Influence of acute pancreatitis on the in vitro responsiveness of rat mesenteric and pulmonary arteries

Detalhes bibliográficos
Autor(a) principal: Camargo, Enilton A.
Data de Publicação: 2008
Outros Autores: Delbin, Maria Andreia [UNESP], Ferreira, Tatiane, Landucci, Elen C. T., Antunes, Edson, Zanesco, Angelina [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1186/1471-230X-8-19
http://hdl.handle.net/11449/20891
Resumo: Background: Acute pancreatitis is an inflammatory disease characterized by local tissue injury and systemic inflammatory response leading to massive nitric oxide (NO) production and haemodynamic disturbances. Therefore, the aim of this work was to evaluate the vascular reactivity of pulmonary and mesenteric artery rings from rats submitted to experimental pancreatitis.Male Wistar rats were divided into three groups: saline (SAL); tauracholate (TAU) and phospholipase A(2) (PLA(2)). Pancreatitis was induced by administration of TAU or PLA(2) from Naja mocambique mocambique into the common bile duct of rats, and after 4 h of duct injection the animals were sacrificed. Concentration-response curves to acetylcholine (ACh), sodium nitroprusside (SNP) and phenylephrine (PHE) in isolated mesenteric and pulmonary arteries were obtained. Potency (pEC(50)) and maximal responses (E(MAX)) were determined. Blood samples were collected for biochemical analysis.Results: In mesenteric rings, the potency for ACh was significantly decreased from animals treated with TAU (about 4.2-fold) or PLA(2) (about 6.9-fold) compared to saline group without changes in the maximal responses. Neither pEC(50) nor E(MAX) values for Ach were altered in pulmonary rings in any group. Similarly, the pEC(50) and the E(MAX) values for SNP were not changed in both preparations in any group. The potency for PHE was significantly decreased in rat mesenteric and pulmonary rings from TAU group compared to SAL group (about 2.2- and 2.69-fold, for mesenteric and pulmonary rings, respectively). No changes were seen in the E(MAX) for PHE. The nitrite/nitrate (NO(x)(-)) levels were markedly increased in animals submitted to acute pancreatitis as compared to SAL group, approximately 76 and 68% in TAU and PLA(2) protocol, respectively.Conclusion: Acute pancreatitis provoked deleterious effects in endothelium-dependent relaxing response for ACh in mesenteric rings that were strongly associated with high plasma NO(x)(-) levels as consequence of intense inflammatory responses. Furthermore, the subsensitivity of contractile response to PHE in both mesenteric and pulmonary rings might be due to the complications of this pathological condition in the early stage of pancreatitis.
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spelling Influence of acute pancreatitis on the in vitro responsiveness of rat mesenteric and pulmonary arteriesBackground: Acute pancreatitis is an inflammatory disease characterized by local tissue injury and systemic inflammatory response leading to massive nitric oxide (NO) production and haemodynamic disturbances. Therefore, the aim of this work was to evaluate the vascular reactivity of pulmonary and mesenteric artery rings from rats submitted to experimental pancreatitis.Male Wistar rats were divided into three groups: saline (SAL); tauracholate (TAU) and phospholipase A(2) (PLA(2)). Pancreatitis was induced by administration of TAU or PLA(2) from Naja mocambique mocambique into the common bile duct of rats, and after 4 h of duct injection the animals were sacrificed. Concentration-response curves to acetylcholine (ACh), sodium nitroprusside (SNP) and phenylephrine (PHE) in isolated mesenteric and pulmonary arteries were obtained. Potency (pEC(50)) and maximal responses (E(MAX)) were determined. Blood samples were collected for biochemical analysis.Results: In mesenteric rings, the potency for ACh was significantly decreased from animals treated with TAU (about 4.2-fold) or PLA(2) (about 6.9-fold) compared to saline group without changes in the maximal responses. Neither pEC(50) nor E(MAX) values for Ach were altered in pulmonary rings in any group. Similarly, the pEC(50) and the E(MAX) values for SNP were not changed in both preparations in any group. The potency for PHE was significantly decreased in rat mesenteric and pulmonary rings from TAU group compared to SAL group (about 2.2- and 2.69-fold, for mesenteric and pulmonary rings, respectively). No changes were seen in the E(MAX) for PHE. The nitrite/nitrate (NO(x)(-)) levels were markedly increased in animals submitted to acute pancreatitis as compared to SAL group, approximately 76 and 68% in TAU and PLA(2) protocol, respectively.Conclusion: Acute pancreatitis provoked deleterious effects in endothelium-dependent relaxing response for ACh in mesenteric rings that were strongly associated with high plasma NO(x)(-) levels as consequence of intense inflammatory responses. Furthermore, the subsensitivity of contractile response to PHE in both mesenteric and pulmonary rings might be due to the complications of this pathological condition in the early stage of pancreatitis.Univ São Paulo State UNESP, Dept Phys Educ, Inst Biosci, Rio Claro, SP, BrazilState Univ Campinas UNICAMP, Dept Pharmacol, Fac Med Sci, Campinas, SP, BrazilUniv São Paulo State UNESP, Dept Phys Educ, Inst Biosci, Rio Claro, SP, BrazilBiomed Central Ltd.Universidade Estadual Paulista (Unesp)Universidade Estadual de Campinas (UNICAMP)Camargo, Enilton A.Delbin, Maria Andreia [UNESP]Ferreira, TatianeLanducci, Elen C. T.Antunes, EdsonZanesco, Angelina [UNESP]2013-09-30T18:49:21Z2014-05-20T13:58:47Z2013-09-30T18:49:21Z2014-05-20T13:58:47Z2008-05-29info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article7application/pdfhttp://dx.doi.org/10.1186/1471-230X-8-19Bmc Gastroenterology. London: Biomed Central Ltd., v. 8, p. 7, 2008.1471-230Xhttp://hdl.handle.net/11449/2089110.1186/1471-230X-8-19WOS:000257345000001WOS000257345000001.pdf4472007237545596Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBMC Gastroenterology2.731info:eu-repo/semantics/openAccess2024-01-23T07:11:00Zoai:repositorio.unesp.br:11449/20891Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T23:47:22.722886Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Influence of acute pancreatitis on the in vitro responsiveness of rat mesenteric and pulmonary arteries
title Influence of acute pancreatitis on the in vitro responsiveness of rat mesenteric and pulmonary arteries
spellingShingle Influence of acute pancreatitis on the in vitro responsiveness of rat mesenteric and pulmonary arteries
Camargo, Enilton A.
