期刊
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 62, 期 14, 页码 3177-3182出版社
AMER CHEMICAL SOC
DOI: 10.1021/jf405639w
关键词
egg white; ACE-inhibitory peptide; Caco-2 cells; transport
The purpose of this study was to investigate the transepithelial transport and cytoprotective effect of Gln-lle-GlyLeu-Phe (QIGLF), an ACE-inhibitory peptide derived from egg white ovalbumin, in human intestinal Caco-2 cell monolayers. The results showed that CZIGLF could be absorbed intact through Caco-2 cell monolayers with a Papp value of (9.11 0.19) x 10(-7) cm/s (transport kinetic parameters: K-m, 32.37 +/- 12.59 mM; V-max, 1.23 +/- 0.49 mu M/min cm(2)). The transport was not significantly decreased by sodium azide and Gly-Pro, an ATP synthesis inhibitor and a peptide transporter 1 (PepT1) substrate, respectively, suggesting that transport of QIGLF was not energy-dependent and carrier-mediated. In addition, wortmannin, a transcytosis inhibitor, had little effect on the transport, suggesting that endocytosis was not involved in the transport of QIGLF. However, the transport of QIGLF was increased significantly in the presence of cytochalasin ll, a tight junction disruptor, suggesting that paracellular transport via tight junctions was the major transport mechanism for intact QIGLF across Caco-2 cell monolayers. Moreover, QIGLF was added to Caco-2 cells followed by addition of H2O2,, and exhibited significant cytoprotective effect in Caco-2 cells against oxidative stress induced by H2O2.
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