Extracellular superoxide dismutase is necessary to maintain renal blood flow during sepsis development

Detalhes bibliográficos
Autor(a) principal: Constantino, Larissa de Souza
Data de Publicação: 2017
Outros Autores: Galant, Leticia Selinger, Vuolo, Franciele Silva, Guarido, Karla Lorena, Kist, Luiza Wilges, Oliveira, Giovanna Medeiros Tavares de, Pasquali, Matheus Augusto de Bittencourt, Souza, Cláudio Teodoro de, Santos, José Eduardo da Silva, Bogo, Mauricio Reis, Moreira, Jose Claudio Fonseca, Ritter, Cristiane, Dal Pizzol, Felipe
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/198565
Resumo: Background: Extracellular superoxide dismutase (ECSOD) protects nitric oxide (NO) bioavailability by decreasing superoxide levels and preventing peroxynitrite generation, which is important in maintaining renal blood flow and in preventing acute kidney injury. However, the profile of ECSOD expression after sepsis is not fully understood. Therefore, we intended to evaluate the content and gene expression of superoxide dismutase (SOD) isoforms in the renal artery and their relation to renal blood flow. Methods: Sepsis was induced in Wistar rats by caecal ligation and perforation. Several times after sepsis induction, renal blood flow (12, 24 and 48 h); the renal arterial content of SOD isoforms, nitrotyrosine, endothelial and inducible nitric oxide synthase (e-NOS and i-NOS), and phosphorylated vasodilator-stimulated phosphoprotein (pVASP); and SOD activity (3, 6 and 12 h) were measured. The influence of a SOD inhibitor was also evaluated. Results: An increase in ECSOD content was associated with decreased 3-nitrotyrosine levels. These events were associated with an increase in pVASP content and maintenance of renal blood flow. Moreover, previous treatment with a SOD inhibitor increased nitrotyrosine content and reduced renal blood flow. Conclusions: ECSOD appears to have a major role in decreasing peroxynitrite formation in the renal artery during the early stages of sepsis development, and its application can be important in renal blood flow control and maintenance during septic insult.
id UFRGS-2_e084e0ff3482355c7c27d9c942017456
oai_identifier_str oai:www.lume.ufrgs.br:10183/198565
network_acronym_str UFRGS-2
network_name_str Repositório Institucional da UFRGS
repository_id_str
spelling Constantino, Larissa de SouzaGalant, Leticia SelingerVuolo, Franciele SilvaGuarido, Karla LorenaKist, Luiza WilgesOliveira, Giovanna Medeiros Tavares dePasquali, Matheus Augusto de BittencourtSouza, Cláudio Teodoro deSantos, José Eduardo da SilvaBogo, Mauricio ReisMoreira, Jose Claudio FonsecaRitter, CristianeDal Pizzol, Felipe2019-08-29T02:34:59Z20172197-425Xhttp://hdl.handle.net/10183/198565001098873Background: Extracellular superoxide dismutase (ECSOD) protects nitric oxide (NO) bioavailability by decreasing superoxide levels and preventing peroxynitrite generation, which is important in maintaining renal blood flow and in preventing acute kidney injury. However, the profile of ECSOD expression after sepsis is not fully understood. Therefore, we intended to evaluate the content and gene expression of superoxide dismutase (SOD) isoforms in the renal artery and their relation to renal blood flow. Methods: Sepsis was induced in Wistar rats by caecal ligation and perforation. Several times after sepsis induction, renal blood flow (12, 24 and 48 h); the renal arterial content of SOD isoforms, nitrotyrosine, endothelial and inducible nitric oxide synthase (e-NOS and i-NOS), and phosphorylated vasodilator-stimulated phosphoprotein (pVASP); and SOD activity (3, 6 and 12 h) were measured. The influence of a SOD inhibitor was also evaluated. Results: An increase in ECSOD content was associated with decreased 3-nitrotyrosine levels. These events were associated with an increase in pVASP content and maintenance of renal blood flow. Moreover, previous treatment with a SOD inhibitor increased nitrotyrosine content and reduced renal blood flow. Conclusions: ECSOD appears to have a major role in decreasing peroxynitrite formation in the renal artery during the early stages of sepsis development, and its application can be important in renal blood flow control and maintenance during septic insult.application/pdfengIntensive care medicine experimental. Heidelberg. Vol. 5 (Dec. 2017), 15, 12 p.SepseÁcido peroxinitrosoSuperóxido dismutaseSepsisAcute renal failureSuperoxideNitric oxideExtracellular superoxide dismutase is necessary to maintain renal blood flow during sepsis developmentEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001098873.pdf.txt001098873.pdf.txtExtracted Texttext/plain40861http://www.lume.ufrgs.br/bitstream/10183/198565/2/001098873.pdf.txtf93ab73b946048c1a5cd1e058f027789MD52ORIGINAL001098873.pdfTexto completo (inglês)application/pdf1169434http://www.lume.ufrgs.br/bitstream/10183/198565/1/001098873.pdfc1c0e982ecc024040609cc73e434246fMD5110183/1985652021-05-07 04:53:04.394342oai:www.lume.ufrgs.br:10183/198565Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-05-07T07:53:04Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Extracellular superoxide dismutase is necessary to maintain renal blood flow during sepsis development
