Absorption and Metabolism of Peptide WDHHAPQLR Derived from Rapeseed Protein and Inhibition of HUVEC Apoptosis under Oxidative Stress

被引:87
作者
Xu, Feiran [1 ,2 ]
Zhang, Jing [2 ]
Wang, Zhigao [1 ,2 ]
Yao, Yijun [1 ,2 ]
Atungulu, Griffiths G. [3 ,4 ]
Ju, Xingrong [1 ,2 ]
Wang, Lifeng [1 ]
机构
[1] Nanjing Univ Finance & Econ, Key Lab Grains & Oils Qual Control & Proc, Coll Food Sci & Engn, Collaborat Innovat Ctr Modem Grain Circulat & Saf, 3 Wenyuan Rd, Nanjing 210023, Jiangsu, Peoples R China
[2] Jiangnan Univ, State Key Lab Food Sci & Technol, 1800 Lihu Ave, Wuxi 214122, Jiangsu, Peoples R China
[3] Univ Arkansas, Grain Proc Engn Dept Food Sci, 2650 North Young Ave, Fayetteville, AR 72701 USA
[4] Univ Arkansas, Div Agr, 2650 North Young Ave, Fayetteville, AR 72701 USA
基金
中国国家自然科学基金;
关键词
rapeseed antioxidant peptide; absorption of intestinal epithelial cells; bioavailability; in vivo metabolism mechanism; inhibition of HUVEC apoptosis; CACO-2 CELL MONOLAYERS; VEIN ENDOTHELIAL-CELLS; ANTIOXIDANT ACTIVITIES; TRANSEPITHELIAL TRANSPORT; PURIFICATION; IDENTIFICATION; PHARMACOKINETICS; CHROMATOGRAPHY; DIGESTION; CASPASES;
D O I
10.1021/acs.jafc.8b01620
中图分类号
S [农业科学];
学科分类号
082806 [农业信息与电气工程];
摘要
WDHHAPQLR (RAP) is an antioxidative peptide derived from rapeseed protein. Although the health benefits from RAP, due to its antioxidant activities, have been determined by chemical methods, a systematic assessment regarding the absorption, metabolism, and antioxidation processes of RAP is still lacking attention. Hence, Caco-2 cell monolayer models and animal experiments were used to evaluate the absorption and bioavailability of RAP. As expected, RAP could be absorbed by intestinal epithelial cells, and the Papp was 0.82 +/- 0.19 X 10(-6) cm/s. Three main fragments, RAP, DHHAPQLR, and WDHHAP were transported by the paracellular pathway, and QLR was transported by PepT1. An important modified product of RAP (EGDHHAPQLR) was found to contribute to the elimination of intracellular reactive oxygen species. The absolute bioavailability of RAP was 3.56%, and three degradation products of RAP were also detected in rat serum. More importantly, RAP exerts its antioxidant activity by inhibiting the apoptosis of oxidative stress cells. RAP could downregulate the expression of Bax and caspase-3 and upregulate the expression of Bcl-2 in H2O2-induced HUVECs (human umbilical vein endothelial cells). In general, using in vitro and in vivo experimental models, the in vivo absorption and transformation processes of RAP and its antioxidative molecular mechanisms by inhibiting apoptosis of cells were revealed.
引用
收藏
页码:5178 / 5189
页数:12
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