Remote ischemic preconditioning and tacrolimus in the fetal small bowel transplant in mice
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S0102-865020160100000006 https://repositorio.unifesp.br/handle/11600/56947 |
Resumo: | PURPOSE: To evaluate the effect of remote ischemic preconditioning (IPC-R) in the fetal small bowel transplantation model. METHODS: Two groups were constituted: The Isogenic transplant (ISO, C57BL/6 mice, n=24) and the allogenic transplant (ALO, BALB/c mice, n=24). In each group, the animals were distributed with and without IPC-R. It was obtained the following subgroups: Tx, IPC-R, Fk, IPC-Fk, in both strains. Intestinal grafts were stained with hematoxylin and eosin and immunohistochemically. RESULTS: The graft development evaluation in ISO group showed that IPC-R reduced the development compared with ISO-Tx (5.2+/-0.4 vs 9.0+/-0.8) and IPC-R-Fk increased the graft development compared with IPC-R (11.2+/-0.7 and 10.2+/-0.8). In ALO group, IPC-Fk increased the development compared with ALO-Tx and ALO with IPC-R (6.0+/-0.8, 9.0+/-1.2, 0.0+/-0.0, 0.5+/-0.3). The PCNA expression was increased in ISO group treated with Fk and IPC-R compared to other groups (12.2+/-0.8 vs Tx: 8.8+/-0.9, IPC-R: 8.0+/-0.4 and Fk: 9.0+/-0.6). The graft rejection was lower in groups treated with IPC-R (-18%), Fk (-68%) or both (-61%) compared with ALO-Tx. CONCLUSION: Remote ischemic preconditioning showed benefic effect even associate with Tacrolimus on the development and acute rejection of the fetal small bowel graft in the Isogenic and Allogenic transplants. |
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Remote ischemic preconditioning and tacrolimus in the fetal small bowel transplant in miceFetal Tissue TransplantationSmall IntestineTacrolimusIschemic PreconditioningMicePURPOSE: To evaluate the effect of remote ischemic preconditioning (IPC-R) in the fetal small bowel transplantation model. METHODS: Two groups were constituted: The Isogenic transplant (ISO, C57BL/6 mice, n=24) and the allogenic transplant (ALO, BALB/c mice, n=24). In each group, the animals were distributed with and without IPC-R. It was obtained the following subgroups: Tx, IPC-R, Fk, IPC-Fk, in both strains. Intestinal grafts were stained with hematoxylin and eosin and immunohistochemically. RESULTS: The graft development evaluation in ISO group showed that IPC-R reduced the development compared with ISO-Tx (5.2+/-0.4 vs 9.0+/-0.8) and IPC-R-Fk increased the graft development compared with IPC-R (11.2+/-0.7 and 10.2+/-0.8). In ALO group, IPC-Fk increased the development compared with ALO-Tx and ALO with IPC-R (6.0+/-0.8, 9.0+/-1.2, 0.0+/-0.0, 0.5+/-0.3). The PCNA expression was increased in ISO group treated with Fk and IPC-R compared to other groups (12.2+/-0.8 vs Tx: 8.8+/-0.9, IPC-R: 8.0+/-0.4 and Fk: 9.0+/-0.6). The graft rejection was lower in groups treated with IPC-R (-18%), Fk (-68%) or both (-61%) compared with ALO-Tx. CONCLUSION: Remote ischemic preconditioning showed benefic effect even associate with Tacrolimus on the development and acute rejection of the fetal small bowel graft in the Isogenic and Allogenic transplants.Univ Fed Sao Paulo UNIFESP, Sch Med, Operat Tech & Expt Surg Div, Sao Paulo, SP, BrazilUniv Sao Paulo, Fac Med, Lab Emergency Med LIM 51, Sao Paulo, BrazilUniv Fed Vale Sao Francisco UNIVASF, Sch Med, Petrolina, PE, BrazilFMUSP, Surg Physiopathol Lab LIM 62, Sao Paulo, SP, BrazilOperative Technique and Experimental Surgery Division, Medical School, Universidade Federal de São Paulo (UNIFESP), BrazilWeb of ScienceActa Cirurgica Brasileira2020-07-31T12:47:37Z2020-07-31T12:47:37Z2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion675-679application/pdfhttp://dx.doi.org/10.1590/S0102-865020160100000006Acta Cirurgica Brasileira. Sao Paulo, v. 31, n. 10, p. 675-679, 2016.10.1590/S0102-865020160100000006S0102-86502016001000675.pdf0102-8650S0102-86502016001000675https://repositorio.unifesp.br/handle/11600/56947WOS:000391432200006engActa Cirurgica BrasileiraSao Pauloinfo:eu-repo/semantics/openAccessMorello, Ricardo José [UNIFESP]Koike, Marcia KiyomiAbrahão, Marcos de Souza [UNIFESP]Saad, Karen RuggeriSaad, Paulo FernandesMontero, Edna Frasson de Souza [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-03T12:59:07Zoai:repositorio.unifesp.br/:11600/56947Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-03T12:59:07Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Remote ischemic preconditioning and tacrolimus in the fetal small bowel transplant in mice |
