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氧化应激以及抗氧化剂和ω-3必需脂肪酸补充剂在精神分裂症中的作用。

Oxidative stress and role of antioxidant and omega-3 essential fatty acid supplementation in schizophrenia.

作者信息

Mahadik S P, Evans D, Lal H

机构信息

Department of Psychiatry and Health Behavior, Medical College of Georgia, Augusta, USA.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2001 Apr;25(3):463-93. doi: 10.1016/s0278-5846(00)00181-0.

Abstract
  1. Schizophrenia is a major mental disorder that has a lifetime risk of 1% and affects at young age (average age at the onset 24 +/- 4.6 years) in many cultures around the world. The etiology is unknown, the pathophysiology is complex, and most of the patients need treatment and care for the rest of their lives. 2. Cellular oxidative stress is inferred from higher tissue levels of reactive oxygen species (ROS, e.g., O2*-, OH*, OH-, NO* and ONOO--) than its antioxidant defense that cause peroxidative cell injury, i.e., peroxidation of membrane phospholipids, particularly esterified essential polyunsaturated fatty acids (EPUFAS), proteins and DNA. 3. Oxidative stress can lead to global cellular with predominantly neuronal peroxidation, since neurons are enriched in highly susceptible EPUFAs and proteins, and damages DNA is not repaired effectively. 4. Such neuronal peroxidation may affect its function (i.e., membrane transport, loss of mitochondrial energy production, gene expression and therefore receptor-mediated phospholipid-dependent signal transduction) that may explain the altered information processing in schizophrenia. 5. It is possible that the oxidative neuronal injury can be prevented by dietary supplementation of antioxidants (e.g., vitamins E, C and A; beta-carotene, Q-enzyme, flavons, etc.) and that membrane phospholipids can be corrected by dietary supplementation of EPUFAs. 6. It may be that the oxidative stress is lower in populations consuming a low caloric diet rich in antioxidants and EPUFAs, and minimizing smoking and drinking. 7. Oxidative stress exists in schizophrenia based on altered antioxidant enzyme defense, increased lipid peroxidation and reduced levels of EPUFAs. The life style of schizophrenic patients is also prooxidative stress, i.e., heavy smoking, drinking, high caloric intake with no physical activity and treatment with pro-oxidant drugs. 8. The patients in developed countries show higher levels of lipid peroxidation and lower levels of membrane phospholipids as compared to patients in the developing countries. 9. Initial observations on the improved outcome of schizophrenia in patients supplemented with EPUFAs and antioxidants suggest the possible beneficial effects of dietary supplementation. 10. Since the oxidative stress exists at or before the onset of psychosis the use of antioxidants from the very onset of psychosis may reduce the oxidative injury and dramatically improve the outcome of illness.
摘要
  1. 精神分裂症是一种主要的精神障碍,终生患病风险为1%,在世界许多文化背景下发病年龄较轻(平均发病年龄为24±4.6岁)。其病因不明,病理生理过程复杂,大多数患者需要终生接受治疗和护理。2. 细胞氧化应激是指组织中活性氧物质(ROS,如超氧阴离子O2•-、羟自由基OH•、氢氧根离子OH-、一氧化氮自由基NO•和过氧亚硝酸盐ONOO-)水平高于其抗氧化防御能力,从而导致细胞发生过氧化损伤,即膜磷脂尤其是酯化必需多不饱和脂肪酸(EPUFA)、蛋白质和DNA的过氧化。3. 氧化应激可导致整体细胞尤其是神经元发生过氧化,因为神经元富含高度易氧化的EPUFA和蛋白质,且受损的DNA无法有效修复。4. 这种神经元过氧化可能会影响其功能(即膜转运、线粒体能量产生丧失、基因表达以及因此受体介导的磷脂依赖性信号转导),这可能解释了精神分裂症中信息处理的改变。5. 通过饮食补充抗氧化剂(如维生素E、C和A;β-胡萝卜素、辅酶Q、黄酮类等)有可能预防氧化神经元损伤,并且通过饮食补充EPUFA可以纠正膜磷脂。6. 食用富含抗氧化剂和EPUFA的低热量饮食、尽量减少吸烟和饮酒的人群中氧化应激可能较低。7. 基于抗氧化酶防御改变、脂质过氧化增加和EPUFA水平降低,精神分裂症患者存在氧化应激。精神分裂症患者的生活方式也会促进氧化应激,即大量吸烟、饮酒、高热量摄入且缺乏体育活动以及使用促氧化药物治疗。8. 与发展中国家的患者相比,发达国家的患者脂质过氧化水平较高,膜磷脂水平较低。9. 对补充EPUFA和抗氧化剂的精神分裂症患者病情改善的初步观察表明饮食补充可能具有有益作用。10. 由于氧化应激在精神病发作时或之前就已存在,从精神病发作一开始就使用抗氧化剂可能会减少氧化损伤并显著改善病情转归。

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