Effects of cyclosporine on ischemia-reperfusion injuries in rat kidneys. An experimental model

Detalhes bibliográficos
Autor(a) principal: Oliveira, Antonio Carlos Cerqueira
Data de Publicação: 2019
Outros Autores: Módolo, Norma Sueli Pinheiro [UNESP], Domingues, Maria Aparecida Custódio [UNESP], Schwingel, Paulo Adriano
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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spelling 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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