Gingerol suppresses sepsis-induced acute kidney injury by modulating methylsulfonylmethane and dimethylamine production
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , , , |
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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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 |
_version_ |
1813028950814752768 |