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Oxidative stress‐related parameters in prostate of rats with experimental autoimmune prostatitis
Author(s) -
Orsilles Miguel A.,
DepianteDepaoli Mirtha
Publication year - 1998
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/(sici)1097-0045(19980301)34:4<270::aid-pros4>3.0.co;2-l
Subject(s) - tbars , oxidative stress , superoxide dismutase , catalase , lipid peroxidation , endocrinology , prostatitis , thiobarbituric acid , antioxidant , medicine , prostate , glutathione , chemistry , glutathione peroxidase , immunology , biochemistry , enzyme , cancer
BACKGROUND Oxidative stress in tissues can be provoked by an augmented metabolic rate, which may sometimes be combined with a decrease in the antioxidant capacity. METHODS In this study we examined the primary enzymatic defense mechanisms against the damage caused by reactive oxygen species (ROS): the superoxide dismutase (SOD) and catalase activities and glutathione content, as well as the levels of total thiobarbituric acid‐reactant substances (TBARS), indicative of lipid peroxidation. These studies were made in prostate homogenates of rats with experimental autoimmune prostatitis (EAP) and of control rats treated with complete Freund's adjuvant (CFA) or nontreated. RESULTS The evaluation of antioxidant defenses revealed a significant diminution of the catalase activity in autoimmune rats without changes in SOD activity and glutathione content. TBARS levels evidenced a significant increase in prostate homogenates from autoimmune rats in relation to control rat samples. CONCLUSIONS The results suggest that in EAP, a marked diminution of catalase activity associated with an enhanced oxidative metabolism of inflammatory macrophages might lead to oxidative damage in this autoimmune disease. Prostate 34:270–274, 1998. © 1998 Wiley‐Liss, Inc.