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Egg white hydrolysates with in vitro biological multiactivities to control complications associated with the metabolic syndrome

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Abstract

The purpose of the present work consisted in the production of egg white hydrolysates with multiple biological activities that would allow the control of some pathologies related to the metabolic syndrome. Eight food-grade enzymes from different sources and specificities were used, and the hydrolysates were analysed for in vitro antioxidant, anti-inflammatory, bile acid-binding, angiotensin I-converting enzyme (ACE)-inhibitory and dipeptidyl peptidase IV-inhibitory activities. The hydrolysate of egg white with Bc Pepsin for 8 h presented a high ACE-inhibitory activity with an IC50 equivalent to, approximately, 50 µg protein/mL, as well as important peroxyl radical-scavenging and bile acid-binding capacities. The hydrolysate with Peptidase 433P for 24 h stood out for its peroxyl radical-scavenging capacity, equivalent to 900–1100 μmol Trolox/g of protein, and its potential hypocholesterolaemic activity. Both hydrolysates also exhibited a moderate DDP IV-inhibitory activity and prevented oxidative damage in RAW 264.7 macrophages, while that with Peptidase 433P also inhibited the release of proinflammatory cytokines induced by LPS in this cell line, in particular, that of IL-6. The multiple properties exerted by these hydrolysates suggest that they could target several symptoms of a complex disease, such as the metabolic syndrome.

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Acknowledgments

This study has received financial support from the Project AGL2012-32387 from MINECO. M. G.-R. acknowledges the financial support of MICINN through a FPI Grant and I. L.-E. that of CSIC through a JAE-Doc Grant.

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Correspondence to Marta Garcés-Rimón.

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Garcés-Rimón, M., López-Expósito, I., López-Fandiño, R. et al. Egg white hydrolysates with in vitro biological multiactivities to control complications associated with the metabolic syndrome. Eur Food Res Technol 242, 61–69 (2016). https://doi.org/10.1007/s00217-015-2518-7

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  • DOI: https://doi.org/10.1007/s00217-015-2518-7

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