutamate transmission have potential anxiolytic action for many different paradigms including fear-potentiated startle, punished responding, and the elevated plus maze. Human clinical drug trials have demonstrated the efficacy of glutamatergic drugs for the treatment of obsessive-compulsive disorder, posttraumatic stress disorder, generalized anxiety disorder, and social phobia. Recent data from magnetic resonance imaging studies provide an additional link between the glutamate system and anxiety. Collectively, the data suggest that future studies on the mechanism of and clinical efficacy of glutamatergic agents in anxiety disorders are appropriately warranted.
焦虑症、应激相关障碍和创伤相关障碍是美国主要的公共卫生问题。分别针对γ-氨基丁酸或血清素能系统的药物,如苯二氮䓬类药物和选择性5-羟色胺再摄取抑制剂,是这些疾病最广泛使用的治疗药物。然而,谷氨酸在焦虑症中的作用越来越受到认可,人们认为通过离子型或代谢型谷氨酸受体调节谷氨酸能功能的药物有可能改善目前对这些严重致残性疾病的治疗。恐惧和焦虑的动物模型为研究谷氨酸在焦虑中的作用提供了一种方法。这项研究表明,改变谷氨酸传递的药物对许多不同的范式具有潜在的抗焦虑作用,包括恐惧增强惊吓反应、惩罚反应和高架十字迷宫实验。人体临床药物试验已经证明了谷氨酸能药物在治疗强迫症、创伤后应激障碍、广泛性焦虑症和社交恐惧症方面的疗效。磁共振成像研究的最新数据为谷氨酸系统和焦虑之间提供了额外的联系。总体而言,这些数据表明,对谷氨酸能药物在焦虑症中的作用机制和临床疗效进行进一步研究是很有必要的。