Effects of diazoxide in experimental acute necrotizing pancreatitis

Detalhes bibliográficos
Autor(a) principal: de Oliveira Andrade, Roberta
Data de Publicação: 2017
Outros Autores: Kunitake, Tiago, Koike, Marcia Kiyomi, Machado, Marcel C.C., Souza, Heraldo Possolo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/128330
Resumo: OBJECTIVE: We aimed to assess the effects of diazoxide on the mortality, pancreatic injury, and inflammatory response in an experimental model of acute pancreatitis. METHODS: Male Wistar rats (200-400 g) were divided randomly into two groups. Fifteen minutes before surgery, animals received physiological (0.9%) saline (3 mL/kg) (control group) or 45 mg/kg diazoxide (treatment group) via the intravenous route. Acute pancreatitis was induced by injection of 2.5% sodium taurocholate via the biliopancreatic duct. Mortality (n=38) was observed for 72 h and analyzed by the Mantel-Cox Log-rank test. To study pancreatic lesions and systemic inflammation, rats (10 from each group) were killed 3 h after acute pancreatitis induction; ascites volume was measured and blood as well as pancreases were collected. Pancreatic injury was assessed according to Schmidt’s scale. Cytokine expression in plasma was evaluated by the multiplex method. RESULTS: Mortality at 72 h was 33% in the control group and 60% in the treatment group (p=0.07). Ascites volumes and plasma levels of cytokines between groups were similar. No difference was observed in edema or infiltration of inflammatory cells in pancreatic tissues from either group. However, necrosis of acinar cells was lower in the treatment group compared to the control group (3.5 vs. 3.75, p=0.015). CONCLUSIONS: Treatment with diazoxide can reduce necrosis of acinar cells in an experimental model of acute pancreatitis, but does not affect the inflammatory response or mortality after 72 h.
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spelling Effects of diazoxide in experimental acute necrotizing pancreatitis OBJECTIVE: We aimed to assess the effects of diazoxide on the mortality, pancreatic injury, and inflammatory response in an experimental model of acute pancreatitis. METHODS: Male Wistar rats (200-400 g) were divided randomly into two groups. Fifteen minutes before surgery, animals received physiological (0.9%) saline (3 mL/kg) (control group) or 45 mg/kg diazoxide (treatment group) via the intravenous route. Acute pancreatitis was induced by injection of 2.5% sodium taurocholate via the biliopancreatic duct. Mortality (n=38) was observed for 72 h and analyzed by the Mantel-Cox Log-rank test. To study pancreatic lesions and systemic inflammation, rats (10 from each group) were killed 3 h after acute pancreatitis induction; ascites volume was measured and blood as well as pancreases were collected. Pancreatic injury was assessed according to Schmidt’s scale. Cytokine expression in plasma was evaluated by the multiplex method. RESULTS: Mortality at 72 h was 33% in the control group and 60% in the treatment group (p=0.07). Ascites volumes and plasma levels of cytokines between groups were similar. No difference was observed in edema or infiltration of inflammatory cells in pancreatic tissues from either group. However, necrosis of acinar cells was lower in the treatment group compared to the control group (3.5 vs. 3.75, p=0.015). CONCLUSIONS: Treatment with diazoxide can reduce necrosis of acinar cells in an experimental model of acute pancreatitis, but does not affect the inflammatory response or mortality after 72 h. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2017-02-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/12833010.6061/clinics/2017(02)10Clinics; Vol. 72 No. 2 (2017); 125-129Clinics; v. 72 n. 2 (2017); 125-129Clinics; Vol. 72 Núm. 2 (2017); 125-1291980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/128330/125202Copyright (c) 2017 Clinicsinfo:eu-repo/semantics/openAccessde Oliveira Andrade, RobertaKunitake, TiagoKoike, Marcia KiyomiMachado, Marcel C.C.Souza, Heraldo Possolo2017-03-16T11:39:13Zoai:revistas.usp.br:article/128330Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2017-03-16T11:39:13Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Effects of diazoxide in experimental acute necrotizing pancreatitis
title Effects of diazoxide in experimental acute necrotizing pancreatitis
spellingShingle Effects of diazoxide in experimental acute necrotizing pancreatitis
de Oliveira Andrade, Roberta
title_short Effects of diazoxide in experimental acute necrotizing pancreatitis
title_full Effects of diazoxide in experimental acute necrotizing pancreatitis
title_fullStr Effects of diazoxide in experimental acute necrotizing pancreatitis
title_full_unstemmed Effects of diazoxide in experimental acute necrotizing pancreatitis
title_sort Effects of diazoxide in experimental acute necrotizing pancreatitis
author de Oliveira Andrade, Roberta
author_facet de Oliveira Andrade, Roberta
Kunitake, Tiago
Koike, Marcia Kiyomi
Machado, Marcel C.C.
Souza, Heraldo Possolo
author_role author
author2 Kunitake, Tiago
Koike, Marcia Kiyomi
Machado, Marcel C.C.
Souza, Heraldo Possolo
author2_role author
author
author
author
dc.contributor.author.fl_str_mv de Oliveira Andrade, Roberta
Kunitake, Tiago
Koike, Marcia Kiyomi
Machado, Marcel C.C.
Souza, Heraldo Possolo
description OBJECTIVE: We aimed to assess the effects of diazoxide on the mortality, pancreatic injury, and inflammatory response in an experimental model of acute pancreatitis. METHODS: Male Wistar rats (200-400 g) were divided randomly into two groups. Fifteen minutes before surgery, animals received physiological (0.9%) saline (3 mL/kg) (control group) or 45 mg/kg diazoxide (treatment group) via the intravenous route. Acute pancreatitis was induced by injection of 2.5% sodium taurocholate via the biliopancreatic duct. Mortality (n=38) was observed for 72 h and analyzed by the Mantel-Cox Log-rank test. To study pancreatic lesions and systemic inflammation, rats (10 from each group) were killed 3 h after acute pancreatitis induction; ascites volume was measured and blood as well as pancreases were collected. Pancreatic injury was assessed according to Schmidt’s scale. Cytokine expression in plasma was evaluated by the multiplex method. RESULTS: Mortality at 72 h was 33% in the control group and 60% in the treatment group (p=0.07). Ascites volumes and plasma levels of cytokines between groups were similar. No difference was observed in edema or infiltration of inflammatory cells in pancreatic tissues from either group. However, necrosis of acinar cells was lower in the treatment group compared to the control group (3.5 vs. 3.75, p=0.015). CONCLUSIONS: Treatment with diazoxide can reduce necrosis of acinar cells in an experimental model of acute pancreatitis, but does not affect the inflammatory response or mortality after 72 h.
publishDate 2017
dc.date.none.fl_str_mv 2017-02-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/128330
10.6061/clinics/2017(02)10
url https://www.revistas.usp.br/clinics/article/view/128330
identifier_str_mv 10.6061/clinics/2017(02)10
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/128330/125202
dc.rights.driver.fl_str_mv Copyright (c) 2017 Clinics
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2017 Clinics
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 72 No. 2 (2017); 125-129
Clinics; v. 72 n. 2 (2017); 125-129
Clinics; Vol. 72 Núm. 2 (2017); 125-129
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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