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Neurotoxic Effects of trans-Glutaconic Acid in Rats

trans-Glutaconic acid (tGA) is an unsaturated C5-dicarboxylic acid which may be found accumulated in glutaric aciduria type I, whose pathophysiology is still uncertain. In the present work it was investigated the in vitro effect of increasing tGA concentrations on neurochemical and oxidative stress...

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Autores principales: Schuck, Patrícia F., Busanello, Estela N. B., Tonin, Anelise M., Viegas, Carolina M., Ferreira, Gustavo C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625603/
https://www.ncbi.nlm.nih.gov/pubmed/23606926
http://dx.doi.org/10.1155/2013/607610
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author Schuck, Patrícia F.
Busanello, Estela N. B.
Tonin, Anelise M.
Viegas, Carolina M.
Ferreira, Gustavo C.
author_facet Schuck, Patrícia F.
Busanello, Estela N. B.
Tonin, Anelise M.
Viegas, Carolina M.
Ferreira, Gustavo C.
author_sort Schuck, Patrícia F.
collection PubMed
description trans-Glutaconic acid (tGA) is an unsaturated C5-dicarboxylic acid which may be found accumulated in glutaric aciduria type I, whose pathophysiology is still uncertain. In the present work it was investigated the in vitro effect of increasing tGA concentrations on neurochemical and oxidative stress parameters in rat cerebral cortex. We observed that Na(+), K(+)-ATPase activity was reduced by tGA, but not creatine kinase, respiratory chain complex IV, and ATP synthase activities. On the other hand, tGA significantly increased lipid peroxidation (thiobarbituric acid-reactive species levels and spontaneous chemiluminescence), as well as protein oxidative damage (oxidation of sulfhydryl groups). tGA also significantly decreased nonenzymatic antioxidant defenses (TRAP and reduced glutathione levels). Our data suggest that tGA may be neurotoxic in rat brain.
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spelling pubmed-36256032013-04-19 Neurotoxic Effects of trans-Glutaconic Acid in Rats Schuck, Patrícia F. Busanello, Estela N. B. Tonin, Anelise M. Viegas, Carolina M. Ferreira, Gustavo C. Oxid Med Cell Longev Research Article trans-Glutaconic acid (tGA) is an unsaturated C5-dicarboxylic acid which may be found accumulated in glutaric aciduria type I, whose pathophysiology is still uncertain. In the present work it was investigated the in vitro effect of increasing tGA concentrations on neurochemical and oxidative stress parameters in rat cerebral cortex. We observed that Na(+), K(+)-ATPase activity was reduced by tGA, but not creatine kinase, respiratory chain complex IV, and ATP synthase activities. On the other hand, tGA significantly increased lipid peroxidation (thiobarbituric acid-reactive species levels and spontaneous chemiluminescence), as well as protein oxidative damage (oxidation of sulfhydryl groups). tGA also significantly decreased nonenzymatic antioxidant defenses (TRAP and reduced glutathione levels). Our data suggest that tGA may be neurotoxic in rat brain. Hindawi Publishing Corporation 2013 2013-03-27 /pmc/articles/PMC3625603/ /pubmed/23606926 http://dx.doi.org/10.1155/2013/607610 Text en Copyright © 2013 Patrícia F. Schuck et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Schuck, Patrícia F.
Busanello, Estela N. B.
Tonin, Anelise M.
Viegas, Carolina M.
Ferreira, Gustavo C.
Neurotoxic Effects of trans-Glutaconic Acid in Rats
title Neurotoxic Effects of trans-Glutaconic Acid in Rats
title_full Neurotoxic Effects of trans-Glutaconic Acid in Rats
title_fullStr Neurotoxic Effects of trans-Glutaconic Acid in Rats
title_full_unstemmed Neurotoxic Effects of trans-Glutaconic Acid in Rats
title_short Neurotoxic Effects of trans-Glutaconic Acid in Rats
title_sort neurotoxic effects of trans-glutaconic acid in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3625603/
https://www.ncbi.nlm.nih.gov/pubmed/23606926
http://dx.doi.org/10.1155/2013/607610
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