Evaluation of potential changes in liver and lung tissue of rats in an ischemia-reperfusion injury model (modified pringle maneuver)
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1371/journal.pone.0178665 http://hdl.handle.net/11449/162869 |
Resumo: | In surgical procedures involving the liver, such as transplantation, resection, and trauma, a temporary occlusion of hepatic vessels may be required. This study was designed to analyze the lesions promoted by ischemia and reperfusion injury of the hepatic pedicle, in the liver and lung, using histopathological and immunohistochemical techniques. In total, 39 Wistar rats were divided into four groups: control group (C n = 3) and ischemia groups subjected to 10, 20, and 30 minutes of hepatic pedicle clamping (I10, n = 12; I20, n = 12; I30, n = 12). Each ischemia group was subdivided into four subgroups of reperfusion (R15, n = 3; R30, n = 3; R60, n = 3; R120, n = 3), after 15, 30, 60, and 120 minutes of reperfusion, respectively. Significant differences were observed in the liver parenchyma (P < 0.05) between the values of microvesicles and hydropic degeneration at different times of ischemia and reperfusion. However, the values of vascular congestion, necrosis, and pyknotic nuclei showed no significant differences (P > 0.05). In the lung parenchyma, a significant difference was observed (P < 0.05) between the values of alveolar septal wall thickening and inflammatory infiltration at different times of ischemia and reperfusion. However, there was no significant difference (P < 0.05) between the values of vascular congestion, bronchial epithelial degeneration, interstitial edema, and hemorrhage. The positive immunoreactivity of caspase-3 protein in the liver parenchyma (indication of ongoing apoptosis), showed no significant differences (P > 0.05) at different times of ischemia and reperfusion. In the pulmonary parenchyma, the immunoreactivity was not specific, and was not quantified. This study demonstrated that the longer the duration of ischemia and reperfusion, the greater are the morphological lesions found in the hepatic and pulmonary parenchyma. |
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Evaluation of potential changes in liver and lung tissue of rats in an ischemia-reperfusion injury model (modified pringle maneuver)In surgical procedures involving the liver, such as transplantation, resection, and trauma, a temporary occlusion of hepatic vessels may be required. This study was designed to analyze the lesions promoted by ischemia and reperfusion injury of the hepatic pedicle, in the liver and lung, using histopathological and immunohistochemical techniques. In total, 39 Wistar rats were divided into four groups: control group (C n = 3) and ischemia groups subjected to 10, 20, and 30 minutes of hepatic pedicle clamping (I10, n = 12; I20, n = 12; I30, n = 12). Each ischemia group was subdivided into four subgroups of reperfusion (R15, n = 3; R30, n = 3; R60, n = 3; R120, n = 3), after 15, 30, 60, and 120 minutes of reperfusion, respectively. Significant differences were observed in the liver parenchyma (P < 0.05) between the values of microvesicles and hydropic degeneration at different times of ischemia and reperfusion. However, the values of vascular congestion, necrosis, and pyknotic nuclei showed no significant differences (P > 0.05). In the lung parenchyma, a significant difference was observed (P < 0.05) between the values of alveolar septal wall thickening and inflammatory infiltration at different times of ischemia and reperfusion. However, there was no significant difference (P < 0.05) between the values of vascular congestion, bronchial epithelial degeneration, interstitial edema, and hemorrhage. The positive immunoreactivity of caspase-3 protein in the liver parenchyma (indication of ongoing apoptosis), showed no significant differences (P > 0.05) at different times of ischemia and reperfusion. In the pulmonary parenchyma, the immunoreactivity was not specific, and was not quantified. This study demonstrated that the longer the duration of ischemia and reperfusion, the greater are the morphological lesions found in the hepatic and pulmonary parenchyma.Foundation for Research Support of Mato Grosso State (FAPEMAT)Univ Cuiaba, Fac Vet Med, Cuiaba, Mato Grosso, BrazilUniv Sao Paulo, Fac Anim Sci & Food Engn, Dept Vet Med, Pirassununga, SP, BrazilUniv Sao Paulo, Fac Anim Sci & Food Engn, Dept Basic Sci, Pirassununga, SP, BrazilPontificia Univ Catolica Parana PUCPR, Sch Agr Sci & Vet Med, Grad Program Anim Sci, Sao Jose Dos Pinhais, Parana, BrazilSao Paulo State Univ Julio de Mesquita Filho, Fac Agr & Vet Sci, Dept Pathol, Jaboticabal, SP, BrazilEduardo Mondlane Univ, Vet Fac, Maputo, MozambiqueSao Paulo State Univ Julio de Mesquita Filho, Fac Agr & Vet Sci, Dept Pathol, Jaboticabal, SP, BrazilPublic Library ScienceUniv CuiabaUniversidade de São Paulo (USP)Pontificia Univ Catolica Parana PUCPRUniversidade Estadual Paulista (Unesp)Eduardo Mondlane UnivFreitas, Silvio HenriqueDoria, Renata G. S.Bueno, Rachel S.Rocha, William B.Filho, Jair R. E.Moraes, Julieta R. E. [UNESP]Vidane, Atanasio SerafinAmbrosio, Carlos E.2018-11-26T17:34:45Z2018-11-26T17:34:45Z2017-06-12info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article13application/pdfhttp://dx.doi.org/10.1371/journal.pone.0178665Plos One. San Francisco: Public Library Science, v. 12, n. 6, 13 p., 2017.1932-6203http://hdl.handle.net/11449/16286910.1371/journal.pone.0178665WOS:000403088400016WOS000403088400016.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPlos One1,164info:eu-repo/semantics/openAccess2024-06-07T13:02:17Zoai:repositorio.unesp.br:11449/162869Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:44:39.611247Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Evaluation of potential changes in liver and lung tissue of rats in an ischemia-reperfusion injury model (modified pringle maneuver) |
