Milk-derived bioactive peptides protect against oxidative stress in a Caco-2 cell model

Milk and milk-derived products are a relevant source of bioactive peptides, which are also potential components of functional foods. Bioactive peptides exert multiple actions including an antioxidant role. In the present paper, four synthetic peptides (NPYVPR, AVPYPQR, KVLPVPEK, and ARHPHPHLSFM), co...

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Veröffentlicht in:Food & function 2018-02, Vol.9 (2), p.1245-1253
Hauptverfasser: Tonolo, F, Sandre, M, Ferro, S, Folda, A, Scalcon, V, Scutari, G, Feller, E, Marin, O, Bindoli, A, Rigobello, M. P
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Sprache:eng
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Zusammenfassung:Milk and milk-derived products are a relevant source of bioactive peptides, which are also potential components of functional foods. Bioactive peptides exert multiple actions including an antioxidant role. In the present paper, four synthetic peptides (NPYVPR, AVPYPQR, KVLPVPEK, and ARHPHPHLSFM), corresponding to milk-derived peptides were studied. Although with different features, as revealed by RP-HPLC chromatography and MS analysis, the obtained peptides were shown to be taken up by Caco-2 cells arranged in an epithelial monolayer formation. The four peptides were all able to preserve cell viability against induced oxidative stress indicating that they might have a role in the control of oxidative stress. Therefore, an estimation of total thiols and glutathione content was performed after cell treatment with oxidants like hydrogen peroxide (H 2 O 2 ) or tert -butyl hydroperoxide (TbOOH). The peptides were able to prevent the decrease of both total thiols and glutathione induced by H 2 O 2 or TbOOH, and, in addition, they showed a protective effect on the thiol-related antioxidant enzymes thioredoxin reductase and glutathione reductase. Finally, they caused a decrease of ROS production induced by TbOOH in Caco-2 cells. The reported results highlight the relevant antioxidant role played by bioactive peptides in cells, which adds to other previously known properties. Milk-derived bioactive peptides are able to prevent oxidative stress in Caco-2 cell model.
ISSN:2042-6496
2042-650X
DOI:10.1039/c7fo01646h