Endothelial, renal and hepatic variables in wistar rats treated with Vancomycin

Detalhes bibliográficos
Autor(a) principal: BRUNIERA,FELIPE R.
Data de Publicação: 2014
Outros Autores: FERREIRA,FELIPE M., SAVIOLI,LUIZ R.M., BACCI,MARCELO R., FEDER,DAVID, PEREIRA,EDIMAR C., PEDREIRA,MAVILDE L.G., PETERLINI,MARIA A.S., PERAZZO,FÁBIO F., AZZALIS,LIGIA A., ROSA,PAULO C.P., JUNQUEIRA,VIRGINIA B.C., SATO,MONICA A., FONSECA,FERNANDO L.A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Anais da Academia Brasileira de Ciências (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652014000401963
Resumo: Vancomycin (VCM) is indicated in combat against Gram-positive infections, but it is not considered a first-choice drug because of its adverse effects. It is believed that oxidative stress is the primary mechanism of endothelial injury and the consequent VCM toxicity, which varies from phlebitis to nephrotoxicity. Moreover, dose recommendations, dilution, rates and types of infusion are still controversial. The aim of this study was to determine the effect of different VCM dilutions in endothelial, liver and kidney injuries by biochemical parameters and histopathological analysis. Wistar rats were randomly divided into six groups and subjected to femoral vein cannulation for drug administration. Control groups received 0.9 ml of saline and the others received VCM (10mg/Kg/day) at dilutions of 5.0 and 10.0 mg/mL for 3 and 7 days. Homocysteine, hs-CRP, AST, ALT, GGT, urea, creatinine, lycopene, alpha-tocopherol, beta-carotene and retinol were analyzed. Kidney, liver and cannulated femoral vein fragments were collected.This study showed alterations in ALT which featured hepatotoxicity. However, drug dilutions were not able to show changes in other biochemical parameters. In contrast, kidney and endothelium pathological changes were observed. More studies are needed to characterize VCM induced kidney and endothelium toxicity and biochemical markers able to show such morphological modifications.
id ABC-1_dba6d09d72d3a433602815eff48cd7eb
oai_identifier_str oai:scielo:S0001-37652014000401963
network_acronym_str ABC-1
network_name_str Anais da Academia Brasileira de Ciências (Online)
repository_id_str
spelling Endothelial, renal and hepatic variables in wistar rats treated with VancomycinVancomycinacute kidney injuryoxidative stresshepatotoxicityendothelial injuryVancomycin (VCM) is indicated in combat against Gram-positive infections, but it is not considered a first-choice drug because of its adverse effects. It is believed that oxidative stress is the primary mechanism of endothelial injury and the consequent VCM toxicity, which varies from phlebitis to nephrotoxicity. Moreover, dose recommendations, dilution, rates and types of infusion are still controversial. The aim of this study was to determine the effect of different VCM dilutions in endothelial, liver and kidney injuries by biochemical parameters and histopathological analysis. Wistar rats were randomly divided into six groups and subjected to femoral vein cannulation for drug administration. Control groups received 0.9 ml of saline and the others received VCM (10mg/Kg/day) at dilutions of 5.0 and 10.0 mg/mL for 3 and 7 days. Homocysteine, hs-CRP, AST, ALT, GGT, urea, creatinine, lycopene, alpha-tocopherol, beta-carotene and retinol were analyzed. Kidney, liver and cannulated femoral vein fragments were collected.This study showed alterations in ALT which featured hepatotoxicity. However, drug dilutions were not able to show changes in other biochemical parameters. In contrast, kidney and endothelium pathological changes were observed. More studies are needed to characterize VCM induced kidney and endothelium toxicity and biochemical markers able to show such morphological modifications.Academia Brasileira de Ciências2014-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652014000401963Anais da Academia Brasileira de Ciências v.86 n.4 2014reponame:Anais da Academia Brasileira de Ciências (Online)instname:Academia Brasileira de Ciências (ABC)instacron:ABC10.1590/0001-3765201420140204info:eu-repo/semantics/openAccessBRUNIERA,FELIPE R.FERREIRA,FELIPE M.SAVIOLI,LUIZ R.M.BACCI,MARCELO R.FEDER,DAVIDPEREIRA,EDIMAR C.PEDREIRA,MAVILDE L.G.PETERLINI,MARIA A.S.PERAZZO,FÁBIO F.AZZALIS,LIGIA A.ROSA,PAULO C.P.JUNQUEIRA,VIRGINIA B.C.SATO,MONICA A.FONSECA,FERNANDO L.A.eng2015-10-27T00:00:00Zoai:scielo:S0001-37652014000401963Revistahttp://www.scielo.br/aabchttps://old.scielo.br/oai/scielo-oai.php||aabc@abc.org.br1678-26900001-3765opendoar:2015-10-27T00:00Anais da Academia Brasileira de Ciências (Online) - Academia Brasileira de Ciências (ABC)false
dc.title.none.fl_str_mv Endothelial, renal and hepatic variables in wistar rats treated with Vancomycin
title Endothelial, renal and hepatic variables in wistar rats treated with Vancomycin
spellingShingle Endothelial, renal and hepatic variables in wistar rats treated with Vancomycin
BRUNIERA,FELIPE R.