title |
Evaluation of potential changes in liver and lung tissue of rats in an ischemia-reperfusion injury model (modified pringle maneuver) |
spellingShingle |
Evaluation of potential changes in liver and lung tissue of rats in an ischemia-reperfusion injury model (modified pringle maneuver) Freitas, Silvio Henrique |
title_short |
Evaluation of potential changes in liver and lung tissue of rats in an ischemia-reperfusion injury model (modified pringle maneuver) |
title_full |
Evaluation of potential changes in liver and lung tissue of rats in an ischemia-reperfusion injury model (modified pringle maneuver) |
title_fullStr |
Evaluation of potential changes in liver and lung tissue of rats in an ischemia-reperfusion injury model (modified pringle maneuver) |
title_full_unstemmed |
Evaluation of potential changes in liver and lung tissue of rats in an ischemia-reperfusion injury model (modified pringle maneuver) |
title_sort |
Evaluation of potential changes in liver and lung tissue of rats in an ischemia-reperfusion injury model (modified pringle maneuver) |
author |
Freitas, Silvio Henrique |
author_facet |
Freitas, Silvio Henrique Doria, Renata G. S. Bueno, Rachel S. Rocha, William B. Filho, Jair R. E. Moraes, Julieta R. E. [UNESP] Vidane, Atanasio Serafin Ambrosio, Carlos E. |
author_role |
author |
author2 |
Doria, Renata G. S. Bueno, Rachel S. Rocha, William B. Filho, Jair R. E. Moraes, Julieta R. E. [UNESP] Vidane, Atanasio Serafin Ambrosio, Carlos E. |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Univ Cuiaba Universidade de São Paulo (USP) Pontificia Univ Catolica Parana PUCPR Universidade Estadual Paulista (Unesp) Eduardo Mondlane Univ |
dc.contributor.author.fl_str_mv |
Freitas, Silvio Henrique Doria, Renata G. S. Bueno, Rachel S. Rocha, William B. Filho, Jair R. E. Moraes, Julieta R. E. [UNESP] Vidane, Atanasio Serafin Ambrosio, Carlos E. |
description |
In surgical procedures involving the liver, such as transplantation, resection, and trauma, a temporary occlusion of hepatic vessels may be required. This study was designed to analyze the lesions promoted by ischemia and reperfusion injury of the hepatic pedicle, in the liver and lung, using histopathological and immunohistochemical techniques. In total, 39 Wistar rats were divided into four groups: control group (C n = 3) and ischemia groups subjected to 10, 20, and 30 minutes of hepatic pedicle clamping (I10, n = 12; I20, n = 12; I30, n = 12). Each ischemia group was subdivided into four subgroups of reperfusion (R15, n = 3; R30, n = 3; R60, n = 3; R120, n = 3), after 15, 30, 60, and 120 minutes of reperfusion, respectively. Significant differences were observed in the liver parenchyma (P < 0.05) between the values of microvesicles and hydropic degeneration at different times of ischemia and reperfusion. However, the values of vascular congestion, necrosis, and pyknotic nuclei showed no significant differences (P > 0.05). In the lung parenchyma, a significant difference was observed (P < 0.05) between the values of alveolar septal wall thickening and inflammatory infiltration at different times of ischemia and reperfusion. However, there was no significant difference (P < 0.05) between the values of vascular congestion, bronchial epithelial degeneration, interstitial edema, and hemorrhage. The positive immunoreactivity of caspase-3 protein in the liver parenchyma (indication of ongoing apoptosis), showed no significant differences (P > 0.05) at different times of ischemia and reperfusion. In the pulmonary parenchyma, the immunoreactivity was not specific, and was not quantified. This study demonstrated that the longer the duration of ischemia and reperfusion, the greater are the morphological lesions found in the hepatic and pulmonary parenchyma. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-06-12 2018-11-26T17:34:45Z 2018-11-26T17:34:45Z |
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/10.1371/journal.pone.0178665 Plos One. San Francisco: Public Library Science, v. 12, n. 6, 13 p., 2017. 1932-6203 http://hdl.handle.net/11449/162869 10.1371/journal.pone.0178665 WOS:000403088400016 WOS000403088400016.pdf |
url |
http://dx.doi.org/10.1371/journal.pone.0178665 http://hdl.handle.net/11449/162869 |
identifier_str_mv |
Plos One. San Francisco: Public Library Science, v. 12, n. 6, 13 p., 2017. 1932-6203 10.1371/journal.pone.0178665 WOS:000403088400016 WOS000403088400016.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Plos One 1,164 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
13 application/pdf |
dc.publisher.none.fl_str_mv |
Public Library Science |
publisher.none.fl_str_mv |
Public Library Science |
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 |
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UNESP |
reponame_str |
Repositório Institucional da UNESP |
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Repositório Institucional da UNESP |
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Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
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1808128972455673856 |