Matsuzawa Daisuke, Obata Takayuki, Shirayama Yukihiko, Nonaka Hiroi, Kanazawa Yoko, Yoshitome Eiji, Takanashi Junichi, Matsuda Tsuyoshi, Shimizu Eiji, Ikehira Hiroo, Iyo Masaomi, Hashimoto Kenji
Department of Psychiatry, Chiba University Graduate School of Medicine, Chiba, Japan.
PLoS One. 2008 Apr 9;3(4):e1944. doi: 10.1371/journal.pone.0001944.
Glutathione (GSH), a major intracellular antioxidant, plays a role in NMDA receptor-mediated neurotransmission, which is involved in the pathophysiology of schizophrenia. In the present study, we aimed to investigate whether GSH levels are altered in the posterior medial frontal cortex of schizophrenic patients. Furthermore, we examined correlations between GSH levels and clinical variables in patients.
Twenty schizophrenia patients and 16 age- and gender-matched normal controls were enrolled to examine the levels of GSH in the posterior medial frontal cortex by using 3T SIGNA EXCITE (1)H-MRS with the spectral editing technique, MEGA-PRESS. Clinical variables of patients were assessed by the Global Assessment of Functioning (GAF), Scale for the Assessment of Negative Symptoms (SANS), Brief Psychiatric Rating Scale (BPRS), Drug-Induced Extra-Pyramidal Symptoms Scale (DIEPSS), and five cognitive performance tests (Word Fluency Test, Stroop Test, Trail Making Test, Wisconsin Card Sorting Test and Digit Span Distractibility Test). Levels of GSH in the posterior medial frontal cortex of schizophrenic patients were not different from those of normal controls. However, we found a significant negative correlation between GSH levels and the severity of negative symptoms (SANS total score and negative symptom subscore on BPRS) in patients. There were no correlations between brain GSH levels and scores on any cognitive performance test except Trail Making Test part A.
These results suggest that GSH levels in the posterior medial frontal cortex may be related to negative symptoms in schizophrenic patients. Therefore, agents that increase GSH levels in the brain could be potential therapeutic drugs for negative symptoms in schizophrenia.
谷胱甘肽(GSH)是一种主要的细胞内抗氧化剂,在N-甲基-D-天冬氨酸(NMDA)受体介导的神经传递中发挥作用,而该神经传递参与了精神分裂症的病理生理学过程。在本研究中,我们旨在调查精神分裂症患者内侧额叶后部皮质中的GSH水平是否发生改变。此外,我们还检查了患者GSH水平与临床变量之间的相关性。
招募了20名精神分裂症患者以及16名年龄和性别匹配的正常对照者,使用3T SIGNA EXCITE(1)H-磁共振波谱(MRS)和频谱编辑技术MEGA-PRESS来检测内侧额叶后部皮质中的GSH水平。通过功能总体评定量表(GAF)、阴性症状评定量表(SANS)、简明精神病评定量表(BPRS)、药物所致锥体外系症状量表(DIEPSS)以及五项认知功能测试(词语流畅性测试、斯特鲁普测试、连线测试、威斯康星卡片分类测试和数字广度分心测试)对患者的临床变量进行评估。精神分裂症患者内侧额叶后部皮质中的GSH水平与正常对照者并无差异。然而,我们发现患者的GSH水平与阴性症状的严重程度(SANS总分以及BPRS上的阴性症状子分数)之间存在显著负相关。除了连线测试A部分外,脑内GSH水平与任何认知功能测试的得分均无相关性。
这些结果表明,内侧额叶后部皮质中的GSH水平可能与精神分裂症患者的阴性症状有关。因此,提高脑内GSH水平的药物可能是治疗精神分裂症阴性症状的潜在药物。