Evaluation of potential changes in liver and lung tissue of rats in an ischemia-reperfusion injury model (modified pringle maneuver)

Detalhes bibliográficos
Autor(a) principal: Freitas, Silvio Henrique
Data de Publicação: 2017
Outros Autores: 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.
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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spelling 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
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language eng
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dc.publisher.none.fl_str_mv Public Library Science
publisher.none.fl_str_mv Public Library Science
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reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
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instname_str Universidade Estadual Paulista (UNESP)
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