Flaxseed protein-derived peptide fractions: Antioxidant properties and inhibition of lipopolysaccharide-induced nitric oxide production in murine macrophages

被引:121
作者
Udenigwe, Chibuike C. [1 ]
Lu, Yeh-Lin [2 ]
Han, Chuan-Hsiao [2 ]
Hou, Wen-Chi [3 ]
Aluko, Rotimi E. [1 ,4 ]
机构
[1] Univ Manitoba, Dept Human Nutr Sci, Winnipeg, MB R3T 2N2, Canada
[2] Taipei Med Univ, Coll Pharm, Sch Pharm, Taipei 110, Taiwan
[3] Taipei Med Univ, Grad Inst Pharmacognosy, Taipei 110, Taiwan
[4] Univ Manitoba, Richardson Ctr Funct Foods & Nutraceut, Winnipeg, MB R3T 2N2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Antioxidant; Flaxseed protein hydrolysates; Nitric oxide; RAW; 264.7; macrophages; Semicarbazide-sensitive amine oxidase; SENSITIVE AMINE OXIDASE; DEGENERATIVE DISEASES; SUPEROXIDE-DISMUTASE; HYDROLYSATE; SYNTHASE; CAPACITY; OVEREXPRESSION; AUTOXIDATION; PYROGALLOL; OXIDATION;
D O I
10.1016/j.foodchem.2009.02.046
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A protein isolate was produced from cellulase-treated defatted flaxseed meal followed by hydrolysis with seven proteases and evaluation of the hydrolysates for antioxidant and anti-inflammatory properties. The flaxseed protein hydrolysates (FPH) were processed by ultrafiltration and ion-exchange chromatography to isolate low molecular weight (LMW) and cationic peptide fractions, respectively. The peptides showed antioxidant properties in scavenging 2,2-diphenyl-1-picrylliydrazyl radical, superoxide anion radical, electron-spin resonance-detected hydroxyl radical and nitric oxide. In addition, all peptide fractions inhibited semicarbazide-sensitive amine oxidase activity. Antioxidant activities of these peptides were dependent on the specificity of proteases and size of the resulting peptides. The LMW fractions from pepsin, ficin and papain FPH also inhibited lipopolysaccharide-induced nitric oxide productions in RAW 264.7 macrophages without apparent cytotoxicity; thus, these peptides may act as anti-inflammatory agents. Thus, flaxseed protein hydrolysates may serve as potential ingredients for the formulation of therapeutic products. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:277 / 284
页数:8
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