Study of Heparin in Intestinal Ischemia and Reperfusion in Rats: Morphologic and Functional Evaluation
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://repositorio.unifesp.br/handle/11600/35307 http://dx.doi.org/10.1016/j.transproceed.2012.07.055 |
Resumo: | To study whether treatment with heparin (HEP) attenuates intestinal dysfunction caused by ischemia (I) and reperfusion (R), rats were treated with HEP (100 U/kg intravenously) or saline solution (SS) before I (60 min), which was produced by occlusion of the superior mesenteric artery, and R (120 min). After I or I/R, we mounted 2-cm jejunal segment in an organ bath to study neurogenic contractions stimulated by electrical pulses or KCl, using a digital recording system. Thin jejunal slices were stained with hematoxylin and eosin for optical microscopy. Compared with the sham group, jejunal contractions were similar in the I + HEP and the I/R + HEP groups, but reduced in the I + SS and the I/R + SS groups. the jejunal enteric nerves were damaged in the I + SS and the I/R + SS, but not in the I + HEP and the I/R + HEP cohorts. These results suggested that HEP attenuated intestinal dysfunction caused by I and I/R. |
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Ghadie, Majid Mohamad [UNIFESP]Miranda-Ferreira, Regiane [UNIFESP]Taha, Nabiha Saadi Abrahão [UNIFESP]Maroso, A. S.Moreti, R. J. Z.Andraus, M. P.Zempulski, P.Monteiro, Hugo Pequeno [UNIFESP]Simões, Manuel de Jesus [UNIFESP]Fagundes, Djalma José [UNIFESP]Caricati-Neto, Afonso [UNIFESP]Taha, Murched Omar [UNIFESP]Universidade Federal de São Paulo (UNIFESP)Fed Univ Great Dourados2016-01-24T14:27:44Z2016-01-24T14:27:44Z2012-10-01Transplantation Proceedings. New York: Elsevier B.V., v. 44, n. 8, p. 2300-2303, 2012.0041-1345http://repositorio.unifesp.br/handle/11600/35307http://dx.doi.org/10.1016/j.transproceed.2012.07.055WOS000309736900012.pdf10.1016/j.transproceed.2012.07.055WOS:000309736900012To study whether treatment with heparin (HEP) attenuates intestinal dysfunction caused by ischemia (I) and reperfusion (R), rats were treated with HEP (100 U/kg intravenously) or saline solution (SS) before I (60 min), which was produced by occlusion of the superior mesenteric artery, and R (120 min). After I or I/R, we mounted 2-cm jejunal segment in an organ bath to study neurogenic contractions stimulated by electrical pulses or KCl, using a digital recording system. Thin jejunal slices were stained with hematoxylin and eosin for optical microscopy. Compared with the sham group, jejunal contractions were similar in the I + HEP and the I/R + HEP groups, but reduced in the I + SS and the I/R + SS groups. the jejunal enteric nerves were damaged in the I + SS and the I/R + SS, but not in the I + HEP and the I/R + HEP cohorts. These results suggested that HEP attenuated intestinal dysfunction caused by I and I/R.Universidade Federal de São Paulo, Escola Paulista Med, Dept Surg, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pharmacol, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biochem, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Morphol, BR-04023900 São Paulo, BrazilFed Univ Great Dourados, Sch Med, Dourados, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Dept Surg, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pharmacol, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biochem, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Morphol, BR-04023900 São Paulo, BrazilWeb of Science2300-2303engElsevier B.V.Transplantation Proceedingshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyinfo:eu-repo/semantics/openAccessStudy of Heparin in Intestinal Ischemia and Reperfusion in Rats: Morphologic and Functional Evaluationinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlereponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALWOS000309736900012.pdfapplication/pdf1144903${dspace.ui.url}/bitstream/11600/35307/1/WOS000309736900012.pdf050872190c0cf0ff882b3921a6323f31MD51open accessTEXTWOS000309736900012.pdf.txtWOS000309736900012.pdf.txtExtracted texttext/plain17902${dspace.ui.url}/bitstream/11600/35307/2/WOS000309736900012.pdf.txtfaa615e99a2620f73c2995a3ef27785fMD52open access11600/353072022-06-02 10:24:17.567open accessoai:repositorio.unifesp.br:11600/35307Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652022-06-02T13:24:17Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.en.fl_str_mv |
Study of Heparin in Intestinal Ischemia and Reperfusion in Rats: Morphologic and Functional Evaluation |
title |
Study of Heparin in Intestinal Ischemia and Reperfusion in Rats: Morphologic and Functional Evaluation |
