Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Francisco Adelvane de Paulo
Data de Publicação: 2018
Outros Autores: Santos, Alan Diego da Conceição, Medeiros, Pedro Henrique Quintela Soares de, Prata, Mara de Moura Gondim, Santos, Tailane Caína de Souza, Silva, James Almada da, Brito, Gerly Anne de Castro, Santos, Armênio Aguiar dos, Silveira, Edilberto Rocha, Lima, Aldo Ângelo Moreira, Havt, Alexandre
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da Universidade Federal do Ceará (UFC)
Texto Completo: http://www.repositorio.ufc.br/handle/riufc/35900
Resumo: Acute kidney injury (AKI) and metabolic dysfunction are critical complications in sepsis syndrome; however, their pathophysiological mechanisms remain poorly understood. Therefore, we evaluated whether the pharmacological properties of 6-gingerol (6G) and 10-gingerol (10G) could modulate AKI and metabolic disruption in a rat model of sepsis (faecal peritonitis). Animals from the sham and AKI groups were intraperitoneally injected with 6G or 10G (25 mg/kg). Septic AKI decreased creatinine clearance and renal antioxidant activity, but enhanced oxidative stress and the renal mRNA levels of tumour necrosis factor-α, interleukin-1β, and transforming growth factor-β. Both phenol compounds repaired kidney function through antioxidant activity related to decreased oxidative/nitrosative stress and proinflammatory cytokines. Metabolomics analysis indicated different metabolic profiles for the sham surgery group, caecal ligation and puncture model alone group, and sepsis groups treated with gingerols. 1H nuclear magnetic resonance analysis detected important increases in urinary creatine, allantoin, and dimethylglycine levels in septic rats. However, dimethylamine and methylsulfonylmethane metabolites were more frequently detected in septic animals treated with 6G or 10G, and were associated with increased survival of septic animals. Gingerols attenuated septic AKI by decreasing renal disturbances, oxidative stress, and inflammatory response through a mechanism possibly correlated with increased production of dimethylamine and methylsulfonylmethane.
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spelling Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine productionSepseSepsisAcute Kidney InjuryLesão Renal AgudaAcute kidney injury (AKI) and metabolic dysfunction are critical complications in sepsis syndrome; however, their pathophysiological mechanisms remain poorly understood. Therefore, we evaluated whether the pharmacological properties of 6-gingerol (6G) and 10-gingerol (10G) could modulate AKI and metabolic disruption in a rat model of sepsis (faecal peritonitis). Animals from the sham and AKI groups were intraperitoneally injected with 6G or 10G (25 mg/kg). Septic AKI decreased creatinine clearance and renal antioxidant activity, but enhanced oxidative stress and the renal mRNA levels of tumour necrosis factor-α, interleukin-1β, and transforming growth factor-β. Both phenol compounds repaired kidney function through antioxidant activity related to decreased oxidative/nitrosative stress and proinflammatory cytokines. Metabolomics analysis indicated different metabolic profiles for the sham surgery group, caecal ligation and puncture model alone group, and sepsis groups treated with gingerols. 1H nuclear magnetic resonance analysis detected important increases in urinary creatine, allantoin, and dimethylglycine levels in septic rats. However, dimethylamine and methylsulfonylmethane metabolites were more frequently detected in septic animals treated with 6G or 10G, and were associated with increased survival of septic animals. Gingerols attenuated septic AKI by decreasing renal disturbances, oxidative stress, and inflammatory response through a mechanism possibly correlated with increased production of dimethylamine and methylsulfonylmethane.Scientific Reports2018-09-25T12:32:37Z2018-09-25T12:32:37Z2018-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfRODRIGUES, F. A. de P. et al. Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production. Scientific Reports, v. 8, p. 1-10, aug. 2018.2045-2322, ESSN: 2045-2322)http://www.repositorio.ufc.br/handle/riufc/35900Rodrigues, Francisco Adelvane de PauloSantos, Alan Diego da ConceiçãoMedeiros, Pedro Henrique Quintela Soares dePrata, Mara de Moura GondimSantos, Tailane Caína de SouzaSilva, James Almada daBrito, Gerly Anne de CastroSantos, Armênio Aguiar dosSilveira, Edilberto RochaLima, Aldo Ângelo MoreiraHavt, Alexandreengreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2019-10-16T16:46:04Zoai:repositorio.ufc.br:riufc/35900Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2024-09-11T18:47:57.500538Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.none.fl_str_mv Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production
title Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production
spellingShingle Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production
Rodrigues, Francisco Adelvane de Paulo
Sepse
Sepsis
Acute Kidney Injury
Lesão Renal Aguda
title_short Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production
title_full Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production
title_fullStr Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production
title_full_unstemmed Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production
title_sort Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production
author Rodrigues, Francisco Adelvane de Paulo
author_facet Rodrigues, Francisco Adelvane de Paulo
Santos, Alan Diego da Conceição
Medeiros, Pedro Henrique Quintela Soares de
Prata, Mara de Moura Gondim
Santos, Tailane Caína de Souza
Silva, James Almada da
Brito, Gerly Anne de Castro
Santos, Armênio Aguiar dos
Silveira, Edilberto Rocha
Lima, Aldo Ângelo Moreira
Havt, Alexandre
author_role author
author2 Santos, Alan Diego da Conceição
Medeiros, Pedro Henrique Quintela Soares de
Prata, Mara de Moura Gondim
Santos, Tailane Caína de Souza
Silva, James Almada da
Brito, Gerly Anne de Castro
Santos, Armênio Aguiar dos
Silveira, Edilberto Rocha
Lima, Aldo Ângelo Moreira
Havt, Alexandre
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Rodrigues, Francisco Adelvane de Paulo
Santos, Alan Diego da Conceição
Medeiros, Pedro Henrique Quintela Soares de
Prata, Mara de Moura Gondim
Santos, Tailane Caína de Souza
Silva, James Almada da
Brito, Gerly Anne de Castro
Santos, Armênio Aguiar dos
Silveira, Edilberto Rocha
Lima, Aldo Ângelo Moreira
Havt, Alexandre
dc.subject.por.fl_str_mv Sepse
Sepsis
Acute Kidney Injury
Lesão Renal Aguda
topic Sepse
Sepsis
Acute Kidney Injury
Lesão Renal Aguda
description Acute kidney injury (AKI) and metabolic dysfunction are critical complications in sepsis syndrome; however, their pathophysiological mechanisms remain poorly understood. Therefore, we evaluated whether the pharmacological properties of 6-gingerol (6G) and 10-gingerol (10G) could modulate AKI and metabolic disruption in a rat model of sepsis (faecal peritonitis). Animals from the sham and AKI groups were intraperitoneally injected with 6G or 10G (25 mg/kg). Septic AKI decreased creatinine clearance and renal antioxidant activity, but enhanced oxidative stress and the renal mRNA levels of tumour necrosis factor-α, interleukin-1β, and transforming growth factor-β. Both phenol compounds repaired kidney function through antioxidant activity related to decreased oxidative/nitrosative stress and proinflammatory cytokines. Metabolomics analysis indicated different metabolic profiles for the sham surgery group, caecal ligation and puncture model alone group, and sepsis groups treated with gingerols. 1H nuclear magnetic resonance analysis detected important increases in urinary creatine, allantoin, and dimethylglycine levels in septic rats. However, dimethylamine and methylsulfonylmethane metabolites were more frequently detected in septic animals treated with 6G or 10G, and were associated with increased survival of septic animals. Gingerols attenuated septic AKI by decreasing renal disturbances, oxidative stress, and inflammatory response through a mechanism possibly correlated with increased production of dimethylamine and methylsulfonylmethane.
publishDate 2018
dc.date.none.fl_str_mv 2018-09-25T12:32:37Z
2018-09-25T12:32:37Z
2018-08
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 RODRIGUES, F. A. de P. et al. Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production. Scientific Reports, v. 8, p. 1-10, aug. 2018.
2045-2322, ESSN: 2045-2322)
http://www.repositorio.ufc.br/handle/riufc/35900
identifier_str_mv RODRIGUES, F. A. de P. et al. Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production. Scientific Reports, v. 8, p. 1-10, aug. 2018.
2045-2322, ESSN: 2045-2322)
url http://www.repositorio.ufc.br/handle/riufc/35900
dc.language.iso.fl_str_mv eng
language eng
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.publisher.none.fl_str_mv Scientific Reports
publisher.none.fl_str_mv Scientific Reports
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal do Ceará (UFC)
instname:Universidade Federal do Ceará (UFC)
instacron:UFC
instname_str Universidade Federal do Ceará (UFC)
instacron_str UFC
institution UFC
reponame_str Repositório Institucional da Universidade Federal do Ceará (UFC)
collection Repositório Institucional da Universidade Federal do Ceará (UFC)
repository.name.fl_str_mv Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)
repository.mail.fl_str_mv bu@ufc.br || repositorio@ufc.br
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