Gingerol fraction from zingiber officinale nephrotoxicity protects against gentamicin-Induced nephrotoxicity
Autor(a) principal: | |
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Data de Publicação: | 2014 |
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/8458 |
Resumo: | Nephrotoxicity is the main complication of gentamicin (GM) treatment. GM induces renal damage by overproduction of reactive oxygen species and inflammation in proximal tubular cells. Phenolic compounds from ginger, called gingerols, have been demonstrated to have antioxidant and anti-inflammatory effects. We investigated if oral treatment with an enriched solution of gingerols (GF) would promote a nephroprotective effect in an animal nephropathy model. The following six groups of male Wistar rats were studied: (i) control group (CT group); (ii) gingerol solution control group (GF group); (iii) gentamicin treatment group (GM group), receiving 100 mg/kg of body weight intraperitoneally (i.p.); and (iv to vi) gentamicin groups also receiving GF, at doses of 6.25, 12.5, and 25 mg/kg, respectively (GM GF groups). Animals from the GM group had a significant decrease in creatinine clearance and higher levels of urinary protein excretion. This was associated with markers of oxidative stress and nitric oxide production. Also, there were increases of the mRNA levels for proinflammatory cytokines (tumor necrosis factor alpha [TNF- ], interleukin-1 [IL-1 ], IL-2, and gamma interferon [IFN- ]). Histopathological findings of tubular degeneration and inflammatory cell infiltration reinforced GM-induced nephrotoxicity. All these alterations were attenuated by previous oral treatment with GF. Animals from the GM GF groups showed amelioration in renal function parameters and reduced lipid peroxidation and nitrosative stress, in addition to an increment in the levels of glutathione (GSH) and superoxide dismutase (SOD) activity. Gingerols also promoted significant reductions in mRNA transcription for TNF- , IL-2, and IFN- . These effects were dose dependent. These results demonstrate that GF promotes a nephroprotective effect on GM-mediated nephropathy by oxidative stress, inflammatory processes, and renal dysfunction. |
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Gingerol fraction from zingiber officinale nephrotoxicity protects against gentamicin-Induced nephrotoxicityGentamicinasNephrotoxicity is the main complication of gentamicin (GM) treatment. GM induces renal damage by overproduction of reactive oxygen species and inflammation in proximal tubular cells. Phenolic compounds from ginger, called gingerols, have been demonstrated to have antioxidant and anti-inflammatory effects. We investigated if oral treatment with an enriched solution of gingerols (GF) would promote a nephroprotective effect in an animal nephropathy model. The following six groups of male Wistar rats were studied: (i) control group (CT group); (ii) gingerol solution control group (GF group); (iii) gentamicin treatment group (GM group), receiving 100 mg/kg of body weight intraperitoneally (i.p.); and (iv to vi) gentamicin groups also receiving GF, at doses of 6.25, 12.5, and 25 mg/kg, respectively (GM GF groups). Animals from the GM group had a significant decrease in creatinine clearance and higher levels of urinary protein excretion. This was associated with markers of oxidative stress and nitric oxide production. Also, there were increases of the mRNA levels for proinflammatory cytokines (tumor necrosis factor alpha [TNF- ], interleukin-1 [IL-1 ], IL-2, and gamma interferon [IFN- ]). Histopathological findings of tubular degeneration and inflammatory cell infiltration reinforced GM-induced nephrotoxicity. All these alterations were attenuated by previous oral treatment with GF. Animals from the GM GF groups showed amelioration in renal function parameters and reduced lipid peroxidation and nitrosative stress, in addition to an increment in the levels of glutathione (GSH) and superoxide dismutase (SOD) activity. Gingerols also promoted significant reductions in mRNA transcription for TNF- , IL-2, and IFN- . These effects were dose dependent. These results demonstrate that GF promotes a nephroprotective effect on GM-mediated nephropathy by oxidative stress, inflammatory processes, and renal dysfunction.Antimicrobial Agents and Chemotherapy2014-07-15T12:11:18Z2014-07-15T12:11:18Z2014-04info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfRODRIGUES, F. A. P. et al. Gingerol fraction from zingiber officinale protects against gentamicin-induced nephrotoxicity. Antimicrobial agents and chemotherapy, Bethesda, v. 58, n. 4, p. 1872–1878, 2014.1098-6596 On linehttp://www.repositorio.ufc.br/handle/riufc/8458Rodrigues, Francisco A. P.Prata, Mara M. G.Oliveira, Iris Cristina MaiaAlves, Natacha Teresa QueirozFreitas, Rosa E. M.Monteiro, Helena S. A.Silva, Jame's A.Vieira, Paulo C.Viana, Daniel A.Libório, Alexandre B.Havt, Alexandreengreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2022-05-02T12:30:12Zoai:repositorio.ufc.br:riufc/8458Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2024-09-11T18:43:41.728902Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false |
