Cascella N G, Macciardi F, Cavallini C, Smeraldi E
Department of Neuropsychiatric Sciences, H. S. Raffaele, University of Milan, School of Medicine, Italy.
J Neural Transm Gen Sect. 1994;95(2):105-11. doi: 10.1007/BF01276429.
D-cycloserine, a partial agonist at the strychnine-insensitive glycine site of the NMDA receptor complex, was tested as adjuvant treatment to conventional neuroleptics in chronic schizophrenic volunteers. The drug was administered, o.a.d., at the daily dose of 250 mg for six weeks. Mental status outcome measures were completed at the end of each week of treatment. The major finding was a deterioration of the patients' clinical condition, specifically of their psychotic symptoms. These preliminary results are discussed among others in view of d-cycloserine pharmacologic properties and recent findings on the interaction between NMDA agonists and dopamine system. This study, finally, suggests the need for a controlled dose-finding trial to establish the activity and a therapeutic "window" of this drug in schizophrenia.
D-环丝氨酸是N-甲基-D-天冬氨酸(NMDA)受体复合物中对士的宁不敏感的甘氨酸位点的部分激动剂,在慢性精神分裂症志愿者中作为传统抗精神病药物的辅助治疗进行了测试。该药物口服给药,每日剂量为250毫克,持续六周。在治疗的每周结束时完成精神状态结果测量。主要发现是患者临床状况恶化,尤其是精神症状。鉴于D-环丝氨酸的药理特性以及最近关于NMDA激动剂与多巴胺系统相互作用的研究结果,对这些初步结果进行了讨论。最后,这项研究表明需要进行一项对照剂量探索试验,以确定该药物在精神分裂症中的活性和治疗“窗口”。