Alfredsson G, Wiesel F A
Department of Psychiatry, Uppsala University, Sweden.
Psychopharmacology (Berl). 1990;101(3):324-31. doi: 10.1007/BF02244049.
Twenty-four acutely ill schizophrenic patients (DSM-III-R), 18-42 years old, were treated for 6 weeks with sulpiride. Sulpiride was administered in three different daily dosages (400, 800 or 1200 mg) according to a double dummy blind randomized administration schedule. The psychopathology of the patients was rated by the Comprehensive Psychopathological Rating Scale (CPRS) and the Nurse's Observation Scale for Inpatient Evaluation (NOSIE). The monoamine metabolites homovanillic acid (HVA), 5-hydroxy-indoleacetic acid (5-HIAA), 4-hydroxy-3-methoxy-phenylglycol (HMPG) and the amino acids tyrosine, tryptophan, glutamate and glutamine were measured in serum before and once a week during sulpiride treatment. There were no significant correlations between the CPRS or the NOSIE morbidity scores and the biochemical measures before drug treatment. HVA levels were not correlated to rating scores during treatment, but after 6 weeks HVA had decreased significantly in the patients with a good response but not in the patients with a poor response. A negative relationship between 5-HIAA levels and depressive and negative symptoms was found. Non-responders according to the subscale for depression had low 5-HIAA levels throughout the treatment. An increase of tryptophan was correlated to improvement in the early part of treatment. High levels of glutamate or glutamine were found in non-responders before treatment. During treatment an increase of the glutamate level was correlated to improvement. Low levels of glutamine were related to improvement according to global and NOSIE (total) rating scores. Peripheral biochemical measures may be a valuable tool in the study of pathophysiological mechanisms and treatment effects in patients with schizophrenia.
24名年龄在18至42岁之间的急性精神分裂症患者(DSM-III-R)接受了为期6周的舒必利治疗。根据双盲随机给药方案,舒必利以三种不同的日剂量(400、800或1200毫克)给药。患者的精神病理学通过综合精神病理学评定量表(CPRS)和护士住院患者评定观察量表(NOSIE)进行评定。在舒必利治疗前及治疗期间每周一次测定血清中的单胺代谢产物高香草酸(HVA)、5-羟吲哚乙酸(5-HIAA)、4-羟基-3-甲氧基苯乙二醇(HMPG)以及氨基酸酪氨酸、色氨酸、谷氨酸和谷氨酰胺。药物治疗前,CPRS或NOSIE发病率评分与生化指标之间无显著相关性。治疗期间,HVA水平与评分无相关性,但6周后,反应良好的患者HVA显著下降,而反应不佳的患者则未下降。发现5-HIAA水平与抑郁和阴性症状呈负相关。根据抑郁分量表评定为无反应者在整个治疗过程中5-HIAA水平较低。色氨酸增加与治疗早期的改善相关。无反应者治疗前谷氨酸或谷氨酰胺水平较高。治疗期间谷氨酸水平升高与改善相关。根据总体和NOSIE(总计)评分,谷氨酰胺水平低与改善相关。外周生化指标可能是研究精神分裂症患者病理生理机制和治疗效果的有价值工具。