title Extracellular superoxide dismutase is necessary to maintain renal blood flow during sepsis development
spellingShingle Extracellular superoxide dismutase is necessary to maintain renal blood flow during sepsis development
Constantino, Larissa de Souza
Sepse
Ácido peroxinitroso
Superóxido dismutase
Sepsis
Acute renal failure
Superoxide
Nitric oxide
title_short Extracellular superoxide dismutase is necessary to maintain renal blood flow during sepsis development
title_full Extracellular superoxide dismutase is necessary to maintain renal blood flow during sepsis development
title_fullStr Extracellular superoxide dismutase is necessary to maintain renal blood flow during sepsis development
title_full_unstemmed Extracellular superoxide dismutase is necessary to maintain renal blood flow during sepsis development
title_sort Extracellular superoxide dismutase is necessary to maintain renal blood flow during sepsis development
author Constantino, Larissa de Souza
author_facet Constantino, Larissa de Souza
Galant, Leticia Selinger
Vuolo, Franciele Silva
Guarido, Karla Lorena
Kist, Luiza Wilges
Oliveira, Giovanna Medeiros Tavares de
Pasquali, Matheus Augusto de Bittencourt
Souza, Cláudio Teodoro de
Santos, José Eduardo da Silva
Bogo, Mauricio Reis
Moreira, Jose Claudio Fonseca
Ritter, Cristiane
Dal Pizzol, Felipe
author_role author
author2 Galant, Leticia Selinger
Vuolo, Franciele Silva
Guarido, Karla Lorena
Kist, Luiza Wilges
Oliveira, Giovanna Medeiros Tavares de
Pasquali, Matheus Augusto de Bittencourt
Souza, Cláudio Teodoro de
Santos, José Eduardo da Silva
Bogo, Mauricio Reis
Moreira, Jose Claudio Fonseca
Ritter, Cristiane
Dal Pizzol, Felipe
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Constantino, Larissa de Souza
Galant, Leticia Selinger
Vuolo, Franciele Silva
Guarido, Karla Lorena
Kist, Luiza Wilges
Oliveira, Giovanna Medeiros Tavares de
Pasquali, Matheus Augusto de Bittencourt
Souza, Cláudio Teodoro de
Santos, José Eduardo da Silva
Bogo, Mauricio Reis
Moreira, Jose Claudio Fonseca
Ritter, Cristiane
Dal Pizzol, Felipe
dc.subject.por.fl_str_mv Sepse
Ácido peroxinitroso
Superóxido dismutase
topic Sepse
Ácido peroxinitroso
Superóxido dismutase
Sepsis
Acute renal failure
Superoxide
Nitric oxide
dc.subject.eng.fl_str_mv Sepsis
Acute renal failure
Superoxide
Nitric oxide
description Background: Extracellular superoxide dismutase (ECSOD) protects nitric oxide (NO) bioavailability by decreasing superoxide levels and preventing peroxynitrite generation, which is important in maintaining renal blood flow and in preventing acute kidney injury. However, the profile of ECSOD expression after sepsis is not fully understood. Therefore, we intended to evaluate the content and gene expression of superoxide dismutase (SOD) isoforms in the renal artery and their relation to renal blood flow. Methods: Sepsis was induced in Wistar rats by caecal ligation and perforation. Several times after sepsis induction, renal blood flow (12, 24 and 48 h); the renal arterial content of SOD isoforms, nitrotyrosine, endothelial and inducible nitric oxide synthase (e-NOS and i-NOS), and phosphorylated vasodilator-stimulated phosphoprotein (pVASP); and SOD activity (3, 6 and 12 h) were measured. The influence of a SOD inhibitor was also evaluated. Results: An increase in ECSOD content was associated with decreased 3-nitrotyrosine levels. These events were associated with an increase in pVASP content and maintenance of renal blood flow. Moreover, previous treatment with a SOD inhibitor increased nitrotyrosine content and reduced renal blood flow. Conclusions: ECSOD appears to have a major role in decreasing peroxynitrite formation in the renal artery during the early stages of sepsis development, and its application can be important in renal blood flow control and maintenance during septic insult.
publishDate 2017
dc.date.issued.fl_str_mv 2017
dc.date.accessioned.fl_str_mv 2019-08-29T02:34:59Z
dc.type.driver.fl_str_mv Estrangeiro
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://hdl.handle.net/10183/198565
dc.identifier.issn.pt_BR.fl_str_mv 2197-425X
dc.identifier.nrb.pt_BR.fl_str_mv 001098873
identifier_str_mv 2197-425X
001098873
url http://hdl.handle.net/10183/198565
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Intensive care medicine experimental. Heidelberg. Vol. 5 (Dec. 2017), 15, 12 p.
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Repositório Institucional da UFRGS
collection Repositório Institucional da UFRGS
bitstream.url.fl_str_mv http://www.lume.ufrgs.br/bitstream/10183/198565/2/001098873.pdf.txt
http://www.lume.ufrgs.br/bitstream/10183/198565/1/001098873.pdf
bitstream.checksum.fl_str_mv f93ab73b946048c1a5cd1e058f027789
c1c0e982ecc024040609cc73e434246f
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv
_version_ 1815447693087997952