Effects of cyclosporine on ischemia-reperfusion injuries in rat kidneys. An experimental model
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1590/s0102-865020190080000006 http://hdl.handle.net/11449/199512 |
Resumo: | Purpose: To assess Cyclosporine A (CsA) therapy at an intraperitoneal dose of 15 mg.kg-1 in a rodent model of non-septic renal ischemia. Methods: Twenty male Wistar rats were randomized to receive CsA therapy or none therapy before undergoing 30 minutes of renal ischemia followed by reperfusion. Additionally, 10 rats were randomized to undergo the same surgical procedure of the aforementioned animals with neither ischemia nor CsA therapy. Twelve hours after kidney ischemia, the left kidneys were evaluated for histological injury according to Park’s criteria. Serum creatinine (Cr), urea nitrogen (Ur) and sodium levels were obtained at different times of the experimental protocol. Results: Rodents in the CsA group showed negative results (p<0.05) in serum variables (Cr: 0.41±0.05mg/ dL vs. 4.17±1.25mg/dL; Ur: 40.90±3.98mg/dL vs. 187.70±22.93mg/dL) even the non CsA or control group (Cr: 0.35±0.07mg/dL vs. 3.80±1.20mg/dL; Ur: 40.10±4.70mg/dL vs. 184.50±49.80mg/dL). The negative results were also verified in histological evaluation, CsA group had 50% in the very severe grade of lesion, 10% in the severe and 40% in the moderate to severe whereas the control group had 90% in the very severe grade. Conclusion: CsA was incapable of preventing the deleterious effects of ischemia-reperfusion injury in rat kidneys. |
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Effects of cyclosporine on ischemia-reperfusion injuries in rat kidneys. An experimental modelAcute kidney injuryCyclosporineKidneyRatsWistarPurpose: To assess Cyclosporine A (CsA) therapy at an intraperitoneal dose of 15 mg.kg-1 in a rodent model of non-septic renal ischemia. Methods: Twenty male Wistar rats were randomized to receive CsA therapy or none therapy before undergoing 30 minutes of renal ischemia followed by reperfusion. Additionally, 10 rats were randomized to undergo the same surgical procedure of the aforementioned animals with neither ischemia nor CsA therapy. Twelve hours after kidney ischemia, the left kidneys were evaluated for histological injury according to Park’s criteria. Serum creatinine (Cr), urea nitrogen (Ur) and sodium levels were obtained at different times of the experimental protocol. Results: Rodents in the CsA group showed negative results (p<0.05) in serum variables (Cr: 0.41±0.05mg/ dL vs. 4.17±1.25mg/dL; Ur: 40.90±3.98mg/dL vs. 187.70±22.93mg/dL) even the non CsA or control group (Cr: 0.35±0.07mg/dL vs. 3.80±1.20mg/dL; Ur: 40.10±4.70mg/dL vs. 184.50±49.80mg/dL). The negative results were also verified in histological evaluation, CsA group had 50% in the very severe grade of lesion, 10% in the severe and 40% in the moderate to severe whereas the control group had 90% in the very severe grade. Conclusion: CsA was incapable of preventing the deleterious effects of ischemia-reperfusion injury in rat kidneys.Department of Anesthesiology and Surgery Complexo Hospitalar Universitário Professor Edgard Santos (HUPES) Universidade Federal da Bahia (UFBA)Department of Anesthesiology Faculdade de Medicina de Botucatu (FMB) Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP)Department of Pathology FMB UNESPHuman Performance Research Laboratory (LAPEDH) Universidade de Peranambuco (UPE)Department of Anesthesiology Faculdade de Medicina de Botucatu (FMB) Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP)Department of Pathology FMB UNESPUniversidade Federal da Bahia (UFBA)Universidade Estadual Paulista (Unesp)Universidade de Peranambuco (UPE)Oliveira, Antonio Carlos CerqueiraMódolo, Norma Sueli Pinheiro [UNESP]Domingues, Maria Aparecida Custódio [UNESP]Schwingel, Paulo Adriano2020-12-12T01:41:54Z2020-12-12T01:41:54Z2019-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.1590/s0102-865020190080000006Acta Cirurgica Brasileira, v. 34, n. 8, 2019.1678-26740102-8650http://hdl.handle.net/11449/19951210.1590/s0102-865020190080000006S0102-865020190008002112-s2.0-85073478003S0102-86502019000800211.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengActa Cirurgica Brasileirainfo:eu-repo/semantics/openAccess2024-09-03T13:14:10Zoai:repositorio.unesp.br:11449/199512Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T13:14:10Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Effects of cyclosporine on ischemia-reperfusion injuries in rat kidneys. An experimental model |
