Bothrops pauloensis snake venom-derived Asp-49 and Lys-49 phospholipases A2 mediates acute kidney injury by oxidative stress and release of inflammatory cytokines

Detalhes bibliográficos
Autor(a) principal: Marinho, Aline Diogo
Data de Publicação: 2021
Outros Autores: Silveira, João Alison de Moraes, Chaves Filho, Adriano José Maia, Jorge, Antônio Rafael Coelho, Nogueira Júnior, Francisco Assis, Pereira, Venúcia Bruna Magalhães, de Aquino, Pedro Everson Alexandre, Pereira, Cássia Arruda Souza, Evangelista, Janaina Serra Azul Monteiro, Macedo, Danielle Silveira, Lima Júnior, Roberto César Pereira, Toyama, Marcos Hikari [UNESP], Jorge, Roberta Jeane Bezerra, Pereira, Gustavo José Silva, 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.2020.12.004
http://hdl.handle.net/11449/208247
Resumo: The envenomation caused by the Bothrops pauloensis snake leads to severe local and systemic effects including acute kidney injury. In this study, we investigated the renal effects by phospholipases A2 (PLA2s), divided into two main subgroups, Asp-49 and Lys-49, isolated from the Bothrops pauloensis snake venom (BpV) in isolated rat kidney system. Both PLA2s (3 μg/mL), added alone to the perfusion system and analyzed for 120 min, had significant effects on isolated rat kidney. Asp-49 reduced Glomerular Filtration Rate (GFR) at 60, 90 and 120 min, and the percentage of total tubular sodium transport (%TNa+) and potassium transport (%TK+) at 120 min. Lys-49 increased Perfusion Pressure (PP) at 120 min and reduced GFR, %TNa+ and the percentage of total tubular chloride transport (%TCl−) at 60, 90 and 120 min. Cytokine release in the kidney tissues were increased with Asp-49 PLA2 (IL-10) and Lys-49 PLA2 (TNF-α, IL-1β, IL-10). Both increased MPO activity. Asp-49 PLA2 decreased Glutathione (GSH) and increased nitrite levels, while Lys-49 PLA2 increased Malondialdehyde (MDA), GSH and nitrite levels. Histological analysis of the perfused kidneys revealed the presence of glomerular degeneration and atrophy, deposit of proteinaceous material in Bowman's space and intratubular with both PLA2s. These findings indicated that both PLA2s modified the functional parameters in an isolated perfused kidney model with increased oxidative stress and cytokine release. PLA2s are one of the components at high concentration in BpV and our results provide important knowledge about their involvement with the nephrotoxic mechanism.
id UNSP_f541f53f81d40c1de0b7eb9fcc15b762
oai_identifier_str oai:repositorio.unesp.br:11449/208247
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Bothrops pauloensis snake venom-derived Asp-49 and Lys-49 phospholipases A2 mediates acute kidney injury by oxidative stress and release of inflammatory cytokinesAcute kidney injuryCytokinesKidney perfusionOxidative stressToxinsTubular damageThe envenomation caused by the Bothrops pauloensis snake leads to severe local and systemic effects including acute kidney injury. In this study, we investigated the renal effects by phospholipases A2 (PLA2s), divided into two main subgroups, Asp-49 and Lys-49, isolated from the Bothrops pauloensis snake venom (BpV) in isolated rat kidney system. Both PLA2s (3 μg/mL), added alone to the perfusion system and analyzed for 120 min, had significant effects on isolated rat kidney. Asp-49 reduced Glomerular Filtration Rate (GFR) at 60, 90 and 120 min, and the percentage of total tubular sodium transport (%TNa+) and potassium transport (%TK+) at 120 min. Lys-49 increased Perfusion Pressure (PP) at 120 min and reduced GFR, %TNa+ and the percentage of total tubular chloride transport (%TCl−) at 60, 90 and 120 min. Cytokine release in the kidney tissues were increased with Asp-49 PLA2 (IL-10) and Lys-49 PLA2 (TNF-α, IL-1β, IL-10). Both increased MPO activity. Asp-49 PLA2 decreased Glutathione (GSH) and increased nitrite levels, while Lys-49 PLA2 increased Malondialdehyde (MDA), GSH and nitrite levels. Histological analysis of the perfused kidneys revealed the presence of glomerular degeneration and atrophy, deposit of proteinaceous material in Bowman's space and intratubular with both PLA2s. These findings indicated that both PLA2s modified the functional parameters in an isolated perfused kidney model with increased oxidative stress and cytokine release. PLA2s are one of the components at high concentration in BpV and our results provide important knowledge about their involvement with the nephrotoxic mechanism.