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Volume 26, Issue 4, Pages 359-366 (April 2010)


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Pomegranate juice polyphenols increase recombinant paraoxonase-1 binding to high-density lipoprotein: Studies in vitro and in diabetic patients

Bianca Fuhrman, D.Sc.Corresponding Author Informationemail address, Nina Volkova, M.Sc., Michael Aviram, D.Sc.

Received 22 February 2009; accepted 5 May 2009. published online 18 September 2009.

Abstract 

Objective

The high-density lipoprotein (HDL)-associated paraoxonase-1 (PON1)/free PON1 ratio is lower in diabetic patients in comparison with healthy controls. Because diabetes is associated with increased oxidative stress, we hypothesized that a labeled recombinant PON1 (rePON1) would detect differences in HDL capacity to bind PON1 under specific experimental conditions, such as oxidation, addition of polyphenols, or in vivo dosing of diabetic patients with polyphenols.

Methods

In the present study we determined labeled rePON1 binding to HDL under various oxidative conditions by using polyacrylamide gel electrophoresis for the separation of free labeled rePON1 from HDL-bound labeled rePON1.

Results

The HDL-rePON1/free rePON1 ratio gradually decreased as the extent of HDL oxidation increased, and the antioxidants vitamin E or pomegranate juice (PJ) inhibited the redistribution of rePON1. PJ or its purified polyphenols, punicalagin, gallic acid, or ellagic acid, increased rePON1 binding also to non-oxidized HDL. Further, rePON1 associated more efficiently with HDLs isolated from diabetic patients after PJ consumption versus HDLs isolated before PJ consumption.

Conclusions

We conclude that 1) oxidative stress impairs binding of fluorescein isothiocyanate–labeled rePON1 to HDL and 2) PJ polyphenols directly increase the HDL-rePON1 association beyond their antioxidative effect.

The Lipid Research Laboratory, Rambam Medical Center, Rappaport Family Institute for Research in Medical Sciences and Technion Faculty of Medicine, Haifa, Israel

Corresponding Author InformationCorresponding author: Tel.: +972-4-829-5278; fax: +972-4-852-0076.

 This research was supported in part by POM Wonderful, Los Angeles, California, USA.

PII: S0899-9007(09)00221-4

doi:10.1016/j.nut.2009.05.003


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