ACE inhibitory activity in vitro and antihypertensive effect in vivo of LSGYGP and its transepithelial transport by Caco-2 cell monolayer

被引:21
|
作者
Zhao Tianrui [1 ]
Liu Bingtong [1 ]
Yuan Ling [1 ]
Sun Liping [1 ]
Zhuang Yongliang [1 ]
机构
[1] Kunming Univ Sci & Technol, Yunnan Inst Food Safety, 727 South Jingming Rd, Kunming 650500, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
LSGYGP; Antihypertensive effect; Molecular docking simulation; Kinetic; Caco-2 cell monolayer; ANGIOTENSIN-CONVERTING ENZYME; BLOOD-PRESSURE; PROTEIN HYDROLYSATE; MOLECULAR DOCKING; PEPTIDES; PURIFICATION; MECHANISM; SILICO; IDENTIFICATION; ANTIOXIDANT;
D O I
10.1016/j.jff.2019.103488
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Leu-Ser-Gly-Tyr-Gly-Pro (LSGYGP) was obtained in our previous study. The angiotensin I-converting enzyme inhibitory (ACEI) activity in vitro and the antihypertensive effect in vivo of LSGYGP were determined in this study. The IC50 value of ACEI activity of LSGYGP was 25.74 mu M, and the ACEI kinetic was noncompetitive. LSGYGP showed a high binding affinity with ACE sites by using seven short hydrogen bonds. LSGYGP had a clear antihypertensive effect on spontaneously hypertensive rats, and the systolic blood and diastolic blood pressures remarkably decreased by 19.81% and 29.92% in 3 h of administration. The ACE activities of serum, kidneys, and lungs were determined at different times, and lung was evaluated as the key target tissue. LSGYGP was completely absorbed by Caco-2 cell monolayer, and the transport degree was 3.5%. Furthermore, several degradations and modifications of LSGYGP, such as SGYGP, LSGY, GYGP, LSGYP, LSSGYGP, and LSLSGYGP, were found during the transport process.
引用
收藏
页数:9
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