化学
一氧化氮
一氧化氮合酶
肽
肿瘤坏死因子α
水解物
炎症
p38丝裂原活化蛋白激酶
磷酸化
生物化学
NF-κB
前列腺素E2
信号转导
促炎细胞因子
激酶
蛋白激酶A
分子生物学
酶
生物
内分泌学
免疫学
有机化学
水解
作者
Mingju Feng,Xiaoya Wang,Hua Xiong,Tingting Qiu,Hua Zhang,Fanghua Guo,Li Jiang,Yong Sun
标识
DOI:10.1016/j.jff.2020.104320
摘要
In the present study, three selenium-enriched brown rice protein hydrolysates were prepared by trypsin, their anti-inflammatory mechanism in vitro were investigated. Results obtained from LPS-induced RAW264.7 cell model showed that the 1.0–3.5 kDa peptide fractions exhibited the most effective anti-inflammatory property through inhibiting the production of nitric oxide (NO), prostaglandin E2 (PGE2) and pro-inflammation cytokines including interleukin-6 (IL-6), interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α). The mRNA and protein expression of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2) were also suppressed by 1.0–3.5 kDa peptide fractions. Additionally, the phosphorylation of nuclear factor-κB (NF-κB) and mitogen-activated protein kinases (MAPKs) signal proteins were blocked after 1.0–3.5 kDa peptide fraction treatments. Above all, the observed anti-inflammatory effects of selenium-enriched brown rice protein hydrolysates were closely related to their Se content. These results illustrated that the 1.0–3.5 kDa peptide fractions could be a novel functional food ingredient for inflammation-related diseases treatment.
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