The combination of atorvastatin and ethanol is not more hepatotoxic to rats than the administration of each drug alone
Autor(a) principal: | |
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Data de Publicação: | 2007 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S0100-879X2007000300009 http://repositorio.unifesp.br/handle/11600/3590 |
Resumo: | Animal studies and premarketing clinical trials have revealed hepatotoxicity of statins, primarily minor elevations in serum alanine aminotransferase levels. The combined chronic use of medicines and eventual ethanol abuse are common and may present a synergistic action regarding liver injury. Our objective was to study the effect of the chronic use of atorvastatin associated with acute ethanol administration on the liver in a rat model. One group of rats was treated daily for 5 days a week for 2 months with 0.8 mg/kg atorvastatin by gavage. At the end of the treatment the livers were perfused with 72 mM ethanol for 60 min. Control groups (at least 4 animals in each group) consisted of a group of 2-month-old male Wistar EPM-1 rats exposed to 10% ethanol (v/v) ad libitum replacing water for 2 months, followed by perfusion of the liver with 61 nM atorvastatin for 60 min, and a group of animals without chronic ethanol treatment whose livers were perfused with atorvastatin and/or ethanol. The combination of atorvastatin with ethanol did not increase the release of injury marker enzymes (alanine aminotransferase, aspartate aminotransferase, and lactic dehydrogenase) from the liver and no change in liver function markers (bromosulfophthalein clearance, and oxygen consumption) was observed. Our results suggest that the combination of atorvastatin with ethanol is not more hepatotoxic than the separate use of each substance. |
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The combination of atorvastatin and ethanol is not more hepatotoxic to rats than the administration of each drug aloneAtorvastatinLiver injuryHepatotoxicAlcoholAnimal studies and premarketing clinical trials have revealed hepatotoxicity of statins, primarily minor elevations in serum alanine aminotransferase levels. The combined chronic use of medicines and eventual ethanol abuse are common and may present a synergistic action regarding liver injury. Our objective was to study the effect of the chronic use of atorvastatin associated with acute ethanol administration on the liver in a rat model. One group of rats was treated daily for 5 days a week for 2 months with 0.8 mg/kg atorvastatin by gavage. At the end of the treatment the livers were perfused with 72 mM ethanol for 60 min. Control groups (at least 4 animals in each group) consisted of a group of 2-month-old male Wistar EPM-1 rats exposed to 10% ethanol (v/v) ad libitum replacing water for 2 months, followed by perfusion of the liver with 61 nM atorvastatin for 60 min, and a group of animals without chronic ethanol treatment whose livers were perfused with atorvastatin and/or ethanol. The combination of atorvastatin with ethanol did not increase the release of injury marker enzymes (alanine aminotransferase, aspartate aminotransferase, and lactic dehydrogenase) from the liver and no change in liver function markers (bromosulfophthalein clearance, and oxygen consumption) was observed. Our results suggest that the combination of atorvastatin with ethanol is not more hepatotoxic than the separate use of each substance.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Departamento de BioquímicaUniversidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Departamento de MedicinaUNIFESP, EPM, Depto. de BioquímicaUNIFESP, EPM, Depto. de MedicinaSciELOAssociação Brasileira de Divulgação CientíficaUniversidade Federal de São Paulo (UNIFESP)Ito, Daniel Takeshi [UNIFESP]Molina, Hercilia Maris [UNIFESP]Andriolo, Adagmar [UNIFESP]Borges, Durval Rosa [UNIFESP]2015-06-14T13:36:47Z2015-06-14T13:36:47Z2007-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion343-348application/pdfhttp://dx.doi.org/10.1590/S0100-879X2007000300009Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 40, n. 3, p. 343-348, 2007.10.1590/S0100-879X2007000300009S0100-879X2007000300009.pdf0100-879XS0100-879X2007000300009http://repositorio.unifesp.br/handle/11600/3590WOS:000244667700009engBrazilian Journal of Medical and Biological Researchinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-05T23:20:48Zoai:repositorio.unifesp.br/:11600/3590Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-05T23:20:48Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
