Goff D C, Henderson D C, Evins A E, Amico E
Psychotic Disorders Program of the Massachusetts General Hospital, Boston, USA.
Biol Psychiatry. 1999 Feb 15;45(4):512-4. doi: 10.1016/s0006-3223(98)00367-9.
D-Cycloserine, a partial agonist at the glycine recognition site of the NMDA receptor, has previously been shown to improve negative symptoms when added to conventional antipsychotics and, in one preliminary dose-finding study, worsened negative symptoms when added to clozapine.
Seventeen schizophrenia outpatients treated with clozapine were assigned in random order to 6-week trials of D-cycloserine 50 mg/day and placebo in a crossover design separated by a 1 week placebo washout.
Eleven patients competed the 13-week study. D-Cycloserine significantly worsened ratings of negative symptoms compared to placebo but did not significantly affect ratings of psychotic symptoms.
The differing effects of D-cycloserine on negative symptoms when added to clozapine compared to conventional antipsychotics suggests that activation of the glycine recognition site may play a role in clozapine's efficacy for negative symptoms.
D-环丝氨酸是N-甲基-D-天冬氨酸(NMDA)受体甘氨酸识别位点的部分激动剂,此前研究表明,将其添加到传统抗精神病药物中可改善阴性症状,而在一项初步剂量探索研究中,添加到氯氮平中时阴性症状却加重。
17名接受氯氮平治疗的精神分裂症门诊患者,采用交叉设计,随机顺序接受为期6周的50毫克/天D-环丝氨酸试验和安慰剂试验,中间有1周的安慰剂洗脱期。
11名患者完成了13周的研究。与安慰剂相比,D-环丝氨酸显著加重了阴性症状评分,但对精神病性症状评分无显著影响。
与传统抗精神病药物相比,D-环丝氨酸添加到氯氮平中对阴性症状的影响不同,这表明甘氨酸识别位点的激活可能在氯氮平治疗阴性症状的疗效中起作用。