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)University of CambridgeFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Physiology and Pharmacology School of Medicine Federal University of Ceara, Coronel Nunes de Melo St., 60.430-275Drug Research and Development Center (NPDM) Federal University of Ceara, Coronel Nunes de Melo St., 60.430-275Department of Pharmacology Escola Paulista de Medicina Universidade Federal de São Paulo, Três de Maio St., 04.044-020Postgraduate Program in Veterinary Science School of Veterinary State University of CearaDepartment of Biological and Environmental Sciences São Paulo State University (UNESP)Department of Biological and Environmental Sciences São Paulo State University (UNESP)FAPESP: 2017/10863-7 (GJSP)Federal University of CearaUniversidade Federal de São Paulo (UNIFESP)State University of CearaUniversidade Estadual Paulista (Unesp)Marinho, Aline DiogoSilveira, João Alison de MoraesChaves Filho, Adriano José MaiaJorge, Antônio Rafael CoelhoNogueira Júnior, Francisco AssisPereira, Venúcia Bruna Magalhãesde Aquino, Pedro Everson AlexandrePereira, Cássia Arruda SouzaEvangelista, Janaina Serra Azul MonteiroMacedo, Danielle SilveiraLima Júnior, Roberto César PereiraToyama, Marcos Hikari [UNESP]Jorge, Roberta Jeane BezerraPereira, Gustavo José SilvaMonteiro, Helena Serra Azul2021-06-25T11:09:01Z2021-06-25T11:09:01Z2021-01-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article31-38http://dx.doi.org/10.1016/j.toxicon.2020.12.004Toxicon, v. 190, p. 31-38.1879-31500041-0101http://hdl.handle.net/11449/20824710.1016/j.toxicon.2020.12.0042-s2.0-85097684826Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengToxiconinfo:eu-repo/semantics/openAccess2021-10-23T18:56:55Zoai:repositorio.unesp.br:11449/208247Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T16:26:32.045919Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Bothrops pauloensis snake venom-derived Asp-49 and Lys-49 phospholipases A2 mediates acute kidney injury by oxidative stress and release of inflammatory cytokines
title Bothrops pauloensis snake venom-derived Asp-49 and Lys-49 phospholipases A2 mediates acute kidney injury by oxidative stress and release of inflammatory cytokines
spellingShingle Bothrops pauloensis snake venom-derived Asp-49 and Lys-49 phospholipases A2 mediates acute kidney injury by oxidative stress and release of inflammatory cytokines
Marinho, Aline Diogo
Acute kidney injury
Cytokines
Kidney perfusion
Oxidative stress
Toxins
Tubular damage
title_short Bothrops pauloensis snake venom-derived Asp-49 and Lys-49 phospholipases A2 mediates acute kidney injury by oxidative stress and release of inflammatory cytokines
title_full Bothrops pauloensis snake venom-derived Asp-49 and Lys-49 phospholipases A2 mediates acute kidney injury by oxidative stress and release of inflammatory cytokines
title_fullStr Bothrops pauloensis snake venom-derived Asp-49 and Lys-49 phospholipases A2 mediates acute kidney injury by oxidative stress and release of inflammatory cytokines
title_full_unstemmed Bothrops pauloensis snake venom-derived Asp-49 and Lys-49 phospholipases A2 mediates acute kidney injury by oxidative stress and release of inflammatory cytokines
title_sort Bothrops pauloensis snake venom-derived Asp-49 and Lys-49 phospholipases A2 mediates acute kidney injury by oxidative stress and release of inflammatory cytokines
author Marinho, Aline Diogo
author_facet Marinho, Aline Diogo
Silveira, João Alison de Moraes
Chaves Filho, Adriano José Maia