Vancomycin
acute kidney injury
oxidative stress
hepatotoxicity
endothelial injury
title_short Endothelial, renal and hepatic variables in wistar rats treated with Vancomycin
title_full Endothelial, renal and hepatic variables in wistar rats treated with Vancomycin
title_fullStr Endothelial, renal and hepatic variables in wistar rats treated with Vancomycin
title_full_unstemmed Endothelial, renal and hepatic variables in wistar rats treated with Vancomycin
title_sort Endothelial, renal and hepatic variables in wistar rats treated with Vancomycin
author BRUNIERA,FELIPE R.
author_facet BRUNIERA,FELIPE R.
FERREIRA,FELIPE M.
SAVIOLI,LUIZ R.M.
BACCI,MARCELO R.
FEDER,DAVID
PEREIRA,EDIMAR C.
PEDREIRA,MAVILDE L.G.
PETERLINI,MARIA A.S.
PERAZZO,FÁBIO F.
AZZALIS,LIGIA A.
ROSA,PAULO C.P.
JUNQUEIRA,VIRGINIA B.C.
SATO,MONICA A.
FONSECA,FERNANDO L.A.
author_role author
author2 FERREIRA,FELIPE M.
SAVIOLI,LUIZ R.M.
BACCI,MARCELO R.
FEDER,DAVID
PEREIRA,EDIMAR C.
PEDREIRA,MAVILDE L.G.
PETERLINI,MARIA A.S.
PERAZZO,FÁBIO F.
AZZALIS,LIGIA A.
ROSA,PAULO C.P.
JUNQUEIRA,VIRGINIA B.C.
SATO,MONICA A.
FONSECA,FERNANDO L.A.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv BRUNIERA,FELIPE R.
FERREIRA,FELIPE M.
SAVIOLI,LUIZ R.M.
BACCI,MARCELO R.
FEDER,DAVID
PEREIRA,EDIMAR C.
PEDREIRA,MAVILDE L.G.
PETERLINI,MARIA A.S.
PERAZZO,FÁBIO F.
AZZALIS,LIGIA A.
ROSA,PAULO C.P.
JUNQUEIRA,VIRGINIA B.C.
SATO,MONICA A.
FONSECA,FERNANDO L.A.
dc.subject.por.fl_str_mv Vancomycin
acute kidney injury
oxidative stress
hepatotoxicity
endothelial injury
topic Vancomycin
acute kidney injury
oxidative stress
hepatotoxicity
endothelial injury
description Vancomycin (VCM) is indicated in combat against Gram-positive infections, but it is not considered a first-choice drug because of its adverse effects. It is believed that oxidative stress is the primary mechanism of endothelial injury and the consequent VCM toxicity, which varies from phlebitis to nephrotoxicity. Moreover, dose recommendations, dilution, rates and types of infusion are still controversial. The aim of this study was to determine the effect of different VCM dilutions in endothelial, liver and kidney injuries by biochemical parameters and histopathological analysis. Wistar rats were randomly divided into six groups and subjected to femoral vein cannulation for drug administration. Control groups received 0.9 ml of saline and the others received VCM (10mg/Kg/day) at dilutions of 5.0 and 10.0 mg/mL for 3 and 7 days. Homocysteine, hs-CRP, AST, ALT, GGT, urea, creatinine, lycopene, alpha-tocopherol, beta-carotene and retinol were analyzed. Kidney, liver and cannulated femoral vein fragments were collected.This study showed alterations in ALT which featured hepatotoxicity. However, drug dilutions were not able to show changes in other biochemical parameters. In contrast, kidney and endothelium pathological changes were observed. More studies are needed to characterize VCM induced kidney and endothelium toxicity and biochemical markers able to show such morphological modifications.
publishDate 2014
dc.date.none.fl_str_mv 2014-12-01
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://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652014000401963
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652014000401963
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/0001-3765201420140204
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Academia Brasileira de Ciências
publisher.none.fl_str_mv Academia Brasileira de Ciências
dc.source.none.fl_str_mv Anais da Academia Brasileira de Ciências v.86 n.4 2014
reponame:Anais da Academia Brasileira de Ciências (Online)
instname:Academia Brasileira de Ciências (ABC)
instacron:ABC
instname_str Academia Brasileira de Ciências (ABC)
instacron_str ABC
institution ABC
reponame_str Anais da Academia Brasileira de Ciências (Online)
collection Anais da Academia Brasileira de Ciências (Online)
repository.name.fl_str_mv Anais da Academia Brasileira de Ciências (Online) - Academia Brasileira de Ciências (ABC)
repository.mail.fl_str_mv ||aabc@abc.org.br
_version_ 1754302860380602368