Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazine

Detalhes bibliográficos
Autor(a) principal: Witaicenis, Aline
Data de Publicação: 2012
Outros Autores: Luchini, Ana C., Hiruma-Lima, Clélia Akiko [UNESP], Felisbino, Sergio L. [UNESP], Garrido-Mesa, Natividad, Utrilla, Pilar, Galvez, Julio, Di Stasi, Luiz C. [UNESP]
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.
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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/openAccess2023-10-12T06:03:12Zoai:repositorio.unesp.br:11449/17491Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-10-12T06:03:12Repositório 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
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