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Food Chem ; 309: 125766, 2020 Mar 30.
Artículo en Inglés | MEDLINE | ID: mdl-31718836

RESUMEN

This study aimed to identify by UPLC-PDA-Q/TOF-MS and quantify by UPLC-PDA phenolic compounds (26 flavonols and 2 phenolic acids) and carotenoids (16) from berries of different cultivars of Hippophaë rhamnoides and determine correlations between these variables and in vitro anticholinergic and on-line antioxidant potential. Isorhamnetin derivatives presented over 65% of total flavonols, but quercetin and kaempferol derivatives were also determined. Carotenes accounted for 19 to 47%, xanthophylls 16 to 81% of total carotenoids. Pearson's correlations between AChE and BuChE inhibition and phenolic acid content were low (r = 0.388 and 0.355), moderate for carotenoids (0.504 and 0.437) and high for flavonols (0.851 and 0.614). The PCA biplot showed the highest correlation between anticholinergic activity and all-trans-ß-cryptoxanthin, quercetin-3-O-glucoside, isorhamnetin-3-O-(2-rhamnosyl)glucoside, kaempferol-3-O-hexoside-7-O-rhamnoside, isorhamnetin-3-O-(6-rhamnosyl)hexoside, isorhamnetin-3-O-rutinoside, and isorhamnetin-3-O-glucoside concentrations. The results obtained can be used to identify sea buckthorn cultivars, develop crops and production, and design functional products rich in flavonols and carotenoids with anticholinergic properties.


Asunto(s)
Antioxidantes/química , Carotenoides/análisis , Inhibidores de la Colinesterasa/análisis , Cromatografía Líquida de Alta Presión/métodos , Hippophae/química , Fenoles/análisis , Acetilcolinesterasa/química , Acetilcolinesterasa/metabolismo , Butirilcolinesterasa/química , Butirilcolinesterasa/metabolismo , Inhibidores de la Colinesterasa/química , Flavonoles/análisis , Frutas/química , Frutas/metabolismo , Hippophae/metabolismo , Análisis de Componente Principal
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