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Promotion of oxidative stress by 3‐hydroxyglutaric acid in rat striatum
Author(s) -
Latini A.,
Scussiato K.,
Leipnitz G.,
DutraFilho C. S.,
Wajner M.
Publication year - 2005
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/s10545-005-3677-7
Subject(s) - oxidative stress , malondialdehyde , chemistry , lipid peroxidation , glutathione , medicine , striatum , antioxidant , endocrinology , biochemistry , biology , enzyme , dopamine
Summary The pathophysiology of the striatum degeneration characteristic of patients affected by the inherited neurometabolic disorder glutaryl‐CoA dehydrogenase deficiency (GDD), also known as glutaric aciduria type I, is still in debate. We have previously reported that 3‐hydroxyglutaric acid (3‐OH‐GA) considered the main neurotoxin in this disorder, induces oxidative stress in rat cerebral cotex. In the present work, we extended these studies by investigating the in vitro effect of 3‐OH‐GA, at concentrations ranging from 0.01 to 1.0 mmol/L on the brain antioxidant defences by measuring total radical‐trapping antioxidant potential (TRAP), total antioxidant reactivity (TAR) and glutathione (GSH) levels, and on the production of hydrogen peroxide (H 2 O 2 ), nitric oxide (NO) and malondialdehyde in striatum homogenates from young rats. We observed that TRAP, TAR and GSH levels were markedly reduced (by up to 50%) when striatum homogenates were treated with 3‐OH‐GA. In contrast, H 2 O 2 (up to 44%), NO (up to 95%) and malondialdehyde levels (up to 28%) were significantly increased by 3‐OH‐GA. These data indicate that total nonenzymatic antioxidant defences (TRAP) and the tissue capacity to handle an increase of reactive species (TAR) were reduced by 3‐OH‐GA in the striatum. Furthermore, the results also reflect an increase of lipid peroxidation, probably secondary to 3‐OH‐GA‐induced free radical production. Thus, it may be presumed that oxidative stress is involved in the neuropathology in GDD.