Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters

Detalhes bibliográficos
Autor(a) principal: Barbosa, Maisie M.
Data de Publicação: 2018
Outros Autores: Araújo, Aurigena A. de, Araújo Júnior, Raimundo F. de, Guerra, Gerlane C. B., Brito, Gerly A. de Castro, Leitão, Renata C., Ribeiro, Susana B., Tavares, Emanuella de Aragão, Vasconcelos, Roseane C., Garcia, Vinícius B., Medeiros, Caroline A. C. X. de
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/35954
Resumo: Oral mucositis (OM) is a common adverse effect resulting from cancer therapy. The OM it has implications that may compromise oncologic treatment and decrease the patient’s quality of life. The therapeutic options to prevent or treat the symptoms of OM are scarce; there is no effective therapy that improves the symptoms. Based on the need for further research for the treatment of OM, the present study objective was to evaluate the effect of telmisartan (TELM) on the OM induced by 5-fluorouracil (5-FU), using as animal model Golden Syrian hamsters. 5-FU followed by mechanical trauma on day 4 was used to induce OM in hamsters. Euthanasia occurred on the day 10. The experiments were constituted by the groups saline, mechanical trauma, 5-FU, and TELM in three doses (1, 5, or 10 mg/kg). Macroscopic, histopathological, and immunohistochemical analyses as well as immunofluorescence experiments were performed on the oral mucosa of the animals. The samples also were used for analysis enzyme-linked immunosorbent assays and quantitative real-time polymerase chain reactions (qPCR). TELM (5 or 10 mg/kg) was able to reduce the inflammatory ulceration and infiltration in the oral mucosa of the animals, decreasing the levels of the cytokines TNF-a and IL-1b. These treatments was minimize the immunostaining for cyclooxygenase-2, matrix metalloproteinase-9, transforming growth factor-b, and smad 2/3. The nuclear transcription factor kappa B (NFkB) p65 and inducible nitric oxide synthase were reduced in the oral mucosa. Finally, TELM (10 mg/kg) increased the PPARg gene expression and reduced STAT1 and NFkB p65 gene expression relative to the 5-FU group. Therefore, TELM prevents the OM produced by 5-FU on animal model.
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spelling Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamstersEstomatiteStomatitisCytokinesCitocinasOral mucositis (OM) is a common adverse effect resulting from cancer therapy. The OM it has implications that may compromise oncologic treatment and decrease the patient’s quality of life. The therapeutic options to prevent or treat the symptoms of OM are scarce; there is no effective therapy that improves the symptoms. Based on the need for further research for the treatment of OM, the present study objective was to evaluate the effect of telmisartan (TELM) on the OM induced by 5-fluorouracil (5-FU), using as animal model Golden Syrian hamsters. 5-FU followed by mechanical trauma on day 4 was used to induce OM in hamsters. Euthanasia occurred on the day 10. The experiments were constituted by the groups saline, mechanical trauma, 5-FU, and TELM in three doses (1, 5, or 10 mg/kg). Macroscopic, histopathological, and immunohistochemical analyses as well as immunofluorescence experiments were performed on the oral mucosa of the animals. The samples also were used for analysis enzyme-linked immunosorbent assays and quantitative real-time polymerase chain reactions (qPCR). TELM (5 or 10 mg/kg) was able to reduce the inflammatory ulceration and infiltration in the oral mucosa of the animals, decreasing the levels of the cytokines TNF-a and IL-1b. These treatments was minimize the immunostaining for cyclooxygenase-2, matrix metalloproteinase-9, transforming growth factor-b, and smad 2/3. The nuclear transcription factor kappa B (NFkB) p65 and inducible nitric oxide synthase were reduced in the oral mucosa. Finally, TELM (10 mg/kg) increased the PPARg gene expression and reduced STAT1 and NFkB p65 gene expression relative to the 5-FU group. Therefore, TELM prevents the OM produced by 5-FU on animal model.Frontiers in Physiology2018-09-26T13:36:31Z2018-09-26T13:36:31Z2018-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfBARBOSA, Maisie M. et al. Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters. Frontiers in Physiology, v. 9, p. 1-12, aug. 2018.1664-042Xhttp://www.repositorio.ufc.br/handle/riufc/35954Barbosa, Maisie M.Araújo, Aurigena A. deAraújo Júnior, Raimundo F. deGuerra, Gerlane C. B.Brito, Gerly A. de CastroLeitão, Renata C.Ribeiro, Susana B.Tavares, Emanuella de AragãoVasconcelos, Roseane C.Garcia, Vinícius B.Medeiros, Caroline A. C. X. deengreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2018-12-14T13:27:16Zoai:repositorio.ufc.br:riufc/35954Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2024-09-11T18:20:49.118594Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.none.fl_str_mv Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters
title Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters
spellingShingle Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters
Barbosa, Maisie M.