Jorge, Antônio Rafael Coelho
Nogueira Júnior, Francisco Assis
Pereira, Venúcia Bruna Magalhães
de Aquino, Pedro Everson Alexandre
Pereira, Cássia Arruda Souza
Evangelista, Janaina Serra Azul Monteiro
Macedo, Danielle Silveira
Lima Júnior, Roberto César Pereira
Toyama, Marcos Hikari [UNESP]
Jorge, Roberta Jeane Bezerra
Pereira, Gustavo José Silva
Monteiro, Helena Serra Azul
author_role author
author2 Silveira, João Alison de Moraes
Chaves Filho, Adriano José Maia
Jorge, Antônio Rafael Coelho
Nogueira Júnior, Francisco Assis
Pereira, Venúcia Bruna Magalhães
de Aquino, Pedro Everson Alexandre
Pereira, Cássia Arruda Souza
Evangelista, Janaina Serra Azul Monteiro
Macedo, Danielle Silveira
Lima Júnior, Roberto César Pereira
Toyama, Marcos Hikari [UNESP]
Jorge, Roberta Jeane Bezerra
Pereira, Gustavo José Silva
Monteiro, Helena Serra Azul
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Federal University of Ceara
Universidade Federal de São Paulo (UNIFESP)
State University of Ceara
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Marinho, Aline Diogo
Silveira, João Alison de Moraes
Chaves Filho, Adriano José Maia
Jorge, Antônio Rafael Coelho
Nogueira Júnior, Francisco Assis
Pereira, Venúcia Bruna Magalhães
de Aquino, Pedro Everson Alexandre
Pereira, Cássia Arruda Souza
Evangelista, Janaina Serra Azul Monteiro
Macedo, Danielle Silveira
Lima Júnior, Roberto César Pereira
Toyama, Marcos Hikari [UNESP]
Jorge, Roberta Jeane Bezerra
Pereira, Gustavo José Silva
Monteiro, Helena Serra Azul
dc.subject.por.fl_str_mv Acute kidney injury
Cytokines
Kidney perfusion
Oxidative stress
Toxins
Tubular damage
topic Acute kidney injury
Cytokines
Kidney perfusion
Oxidative stress
Toxins
Tubular damage
description The envenomation caused by the Bothrops pauloensis snake leads to severe local and systemic effects including acute kidney injury. In this study, we investigated the renal effects by phospholipases A2 (PLA2s), divided into two main subgroups, Asp-49 and Lys-49, isolated from the Bothrops pauloensis snake venom (BpV) in isolated rat kidney system. Both PLA2s (3 μg/mL), added alone to the perfusion system and analyzed for 120 min, had significant effects on isolated rat kidney. Asp-49 reduced Glomerular Filtration Rate (GFR) at 60, 90 and 120 min, and the percentage of total tubular sodium transport (%TNa+) and potassium transport (%TK+) at 120 min. Lys-49 increased Perfusion Pressure (PP) at 120 min and reduced GFR, %TNa+ and the percentage of total tubular chloride transport (%TCl−) at 60, 90 and 120 min. Cytokine release in the kidney tissues were increased with Asp-49 PLA2 (IL-10) and Lys-49 PLA2 (TNF-α, IL-1β, IL-10). Both increased MPO activity. Asp-49 PLA2 decreased Glutathione (GSH) and increased nitrite levels, while Lys-49 PLA2 increased Malondialdehyde (MDA), GSH and nitrite levels. Histological analysis of the perfused kidneys revealed the presence of glomerular degeneration and atrophy, deposit of proteinaceous material in Bowman's space and intratubular with both PLA2s. These findings indicated that both PLA2s modified the functional parameters in an isolated perfused kidney model with increased oxidative stress and cytokine release. PLA2s are one of the components at high concentration in BpV and our results provide important knowledge about their involvement with the nephrotoxic mechanism.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T11:09:01Z
2021-06-25T11:09:01Z
2021-01-30
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.2020.12.004
Toxicon, v. 190, p. 31-38.
1879-3150
0041-0101
http://hdl.handle.net/11449/208247
10.1016/j.toxicon.2020.12.004
2-s2.0-85097684826
url http://dx.doi.org/10.1016/j.toxicon.2020.12.004
http://hdl.handle.net/11449/208247
identifier_str_mv Toxicon, v. 190, p. 31-38.
1879-3150
0041-0101
10.1016/j.toxicon.2020.12.004
2-s2.0-85097684826
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 31-38
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
_version_ 1808128652015042560