Bothrops pauloensis snake venom-derived Asp-49 and Lys-49 phospholipases A2 mediates acute kidney injury by oxidative stress and release of inflammatory cytokines
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , , , , , |
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. |
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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 |