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LIBRO-CONGRESO-CITRUS

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S20<br />

dysfunction. Microarray studies performed on aortas demonstrated differentially expressed genes encoding<br />

proteins involved in cell adhesion, actin cytoskeleton organization or focal adhesion. Expression profile of<br />

these genes suggested limited immune cell adhesion to endothelial cells (ECs) and infiltration in the intima<br />

of vascular wall. This hypothesis was strengthened by in-vitro experiments on ECs using naringin metabolites<br />

at physiologically relevant concentrations. These metabolites significantly reduced monocyte adhesion to<br />

TNFα-activated ECs. Exposure of both monocytes and ECs to naringin metabolites potentiated their inhibitory<br />

effect on monocyte adhesion, suggesting that monocytes may also be targets for naringenin metabolites. In<br />

conclusion, this study revealed that the atheroprotective effect of dietary naringin could be linked to its effect<br />

on gene networks and cell functions related to leukocyte adhesion and transendothelial migration, processes<br />

highly involved in the early steps of atherosclerosis development.<br />

S20P02<br />

Effect of membrane processing on the radical scavenging activity of juice from IGP product Citrus<br />

limon from “Rocca imperiale” (south Italy)<br />

Loizzo M.R. 1 , Tundis R1 , Bonesi M. 1 , Pugliese A. 1 , Di Sanzo G. 2 , Balducchi R. 2 , Verardi A. 3 , and Calabro V. 3<br />

1University of Calabria (UNICAL), Department of Pharmacy, Health Sciences and Nutrition, Italy; 2ENEA C.R. Trisaia (ENEA), Laboratorio<br />

Biotecnologie (UTTRI-BIOTEC), Italy; and 3University of Calabria (UNICAL), Department of Engineering Modeling, Italy.<br />

vincenza.calabro@unical.it<br />

Citrus limon from “Rocca imperiale” was awarded the IGP (Protected Geographical Indication) denomination<br />

in 2012. The juice is characterized by yellow colour and a sweet taste. Juice obtained by manual pressure of<br />

C. limon was firstly centrifuged and then concentrated with ultrafiltration process (carried out on Osmonics®<br />

module, by using a polysulphone membrane, cut off 150 kDa, under d transmembrane membrane pressure<br />

ranging from 0.5 to 2 bar) with the aim to concentrate and separate the antioxidants. Samples of permeate<br />

and retentate were continuously collected and analysed in order to measure the amount of antioxidant in<br />

each flow stream. Considering that antioxidant compounds may act in vivo through different mechanisms of<br />

action, no single method can fully evaluate the antioxidant capacity of food since levels of single antioxidant<br />

in food do not necessarily reflect their antioxidant activity. For this reason permeate and retentate juices<br />

were evaluated for their radical scavenging activity through DPPH and ABTS assay. Permeate samples showed<br />

a percentage of inhibition of ABTS∙ from 35.97 to 54.27 using pure products while retentate samples exhibited<br />

a percentage of inhibition 22.67 to 43.66 using pure products. In DPPH assay IC50 values v/v -ranging from<br />

3.46.64 to 10.64 for permeate and from 7.64 to 8.70 for retentate, respectively.<br />

S20P03<br />

The effect of time and refrigeration on bioavailability of flavanones in healthy volunteers after<br />

fresh squeezed orange juice consumption<br />

Tomas-Navarro M., Vallejo F., and Tomás-Barberán F.A.<br />

Centro de Edafología y Biología Aplicada del Segura (CEBAS-CSIC), Ciencia y Tecnología de los Alimentos, Spain.<br />

mtomas@cebas.csic.es<br />

The effect of both temperature and time is unclear yet on flavanones bioavailability. A comparison between<br />

ingestion of freshly squeezed orange ‘Lane Late’ juice and the same juice after a 24h refrigeration period<br />

(8 ºC) in the fridge was carried out. This study was developed in healthy volunteers (n=7) following the<br />

administration of 400 mL of freshly squeezed orange juice (FS) and 24 h urine collection. The same operation<br />

was done with the refrigerated one (FR). The determination of the total amount of flavanones present in the<br />

supernatant and pellet of both juices was measured by HPLC-MS. Significant differences were observed in<br />

flavanones precipitation (pellet) after 24 h refrigeration (FR) compared to the freshly squeezed one (FS). The<br />

total excretion of flavanone metabolites in all volunteers decreased between 2 and 5-fold after storage for 24<br />

h at 8 ºC (FR). The results show that research on technological and biotechnological methods to preserve the<br />

bioavailability of the freshly squeezed juice are necessary in order to obtain processed juice with the highest<br />

bioavailability.<br />

346 - VALENCIA CONFERENCE CENTER, 18th-23rd NOVEMBER 2012

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