dc.title.none.fl_str_mv |
Gingerol fraction from zingiber officinale nephrotoxicity protects against gentamicin-Induced nephrotoxicity |
title |
Gingerol fraction from zingiber officinale nephrotoxicity protects against gentamicin-Induced nephrotoxicity |
spellingShingle |
Gingerol fraction from zingiber officinale nephrotoxicity protects against gentamicin-Induced nephrotoxicity Rodrigues, Francisco A. P. Gentamicinas |
title_short |
Gingerol fraction from zingiber officinale nephrotoxicity protects against gentamicin-Induced nephrotoxicity |
title_full |
Gingerol fraction from zingiber officinale nephrotoxicity protects against gentamicin-Induced nephrotoxicity |
title_fullStr |
Gingerol fraction from zingiber officinale nephrotoxicity protects against gentamicin-Induced nephrotoxicity |
title_full_unstemmed |
Gingerol fraction from zingiber officinale nephrotoxicity protects against gentamicin-Induced nephrotoxicity |
title_sort |
Gingerol fraction from zingiber officinale nephrotoxicity protects against gentamicin-Induced nephrotoxicity |
author |
Rodrigues, Francisco A. P. |
author_facet |
Rodrigues, Francisco A. P. Prata, Mara M. G. Oliveira, Iris Cristina Maia Alves, Natacha Teresa Queiroz Freitas, Rosa E. M. Monteiro, Helena S. A. Silva, Jame's A. Vieira, Paulo C. Viana, Daniel A. Libório, Alexandre B. Havt, Alexandre |
author_role |
author |
author2 |
Prata, Mara M. G. Oliveira, Iris Cristina Maia Alves, Natacha Teresa Queiroz Freitas, Rosa E. M. Monteiro, Helena S. A. Silva, Jame's A. Vieira, Paulo C. Viana, Daniel A. Libório, Alexandre B. Havt, Alexandre |
author2_role |
author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Rodrigues, Francisco A. P. Prata, Mara M. G. Oliveira, Iris Cristina Maia Alves, Natacha Teresa Queiroz Freitas, Rosa E. M. Monteiro, Helena S. A. Silva, Jame's A. Vieira, Paulo C. Viana, Daniel A. Libório, Alexandre B. Havt, Alexandre |
dc.subject.por.fl_str_mv |
Gentamicinas |
topic |
Gentamicinas |
description |
Nephrotoxicity is the main complication of gentamicin (GM) treatment. GM induces renal damage by overproduction of reactive oxygen species and inflammation in proximal tubular cells. Phenolic compounds from ginger, called gingerols, have been demonstrated to have antioxidant and anti-inflammatory effects. We investigated if oral treatment with an enriched solution of gingerols (GF) would promote a nephroprotective effect in an animal nephropathy model. The following six groups of male Wistar rats were studied: (i) control group (CT group); (ii) gingerol solution control group (GF group); (iii) gentamicin treatment group (GM group), receiving 100 mg/kg of body weight intraperitoneally (i.p.); and (iv to vi) gentamicin groups also receiving GF, at doses of 6.25, 12.5, and 25 mg/kg, respectively (GM GF groups). Animals from the GM group had a significant decrease in creatinine clearance and higher levels of urinary protein excretion. This was associated with markers of oxidative stress and nitric oxide production. Also, there were increases of the mRNA levels for proinflammatory cytokines (tumor necrosis factor alpha [TNF- ], interleukin-1 [IL-1 ], IL-2, and gamma interferon [IFN- ]). Histopathological findings of tubular degeneration and inflammatory cell infiltration reinforced GM-induced nephrotoxicity. All these alterations were attenuated by previous oral treatment with GF. Animals from the GM GF groups showed amelioration in renal function parameters and reduced lipid peroxidation and nitrosative stress, in addition to an increment in the levels of glutathione (GSH) and superoxide dismutase (SOD) activity. Gingerols also promoted significant reductions in mRNA transcription for TNF- , IL-2, and IFN- . These effects were dose dependent. These results demonstrate that GF promotes a nephroprotective effect on GM-mediated nephropathy by oxidative stress, inflammatory processes, and renal dysfunction. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-07-15T12:11:18Z 2014-07-15T12:11:18Z 2014-04 |
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. P. et al. Gingerol fraction from zingiber officinale protects against gentamicin-induced nephrotoxicity. Antimicrobial agents and chemotherapy, Bethesda, v. 58, n. 4, p. 1872–1878, 2014. 1098-6596 On line http://www.repositorio.ufc.br/handle/riufc/8458 |
identifier_str_mv |
RODRIGUES, F. A. P. et al. Gingerol fraction from zingiber officinale protects against gentamicin-induced nephrotoxicity. Antimicrobial agents and chemotherapy, Bethesda, v. 58, n. 4, p. 1872–1878, 2014. 1098-6596 On line |
url |
http://www.repositorio.ufc.br/handle/riufc/8458 |
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 |
Antimicrobial Agents and Chemotherapy |
publisher.none.fl_str_mv |
Antimicrobial Agents and Chemotherapy |
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_ |
1813028922564018176 |