Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazine
Autor(a) principal: | |
---|---|
Data de Publicação: | 2012 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.cbi.2011.11.004 http://hdl.handle.net/11449/17491 |
Resumo: | The aim of the present study was to compare the effects of the 4-methylesculetin with those produced by prednisolone and sulphasalazine and to elucidate the mechanisms involved in its action. Colitis was induced in rat by instillation of trinitrobenzenesulphonic acid (TNBS). The colon damage was evaluated using macroscopic, microscopic and biochemical analysis. In addition, in vitro studies were performed to evaluate cytokine production in cell cultures using the murine macrophage cell line RAW264.7, mouse splenocytes and the human colonic epithelial cell line Caco-2. 4-Methylesculetin produced a reduction of the macroscopic damage score and the recovery of the intestinal cytoarchitecture. These effects were associated with a prevention of the GSH depletion and an inhibition in AP activity. After colitis relapse, 4-methylesculetin improved the colonic inflammatory status as evidenced by histological findings, with a reduction in apoptosis, as well as biochemically by inhibition of colonic myeloperoxidase, alkaline phosphatase and metalloproteinase 9 activities. Paired with this inhibitive activity, there was a decrease in malondialdehyde content and in IL-1 beta levels. In vitro assays revealed that 4-methylesculetin promoted an inhibition in IL-1 beta, IL-8, IL-2 and IFN-gamma production in cell cultures. In conclusion, 4-methylesculetin showed similar efficacy to that obtained with either prednisolone or sulphasalazine, both in the acute phase of colitis as well as following a curative protocol. The intestinal anti-inflammatory activity by 4-methylesculetin is likely related to its ability in reduce colonic oxidative stress and inhibit pro-inflammatory cytokine production. (C) 2011 Elsevier B.V. All rights reserved. |
id |
UNSP_0075ea2ea553b3017dd81d3a910b79be |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/17491 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
spelling |
Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazineIBD4-MethylesculetinTNBSMetalloproteinaseApoptosisThe aim of the present study was to compare the effects of the 4-methylesculetin with those produced by prednisolone and sulphasalazine and to elucidate the mechanisms involved in its action. Colitis was induced in rat by instillation of trinitrobenzenesulphonic acid (TNBS). The colon damage was evaluated using macroscopic, microscopic and biochemical analysis. In addition, in vitro studies were performed to evaluate cytokine production in cell cultures using the murine macrophage cell line RAW264.7, mouse splenocytes and the human colonic epithelial cell line Caco-2. 4-Methylesculetin produced a reduction of the macroscopic damage score and the recovery of the intestinal cytoarchitecture. These effects were associated with a prevention of the GSH depletion and an inhibition in AP activity. After colitis relapse, 4-methylesculetin improved the colonic inflammatory status as evidenced by histological findings, with a reduction in apoptosis, as well as biochemically by inhibition of colonic myeloperoxidase, alkaline phosphatase and metalloproteinase 9 activities. Paired with this inhibitive activity, there was a decrease in malondialdehyde content and in IL-1 beta levels. In vitro assays revealed that 4-methylesculetin promoted an inhibition in IL-1 beta, IL-8, IL-2 and IFN-gamma production in cell cultures. In conclusion, 4-methylesculetin showed similar efficacy to that obtained with either prednisolone or sulphasalazine, both in the acute phase of colitis as well as following a curative protocol. The intestinal anti-inflammatory activity by 4-methylesculetin is likely related to its ability in reduce colonic oxidative stress and inhibit pro-inflammatory cytokine production. (C) 2011 Elsevier B.V. All rights reserved.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Spanish Ministry of Science and InnovationEuropean UnionJunta de AndaluciaUniv Estadual Paulista UNESP, Inst Biosci, Dept Pharmacol, Lab Phytomed, BR-18618970 Botucatu, SP, BrazilUniv Estadual Paulista UNESP, Inst Biosci, Dept Physiol, BR-18618970 Botucatu, SP, BrazilUniv Estadual Paulista UNESP, Inst Biosci, Dept Morphol, Botucatu, SP, BrazilUniv Granada, Dept Pharmacol, CIBER EHD, Ctr Biomed Res, Granada, SpainUniv Estadual Paulista UNESP, Inst Biosci, Dept Pharmacol, Lab Phytomed, BR-18618970 Botucatu, SP, BrazilUniv Estadual Paulista UNESP, Inst Biosci, Dept Physiol, BR-18618970 Botucatu, SP, BrazilUniv Estadual Paulista UNESP, Inst Biosci, Dept Morphol, Botucatu, SP, BrazilFAPESP: 03/09324-1FAPESP: 06/55209-9FAPESP: 07/54516-7Spanish Ministry of Science and Innovation: SAF2008-02616Junta de Andalucia: CTS 164Elsevier B.V.Universidade Estadual Paulista (Unesp)Univ GranadaWitaicenis, AlineLuchini, Ana C.Hiruma-Lima, Clélia Akiko [UNESP]Felisbino, Sergio L. [UNESP]Garrido-Mesa, NatividadUtrilla, PilarGalvez, JulioDi Stasi, Luiz C. [UNESP]2014-05-20T13:49:07Z2014-05-20T13:49:07Z2012-01-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article76-85application/pdfhttp://dx.doi.org/10.1016/j.cbi.2011.11.004Chemico-biological Interactions. Clare: Elsevier B.V., v. 195, n. 1, p. 76-85, 2012.0009-2797http://hdl.handle.net/11449/1749110.1016/j.cbi.2011.11.004WOS:000299917700010WOS000299917700010.pdf38145049013868440000-0002-8645-3777Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengChemico-biological Interactions3.2961,033info:eu-repo/semantics/openAccess2024-10-14T19:14:34Zoai:repositorio.unesp.br:11449/17491Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-10-14T19:14:34Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazine |
title |
Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazine |
spellingShingle |
Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazine Witaicenis, Aline IBD 4-Methylesculetin TNBS Metalloproteinase Apoptosis |
title_short |
Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazine |
title_full |
Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazine |
title_fullStr |
Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazine |
title_full_unstemmed |
Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazine |
title_sort |
Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazine |
author |
Witaicenis, Aline |
author_facet |
Witaicenis, Aline Luchini, Ana C. Hiruma-Lima, Clélia Akiko [UNESP] Felisbino, Sergio L. [UNESP] Garrido-Mesa, Natividad Utrilla, Pilar Galvez, Julio Di Stasi, Luiz C. [UNESP] |
author_role |
author |
author2 |
Luchini, Ana C. Hiruma-Lima, Clélia Akiko [UNESP] Felisbino, Sergio L. [UNESP] Garrido-Mesa, Natividad Utrilla, Pilar Galvez, Julio Di Stasi, Luiz C. [UNESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Univ Granada |
dc.contributor.author.fl_str_mv |
Witaicenis, Aline Luchini, Ana C. Hiruma-Lima, Clélia Akiko [UNESP] Felisbino, Sergio L. [UNESP] Garrido-Mesa, Natividad Utrilla, Pilar Galvez, Julio Di Stasi, Luiz C. [UNESP] |
dc.subject.por.fl_str_mv |
IBD 4-Methylesculetin TNBS Metalloproteinase Apoptosis |
topic |
IBD 4-Methylesculetin TNBS Metalloproteinase Apoptosis |
description |
The aim of the present study was to compare the effects of the 4-methylesculetin with those produced by prednisolone and sulphasalazine and to elucidate the mechanisms involved in its action. Colitis was induced in rat by instillation of trinitrobenzenesulphonic acid (TNBS). The colon damage was evaluated using macroscopic, microscopic and biochemical analysis. In addition, in vitro studies were performed to evaluate cytokine production in cell cultures using the murine macrophage cell line RAW264.7, mouse splenocytes and the human colonic epithelial cell line Caco-2. 4-Methylesculetin produced a reduction of the macroscopic damage score and the recovery of the intestinal cytoarchitecture. These effects were associated with a prevention of the GSH depletion and an inhibition in AP activity. After colitis relapse, 4-methylesculetin improved the colonic inflammatory status as evidenced by histological findings, with a reduction in apoptosis, as well as biochemically by inhibition of colonic myeloperoxidase, alkaline phosphatase and metalloproteinase 9 activities. Paired with this inhibitive activity, there was a decrease in malondialdehyde content and in IL-1 beta levels. In vitro assays revealed that 4-methylesculetin promoted an inhibition in IL-1 beta, IL-8, IL-2 and IFN-gamma production in cell cultures. In conclusion, 4-methylesculetin showed similar efficacy to that obtained with either prednisolone or sulphasalazine, both in the acute phase of colitis as well as following a curative protocol. The intestinal anti-inflammatory activity by 4-methylesculetin is likely related to its ability in reduce colonic oxidative stress and inhibit pro-inflammatory cytokine production. (C) 2011 Elsevier B.V. All rights reserved. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-01-05 2014-05-20T13:49:07Z 2014-05-20T13:49:07Z |
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 |
http://dx.doi.org/10.1016/j.cbi.2011.11.004 Chemico-biological Interactions. Clare: Elsevier B.V., v. 195, n. 1, p. 76-85, 2012. 0009-2797 http://hdl.handle.net/11449/17491 10.1016/j.cbi.2011.11.004 WOS:000299917700010 WOS000299917700010.pdf 3814504901386844 0000-0002-8645-3777 |
url |
http://dx.doi.org/10.1016/j.cbi.2011.11.004 http://hdl.handle.net/11449/17491 |
identifier_str_mv |
Chemico-biological Interactions. Clare: Elsevier B.V., v. 195, n. 1, p. 76-85, 2012. 0009-2797 10.1016/j.cbi.2011.11.004 WOS:000299917700010 WOS000299917700010.pdf 3814504901386844 0000-0002-8645-3777 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Chemico-biological Interactions 3.296 1,033 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
76-85 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1826303584344473600 |