• Aucun résultat trouvé

Citrus flavanones enhance carotenoid uptake by human intestinal Caco-2 cells Dhuique-Mayer Claudie*

N/A
N/A
Protected

Academic year: 2021

Partager "Citrus flavanones enhance carotenoid uptake by human intestinal Caco-2 cells Dhuique-Mayer Claudie*"

Copied!
1
0
0

Texte intégral

(1)

Citrus flavanones enhance carotenoid uptake by human intestinal Caco-2 cells

Dhuique-Mayer Claudie*

1

, During Alexandrine

2

, Caporiccio Bertrand

3

Tourniaire Franck

4

,

Amiot Marie-Josèphe

4

.

1

CIRAD-Dept persyst-UMR Qualisud, TA B95/16 34398 Montpellier cedex 5, France

2

Université catholique de Louvain, Institut des Sciences de la Vie, BCNT, Croix du Sud, 5,

B_1348, Louvain-la-Neuve, Belgique

3

Université Montpellier II UMR Nutripass, 34095 Montpellier cedex 5, France.

4

UMR 476 INSERM (National Institute of Health and Medical Research)/1260 INRA

(National Institute for Agronomic Research), Université de la Méditerranée, Faculté de

Médecine de la Timone, 13385 Marseille cedex 05, France.

• corresponding author claudie.dhuique-mayer@cirad.fr

The health benefit of a diet rich in fruits and vegetables could be attributed to the complex mixture of phytochemicals. It is now widely believed that the actions of the antioxidant microconstituents is a result of additive and/or synergistic effects of these phytochemicals present in whole food. Because citrus juices are considered as a rich source of antioxidants including ascorbic acid (or vitamin C), phenolics compounds, and carotenoids, these different molecules may affect bioavailability or intestinal absorption of each other microconstituent. For these reasons, our study focused on effects of flavonoids and acid ascorbic on intestinal carotenoid uptake. This study was conducted using the differentiated Caco-2 cellline as experimental in vitro model and interactions of different flavanones such as hesperidin (HES-G) and hesperetin (HES) with carotenoid uptake were examined. Effect of ascorbic acid (AA) added to HES-G was also investigated. The data showed an enhancing effect of HES-G and HES on β-carotene (b-C) and β-cryptoxanthin (b-CX) uptake. For instance, at 5h incubation in presence of a mixture b-C:b-CX, HES-G and HES significantly increased total carotenoid uptake by 1.7 and 1.6-fold, respectively. Moreover, AA was able to cancel the enhancing effect of HES-G by decreasing significantly the cellular uptake of carotenoids from 48.2 to 39.8 % (P<0.05). In order to attribute the enhancing effect of HES-G to its already known iron-chelating effect, another experiment was conducted by incubating cells with b-CX in presence of either iron or a metal chelator (deferoxamine). b-CX uptake decreases in presence of iron and increases in presence of deferoxamine In sum, the results indicate that citrus flavanones enhance the carotenoid uptake by intestinal cells and that iron inhibits this process. Thus, the present data suggest that the citrus polyphenols could act through their iron-chelating properties.

Références

Documents relatifs

❚ ❚ The results indicate that citrus flavanones enhance the carotenoid uptake by intestinal cells and that addition of ascorbic acid counteract this effect. We supposed that HES-G has

Both figures show different polyphenol assimilative rate via human intestinal Caco-2 cell lines : the quercetin is remarkably reduced faster than the hesperidin at

In the present study, two polyphenols (quercetin, and hesperidin) chosen according to their structural characteristics, were used to evaluate the localization from their

Caco-2 cells were grown and differentiated in 75 cm² cell culture flasks incubated for 24 h with different species and concentrations of Al by adding 1 mL of Al-containing

As studies exploring the comparison of toxicological mechanisms induced by OA, DTX-1, and DTX-2 are lacking, we investigated and compared the cellular and molecular mechanisms

However, additional biological functions (DNA damage response of cells, repair of DNA, and modification of DNA), which include genes coding for proteins implied in the regulation

Our results provide evidence for an important role of the 5- domain trans-membrane molecule CD133 in the regulation of cellular cross-talk with the extracellular

Speci fically, our aims were (1) to evaluate the bioaccessibility of carotenoids with and without added DPs micro-encapsulated with maltodextrin and (2) to understand if these