Extracellular superoxide dismutase is necessary to maintain renal blood flow during sepsis development
Autor(a) principal: | |
---|---|
Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , , , , |
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 |