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

Mahadik, Sahebarao P., Denise Evans and Harbans Lal: Oxidative Stress and Role of Antioxidant and ω3 Essential Fatty Acid Supplementation in Schizophrenia. Prog. Neuropsychopharmacol. Biol. Psychiat. 1. Schizophrenia is a major mental disorder that has a lifetime risk of 1% and affects at young age...

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Veröffentlicht in:Progress in neuro-psychopharmacology & biological psychiatry 2001-04, Vol.25 (3), p.463-493
Hauptverfasser: Mahadik, Sahebarao P., Evans, Denise, Lal, Harbns
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Sprache:eng
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Zusammenfassung:Mahadik, Sahebarao P., Denise Evans and Harbans Lal: Oxidative Stress and Role of Antioxidant and ω3 Essential Fatty Acid Supplementation in Schizophrenia. Prog. Neuropsychopharmacol. Biol. Psychiat. 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., O 2 — , 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; β-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 pro-oxidative 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 ex
ISSN:0278-5846
1878-4216
DOI:10.1016/S0278-5846(00)00181-0