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蛋黄卵转铁蛋白(α、β 和 γ-卵转铁蛋白)馏分及其酶解产物对脂多糖诱导的 RAW 264.7 巨噬细胞的抗炎作用。

Anti-inflammatory effects of egg yolk livetins (α, β, and γ-livetin) fraction and its enzymatic hydrolysates in lipopolysaccharide-induced RAW 264.7 macrophages.

机构信息

Department of Agricultural, Food and Nutritional Science (AFNS), 4-10 Ag/For Centre, University of Alberta, Edmonton, Alberta, Canada.

Department of Agricultural, Food and Nutritional Science (AFNS), 4-10 Ag/For Centre, University of Alberta, Edmonton, Alberta, Canada.

出版信息

Food Res Int. 2017 Oct;100(Pt 1):449-459. doi: 10.1016/j.foodres.2017.07.032. Epub 2017 Jul 18.

DOI:10.1016/j.foodres.2017.07.032
PMID:28873708
Abstract

In this study, the egg yolk livetins (α, β, and γ-livetin) fraction and its hydrolysates, prepared by pepsin and Alcalase, were evaluated for their anti-inflammatory effects using lipopolysaccharide (LPS)-induced RAW 264.7 macrophages as an in vitro model. Enzymatic hydrolysis by pepsin and Alcalase successfully transformed the large molecular weight livetins into low molecular mass peptides mostly below 10kDa. Results revealed that livetins and its hydrolysates (peptides) treatment significantly reduced the inflammatory responses as evidenced by inhibition of production of nitric oxide (NO) (22.7-39.2%), pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α) (36.9-43.2%), interleukin-1β (IL-1β) (26.1-50.9%) and interleukin-6 (IL-6) (60.4-69.0%), and the expression of inducible nitric oxide synthase (iNOS) (58.6-62%). Alcalase hydrolysate showed more effects in inhibiting prostaglandin-E2 (PGE2) production (30.3%) as well as expression of cyclooxygenase-2 (COX-2) (55.7%). In addition, effect of livetins and its hydrolysates on phagocytic capacity of the macrophages was also evaluated. The results indicate that livetins and its enzymatic hydrolysates significantly (p<0.001, 0.05) enhanced the phagocytic activity of the macrophages. The results suggest that egg yolk livetins and its hydrolysates with anti-inflammatory activity can potentially be used in health food/nutraceutical/pharmaceutical industry for various applications.

摘要

在这项研究中,使用脂多糖 (LPS) 诱导的 RAW 264.7 巨噬细胞作为体外模型,评估了蛋黄卵黄蛋白(α、β 和 γ-卵黄蛋白)馏分及其由胃蛋白酶和碱性蛋白酶制备的水解产物的抗炎作用。胃蛋白酶和碱性蛋白酶的酶解成功地将大分子量的卵黄蛋白转化为低分子量的肽,大部分分子量低于 10 kDa。结果表明,卵黄蛋白及其水解产物(肽)处理显著抑制了炎症反应,表现为一氧化氮(NO)产生的抑制(22.7-39.2%)、促炎细胞因子如肿瘤坏死因子-α(TNF-α)(36.9-43.2%)、白细胞介素-1β(IL-1β)(26.1-50.9%)和白细胞介素-6(IL-6)(60.4-69.0%),以及诱导型一氧化氮合酶(iNOS)的表达(58.6-62%)。碱性蛋白酶水解产物在抑制前列腺素-E2(PGE2)产生(30.3%)和环氧化酶-2(COX-2)表达(55.7%)方面表现出更多的效果。此外,还评估了卵黄蛋白及其水解产物对巨噬细胞吞噬能力的影响。结果表明,卵黄蛋白及其酶解产物显著(p<0.001,0.05)增强了巨噬细胞的吞噬活性。这些结果表明,具有抗炎活性的蛋黄卵黄蛋白及其水解产物可潜在应用于保健食品/营养保健品/制药行业,用于各种应用。

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