Show simple item record

Authordc.contributor.authorMuñoz Ramírez, Alejandra 
Authordc.contributor.authorMascayano Collado, Carolina 
Authordc.contributor.authorBarriga, Andrés 
Authordc.contributor.authorEcheverría, Javier 
Authordc.contributor.authorUrzúa, Alejandro 
Admission datedc.date.accessioned2021-06-11T20:15:01Z
Available datedc.date.available2021-06-11T20:15:01Z
Publication datedc.date.issued2020
Cita de ítemdc.identifier.citationFrontiers in Pharmacology November 2020 | Volume 11 | Article 594257es_ES
Identifierdc.identifier.other10.3389/fphar.2020.594257
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/180103
Abstractdc.description.abstractLithraea caustica (Molina) Hook. and Arn. (Anacardiaceae), common name Litre, is an evergreen endemic plant used in the Mapuche Chilean folk medicine. The stem juice of L. caustica mixed with Rubus ulmifolius (blackberry) is used to treat cough and the infusion of leaves is used in baths to treat joint inflammations. In this study, the activities of 3-n-alk(en)yl-catechols, obtained from the dichloromethane extract of the epicuticular compounds of fresh leaves (DCME), stem bark petroleum ether extract (PEE), fractions of phenols and phenol-acid compounds obtained from the methanolic extract (methanolic extract) of defatted leaves and aqueous infusion (AE) from fresh leaves, were evaluated as in vitro inhibitors of soybean 15-lipoxygenase (15-sLOX) and human 5-lipoxygenase (5-hLOX), one of the inflammation pathways. The 3-n-alk(en)yl-catechols were characterized by gas chromatography-mass spectrometry and 1D and 2D nuclear magnetic resonance analysis as mixtures of 3-[(10E)-pentadec-10 '-en-1-yl]-catechol, 3-[(10Z)-pentadec-10 '-en-1-yl]-catechol and 3-n-pentadecylcatechol. In addition, two fractions, obtained from MeOHE, were characterized by liquid chromatography electrospray ionization tandem mass spectrometric as complex mixtures of known acids and phenolic compounds. DCME, MeOHE and ethyl acetate extract (AcOEtE) extracts showed inhibition against 15-sLOX, and the AE of fresh leaves, showed the best inhibition against 5-hLOX. The mixture of 3-n-alk(en)yl-catechols showed inhibition of 15-sLOX and 5-hLOX. The compounds 3-[(10Z)-pentadec-10 '-en-1-yl]-catechol (IC50 2.09 mu M) and 3-n-pentadecylcatechol (IC50 2.74 mu M) showed inhibition against 5-hLOX. The inhibition values obtained for the 3-n-alk(en)yl-catechols are in the range of well-known inhibitors of 5-hLOX. Acetylation of the 3-n-alk(en)yl-catechols blocks the inhibitory activity, indicating that the free catechol function is necessary for the enzyme inhibition. In addition, the fractions of phenols and phenol-acid compounds showed inhibitory activity against 15-sLOX and the AE, showed a good inhibition against 5-hLOX. These results would be in agreement with the use of L. caustica, as an anti-inflammatory in Mapuche ethnomedicine.es_ES
Patrocinadordc.description.sponsorshipEntidad financiadoraMostrar más información Número de concesión Universidad de Santiago de Chile USA1799-VRIDEI 021941MC-PAP USA2055_DICYT Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) 79160109 CONICYT: CONICYT-PCHA/Doctorado Nacional 21140089es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherFrontiers Mediaes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceFrontiers in Pharmacologyes_ES
Keywordsdc.subjectLithraea causticaes_ES
Keywordsdc.subjectAnacardiaceaees_ES
Keywordsdc.subject3-n-alk(en)yl-catecholses_ES
Keywordsdc.subjectSoybean 15-lipoxygenasees_ES
Keywordsdc.subjectHuman 5-lipoxygenasees_ES
Keywordsdc.subjectAnti-inflammatory activityes_ES
Títulodc.titleInhibition of soybean 15-lipoxygenase and human 5-lipoxygenase by extracts of leaves, stem bark, phenols and catechols isolated from lithraea caustica (Anacardiaceae)es_ES
Document typedc.typeArtículo de revistaes_ES
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorcfres_ES
Indexationuchile.indexArtículo de publicación ISI
Indexationuchile.indexArtículo de publicación SCOPUS


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record

Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile