%N 8
%A Francesca Giampieri
%A Sadia Afrin
%A Derek Stewart
%A Gordon McDougall
%A Rex Brennan
%A Lesley Blyth
%A Massimiliano Gasparrini
%A Luca Mazzoni
%A Franco Capocasa
%A José M. Alvarez-Suarez
%A Stefano Bompadre
%A Pedro Nogueira Brás de Oliveira
%A Claudia N. Santos
%A Manuel Masias Vergara
%A Pablo Agudo Toyos
%A Jorge Crespo-Álvarez
%A Bruno Mezzetti
%A Tamara Y. Forbes-Hernandez
%A Maurizio Battino
%J Molecules
%K Berry; Polyphenols; In vitro gastrointestinal digestion; Bioavailability; Cytotoxicity.
%V 23
%T Phytochemical Composition and Cytotoxic Effects on Liver Hepatocellular Carcinoma Cells of Different Berries Following a Simulated In Vitro Gastrointestinal Digestion
%D 2018
%L uneatlantico130
%P 1918
%X Berry fruits are rich in nutrients and polyphenols, providing potential health benefits. Understanding the factors that affect their bioavailability is becoming of utmost importance for evaluating their biological significance and efficacy as functional food. In this study, the phytochemical composition and the total antioxidant capacity of different varieties of five berries (blackberry, blackcurrant, blueberry, raspberry, and strawberry) were evaluated after an in vitro gastrointestinal digestion process. The cultivar of each berry that showed the higher content of total phenols and flavonoids was selected to study its cytotoxic effect on human hepatoma cells. Digestion resulted in a high reduction (p ˂ 0.05) of total phenolic, flavonoid and anthocyanin contents and total antioxidant capacity, in the “IN” samples compared to the “OUT” extracts, which represent the “serum-available” and the “colon-available” fractions, respectively. Incubation of the digested fraction for 24 h didn’t exert any effect on cellular viability, while a dose- and time-dependent cytotoxicity was observed after 48 h and 72 h of incubation for all the berries analyzed. Our results suggest that the approach proposed in this work may represent a rapid tool for evaluating and identifying new berries with increased phytochemical bioavailability, highlighting their antiproliferative agents after an in vitro digestion.
%R doi:10.3390/molecules23081918