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• W2325151616 abstract "α-Casozepine and f91–97, peptides from αs1-casein, display anxiolytic activity in rats and may have to cross the intestinal epithelium to exert this central effect. We evaluated their resistance to hydrolysis by the peptidases of Caco-2 cells and their ability to cross the cell monolayer. To mimic physiological conditions, two preparations of bile salts were used in noncytotoxic concentrations: porcine bile extract and an equimolar mixture of taurocholate, cholate, and deoxycholate. The presence and composition of bile salts appeared to modulate the peptidase activities of the Caco-2 cells involved (i) in the hydrolysis of α-casozepine, leading to much higher formation of fragments f91–99, f91–98, and f91–97, and (ii) in the hydrolysis of f91–97, leading to lower degradation of this peptide. Transport of α-casozepine across Caco-2 monolayer increased significantly, in the presence of bile extract, and of fragment f91–97, in the presence of bile salts." @default.
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• W2325151616 date "2011-10-24" @default.
• W2325151616 modified "2023-09-23" @default.
• W2325151616 title "Transport Across Caco-2 Cell Monolayer and Sensitivity to Hydrolysis of Two Anxiolytic Peptides from α_s1-Casein, α-Casozepine, and α_s1-Casein-(f91–97): Effect of Bile Salts" @default.
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• W2325151616 doi "https://doi.org/10.1021/jf202890e" @default.
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