Estomatite
Stomatitis
Cytokines
Citocinas
title_short Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters
title_full Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters
title_fullStr Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters
title_full_unstemmed Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters
title_sort Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters
author Barbosa, Maisie M.
author_facet Barbosa, Maisie M.
Araújo, Aurigena A. de
Araújo Júnior, Raimundo F. de
Guerra, Gerlane C. B.
Brito, Gerly A. de Castro
Leitão, Renata C.
Ribeiro, Susana B.
Tavares, Emanuella de Aragão
Vasconcelos, Roseane C.
Garcia, Vinícius B.
Medeiros, Caroline A. C. X. de
author_role author
author2 Araújo, Aurigena A. de
Araújo Júnior, Raimundo F. de
Guerra, Gerlane C. B.
Brito, Gerly A. de Castro
Leitão, Renata C.
Ribeiro, Susana B.
Tavares, Emanuella de Aragão
Vasconcelos, Roseane C.
Garcia, Vinícius B.
Medeiros, Caroline A. C. X. de
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Barbosa, Maisie M.
Araújo, Aurigena A. de
Araújo Júnior, Raimundo F. de
Guerra, Gerlane C. B.
Brito, Gerly A. de Castro
Leitão, Renata C.
Ribeiro, Susana B.
Tavares, Emanuella de Aragão
Vasconcelos, Roseane C.
Garcia, Vinícius B.
Medeiros, Caroline A. C. X. de
dc.subject.por.fl_str_mv Estomatite
Stomatitis
Cytokines
Citocinas
topic Estomatite
Stomatitis
Cytokines
Citocinas
description Oral mucositis (OM) is a common adverse effect resulting from cancer therapy. The OM it has implications that may compromise oncologic treatment and decrease the patient’s quality of life. The therapeutic options to prevent or treat the symptoms of OM are scarce; there is no effective therapy that improves the symptoms. Based on the need for further research for the treatment of OM, the present study objective was to evaluate the effect of telmisartan (TELM) on the OM induced by 5-fluorouracil (5-FU), using as animal model Golden Syrian hamsters. 5-FU followed by mechanical trauma on day 4 was used to induce OM in hamsters. Euthanasia occurred on the day 10. The experiments were constituted by the groups saline, mechanical trauma, 5-FU, and TELM in three doses (1, 5, or 10 mg/kg). Macroscopic, histopathological, and immunohistochemical analyses as well as immunofluorescence experiments were performed on the oral mucosa of the animals. The samples also were used for analysis enzyme-linked immunosorbent assays and quantitative real-time polymerase chain reactions (qPCR). TELM (5 or 10 mg/kg) was able to reduce the inflammatory ulceration and infiltration in the oral mucosa of the animals, decreasing the levels of the cytokines TNF-a and IL-1b. These treatments was minimize the immunostaining for cyclooxygenase-2, matrix metalloproteinase-9, transforming growth factor-b, and smad 2/3. The nuclear transcription factor kappa B (NFkB) p65 and inducible nitric oxide synthase were reduced in the oral mucosa. Finally, TELM (10 mg/kg) increased the PPARg gene expression and reduced STAT1 and NFkB p65 gene expression relative to the 5-FU group. Therefore, TELM prevents the OM produced by 5-FU on animal model.
publishDate 2018
dc.date.none.fl_str_mv 2018-09-26T13:36:31Z
2018-09-26T13:36:31Z
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 BARBOSA, Maisie M. et al. Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters. Frontiers in Physiology, v. 9, p. 1-12, aug. 2018.
1664-042X
http://www.repositorio.ufc.br/handle/riufc/35954
identifier_str_mv BARBOSA, Maisie M. et al. Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters. Frontiers in Physiology, v. 9, p. 1-12, aug. 2018.
1664-042X
url http://www.repositorio.ufc.br/handle/riufc/35954
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 Frontiers in Physiology
publisher.none.fl_str_mv Frontiers in Physiology
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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