Literature DB >> 24388910

Impact of long term Fe³⁺ toxicity on expression of glutathione system in rat liver.

Harun Budak1, Nurdan Gonul2, Hamid Ceylan2, Enver Fehim Kocpinar3.   

Abstract

The free radicals within the body, produced by metabolic activities or derived from environmental sources are relatively related to hepatoxicity. Since heavy metals including iron have the ability to produce free radicals, the liver glutathione system neutralizes them to protect cells against any damage. The objective of this study is to indicate the toxic effects of iron on the glutathione system at the enzymatic and molecular level. Thus, any possible correlation between enzymatic and molecular levels can be determined. According to our results, while mRNA expression of glutathione reductase (Gsr) and glutathione S-transferases (Gsta5) genes were not affected by long-term exposure to various concentrations of iron (Fe(3+)), transcription level of glutathione peroxidase (Gpx2) was influenced in the presence of toxic iron. Whereas the enzyme activites of GSR (GR), GPX and GST were significantly affected in rat liver.
Copyright © 2013 Elsevier B.V. All rights reserved.

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Keywords:  Enzyme activity; Glutathione system; Iron; Toxic effects; mRNA expression

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Year:  2013        PMID: 24388910     DOI: 10.1016/j.etap.2013.12.007

Source DB:  PubMed          Journal:  Environ Toxicol Pharmacol        ISSN: 1382-6689            Impact factor:   4.860


  1 in total

1.  Tip60/Kat5 may be a novel candidate histone acetyltransferase for the regulation of liver iron localization via acetylation.

Authors:  Nurdan Gönül Baltacı; Emine Toraman; Mesut Akyüz; Şeyda Nur Kalın; Harun Budak
Journal:  Biometals       Date:  2022-08-20       Impact factor: 3.378

  1 in total

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