The combination of atorvastatin and ethanol is not more hepatotoxic to rats than the administration of each drug alone |
title |
The combination of atorvastatin and ethanol is not more hepatotoxic to rats than the administration of each drug alone |
spellingShingle |
The combination of atorvastatin and ethanol is not more hepatotoxic to rats than the administration of each drug alone Ito, Daniel Takeshi [UNIFESP] Atorvastatin Liver injury Hepatotoxic Alcohol |
title_short |
The combination of atorvastatin and ethanol is not more hepatotoxic to rats than the administration of each drug alone |
title_full |
The combination of atorvastatin and ethanol is not more hepatotoxic to rats than the administration of each drug alone |
title_fullStr |
The combination of atorvastatin and ethanol is not more hepatotoxic to rats than the administration of each drug alone |
title_full_unstemmed |
The combination of atorvastatin and ethanol is not more hepatotoxic to rats than the administration of each drug alone |
title_sort |
The combination of atorvastatin and ethanol is not more hepatotoxic to rats than the administration of each drug alone |
author |
Ito, Daniel Takeshi [UNIFESP] |
author_facet |
Ito, Daniel Takeshi [UNIFESP] Molina, Hercilia Maris [UNIFESP] Andriolo, Adagmar [UNIFESP] Borges, Durval Rosa [UNIFESP] |
author_role |
author |
author2 |
Molina, Hercilia Maris [UNIFESP] Andriolo, Adagmar [UNIFESP] Borges, Durval Rosa [UNIFESP] |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Ito, Daniel Takeshi [UNIFESP] Molina, Hercilia Maris [UNIFESP] Andriolo, Adagmar [UNIFESP] Borges, Durval Rosa [UNIFESP] |
dc.subject.por.fl_str_mv |
Atorvastatin Liver injury Hepatotoxic Alcohol |
topic |
Atorvastatin Liver injury Hepatotoxic Alcohol |
description |
Animal studies and premarketing clinical trials have revealed hepatotoxicity of statins, primarily minor elevations in serum alanine aminotransferase levels. The combined chronic use of medicines and eventual ethanol abuse are common and may present a synergistic action regarding liver injury. Our objective was to study the effect of the chronic use of atorvastatin associated with acute ethanol administration on the liver in a rat model. One group of rats was treated daily for 5 days a week for 2 months with 0.8 mg/kg atorvastatin by gavage. At the end of the treatment the livers were perfused with 72 mM ethanol for 60 min. Control groups (at least 4 animals in each group) consisted of a group of 2-month-old male Wistar EPM-1 rats exposed to 10% ethanol (v/v) ad libitum replacing water for 2 months, followed by perfusion of the liver with 61 nM atorvastatin for 60 min, and a group of animals without chronic ethanol treatment whose livers were perfused with atorvastatin and/or ethanol. The combination of atorvastatin with ethanol did not increase the release of injury marker enzymes (alanine aminotransferase, aspartate aminotransferase, and lactic dehydrogenase) from the liver and no change in liver function markers (bromosulfophthalein clearance, and oxygen consumption) was observed. Our results suggest that the combination of atorvastatin with ethanol is not more hepatotoxic than the separate use of each substance. |
publishDate |
2007 |
dc.date.none.fl_str_mv |
2007-03-01 2015-06-14T13:36:47Z 2015-06-14T13:36:47Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S0100-879X2007000300009 Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 40, n. 3, p. 343-348, 2007. 10.1590/S0100-879X2007000300009 S0100-879X2007000300009.pdf 0100-879X S0100-879X2007000300009 http://repositorio.unifesp.br/handle/11600/3590 WOS:000244667700009 |
url |
http://dx.doi.org/10.1590/S0100-879X2007000300009 http://repositorio.unifesp.br/handle/11600/3590 |
identifier_str_mv |
Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 40, n. 3, p. 343-348, 2007. 10.1590/S0100-879X2007000300009 S0100-879X2007000300009.pdf 0100-879X S0100-879X2007000300009 WOS:000244667700009 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Brazilian Journal of Medical and Biological Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
343-348 application/pdf |
dc.publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268305532256256 |