Dietrich-Muszalska Anna, Olas Beata
II Department of Psychiatry, Medical University of Lodz, Poland.
World J Biol Psychiatry. 2009;10(1):27-33. doi: 10.1080/15622970701361263.
Free radicals induce oxidative stress and damage to all types of biological molecules and may be involved in pathology of schizophrenia. A cell membrane dysfunction caused by lipid peroxidation can be secondary to a free radical-mediated pathology and may contribute to specific aspects of schizophrenic symptomatology and complications of its treatment.
The aim of our study was to estimate oxidative stress in a group of schizophrenic patients by using different biomarkers of free radicals-induced lipid peroxidation (isoprostanes, thiobarbituric acid reactive substances (TBARS)). We also determined the products of enzymatic peroxidation of arachidonic acid, such as thromboxane B2 (TXB2) and its metabolite 11-dehydrothromboxane B2. Isoprostanes (IPs) are a family of novel prostaglandin isomers and are produced in free radical-catalysed reactions from arachidonic acid. They are useful as a specific, sensitive, chemically stable, noninvasive index of free radical generation in vivo. We therefore assessed in schizophrenic patients and control subjects the level of urinary excretion of isoprostane--8-epi-prostaglandin F2 alpha, (8-isoPGF2 alpha)--a marker of lipid peroxidation induced by free radicals using an immunoassay kit. We also studied the level of the other marker of enzymatic arachidonic acid peroxidation--11-dehydrothromboxane B2--in urine from schizophrenic patients and healthy volunteers. Moreover, we estimated the production of TBARS and TXB2 in plasma from schizophrenic patients and the control group. Patients hospitalised in the II Psychiatric Department of Medical University in Lodz, Poland, were interviewed with a special questionnaire (treatment, course of diseases, dyskinesis and other EPS). According to DSM-IV criteria, all patients had diagnosis of paranoid type. All patients were treated with second-generation antipsychotic drugs (risperidone, clozapine, and olanzapine). Mean time of schizophrenia duration was about 2 years.
We observed a statistically increased level of TBARS in plasma (P=0.000162) and isoprostanes (P=3.5 x 10(-12)) in urine of schizophrenic patients in comparison with the control group. The level of markers of enzymatic oxidation of arachidonic acid (TXB2 and its metabolite, 11-dehydrothromboxane B2) did not change. This indicates that free radicals induce peroxidation of unsaturated fatty acid in schizophrenic patients.
Considering the data presented in this study, we suggest that non-invasive measurement of 8-isoPGF2 alpha, is a valuable and sensitive (contrary to TBARS) indicator of oxidative stress status in vivo in schizophrenia.
自由基可诱导氧化应激并对所有类型的生物分子造成损害,可能参与精神分裂症的病理过程。脂质过氧化引起的细胞膜功能障碍可能继发于自由基介导的病理过程,并可能导致精神分裂症症状的特定方面及其治疗并发症。
我们研究的目的是通过使用自由基诱导脂质过氧化的不同生物标志物(异前列腺素、硫代巴比妥酸反应性物质(TBARS))来评估一组精神分裂症患者的氧化应激。我们还测定了花生四烯酸酶促过氧化产物,如血栓素B2(TXB2)及其代谢物11-脱氢血栓素B2。异前列腺素(IPs)是一类新型前列腺素异构体,由花生四烯酸在自由基催化反应中产生。它们作为体内自由基生成的特异性、敏感性、化学稳定性、非侵入性指标很有用。因此,我们使用免疫分析试剂盒评估了精神分裂症患者和对照受试者尿液中异前列腺素——8-表-前列腺素F2α(8-isoPGF2α)——自由基诱导脂质过氧化的标志物的排泄水平。我们还研究了精神分裂症患者和健康志愿者尿液中花生四烯酸酶促过氧化的另一个标志物——11-脱氢血栓素B2的水平。此外,我们估计了精神分裂症患者和对照组血浆中TBARS和TXB2的产生。对波兰罗兹医科大学第二精神科住院的患者进行了一份特殊问卷(治疗、病程、运动障碍和其他锥体外系反应)的访谈。根据《精神疾病诊断与统计手册》第四版标准,所有患者均诊断为偏执型。所有患者均接受第二代抗精神病药物(利培酮、氯氮平、奥氮平)治疗。精神分裂症的平均病程约为2年。
与对照组相比,我们观察到精神分裂症患者血浆中TBARS水平(P = 0.000162)和尿液中异前列腺素水平(P = (^{}3.5\times10^{-12}))在统计学上显著升高。花生四烯酸酶促氧化标志物(TXB2及其代谢物11-脱氢血栓素B2)水平未发生变化。这表明自由基在精神分裂症患者中诱导不饱和脂肪酸过氧化。
考虑到本研究中呈现的数据,我们认为非侵入性测量8-isoPGF2α是精神分裂症体内氧化应激状态的有价值且敏感(与TBARS相反)的指标。