title |
Remote ischemic preconditioning and tacrolimus in the fetal small bowel transplant in mice |
spellingShingle |
Remote ischemic preconditioning and tacrolimus in the fetal small bowel transplant in mice Morello, Ricardo José [UNIFESP] Fetal Tissue Transplantation Small Intestine Tacrolimus Ischemic Preconditioning Mice |
title_short |
Remote ischemic preconditioning and tacrolimus in the fetal small bowel transplant in mice |
title_full |
Remote ischemic preconditioning and tacrolimus in the fetal small bowel transplant in mice |
title_fullStr |
Remote ischemic preconditioning and tacrolimus in the fetal small bowel transplant in mice |
title_full_unstemmed |
Remote ischemic preconditioning and tacrolimus in the fetal small bowel transplant in mice |
title_sort |
Remote ischemic preconditioning and tacrolimus in the fetal small bowel transplant in mice |
author |
Morello, Ricardo José [UNIFESP] |
author_facet |
Morello, Ricardo José [UNIFESP] Koike, Marcia Kiyomi Abrahão, Marcos de Souza [UNIFESP] Saad, Karen Ruggeri Saad, Paulo Fernandes Montero, Edna Frasson de Souza [UNIFESP] |
author_role |
author |
author2 |
Koike, Marcia Kiyomi Abrahão, Marcos de Souza [UNIFESP] Saad, Karen Ruggeri Saad, Paulo Fernandes Montero, Edna Frasson de Souza [UNIFESP] |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Morello, Ricardo José [UNIFESP] Koike, Marcia Kiyomi Abrahão, Marcos de Souza [UNIFESP] Saad, Karen Ruggeri Saad, Paulo Fernandes Montero, Edna Frasson de Souza [UNIFESP] |
dc.subject.por.fl_str_mv |
Fetal Tissue Transplantation Small Intestine Tacrolimus Ischemic Preconditioning Mice |
topic |
Fetal Tissue Transplantation Small Intestine Tacrolimus Ischemic Preconditioning Mice |
description |
PURPOSE: To evaluate the effect of remote ischemic preconditioning (IPC-R) in the fetal small bowel transplantation model. METHODS: Two groups were constituted: The Isogenic transplant (ISO, C57BL/6 mice, n=24) and the allogenic transplant (ALO, BALB/c mice, n=24). In each group, the animals were distributed with and without IPC-R. It was obtained the following subgroups: Tx, IPC-R, Fk, IPC-Fk, in both strains. Intestinal grafts were stained with hematoxylin and eosin and immunohistochemically. RESULTS: The graft development evaluation in ISO group showed that IPC-R reduced the development compared with ISO-Tx (5.2+/-0.4 vs 9.0+/-0.8) and IPC-R-Fk increased the graft development compared with IPC-R (11.2+/-0.7 and 10.2+/-0.8). In ALO group, IPC-Fk increased the development compared with ALO-Tx and ALO with IPC-R (6.0+/-0.8, 9.0+/-1.2, 0.0+/-0.0, 0.5+/-0.3). The PCNA expression was increased in ISO group treated with Fk and IPC-R compared to other groups (12.2+/-0.8 vs Tx: 8.8+/-0.9, IPC-R: 8.0+/-0.4 and Fk: 9.0+/-0.6). The graft rejection was lower in groups treated with IPC-R (-18%), Fk (-68%) or both (-61%) compared with ALO-Tx. CONCLUSION: Remote ischemic preconditioning showed benefic effect even associate with Tacrolimus on the development and acute rejection of the fetal small bowel graft in the Isogenic and Allogenic transplants. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 2020-07-31T12:47:37Z 2020-07-31T12:47:37Z |
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://dx.doi.org/10.1590/S0102-865020160100000006 Acta Cirurgica Brasileira. Sao Paulo, v. 31, n. 10, p. 675-679, 2016. 10.1590/S0102-865020160100000006 S0102-86502016001000675.pdf 0102-8650 S0102-86502016001000675 https://repositorio.unifesp.br/handle/11600/56947 WOS:000391432200006 |
url |
http://dx.doi.org/10.1590/S0102-865020160100000006 https://repositorio.unifesp.br/handle/11600/56947 |
identifier_str_mv |
Acta Cirurgica Brasileira. Sao Paulo, v. 31, n. 10, p. 675-679, 2016. 10.1590/S0102-865020160100000006 S0102-86502016001000675.pdf 0102-8650 S0102-86502016001000675 WOS:000391432200006 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Acta Cirurgica Brasileira |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
675-679 application/pdf |
dc.coverage.none.fl_str_mv |
Sao Paulo |
dc.publisher.none.fl_str_mv |
Acta Cirurgica Brasileira |
publisher.none.fl_str_mv |
Acta Cirurgica Brasileira |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268331796987904 |