Publicação:
Gastroprotective mechanisms of Citrus lemon (Rutaceae) essential oil and its majority compounds limonene and beta-pinene: Involvement of heat-shock protein-70, vasoactive intestinal peptide, glutathione, sulfhydryl compounds, nitric oxide and prostaglandin E-2

dc.contributor.authorRozza, Ariane Leite [UNESP]
dc.contributor.authorMoraes, Thiago de Mello [UNESP]
dc.contributor.authorKushima, Helio [UNESP]
dc.contributor.authorTanimoto, Alexandre [UNESP]
dc.contributor.authorMayo Marques, Marcia Ortiz
dc.contributor.authorBauab, Taís Maria [UNESP]
dc.contributor.authorHiruma-Lima, Clélia Akiko [UNESP]
dc.contributor.authorPellizzon, Claudia Helena [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionCampinas Agron Inst
dc.date.accessioned2014-05-20T13:49:51Z
dc.date.available2014-05-20T13:49:51Z
dc.date.issued2011-01-15
dc.description.abstractCitrus lemon (CL) belongs to Rutaceae family and is popularly known in Brazil as lima() siciliano. The phytochemical analysis of CL fruit bark essential oil showed two majority components, limonene (LIM) and beta-pinene (PIN). This study aimed to evaluate the gastroprotective mechanism of action from CL, LIM and PIN in ethanol- and indomethacin-induced gastric ulcers and its in vitro anti-Helicobacter pylori activity. After ethanol-induced gastric ulcer, the ulcer area was measured and the stomachs were destined to histology (HE and PAS), immunohistochemistry for HSP-70 and VIP and glutathione (GSH) measurement. The involvement of nitric oxide (NO) and sulfhydryl (SH) compounds was determined. The ulcer area for indomethacin-induced gastric ulcers was measured. PGE(2) concentration was biochemically measured. The minimum inhibitory concentration (MIC) against H. pylori was determined in vitro. In ethanol model. CL and LIM demonstrated 100% of gastroprotection, while PIN did not exert effective gastroprotection (53.26%). In the indomethacin model, CL and LIM offered effective gastroprotection but PIN did not show gastroprotective effect. The gastric ulcer area of rats pretreated with NO-synthase inhibitor or SH-blocker was decreased in comparison to the control group. The MIC obtained for CL was 125 mu g/mL, for LIM was 75 mu g/mL and for PIN was 500 mu g/mL. The gastroprotective effect of CL and LIM was involved with increasing in mucus secretion, HSP-70 and VIP, but not with GSH. NO or SH compounds. CL gastroprotective mechanism is involved with PGE(2). PIN did not present gastroprotective activity. (C) 2010 Elsevier B.V. All rights reserved.en
dc.description.affiliationUNESP Univ Estadual Paulista, Dept Morphol, Biosci Inst, BR-18618970 Botucatu, SP, Brazil
dc.description.affiliationUNESP Univ Estadual Paulista, Dept Physiol, Biosci Inst, BR-18618970 Botucatu, SP, Brazil
dc.description.affiliationCampinas Agron Inst, BR-13020902 Campinas, SP, Brazil
dc.description.affiliationUNESP Univ Estadual Paulista, Dept Biol Sci, Sch Pharmaceut Sci, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUnespUNESP Univ Estadual Paulista, Dept Morphol, Biosci Inst, BR-18618970 Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP Univ Estadual Paulista, Dept Physiol, Biosci Inst, BR-18618970 Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP Univ Estadual Paulista, Dept Biol Sci, Sch Pharmaceut Sci, BR-14801902 Araraquara, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 07/53128-3
dc.description.sponsorshipIdFAPESP: 06/55542-9
dc.format.extent82-89
dc.identifierhttp://dx.doi.org/10.1016/j.cbi.2010.09.031
dc.identifier.citationChemico-biological Interactions. Clare: Elsevier B.V., v. 189, n. 1-2, p. 82-89, 2011.
dc.identifier.doi10.1016/j.cbi.2010.09.031
dc.identifier.issn0009-2797
dc.identifier.lattes0019393779801069
dc.identifier.lattes3814504901386844
dc.identifier.orcid0000-0002-8645-3777
dc.identifier.orcid0000-0002-4494-4180
dc.identifier.urihttp://hdl.handle.net/11449/17784
dc.identifier.wosWOS:000287004200010
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofChemico-biological Interactions
dc.relation.ispartofjcr3.296
dc.relation.ispartofsjr1,033
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectCitrus lemon essential oilen
dc.subjectLimoneneen
dc.subjectGastroprotectionen
dc.subjectPGE(2)en
dc.subjectSulfhydryl compoundsen
dc.titleGastroprotective mechanisms of Citrus lemon (Rutaceae) essential oil and its majority compounds limonene and beta-pinene: Involvement of heat-shock protein-70, vasoactive intestinal peptide, glutathione, sulfhydryl compounds, nitric oxide and prostaglandin E-2en
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes2328604224911233[1]
unesp.author.lattes0019393779801069[8]
unesp.author.lattes3814504901386844[7]
unesp.author.orcid0000-0002-4198-0135[1]
unesp.author.orcid0000-0002-8645-3777[7]
unesp.author.orcid0000-0002-4494-4180[8]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências, Botucatupt
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentCiências Biológicas - FCFpt
unesp.departmentFisiologia - IBBpt
unesp.departmentMorfologia - IBBpt

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