Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venom

Detalhes bibliográficos
Autor(a) principal: Jorge, Antônio Rafael Coelho
Data de Publicação: 2021
Outros Autores: Marinho, Aline Diogo, Silveira, João Alison de Moraes, Nogueira Junior, Francisco Assis, de Aquino, Pedro Everson Alexandre, Alves, Ana Paula Negreiros Nunes, Jorge, Roberta Jeane Bezerra, Ferreira Junior, Rui Seabra [UNESP], Monteiro, Helena Serra Azul
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.toxicon.2021.08.024
http://hdl.handle.net/11449/229577
Resumo: Acute kidney injury pathogenesis in envenoming by snakes is multifactorial and involves immunologic reactions, hemodynamic disturbances, and direct nephrotoxicity. Sildenafil (SFC), a phosphodiesterase 5 inhibitor, has been reported to protect against pathological kidney changes. Objective: This study aimed to investigate the protective effect of sildenafil against Bothrops alternatus snake venom (BaV)-induced nephrotoxicity. Methods: Kidneys from Wistar rats (n = 6, weighing 260–300 g) were isolated and divided into four groups: (1) perfused with a modified Krebs-Henseleit solution (MKHS) containing 6 g% of bovine serum albumin; (2) administered 3 μg/mL SFC; (3) perfused with 3 μg/mL BaV; and (4) administered SFC + BaV, both at 3 μg/mL. Subsequently, the perfusion pressure (PP), renal vascular resistance (RVR), urinary flow (UF), glomerular filtration rate (GFR), and percentage of electrolyte tubular sodium and chloride transport (%TNa+, %TCl−, respectively) were evaluated. The cyclic guanosine monophosphate (cGMP) levels were analyzed in the perfusate, and the kidneys were removed to perform oxidative stress and histopathological analyses. Results: All renal parameters evaluated were reduced with BaV. In the SFC + BaV group, SFC restored PP to normal values and promoted a significant increase in %TNa+ and %TCl−. cGMP levels were increased in the SFC + BaV group. The oxidative stress biomarkers, malondialdehyde (MDA) and glutathione (GSH), were reduced by BaV. In the SFC + BaV group, a decrease in MDA without an increase in GSH was observed. These findings were confirmed by histological analysis, which showed improvement mainly in tubulis. Conclusion: Our data suggest the involvement of phosphodiesterase-5 and cGMP in BaV-induced nephrotoxicity since its effects were attenuated by the administration of SFC.
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spelling Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venomAcute kidney injuryKidney perfusionSildenafilSnake venomAcute kidney injury pathogenesis in envenoming by snakes is multifactorial and involves immunologic reactions, hemodynamic disturbances, and direct nephrotoxicity. Sildenafil (SFC), a phosphodiesterase 5 inhibitor, has been reported to protect against pathological kidney changes. Objective: This study aimed to investigate the protective effect of sildenafil against Bothrops alternatus snake venom (BaV)-induced nephrotoxicity. Methods: Kidneys from Wistar rats (n = 6, weighing 260–300 g) were isolated and divided into four groups: (1) perfused with a modified Krebs-Henseleit solution (MKHS) containing 6 g% of bovine serum albumin; (2) administered 3 μg/mL SFC; (3) perfused with 3 μg/mL BaV; and (4) administered SFC + BaV, both at 3 μg/mL. Subsequently, the perfusion pressure (PP), renal vascular resistance (RVR), urinary flow (UF), glomerular filtration rate (GFR), and percentage of electrolyte tubular sodium and chloride transport (%TNa+, %TCl−, respectively) were evaluated. The cyclic guanosine monophosphate (cGMP) levels were analyzed in the perfusate, and the kidneys were removed to perform oxidative stress and histopathological analyses. Results: All renal parameters evaluated were reduced with BaV. In the SFC + BaV group, SFC restored PP to normal values and promoted a significant increase in %TNa+ and %TCl−. cGMP levels were increased in the SFC + BaV group. The oxidative stress biomarkers, malondialdehyde (MDA) and glutathione (GSH), were reduced by BaV. In the SFC + BaV group, a decrease in MDA without an increase in GSH was observed. These findings were confirmed by histological analysis, which showed improvement mainly in tubulis. Conclusion: Our data suggest the involvement of phosphodiesterase-5 and cGMP in BaV-induced nephrotoxicity since its effects were attenuated by the administration of SFC.Department of Physiology and Pharmacology School of Medicine Federal University of Ceara, Coronel Nunes de Melo St., 1127Drug Research and Development Center (NPDM) Federal University of Ceara, Coronel Nunes de Melo St., 1000Department of Dental Clinic School of Pharmacy Dentistry and Nursing Federal University of Ceara, Monsenhor Furtado St.Center for the Study of Venoms and Venomous Animals Fazenda Experimental Lageado São Paulo State University, José Barbosa de Barros St. 1780Center for the Study of Venoms and Venomous Animals Fazenda Experimental Lageado São Paulo State University, José Barbosa de Barros St. 1780Federal University of CearaUniversidade Estadual Paulista (UNESP)Jorge, Antônio Rafael CoelhoMarinho, Aline DiogoSilveira, João Alison de MoraesNogueira Junior, Francisco Assisde Aquino, Pedro Everson AlexandreAlves, Ana Paula Negreiros NunesJorge, Roberta Jeane BezerraFerreira Junior, Rui Seabra [UNESP]Monteiro, Helena Serra Azul2022-04-29T08:33:17Z2022-04-29T08:33:17Z2021-10-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article46-52http://dx.doi.org/10.1016/j.toxicon.2021.08.024Toxicon, v. 202, p. 46-52.1879-31500041-0101http://hdl.handle.net/11449/22957710.1016/j.toxicon.2021.08.0242-s2.0-85115635243Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengToxiconinfo:eu-repo/semantics/openAccess2024-04-11T15:28:26Zoai:repositorio.unesp.br:11449/229577Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:46:59.738283Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venom
title Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venom
spellingShingle Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venom
Jorge, Antônio Rafael Coelho
Acute kidney injury
Kidney perfusion
Sildenafil
Snake venom
title_short Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venom
title_full Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venom
title_fullStr Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venom
title_full_unstemmed Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venom
title_sort Phosphodiesterase-5 inhibitor sildenafil attenuates kidney injury induced by Bothrops alternatus snake venom
author Jorge, Antônio Rafael Coelho
author_facet Jorge, Antônio Rafael Coelho
Marinho, Aline Diogo
Silveira, João Alison de Moraes
Nogueira Junior, Francisco Assis
de Aquino, Pedro Everson Alexandre
Alves, Ana Paula Negreiros Nunes
Jorge, Roberta Jeane Bezerra
Ferreira Junior, Rui Seabra [UNESP]
Monteiro, Helena Serra Azul
author_role author
author2 Marinho, Aline Diogo
Silveira, João Alison de Moraes
Nogueira Junior, Francisco Assis
de Aquino, Pedro Everson Alexandre
Alves, Ana Paula Negreiros Nunes
Jorge, Roberta Jeane Bezerra
Ferreira Junior, Rui Seabra [UNESP]
Monteiro, Helena Serra Azul
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Federal University of Ceara
Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Jorge, Antônio Rafael Coelho
Marinho, Aline Diogo
Silveira, João Alison de Moraes
Nogueira Junior, Francisco Assis
de Aquino, Pedro Everson Alexandre
Alves, Ana Paula Negreiros Nunes
Jorge, Roberta Jeane Bezerra
Ferreira Junior, Rui Seabra [UNESP]
Monteiro, Helena Serra Azul
dc.subject.por.fl_str_mv Acute kidney injury
Kidney perfusion
Sildenafil
Snake venom
topic Acute kidney injury
Kidney perfusion
Sildenafil
Snake venom
description Acute kidney injury pathogenesis in envenoming by snakes is multifactorial and involves immunologic reactions, hemodynamic disturbances, and direct nephrotoxicity. Sildenafil (SFC), a phosphodiesterase 5 inhibitor, has been reported to protect against pathological kidney changes. Objective: This study aimed to investigate the protective effect of sildenafil against Bothrops alternatus snake venom (BaV)-induced nephrotoxicity. Methods: Kidneys from Wistar rats (n = 6, weighing 260–300 g) were isolated and divided into four groups: (1) perfused with a modified Krebs-Henseleit solution (MKHS) containing 6 g% of bovine serum albumin; (2) administered 3 μg/mL SFC; (3) perfused with 3 μg/mL BaV; and (4) administered SFC + BaV, both at 3 μg/mL. Subsequently, the perfusion pressure (PP), renal vascular resistance (RVR), urinary flow (UF), glomerular filtration rate (GFR), and percentage of electrolyte tubular sodium and chloride transport (%TNa+, %TCl−, respectively) were evaluated. The cyclic guanosine monophosphate (cGMP) levels were analyzed in the perfusate, and the kidneys were removed to perform oxidative stress and histopathological analyses. Results: All renal parameters evaluated were reduced with BaV. In the SFC + BaV group, SFC restored PP to normal values and promoted a significant increase in %TNa+ and %TCl−. cGMP levels were increased in the SFC + BaV group. The oxidative stress biomarkers, malondialdehyde (MDA) and glutathione (GSH), were reduced by BaV. In the SFC + BaV group, a decrease in MDA without an increase in GSH was observed. These findings were confirmed by histological analysis, which showed improvement mainly in tubulis. Conclusion: Our data suggest the involvement of phosphodiesterase-5 and cGMP in BaV-induced nephrotoxicity since its effects were attenuated by the administration of SFC.
publishDate 2021
dc.date.none.fl_str_mv 2021-10-30
2022-04-29T08:33:17Z
2022-04-29T08:33:17Z
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/10.1016/j.toxicon.2021.08.024
Toxicon, v. 202, p. 46-52.
1879-3150
0041-0101
http://hdl.handle.net/11449/229577
10.1016/j.toxicon.2021.08.024
2-s2.0-85115635243
url http://dx.doi.org/10.1016/j.toxicon.2021.08.024
http://hdl.handle.net/11449/229577
identifier_str_mv Toxicon, v. 202, p. 46-52.
1879-3150
0041-0101
10.1016/j.toxicon.2021.08.024
2-s2.0-85115635243
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Toxicon
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 46-52
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
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