title_short Influence of acute pancreatitis on the in vitro responsiveness of rat mesenteric and pulmonary arteries
title_full Influence of acute pancreatitis on the in vitro responsiveness of rat mesenteric and pulmonary arteries
title_fullStr Influence of acute pancreatitis on the in vitro responsiveness of rat mesenteric and pulmonary arteries
title_full_unstemmed Influence of acute pancreatitis on the in vitro responsiveness of rat mesenteric and pulmonary arteries
title_sort Influence of acute pancreatitis on the in vitro responsiveness of rat mesenteric and pulmonary arteries
author Camargo, Enilton A.
author_facet Camargo, Enilton A.
Delbin, Maria Andreia [UNESP]
Ferreira, Tatiane
Landucci, Elen C. T.
Antunes, Edson
Zanesco, Angelina [UNESP]
author_role author
author2 Delbin, Maria Andreia [UNESP]
Ferreira, Tatiane
Landucci, Elen C. T.
Antunes, Edson
Zanesco, Angelina [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade Estadual de Campinas (UNICAMP)
dc.contributor.author.fl_str_mv Camargo, Enilton A.
Delbin, Maria Andreia [UNESP]
Ferreira, Tatiane
Landucci, Elen C. T.
Antunes, Edson
Zanesco, Angelina [UNESP]
description Background: Acute pancreatitis is an inflammatory disease characterized by local tissue injury and systemic inflammatory response leading to massive nitric oxide (NO) production and haemodynamic disturbances. Therefore, the aim of this work was to evaluate the vascular reactivity of pulmonary and mesenteric artery rings from rats submitted to experimental pancreatitis.Male Wistar rats were divided into three groups: saline (SAL); tauracholate (TAU) and phospholipase A(2) (PLA(2)). Pancreatitis was induced by administration of TAU or PLA(2) from Naja mocambique mocambique into the common bile duct of rats, and after 4 h of duct injection the animals were sacrificed. Concentration-response curves to acetylcholine (ACh), sodium nitroprusside (SNP) and phenylephrine (PHE) in isolated mesenteric and pulmonary arteries were obtained. Potency (pEC(50)) and maximal responses (E(MAX)) were determined. Blood samples were collected for biochemical analysis.Results: In mesenteric rings, the potency for ACh was significantly decreased from animals treated with TAU (about 4.2-fold) or PLA(2) (about 6.9-fold) compared to saline group without changes in the maximal responses. Neither pEC(50) nor E(MAX) values for Ach were altered in pulmonary rings in any group. Similarly, the pEC(50) and the E(MAX) values for SNP were not changed in both preparations in any group. The potency for PHE was significantly decreased in rat mesenteric and pulmonary rings from TAU group compared to SAL group (about 2.2- and 2.69-fold, for mesenteric and pulmonary rings, respectively). No changes were seen in the E(MAX) for PHE. The nitrite/nitrate (NO(x)(-)) levels were markedly increased in animals submitted to acute pancreatitis as compared to SAL group, approximately 76 and 68% in TAU and PLA(2) protocol, respectively.Conclusion: Acute pancreatitis provoked deleterious effects in endothelium-dependent relaxing response for ACh in mesenteric rings that were strongly associated with high plasma NO(x)(-) levels as consequence of intense inflammatory responses. Furthermore, the subsensitivity of contractile response to PHE in both mesenteric and pulmonary rings might be due to the complications of this pathological condition in the early stage of pancreatitis.
publishDate 2008
dc.date.none.fl_str_mv 2008-05-29
2013-09-30T18:49:21Z
2013-09-30T18:49:21Z
2014-05-20T13:58:47Z
2014-05-20T13:58:47Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/1471-230X-8-19
Bmc Gastroenterology. London: Biomed Central Ltd., v. 8, p. 7, 2008.
1471-230X
http://hdl.handle.net/11449/20891
10.1186/1471-230X-8-19
WOS:000257345000001
WOS000257345000001.pdf
4472007237545596
url http://dx.doi.org/10.1186/1471-230X-8-19
http://hdl.handle.net/11449/20891
identifier_str_mv Bmc Gastroenterology. London: Biomed Central Ltd., v. 8, p. 7, 2008.
1471-230X
10.1186/1471-230X-8-19
WOS:000257345000001
WOS000257345000001.pdf
4472007237545596
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv BMC Gastroenterology
2.731
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eu_rights_str_mv openAccess
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application/pdf
dc.publisher.none.fl_str_mv Biomed Central Ltd.
publisher.none.fl_str_mv Biomed Central Ltd.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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