Diethylcarbamazine Reduces Chronic Inflammation and Fibrosis in Carbon Tetrachloride- (CCl4-) Induced Liver Injury in Mice

This study investigated the anti-inflammatory effects of DEC on the CCl4-induced hepatotoxicity in C57BL/6 mice. Chronic inflammation was induced by i.p. administration of CCl4 0.5 μL/g of body weight through two injections a week for 6 weeks. DEC (50 mg/kg) was administered by gavage for 12 days be...

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Main Authors: Sura Wanessa Santos Rocha, Maria Eduarda Rocha de França, Gabriel Barros Rodrigues, Karla Patrícia Sousa Barbosa, Ana Karolina Santana Nunes, André Filipe Pastor, Anne Gabrielle Vasconcelos Oliveira, Wilma Helena Oliveira, Rayana Leal Almeida Luna, Christina Alves Peixoto
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2014/696383
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author Sura Wanessa Santos Rocha
Maria Eduarda Rocha de França
Gabriel Barros Rodrigues
Karla Patrícia Sousa Barbosa
Ana Karolina Santana Nunes
André Filipe Pastor
Anne Gabrielle Vasconcelos Oliveira
Wilma Helena Oliveira
Rayana Leal Almeida Luna
Christina Alves Peixoto
author_facet Sura Wanessa Santos Rocha
Maria Eduarda Rocha de França
Gabriel Barros Rodrigues
Karla Patrícia Sousa Barbosa
Ana Karolina Santana Nunes
André Filipe Pastor
Anne Gabrielle Vasconcelos Oliveira
Wilma Helena Oliveira
Rayana Leal Almeida Luna
Christina Alves Peixoto
author_sort Sura Wanessa Santos Rocha
collection DOAJ
description This study investigated the anti-inflammatory effects of DEC on the CCl4-induced hepatotoxicity in C57BL/6 mice. Chronic inflammation was induced by i.p. administration of CCl4 0.5 μL/g of body weight through two injections a week for 6 weeks. DEC (50 mg/kg) was administered by gavage for 12 days before finishing the CCl4 induction. Histological analyses of the DEC-treated group exhibited reduced inflammatory process and prevented liver necrosis and fibrosis. Immunohistochemical and immunofluorescence analyses of the DEC-treated group showed reduced COX-2, IL1β, MDA, TGF-β, and αSMA immunopositivity, besides exhibiting decreased IL1β, COX-2, NFκB, IFNγ, and TGFβ expressions in the western blot analysis. The DEC group enhanced significantly the IL-10 expression. The reduction of hepatic injury in the DEC-treated group was confirmed by the COX-2 and iNOS mRNA expression levels. Based on the results of the present study, DEC can be used as a potential anti-inflammatory drug for chronic hepatic inflammation.
