Serum S100B and antioxidant enzymes in bipolar patients

被引:239
作者
Andreazza, Ana Cristina
Cassini, Carina
Rosa, Adriane Ribeiro
Leite, Marina Conch
de Almeida, Lucia M. V.
Nardin, Patricia
Cunha, Angelo B. N.
Cereser, Keila Maria
Santin, Aida
Gottfried, Carmem
Salvador, Mirian
Kapczinski, Flavio
Goncalves, Carlos Alberto
机构
[1] Univ Fed Rio Grande do Sul, Inst Ciencias Basicas Saude, Dept Bioquim, BR-90035003 Porto Alegre, RS, Brazil
[2] Hosp Clin Porto Alegre, Ctr Pesquisas, Programa Desordens Bipolares, BR-90035003 Porto Alegre, RS, Brazil
[3] Univ Caxias Sul, Inst Biotecnol, BR-95070560 Caxias Do Sul, RS, Brazil
关键词
bipolar disorder; catalase; glutathione peroxidase; oxidative stress; superoxide dismutase; S100B;
D O I
10.1016/j.jpsychires.2006.07.013
中图分类号
R749 [精神病学];
学科分类号
100205 [精神病与精神卫生学];
摘要
Bipolar disorder (BD) is a chronic, severe, and highly disabling psychiatric disorder; peripheral markers have been used to assess biochemical alterations associated with BD and/or possibly involved in its pathophysiology. Beyond neuronal commitment, many groups have proposed the involvement of glial activity in psychiatric disorders. Other biochemical markers, particularly associated with oxidative stress, have been studied in BD. In the present study, we evaluated glial involvement and oxidative stress in patients with BD. Glial activity was assessed by measuring serum S100B content; oxidative stress was assessed using serum thiobarbituric acid reactive substances (TBARS) and activities of antioxidant enzymes in BD patients during different episodes of disease. We found a significant increment of serum S100B during episodes of mania and depression, but not in euthymic patients. Superoxide dismutase (SOD) activity, as well the SOD/glutathione peroxidase plus catalase ratio, was also increased in manic and depressed patients. On the other hand, TBARS levels were increased in BD patients regardless of the phase of the disorder. These findings suggest a potential oxidative damage in BD patients. This peripheral oxidative imbalance indicates that systemic changes are taking place during the active phases of the illness. Such changes appear to relate to astrocyte function, as indicated by serum S100B elevation. (c) 2006 Published by Elsevier Ltd.
引用
收藏
页码:523 / 529
页数:7
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