title |
Effects of cyclosporine on ischemia-reperfusion injuries in rat kidneys. An experimental model |
spellingShingle |
Effects of cyclosporine on ischemia-reperfusion injuries in rat kidneys. An experimental model Oliveira, Antonio Carlos Cerqueira Acute kidney injury Cyclosporine Kidney Rats Wistar |
title_short |
Effects of cyclosporine on ischemia-reperfusion injuries in rat kidneys. An experimental model |
title_full |
Effects of cyclosporine on ischemia-reperfusion injuries in rat kidneys. An experimental model |
title_fullStr |
Effects of cyclosporine on ischemia-reperfusion injuries in rat kidneys. An experimental model |
title_full_unstemmed |
Effects of cyclosporine on ischemia-reperfusion injuries in rat kidneys. An experimental model |
title_sort |
Effects of cyclosporine on ischemia-reperfusion injuries in rat kidneys. An experimental model |
author |
Oliveira, Antonio Carlos Cerqueira |
author_facet |
Oliveira, Antonio Carlos Cerqueira Módolo, Norma Sueli Pinheiro [UNESP] Domingues, Maria Aparecida Custódio [UNESP] Schwingel, Paulo Adriano |
author_role |
author |
author2 |
Módolo, Norma Sueli Pinheiro [UNESP] Domingues, Maria Aparecida Custódio [UNESP] Schwingel, Paulo Adriano |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal da Bahia (UFBA) Universidade Estadual Paulista (Unesp) Universidade de Peranambuco (UPE) |
dc.contributor.author.fl_str_mv |
Oliveira, Antonio Carlos Cerqueira Módolo, Norma Sueli Pinheiro [UNESP] Domingues, Maria Aparecida Custódio [UNESP] Schwingel, Paulo Adriano |
dc.subject.por.fl_str_mv |
Acute kidney injury Cyclosporine Kidney Rats Wistar |
topic |
Acute kidney injury Cyclosporine Kidney Rats Wistar |
description |
Purpose: To assess Cyclosporine A (CsA) therapy at an intraperitoneal dose of 15 mg.kg-1 in a rodent model of non-septic renal ischemia. Methods: Twenty male Wistar rats were randomized to receive CsA therapy or none therapy before undergoing 30 minutes of renal ischemia followed by reperfusion. Additionally, 10 rats were randomized to undergo the same surgical procedure of the aforementioned animals with neither ischemia nor CsA therapy. Twelve hours after kidney ischemia, the left kidneys were evaluated for histological injury according to Park’s criteria. Serum creatinine (Cr), urea nitrogen (Ur) and sodium levels were obtained at different times of the experimental protocol. Results: Rodents in the CsA group showed negative results (p<0.05) in serum variables (Cr: 0.41±0.05mg/ dL vs. 4.17±1.25mg/dL; Ur: 40.90±3.98mg/dL vs. 187.70±22.93mg/dL) even the non CsA or control group (Cr: 0.35±0.07mg/dL vs. 3.80±1.20mg/dL; Ur: 40.10±4.70mg/dL vs. 184.50±49.80mg/dL). The negative results were also verified in histological evaluation, CsA group had 50% in the very severe grade of lesion, 10% in the severe and 40% in the moderate to severe whereas the control group had 90% in the very severe grade. Conclusion: CsA was incapable of preventing the deleterious effects of ischemia-reperfusion injury in rat kidneys. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-01-01 2020-12-12T01:41:54Z 2020-12-12T01:41:54Z |
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/10.1590/s0102-865020190080000006 Acta Cirurgica Brasileira, v. 34, n. 8, 2019. 1678-2674 0102-8650 http://hdl.handle.net/11449/199512 10.1590/s0102-865020190080000006 S0102-86502019000800211 2-s2.0-85073478003 S0102-86502019000800211.pdf |
url |
http://dx.doi.org/10.1590/s0102-865020190080000006 http://hdl.handle.net/11449/199512 |
identifier_str_mv |
Acta Cirurgica Brasileira, v. 34, n. 8, 2019. 1678-2674 0102-8650 10.1590/s0102-865020190080000006 S0102-86502019000800211 2-s2.0-85073478003 S0102-86502019000800211.pdf |
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 |
application/pdf |
dc.source.none.fl_str_mv |
Scopus 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) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1810021356442484736 |