| Literature DB >> 28784530 |
Siluana Katia Tischer Seraglio1, Andressa Camargo Valese2, Heitor Daguer2, Greici Bergamo1, Mônia Stremel Azevedo1, Priscila Nehring1, Luciano Valdemiro Gonzaga1, Roseane Fett1, Ana Carolina Oliveira Costa3.
Abstract
Honey is a product traditionally consumed due to its possible health benefits promoted by natural antioxidants. However, few studies have evaluated the effect of in vitro gastrointestinal digestion on these compounds in honeys. To improve the knowledge of this subject, the present study aimed to investigate the influence of simulated digestion on the stability of antioxidant capacity (FRAP, DPPH, and Folin-Ciocalteu assays), phenolic compounds (LC-ESI-MS/MS), and minerals (CE-DAD) in Mimosa scabrella Bentham honeydew honeys. The results show that the digestive system, mainly after duodenal digestion, significantly decreased the antioxidant capacity assessed by FRAP (410.3±18.3 to 564.7±8.4μmolFe+2100g-1), DPPH (30.1±0.8 to 33.9±1.4mgAAE100g-1), and Folin-Ciocalteu assays (58.3±2.6 to 142.0±1.6mgGAE100g-1) of this honey. However, phenolic compounds and minerals showed high stability and in some cases, significantly increased after the simulated digestion, presenting a bioaccessible fraction that ranged from 78.2±6.4 to 174.38±6.82% and 94.0±4.3 to 220.5±3.4%, respectively. Therefore, these honey constituents may be considered highly bioaccessible and potentially bioavailable. Additionally, the correlation between the investigated parameters suggests that other honey constituents could also possibly affect antioxidant capacity of this honey. In conclusion, the bracatinga (Mimosa scabrella Benth.) honeydew honey can be highlighted as an important natural source of bioaccessible polyphenols, besides presenting highly bioaccessible minerals in its composition, maintaining a satisfactory antioxidant capacity.Entities:
Keywords: Antioxidant activity; Bioactive compounds; Bracatinga; Capillary electrophoresis; Liquid chromatography–tandem mass spectrometry; Simulated gastrointestinal digestion
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Year: 2017 PMID: 28784530 DOI: 10.1016/j.foodres.2017.06.024
Source DB: PubMed Journal: Food Res Int ISSN: 0963-9969 Impact factor: 6.475