Serum Oxidative Stress Marker Levels in Unmedicated and Medicated Patients with Schizophrenia

被引:65
作者
Bai, Zhi-Le [1 ]
Li, Xue-Song [2 ]
Chen, Guang-Yang [2 ]
Du, Yang [1 ]
Wei, Ze-Xu [1 ]
Chen, Xi [1 ]
Zheng, Guang-En [2 ]
Deng, Wen [2 ]
Cheng, Yong [1 ]
机构
[1] Minzu Univ China, Coll Life & Environm Sci, Ctr Translat Neurosci, Key Lab Ethnomed,Minist Educ, 27 South Zhongguancun Ave, Beijing 100081, Peoples R China
[2] Third Hosp Fuoshan, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Schizophrenia; Antipsychotics; Oxidative stress; Superoxide dismutase; Glutathione peroxidase; Total antioxidant capacity; Malondialdehyde; ANTIOXIDANT DEFENSE SYSTEM; ACID REACTIVE SUBSTANCES; LIPID-PEROXIDATION; CEREBROSPINAL-FLUID; PREFRONTAL CORTEX; BIPOLAR DISORDER; DIFFERENT FORMS; ENZYMES; BRAIN; GLUTATHIONE;
D O I
10.1007/s12031-018-1165-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oxidative stress has been suggested to be involved in schizophrenia, but studies have demonstrated inconsistent results on oxidative stress marker level/activity in patients with schizophrenia. In order to clarify the circulating oxidative stress marker level/activity in patients with schizophrenia, this study recruited 80 schizophrenia patients (40 first-episode, drug-free and 40 chronically medicated patients) and 80 controls to analyze serum activities of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and total antioxidant capacity (T-AOC), and levels of lipid peroxidation marker malondialdehyde (MDA) in schizophrenia patients, and whether they associate with the severity of the disease. We showed that only serum GSH-Px activity was significantly reduced in unmedicated patients with schizophrenia when compared with control subjects, whereas the other three analyzed oxidative stress markers did not show significant differences between cases and controls. Moreover, our results demonstrated that chronic medication increased GSH-Px activity and MDA levels in patients with schizophrenia, but reduced SOD activity in the patients. We also found that short-term antipsychotic treatments on the patients with schizophrenia reduced the SOD activity. Correlation analyses indicated that the oxidative stress marker activity/level is not significantly associated with the severity of schizophrenia, except that SOD level correlated with PANSS positive score significantly. Taken together, the data from the present study suggested that the dysfunctions of oxidative stress markers in patients with schizophrenia were mainly caused by antipsychotics, emphasizing increased oxidative stress as a potential side effect of antipsychotics on the patients.
引用
收藏
页码:428 / 436
页数:9
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