spellingShingle |
Study of Heparin in Intestinal Ischemia and Reperfusion in Rats: Morphologic and Functional Evaluation Ghadie, Majid Mohamad [UNIFESP] |
title_short |
Study of Heparin in Intestinal Ischemia and Reperfusion in Rats: Morphologic and Functional Evaluation |
title_full |
Study of Heparin in Intestinal Ischemia and Reperfusion in Rats: Morphologic and Functional Evaluation |
title_fullStr |
Study of Heparin in Intestinal Ischemia and Reperfusion in Rats: Morphologic and Functional Evaluation |
title_full_unstemmed |
Study of Heparin in Intestinal Ischemia and Reperfusion in Rats: Morphologic and Functional Evaluation |
title_sort |
Study of Heparin in Intestinal Ischemia and Reperfusion in Rats: Morphologic and Functional Evaluation |
author |
Ghadie, Majid Mohamad [UNIFESP] |
author_facet |
Ghadie, Majid Mohamad [UNIFESP] Miranda-Ferreira, Regiane [UNIFESP] Taha, Nabiha Saadi Abrahão [UNIFESP] Maroso, A. S. Moreti, R. J. Z. Andraus, M. P. Zempulski, P. Monteiro, Hugo Pequeno [UNIFESP] Simões, Manuel de Jesus [UNIFESP] Fagundes, Djalma José [UNIFESP] Caricati-Neto, Afonso [UNIFESP] Taha, Murched Omar [UNIFESP] |
author_role |
author |
author2 |
Miranda-Ferreira, Regiane [UNIFESP] Taha, Nabiha Saadi Abrahão [UNIFESP] Maroso, A. S. Moreti, R. J. Z. Andraus, M. P. Zempulski, P. Monteiro, Hugo Pequeno [UNIFESP] Simões, Manuel de Jesus [UNIFESP] Fagundes, Djalma José [UNIFESP] Caricati-Neto, Afonso [UNIFESP] Taha, Murched Omar [UNIFESP] |
author2_role |
author author author author author author author author author author author |
dc.contributor.institution.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Fed Univ Great Dourados |
dc.contributor.author.fl_str_mv |
Ghadie, Majid Mohamad [UNIFESP] Miranda-Ferreira, Regiane [UNIFESP] Taha, Nabiha Saadi Abrahão [UNIFESP] Maroso, A. S. Moreti, R. J. Z. Andraus, M. P. Zempulski, P. Monteiro, Hugo Pequeno [UNIFESP] Simões, Manuel de Jesus [UNIFESP] Fagundes, Djalma José [UNIFESP] Caricati-Neto, Afonso [UNIFESP] Taha, Murched Omar [UNIFESP] |
description |
To study whether treatment with heparin (HEP) attenuates intestinal dysfunction caused by ischemia (I) and reperfusion (R), rats were treated with HEP (100 U/kg intravenously) or saline solution (SS) before I (60 min), which was produced by occlusion of the superior mesenteric artery, and R (120 min). After I or I/R, we mounted 2-cm jejunal segment in an organ bath to study neurogenic contractions stimulated by electrical pulses or KCl, using a digital recording system. Thin jejunal slices were stained with hematoxylin and eosin for optical microscopy. Compared with the sham group, jejunal contractions were similar in the I + HEP and the I/R + HEP groups, but reduced in the I + SS and the I/R + SS groups. the jejunal enteric nerves were damaged in the I + SS and the I/R + SS, but not in the I + HEP and the I/R + HEP cohorts. These results suggested that HEP attenuated intestinal dysfunction caused by I and I/R. |
publishDate |
2012 |
dc.date.issued.fl_str_mv |
2012-10-01 |
dc.date.accessioned.fl_str_mv |
2016-01-24T14:27:44Z |
dc.date.available.fl_str_mv |
2016-01-24T14:27:44Z |
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.citation.fl_str_mv |
Transplantation Proceedings. New York: Elsevier B.V., v. 44, n. 8, p. 2300-2303, 2012. |
dc.identifier.uri.fl_str_mv |
http://repositorio.unifesp.br/handle/11600/35307 http://dx.doi.org/10.1016/j.transproceed.2012.07.055 |
dc.identifier.issn.none.fl_str_mv |
0041-1345 |
dc.identifier.file.none.fl_str_mv |
WOS000309736900012.pdf |
dc.identifier.doi.none.fl_str_mv |
10.1016/j.transproceed.2012.07.055 |
dc.identifier.wos.none.fl_str_mv |
WOS:000309736900012 |
identifier_str_mv |
Transplantation Proceedings. New York: Elsevier B.V., v. 44, n. 8, p. 2300-2303, 2012. 0041-1345 WOS000309736900012.pdf 10.1016/j.transproceed.2012.07.055 WOS:000309736900012 |
url |
http://repositorio.unifesp.br/handle/11600/35307 http://dx.doi.org/10.1016/j.transproceed.2012.07.055 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.none.fl_str_mv |
Transplantation Proceedings |
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http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy info:eu-repo/semantics/openAccess |
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http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
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openAccess |
dc.format.none.fl_str_mv |
2300-2303 |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
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