Structural and functional characterization of hemp seed (Cannabis sativa L.) protein-derived antioxidant and antihypertensive peptides

被引:212
作者
Girgih, Abraham T. [1 ]
He, Rong [1 ,3 ]
Malomo, Sunday [1 ]
Offengenden, Marina [2 ]
Wu, Jianping [2 ]
Aluko, Rotimi E. [1 ]
机构
[1] Univ Manitoba, Richardson Ctr Funct Foods & Nutraceut, Dept Human Nutr Sci, Winnipeg, MB R3T 2N2, Canada
[2] Univ Alberta, Dept Agr Food & Nutr Sci, Edmonton, AB T6G 2P5, Canada
[3] Nanjing Univ Finance & Econ, Coll Food Sci & Engn, Nanjing 210046, Jiangsu, Peoples R China
基金
加拿大自然科学与工程研究理事会;
关键词
Hemp seed; Angiotensin converting enzyme; Renin; Antihypertensive peptides; Antioxidant peptides; Spontaneously hypertensive rats; I-CONVERTING-ENZYME; SPONTANEOUSLY HYPERTENSIVE-RATS; RADICAL-SCAVENGING PEPTIDE; INHIBITORY PEPTIDES; FLAXSEED PROTEIN; FOOD PROTEINS; HYDROLYSATE; PURIFICATION; FRACTIONS; IDENTIFICATION;
D O I
10.1016/j.jff.2013.11.005
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
The aim of this study was to identify and test efficacy of antioxidant and antihypertensive peptides present in hemp seed protein hydrolysate (HPH), which was produced through simulated gastrointestinal tract digestion of hemp seed proteins. Consecutive fractionation of HPH by reverse-phase HPLC followed by tandem mass spectrometry analysis of active peaks led to identification of 23 short-chain (<= 5 amino acids) peptides. At 0.5 mg/mL, Trp-Val-Tyr-Tyr (WVYY) and Pro-Ser-Leu-Pro-Ala (PSLPA) were the most active antioxidant peptides with 67% and 58% DPPH scavenging and metal chelation activity of 94% and 96%, respectively. WVYY and PSLPA showed maximum systolic blood pressure (SBP) reduction in spontaneously hypertensive rats by 34 (2 h) and 40 mmHg (4 h), respectively, after oral administration of 30 mg/kg body weight dose. Trp-Tyr-Thr (WYT) at 2 h, Ser-Val-Tyr-Thr (SVYT) at 6 h, and Ile-Pro-Ala-Gly-Val (IPAGV) at 4 h, each at 30 mg/kg body weight dose had maximum SBP reductions of 13, 24, and 36 mmHg, respectively. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:384 / 394
页数:11
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