Peptide fraction from sturgeon muscle by pepsin hydrolysis exerts anti-inflammatory effects in LPS-stimulated RAW264.7 macrophages via MAPK and NF-κB pathways

被引:54
作者
Gao, Ruichang [1 ,2 ]
Shu, Wanghui [1 ]
Shen, Yang [1 ]
Sun, Quancai [1 ]
Jin, Wengang [2 ]
Li, Dajing [3 ]
Li, Ying [3 ]
Yuan, Li [1 ]
机构
[1] Jiangsu Univ, Sch Food & Biol Engn, 301 Xuefu Rd, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Shaanxi Univ Technol, Sch Biosci & Engn, Bioresources Key Lab Shaanxi Prov, Hanzhong 723001, Peoples R China
[3] Jiangsu Acad Agr Sci, Inst Agroprod Proc, Nanjing 210014, Jiangsu, Peoples R China
关键词
Sturgeon; Enzymatic hydrolysis; Antioxidant; Anti-inflammation mechanism; RAW264.7; macrophages; ANTIOXIDANT PROPERTIES; ENZYMATIC-HYDROLYSIS; PURIFICATION; IDENTIFICATION; PROTEINS; INSIGHTS; STRESS; CANCER; ALPHA;
D O I
10.1016/j.fshw.2020.04.014
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Previous studies have suggested that polypeptides extracted from milk, soybean, fish, eggs, and meat possess potential anti-inflammatory effects. To date, few studies have reported the anti-inflammatory function of sturgeon peptides and their underlying mechanisms are unknown. The current study was therefore to determine the anti-inflammatory potential of sturgeon peptides with lipopolysaccharide (LPS)-induced RAW264.7 inflammatory model. Pepsin hydrolysate (PeH) was purified by ultrafiltration and Sephadex G-15 gel filtration chromatography. PeH significantly reduced the inflammatory mediator (NO) and inflammatory cytokines (IL-6, TNF-alpha. and IL-1 beta) expression in a dose-dependent manner. Moreover, the purified sturgeon peptide (F2) possessed strong antioxidant potential and effectively inhibited DPPH and ABTS free radicals. F2 significantly suppressed the expression of MAPK, I kappa B alpha, and NF-kappa B p65, indicating that F2 exerted anti-inflammatory influence by the inhibition of MAPK and NF-kappa B pathways. (C) 2021 Beijing Academy of Food Sciences. Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.
引用
收藏
页码:103 / 111
页数:9
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