Telmisartan modulates the oral mucositis induced by 5-Fluorouracil in hamsters
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/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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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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1813028765022814208 |