Literature DB >> 24838005

Rat liver antioxidant response to iron and copper overloads.

Rosario Musacco-Sebio1, Christian Saporito-Magriñá1, Jimena Semprine1, Horacio Torti2, Nidia Ferrarotti3, Mauricio Castro-Parodi4, Alicia Damiano4, Alberto Boveris1, Marisa G Repetto5.   

Abstract

The rat liver antioxidant response to Fe and Cu overloads (0-60mg/kg) was studied. Dose- and time-responses were determined and summarized by t1/2 and C50, the time and the liver metal content for half maximal oxidative responses. Liver GSH (reduced glutathione) and GSSG (glutathione disulfide) were determined. The GSH content and the GSH/GSSG ratio markedly decreased after Fe (58-66%) and Cu (79-81%) loads, with t1/2 of 4.0 and 2.0h. The C50 were in a similar range for all the indicators (110-124μgFe/g and 40-50μgCu/g) and suggest a unique free-radical mediated process. Hydrophilic antioxidants markedly decreased after Fe and Cu (60-75%; t1/2: 4.5 and 4.0h). Lipophilic antioxidants were also decreased (30-92%; t1/2: 7.0 and 5.5h) after Fe and Cu. Superoxide dismutase (SOD) activities (Cu,Zn-SOD and Mn-SOD) and protein expression were adaptively increased after metal overloads (Cu,Zn-SOD: t1/2: 8-8.5h and Mn-SOD: t1/2: 8.5-8.0h). Catalase activity was increased after Fe (65%; t1/2: 8.5h) and decreased after Cu (26%; t1/2: 8.0h), whereas catalase expression was increased after Fe and decreased after Cu overloads. Glutathione peroxidase activity decreased after metal loads by 22-39% with a t1/2 of 4.5h and with unchanged protein expression. GSH is the main and fastest responder antioxidant in Fe and Cu overloads. The results indicate that thiol (SH) content and antioxidant enzyme activities are central to the antioxidant defense in the oxidative stress and damage after Fe and Cu overloads.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Antioxidants; Copper; Glutathione; Iron; Liver chemiluminescence; Oxidative damage

Mesh:

Substances:

Year:  2014        PMID: 24838005     DOI: 10.1016/j.jinorgbio.2014.04.014

Source DB:  PubMed          Journal:  J Inorg Biochem        ISSN: 0162-0134            Impact factor:   4.155


  5 in total

1.  Oxidative damage induced by copper in mouse primary hepatocytes by single-cell analysis.

Authors:  Mingyang Jing; Yang Liu; Wei Song; Yunxing Yan; Wenbao Yan; Rutao Liu
Journal:  Environ Sci Pollut Res Int       Date:  2015-09-11       Impact factor: 4.223

2.  Nitric oxide, chronic iron and copper overloads and regulation of redox homeostasis in rat liver.

Authors:  Fabiana Lairion; Christian Saporito-Magriñá; Rosario Musacco-Sebio; Julian Fuda; Horacio Torti; Marisa Gabriela Repetto
Journal:  J Biol Inorg Chem       Date:  2021-11-17       Impact factor: 3.358

3.  Biochemical regulatory processes in the control of oxidants and antioxidants production in the brain of rats with iron and copper chronic overloads.

Authors:  Christian Saporito-Magriñá; Fabiana Lairion; Rosario Musacco-Sebio; Julian Fuda; Horacio Torti; Marisa Gabriela Repetto
Journal:  J Biol Inorg Chem       Date:  2022-09-29       Impact factor: 3.862

Review 4.  Oxidative Stress and Inflammation in Hepatic Diseases: Therapeutic Possibilities of N-Acetylcysteine.

Authors:  Kívia Queiroz de Andrade; Fabiana Andréa Moura; John Marques dos Santos; Orlando Roberto Pimentel de Araújo; Juliana Célia de Farias Santos; Marília Oliveira Fonseca Goulart
Journal:  Int J Mol Sci       Date:  2015-12-18       Impact factor: 5.923

5.  Protective Mechanism of Gandou Decoction in a Copper-Laden Hepatolenticular Degeneration Model: In Vitro Pharmacology and Cell Metabolomics.

Authors:  Fengxia Yin; Mengnan Nian; Na Wang; Hongfei Wu; Huan Wu; Wenchen Zhao; Shijian Cao; Peng Wu; An Zhou
Journal:  Front Pharmacol       Date:  2022-03-23       Impact factor: 5.810

  5 in total

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