Antioxidant enzyme activities and oxidative stress in affective disorders

Recent data from several reports indicate that free radicals are involved in the biochemical mechanisms underlying neuropsychiatric disorders in human. The results of several reports suggest that lower antioxidant defences against lipid peroxidation exist in patients with depression and that there is a therapeutic benefit from antioxidant supplementation in unstable manic-depressive patients. We investigated the antioxidant enzyme status and the indices of oxidative stress and lipid peroxidation end products in erythrocytes from patients with affective disorder. For this purpose, we measured superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) and catalase (CAT) activities, as well as malondialdehyde (MDA) and nitric oxide (NO) levels in patients with affective disorders (n=30) in both pre- and post-treatment periods, and in a control group (n=21). CAT activities were significantly decreased in both pre-, and post-treatment periods in patients compared to the control group. GSH-Px activity in the pre-treatment period in the patients was significantly lower than both post-treatment patient and control groups. MDA levels were increased in both pre-, and post-treatment patient groups compared to the control group. NO level was lower in the pre-treatment patient group than in the control group. There were statistically significant correlations between SOD and MDA, and SOD and NO in the pre-treatment patient and control groups. Because the overall study sample was small, and the post-treatment patient group was even smaller, it can tentatively be suggested that the antioxidant system is impaired during a mood episode in patients with affective disorders, normalizing at the end of the episode.

[1]  Y. Lu,et al.  Expression of Inducible Nitric Oxide Synthase after Focal Cerebral Ischemia Stimulates Neurogenesis in the Adult Rodent Dentate Gyrus , 2003, The Journal of Neuroscience.

[2]  C. Nemeroff,et al.  Depression in Patients With Cancer: Diagnosis, Biology, and Treatment , 1995 .

[3]  H. Mermelstein,et al.  Depression in patients with cancer , 1992 .

[4]  N. Mcintyre Familial LCAT deficiency and fish-eye disease , 1988, Journal of Inherited Metabolic Disease.

[5]  J. Richardson,et al.  Oxygen free radicals and brain dysfunction. , 1991, The International journal of neuroscience.

[6]  W. Crocker Catalase , 1911, Botanical Gazette.

[7]  G. Rubanyi,et al.  Cytoprotective function of nitric oxide: inactivation of superoxide radicals produced by human leukocytes. , 1991, Biochemical and biophysical research communications.

[8]  M. Yoshioka,et al.  Aminoguanidine prevented the impairment of learning behavior and hippocampal long-term potentiation following transient cerebral ischemia , 2001, Behavioural Brain Research.

[9]  M. Dikshit,et al.  A study on nitric oxide, beta-adrenergic receptors and antioxidant status in the polymorphonuclear leukocytes from the patients of depression. , 2002, Journal of affective disorders.

[10]  H. Esumi,et al.  Reciprocal regulation between nitric oxide and vascular endothelial growth factor in angiogenesis. , 2003, Acta biochimica Polonica.

[11]  W. Wąsowicz,et al.  Optimized steps in fluorometric determination of thiobarbituric acid-reactive substances in serum: importance of extraction pH and influence of sample preservation and storage. , 1993, Clinical chemistry.

[12]  Glenda M MacQueen,et al.  Course of illness, hippocampal function, and hippocampal volume in major depression , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[13]  Y. Sagara Induction of Reactive Oxygen Species in Neurons by Haloperidol , 1998, Journal of neurochemistry.

[14]  H. Ishida,et al.  Nitric oxide reversibly suppresses xanthine oxidase activity. , 1994, Free radical research.

[15]  M. Wilson,et al.  Regional changes in rat brain inositol monophosphatase 1 (IMPase 1) activity with chronic lithium treatment , 2003, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

[16]  S. Rapoport,et al.  Lithium decreases turnover of arachidonate in several brain phospholipids , 1996, Neuroscience Letters.

[17]  D. Kammen,et al.  Effects of haloperidol on antioxidant defense system enzymes in schizophrenia. , 1998, Journal of psychiatric research.

[18]  R. Cuppini,et al.  Tocopherols enhance neurogenesis in dentate gyrus of adult rats. , 2002, International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition.

[19]  B. Leonard,et al.  Catalase, superoxide dismutase and glutathione peroxidase activity in neutrophils of sham-operated and olfactory-bulbectomised rats following chronic treatment with desipramine and lithium chloride. , 1994, Neuropsychobiology.

[20]  Etelvino J. H. Bechara,et al.  Activities of superoxide dismutase and glutathione peroxidase in schizophrenic and manic-depressive patients. , 1986, Clinical chemistry.

[21]  S. Cory,et al.  The Bcl-2 protein family: arbiters of cell survival. , 1998, Science.

[22]  J. Coyle,et al.  Finding the Intracellular Signaling Pathways Affected by Mood Disorder Treatments , 2003, Neuron.

[23]  M. Papa,et al.  Nitric Oxide and Long‐Term Habituation to Novelty in the Rat a , 1994, Annals of the New York Academy of Sciences.

[24]  W. Valentine,et al.  Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. , 1967, The Journal of laboratory and clinical medicine.

[25]  D. Horrobin,et al.  Depletion of Omega-3 Fatty Acid Levels in Red Blood Cell Membranes of Depressive Patients , 1998, Biological Psychiatry.

[26]  R. Pioli,et al.  Lower serum vitamin E concentrations in major depression. Another marker of lowered antioxidant defenses in that illness. , 2000, Journal of affective disorders.

[27]  M. Bekaroǧlu,et al.  Antioxidative enzyme activities and lipid peroxidation in major depression: alterations by antidepressant treatments. , 2001, Journal of affective disorders.

[28]  M. Chopp,et al.  A nitric oxide donor induces neurogenesis and reduces functional deficits after stroke in rats , 2001, Annals of neurology.

[29]  K. A. Kirkebøen,et al.  The role of nitric oxide in sepsis – an overview , 1999, Acta anaesthesiologica Scandinavica.

[30]  James B. Mitchell,et al.  Nitric oxide protects against cellular damage and cytotoxicity from reactive oxygen species. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[31]  R. Dean Free radicals, membrane damage and cell-mediated cytolysis. , 1987, The British journal of cancer. Supplement.

[32]  Y. Sun,et al.  A simple method for clinical assay of superoxide dismutase. , 1988, Clinical chemistry.

[33]  H. Manji,et al.  Enhancing neuronal plasticity and cellular resilience to develop novel, improved therapeutics for Difficult-to-Treat depression , 2003, Biological Psychiatry.

[34]  H. Li,et al.  Deciphering the pathways of life and death. , 1999, Current opinion in cell biology.

[35]  N. Cortas,et al.  Determination of inorganic nitrate in serum and urine by a kinetic cadmium-reduction method. , 1990, Clinical chemistry.