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institution Kabale University
issn 0962-9351
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language English
publishDate 2014-01-01
publisher Wiley
record_format Article
series Mediators of Inflammation
spelling doaj-art-108a0b36a6494955acaabd5a931864b22025-02-03T01:31:16ZengWileyMediators of Inflammation0962-93511466-18612014-01-01201410.1155/2014/696383696383Diethylcarbamazine Reduces Chronic Inflammation and Fibrosis in Carbon Tetrachloride- (CCl4-) Induced Liver Injury in MiceSura Wanessa Santos Rocha0Maria Eduarda Rocha de França1Gabriel Barros Rodrigues2Karla Patrícia Sousa Barbosa3Ana Karolina Santana Nunes4André Filipe Pastor5Anne Gabrielle Vasconcelos Oliveira6Wilma Helena Oliveira7Rayana Leal Almeida Luna8Christina Alves Peixoto9Laboratory of Ultrastructure, Aggeu Magalhães Research Center (CPqAM), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50740-465 Recife, PE, BrazilLaboratory of Ultrastructure, Aggeu Magalhães Research Center (CPqAM), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50740-465 Recife, PE, BrazilLaboratory of Ultrastructure, Aggeu Magalhães Research Center (CPqAM), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50740-465 Recife, PE, BrazilLaboratory of Ultrastructure, Aggeu Magalhães Research Center (CPqAM), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50740-465 Recife, PE, BrazilLaboratory of Ultrastructure, Aggeu Magalhães Research Center (CPqAM), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50740-465 Recife, PE, BrazilLaboratory of Virology and Experimental Therapy, Aggeu Magalhães Research Center (CPqAM), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50740-465 Recife, PE, BrazilLaboratory of Microscopy and Microanalisis, Northeastern Center for Strategic Technologies (CETENE), Avenida Professor Luiz Freire, Cidade Universitária, 50740-540 Recife, PE, BrazilLaboratory of Ultrastructure, Aggeu Magalhães Research Center (CPqAM), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50740-465 Recife, PE, BrazilLaboratory of Ultrastructure, Aggeu Magalhães Research Center (CPqAM), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50740-465 Recife, PE, BrazilLaboratory of Ultrastructure, Aggeu Magalhães Research Center (CPqAM), Avenida Professor Moraes Rego, s/n, Cidade Universitária, 50740-465 Recife, PE, BrazilThis study investigated the anti-inflammatory effects of DEC on the CCl4-induced hepatotoxicity in C57BL/6 mice. Chronic inflammation was induced by i.p. administration of CCl4 0.5 μL/g of body weight through two injections a week for 6 weeks. DEC (50 mg/kg) was administered by gavage for 12 days before finishing the CCl4 induction. Histological analyses of the DEC-treated group exhibited reduced inflammatory process and prevented liver necrosis and fibrosis. Immunohistochemical and immunofluorescence analyses of the DEC-treated group showed reduced COX-2, IL1β, MDA, TGF-β, and αSMA immunopositivity, besides exhibiting decreased IL1β, COX-2, NFκB, IFNγ, and TGFβ expressions in the western blot analysis. The DEC group enhanced significantly the IL-10 expression. The reduction of hepatic injury in the DEC-treated group was confirmed by the COX-2 and iNOS mRNA expression levels. Based on the results of the present study, DEC can be used as a potential anti-inflammatory drug for chronic hepatic inflammation.http://dx.doi.org/10.1155/2014/696383
spellingShingle Sura Wanessa Santos Rocha
Maria Eduarda Rocha de França
Gabriel Barros Rodrigues
Karla Patrícia Sousa Barbosa
Ana Karolina Santana Nunes
André Filipe Pastor
Anne Gabrielle Vasconcelos Oliveira
Wilma Helena Oliveira
Rayana Leal Almeida Luna
Christina Alves Peixoto
Diethylcarbamazine Reduces Chronic Inflammation and Fibrosis in Carbon Tetrachloride- (CCl4-) Induced Liver Injury in Mice
Mediators of Inflammation
title Diethylcarbamazine Reduces Chronic Inflammation and Fibrosis in Carbon Tetrachloride- (CCl4-) Induced Liver Injury in Mice
title_full Diethylcarbamazine Reduces Chronic Inflammation and Fibrosis in Carbon Tetrachloride- (CCl4-) Induced Liver Injury in Mice
title_fullStr Diethylcarbamazine Reduces Chronic Inflammation and Fibrosis in Carbon Tetrachloride- (CCl4-) Induced Liver Injury in Mice
title_full_unstemmed Diethylcarbamazine Reduces Chronic Inflammation and Fibrosis in Carbon Tetrachloride- (CCl4-) Induced Liver Injury in Mice
title_short Diethylcarbamazine Reduces Chronic Inflammation and Fibrosis in Carbon Tetrachloride- (CCl4-) Induced Liver Injury in Mice
title_sort diethylcarbamazine reduces chronic inflammation and fibrosis in carbon tetrachloride ccl4 induced liver injury in mice
url http://dx.doi.org/10.1155/2014/696383
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