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Anti-inflammatory effects of three selenium-enriched brown rice protein hydrolysates in LPS-induced RAW264.7 macrophages via NF-κB/MAPKs signaling pathways.

Authors :
Feng, Mingju
Wang, Xiaoya
Xiong, Hua
Qiu, Tingting
Zhang, Hua
Guo, Fanghua
Jiang, Li
Sun, Yong
Source :
Journal of Functional Foods; Jan2021, Vol. 76, pN.PAG-N.PAG, 1p
Publication Year :
2021

Abstract

The anti-inflammatory mechanism of peptide fractions. • Three Se-enriched brown rice protein hydrolysates were prepared. • The anti-inflammatory property of protein hydrolysates was investigated. • The relationship between anti-inflammatory property and molecular weight. 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 E 2 (PGE 2) 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17564646
Volume :
76
Database :
Supplemental Index
Journal :
Journal of Functional Foods
Publication Type :
Academic Journal
Accession number :
147855763
Full Text :
https://doi.org/10.1016/j.jff.2020.104320