Expression of Glutathione Peroxidase and Glutathione Reductase and Level of Free Radical Processes under Toxic Hepatitis in Rats

Correlation between intensity of free radical processes estimated by biochemiluminesce parameters, content of lipoperoxidation products, and changes of glutathione peroxidase (GP, EC 1.11.1.9) and glutathione reductase (GR, EC 1.6.4.2) activities at rats liver injury, after 12, 36, 70, 96, 110, and...

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Main Authors: Igor Y. Iskusnykh, Tatyana N. Popova, Aleksander A. Agarkov, Miguel Â. A. Pinheiro de Carvalho, Stanislav G. Rjevskiy
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Journal of Toxicology
Online Access:http://dx.doi.org/10.1155/2013/870628
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author Igor Y. Iskusnykh
Tatyana N. Popova
Aleksander A. Agarkov
Miguel Â. A. Pinheiro de Carvalho
Stanislav G. Rjevskiy
author_facet Igor Y. Iskusnykh
Tatyana N. Popova
Aleksander A. Agarkov
Miguel Â. A. Pinheiro de Carvalho
Stanislav G. Rjevskiy
author_sort Igor Y. Iskusnykh
collection DOAJ
description Correlation between intensity of free radical processes estimated by biochemiluminesce parameters, content of lipoperoxidation products, and changes of glutathione peroxidase (GP, EC 1.11.1.9) and glutathione reductase (GR, EC 1.6.4.2) activities at rats liver injury, after 12, 36, 70, 96, 110, and 125 hours & tetrachloromethane administration have been investigated. The histological examination of the liver sections of rats showed that prominent hepatocytes with marked vacuolisation and inflammatory cells which were arranged around the necrotic tissue are more at 96 h after exposure to CCl4. Moreover maximum increase in GR and GP activities, 2.1 and 2.5 times, respectively, was observed at 96 h after exposure to CCl4, what coincided with the maximum of free radical oxidation processes. Using a combination of reverse transcription and real-time polymerase chain reaction, expression of the glutathione peroxidase and glutathione reductase genes (Gpx1 and Gsr) was analyzed by the determination of their respective mRNAs in the rat liver tissue under toxic hepatitis conditions. The analyses of Gpx1 and Gsr expression revealed that the transcript levels increased in 2.5- and 3.0-folds, respectively. Western blot analysis revealed that the amounts of hepatic Gpx1 and Gsr proteins increased considerably after CCl4 administration. It can be proposed that the overexpression of these enzymes could be a mechanism of enhancement of hepatocytes tolerance to oxidative stress.
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spelling doaj-art-2aa122fade904ec886748a2ba3f990222025-02-03T01:26:20ZengWileyJournal of Toxicology1687-81911687-82052013-01-01201310.1155/2013/870628870628Expression of Glutathione Peroxidase and Glutathione Reductase and Level of Free Radical Processes under Toxic Hepatitis in RatsIgor Y. Iskusnykh0Tatyana N. Popova1Aleksander A. Agarkov2Miguel Â. A. Pinheiro de Carvalho3Stanislav G. Rjevskiy4Department of Medical Biochemistry and Microbiology, Voronezh State University, University Square 1, Voronezh 394006, RussiaDepartment of Medical Biochemistry and Microbiology, Voronezh State University, University Square 1, Voronezh 394006, RussiaDepartment of Medical Biochemistry and Microbiology, Voronezh State University, University Square 1, Voronezh 394006, RussiaISOPlexis Gene Bank, University of Madeira, Campus da Penteada, 9000-390 Funchal, PortugalDepartment of Medical Biochemistry and Microbiology, Voronezh State University, University Square 1, Voronezh 394006, RussiaCorrelation between intensity of free radical processes estimated by biochemiluminesce parameters, content of lipoperoxidation products, and changes of glutathione peroxidase (GP, EC 1.11.1.9) and glutathione reductase (GR, EC 1.6.4.2) activities at rats liver injury, after 12, 36, 70, 96, 110, and 125 hours & tetrachloromethane administration have been investigated. The histological examination of the liver sections of rats showed that prominent hepatocytes with marked vacuolisation and inflammatory cells which were arranged around the necrotic tissue are more at 96 h after exposure to CCl4. Moreover maximum increase in GR and GP activities, 2.1 and 2.5 times, respectively, was observed at 96 h after exposure to CCl4, what coincided with the maximum of free radical oxidation processes. Using a combination of reverse transcription and real-time polymerase chain reaction, expression of the glutathione peroxidase and glutathione reductase genes (Gpx1 and Gsr) was analyzed by the determination of their respective mRNAs in the rat liver tissue under toxic hepatitis conditions. The analyses of Gpx1 and Gsr expression revealed that the transcript levels increased in 2.5- and 3.0-folds, respectively. Western blot analysis revealed that the amounts of hepatic Gpx1 and Gsr proteins increased considerably after CCl4 administration. It can be proposed that the overexpression of these enzymes could be a mechanism of enhancement of hepatocytes tolerance to oxidative stress.http://dx.doi.org/10.1155/2013/870628
spellingShingle Igor Y. Iskusnykh
Tatyana N. Popova
Aleksander A. Agarkov
Miguel Â. A. Pinheiro de Carvalho
Stanislav G. Rjevskiy
Expression of Glutathione Peroxidase and Glutathione Reductase and Level of Free Radical Processes under Toxic Hepatitis in Rats
Journal of Toxicology
title Expression of Glutathione Peroxidase and Glutathione Reductase and Level of Free Radical Processes under Toxic Hepatitis in Rats
title_full Expression of Glutathione Peroxidase and Glutathione Reductase and Level of Free Radical Processes under Toxic Hepatitis in Rats
title_fullStr Expression of Glutathione Peroxidase and Glutathione Reductase and Level of Free Radical Processes under Toxic Hepatitis in Rats
title_full_unstemmed Expression of Glutathione Peroxidase and Glutathione Reductase and Level of Free Radical Processes under Toxic Hepatitis in Rats
title_short Expression of Glutathione Peroxidase and Glutathione Reductase and Level of Free Radical Processes under Toxic Hepatitis in Rats
title_sort expression of glutathione peroxidase and glutathione reductase and level of free radical processes under toxic hepatitis in rats
url http://dx.doi.org/10.1155/2013/870628
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