Mostrar el registro sencillo del ítem

dc.rights.licenseopenen_US
dc.contributor.authorARRAKI, Kamel
dc.contributor.authorTOTOSON, Perle
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorDECENDIT, Alain
dc.contributor.authorZEDET, Andy
dc.contributor.authorMAROILLEY, Justine
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorBADOC, Alain
dc.contributor.authorDEMOUGEOT, Céline
dc.contributor.authorGIRARD, C.
dc.contributor.authorGIRARD, Corine
dc.date.accessioned2022-01-05T14:30:03Z
dc.date.available2022-01-05T14:30:03Z
dc.date.issued2021-03-18
dc.identifier.issn1420-3049en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/124323
dc.description.abstractEnPolyphenolic enriched extracts from two species of Cyperus, Cyperus glomeratus and Cyperus thunbergii, possess mammalian arginase inhibitory capacities, with the percentage inhibition ranging from 80% to 95% at 100 µg/mL and 40% to 64% at 10 µg/mL. Phytochemical investigation of these species led to the isolation and identification of two new natural stilbene oligomers named thunbergin A-B (1-2), together with three other stilbenes, trans-resveratrol (3), trans-scirpusin A (4), trans-cyperusphenol A (6), and two flavonoids, aureusidin (5) and luteolin (7), which were isolated for the first time from C. thunbergii and C. glomeratus. Structures were established on the basis of the spectroscopic data from MS and NMR experiments. The arginase inhibitory activity of compounds 1-7 was evaluated through an in vitro arginase inhibitory assay using purified liver bovine arginase. As a result, five compounds (1, 4-7) showed significant inhibition of arginase, with IC50 values between 17.6 and 60.6 µM, in the range of those of the natural arginase inhibitor piceatannol (12.6 µM). In addition, methanolic extract from Cyperus thunbergii exhibited an endothelium and NO-dependent vasorelaxant effect on thoracic aortic rings from rats and improved endothelial dysfunction in an adjuvant-induced arthritis rat model.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enCyperus thunbergii
dc.subject.enCyperus glomeratus
dc.subject.enArginase inhibitors
dc.subject.enVasorelaxante activity
dc.subject.enStilbenes
dc.subject.enFlavonoids
dc.title.enMammalian arginase inhibitory activity of methanolic extracts and isolated compounds from cyperus species
dc.typeArticle de revueen_US
dc.identifier.doi10.3390/molecules26061694en_US
dc.subject.halSciences du Vivant [q-bio]/Biologie végétaleen_US
bordeaux.journalMoleculesen_US
bordeaux.volume26en_US
bordeaux.hal.laboratoriesUnité de Recherche Oenologie - EA 4577en_US
bordeaux.issue6en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionINRAEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.exportfalse
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Molecules&rft.date=2021-03-18&rft.volume=26&rft.issue=6&rft.eissn=1420-3049&rft.issn=1420-3049&rft.au=ARRAKI,%20Kamel&TOTOSON,%20Perle&DECENDIT,%20Alain&ZEDET,%20Andy&MAROILLEY,%20Justine&rft.genre=article


Archivos en el ítem

Thumbnail
Thumbnail

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem