Effect of atenolol pre-treatment in heart damage in a model of intestinal ischemia-reperfusion

Detalhes bibliográficos
Autor(a) principal: Okada,Mieko
Data de Publicação: 2017
Outros Autores: Falcão,Luiz Fernando Reis, Ferez,David, Martins,José Luiz, Errante,Paolo Ruggero, Rodrigues,Francisco Sandro Menezes, Caricati-Neto,Afonso, Marinho,Márcia, Fenelon,Guilherme, Oliveira-Júnior,Itamar Souza
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Acta Cirúrgica Brasileira (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86502017001100964
Resumo: Abstract Purpose: To investigate the effects of atenolol in inflammatory mediator and oxidative stress in a myocardial injury by intestinal ischemia/reperfusion in rat model. Methods: Adult Wistar male rats were randomly (n=8), anesthetized and divided in: Sham: submitted to operation only; group SS+IR: intravenous saline infusion following superior mesenteric artery occlusion during 60 minutes (ischemia) and open for 120 minutes (reperfusion); group AT+IR: intravenous atenolol infusion (2 mg/kg) following superior mesenteric artery occlusion during 60 minutes (ischemia) and open for 120 minutes (reperfusion); and group AT+I+AT+R: intravenous atenolol infusion following superior mesenteric artery occlusion during 60 minutes (ischemia) and in the time 45 minutes other atenolol doses were administrated and the artery was open for 120 minutes (reperfusion), all animals were submitted to muscular relaxation for mechanical ventilation. In the end of experiment the animals were euthanized and the hearts tissue were morphology analyzed by histology and malondialdehyde by ELISA, and the plasma were analyzed for tumor necrosis factor-alpha by ELISA. Results: The group SS+IR demonstrated the higher malondialdehyde levels when compared with the atenolol treated-groups (p=0.001) in the heart tissue. The tumor necrosis factor-alpha level in plasma decrease in the treated groups when compared with SS+IR group (p=0.001). Histology analyses demonstrate pyknosis, edema, cellular vacuolization, presence of inflammatory infiltrate and band contraction in the heart tissue of the rats. Conclusion: Atenolol significantly reduce the degree of cardiac damage after intestinal ischemia-reperfusion.
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spelling Effect of atenolol pre-treatment in heart damage in a model of intestinal ischemia-reperfusionAdrenergic AntagonistsAtenololIschemiaReperfusionCytokinesOxidative StressRats.Abstract Purpose: To investigate the effects of atenolol in inflammatory mediator and oxidative stress in a myocardial injury by intestinal ischemia/reperfusion in rat model. Methods: Adult Wistar male rats were randomly (n=8), anesthetized and divided in: Sham: submitted to operation only; group SS+IR: intravenous saline infusion following superior mesenteric artery occlusion during 60 minutes (ischemia) and open for 120 minutes (reperfusion); group AT+IR: intravenous atenolol infusion (2 mg/kg) following superior mesenteric artery occlusion during 60 minutes (ischemia) and open for 120 minutes (reperfusion); and group AT+I+AT+R: intravenous atenolol infusion following superior mesenteric artery occlusion during 60 minutes (ischemia) and in the time 45 minutes other atenolol doses were administrated and the artery was open for 120 minutes (reperfusion), all animals were submitted to muscular relaxation for mechanical ventilation. In the end of experiment the animals were euthanized and the hearts tissue were morphology analyzed by histology and malondialdehyde by ELISA, and the plasma were analyzed for tumor necrosis factor-alpha by ELISA. Results: The group SS+IR demonstrated the higher malondialdehyde levels when compared with the atenolol treated-groups (p=0.001) in the heart tissue. The tumor necrosis factor-alpha level in plasma decrease in the treated groups when compared with SS+IR group (p=0.001). Histology analyses demonstrate pyknosis, edema, cellular vacuolization, presence of inflammatory infiltrate and band contraction in the heart tissue of the rats. Conclusion: Atenolol significantly reduce the degree of cardiac damage after intestinal ischemia-reperfusion.Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia2017-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86502017001100964Acta Cirúrgica Brasileira v.32 n.11 2017reponame:Acta Cirúrgica Brasileira (Online)instname:Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia (SBDPC)instacron:SBDPC10.1590/s0102-865020170110000008info:eu-repo/semantics/openAccessOkada,MiekoFalcão,Luiz Fernando ReisFerez,DavidMartins,José LuizErrante,Paolo RuggeroRodrigues,Francisco Sandro MenezesCaricati-Neto,AfonsoMarinho,MárciaFenelon,GuilhermeOliveira-Júnior,Itamar Souzaeng2017-12-19T00:00:00Zoai:scielo:S0102-86502017001100964Revistahttps://www.bvs-vet.org.br/vetindex/periodicos/acta-cirurgica-brasileira/https://old.scielo.br/oai/scielo-oai.php||sgolden@terra.com.br0102-86501678-2674opendoar:2017-12-19T00:00Acta Cirúrgica Brasileira (Online) - Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia (SBDPC)false
dc.title.none.fl_str_mv Effect of atenolol pre-treatment in heart damage in a model of intestinal ischemia-reperfusion
title Effect of atenolol pre-treatment in heart damage in a model of intestinal ischemia-reperfusion
spellingShingle Effect of atenolol pre-treatment in heart damage in a model of intestinal ischemia-reperfusion
Okada,Mieko
Adrenergic Antagonists
Atenolol
Ischemia
Reperfusion
Cytokines
Oxidative Stress
Rats.
title_short Effect of atenolol pre-treatment in heart damage in a model of intestinal ischemia-reperfusion
title_full Effect of atenolol pre-treatment in heart damage in a model of intestinal ischemia-reperfusion
title_fullStr Effect of atenolol pre-treatment in heart damage in a model of intestinal ischemia-reperfusion
title_full_unstemmed Effect of atenolol pre-treatment in heart damage in a model of intestinal ischemia-reperfusion
title_sort Effect of atenolol pre-treatment in heart damage in a model of intestinal ischemia-reperfusion
author Okada,Mieko
author_facet Okada,Mieko
Falcão,Luiz Fernando Reis
Ferez,David
Martins,José Luiz
Errante,Paolo Ruggero
Rodrigues,Francisco Sandro Menezes
Caricati-Neto,Afonso
Marinho,Márcia
Fenelon,Guilherme
Oliveira-Júnior,Itamar Souza
author_role author
author2 Falcão,Luiz Fernando Reis
Ferez,David
Martins,José Luiz
Errante,Paolo Ruggero
Rodrigues,Francisco Sandro Menezes
Caricati-Neto,Afonso
Marinho,Márcia
Fenelon,Guilherme
Oliveira-Júnior,Itamar Souza
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Okada,Mieko
Falcão,Luiz Fernando Reis
Ferez,David
Martins,José Luiz
Errante,Paolo Ruggero
Rodrigues,Francisco Sandro Menezes
Caricati-Neto,Afonso
Marinho,Márcia
Fenelon,Guilherme
Oliveira-Júnior,Itamar Souza
dc.subject.por.fl_str_mv Adrenergic Antagonists
Atenolol
Ischemia
Reperfusion
Cytokines
Oxidative Stress
Rats.
topic Adrenergic Antagonists
Atenolol
Ischemia
Reperfusion
Cytokines
Oxidative Stress
Rats.
description Abstract Purpose: To investigate the effects of atenolol in inflammatory mediator and oxidative stress in a myocardial injury by intestinal ischemia/reperfusion in rat model. Methods: Adult Wistar male rats were randomly (n=8), anesthetized and divided in: Sham: submitted to operation only; group SS+IR: intravenous saline infusion following superior mesenteric artery occlusion during 60 minutes (ischemia) and open for 120 minutes (reperfusion); group AT+IR: intravenous atenolol infusion (2 mg/kg) following superior mesenteric artery occlusion during 60 minutes (ischemia) and open for 120 minutes (reperfusion); and group AT+I+AT+R: intravenous atenolol infusion following superior mesenteric artery occlusion during 60 minutes (ischemia) and in the time 45 minutes other atenolol doses were administrated and the artery was open for 120 minutes (reperfusion), all animals were submitted to muscular relaxation for mechanical ventilation. In the end of experiment the animals were euthanized and the hearts tissue were morphology analyzed by histology and malondialdehyde by ELISA, and the plasma were analyzed for tumor necrosis factor-alpha by ELISA. Results: The group SS+IR demonstrated the higher malondialdehyde levels when compared with the atenolol treated-groups (p=0.001) in the heart tissue. The tumor necrosis factor-alpha level in plasma decrease in the treated groups when compared with SS+IR group (p=0.001). Histology analyses demonstrate pyknosis, edema, cellular vacuolization, presence of inflammatory infiltrate and band contraction in the heart tissue of the rats. Conclusion: Atenolol significantly reduce the degree of cardiac damage after intestinal ischemia-reperfusion.
publishDate 2017
dc.date.none.fl_str_mv 2017-11-01
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=S0102-86502017001100964
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86502017001100964
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/s0102-865020170110000008
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 Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia
publisher.none.fl_str_mv Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia
dc.source.none.fl_str_mv Acta Cirúrgica Brasileira v.32 n.11 2017
reponame:Acta Cirúrgica Brasileira (Online)
instname:Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia (SBDPC)
instacron:SBDPC
instname_str Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia (SBDPC)
instacron_str SBDPC
institution SBDPC
reponame_str Acta Cirúrgica Brasileira (Online)
collection Acta Cirúrgica Brasileira (Online)
repository.name.fl_str_mv Acta Cirúrgica Brasileira (Online) - Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia (SBDPC)
repository.mail.fl_str_mv ||sgolden@terra.com.br
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