The Anti-Inflammatory Effect of Low Molecular Weight Fucoidan from Sargassum siliquastrum in Lipopolysaccharide-Stimulated RAW 264.7 Macrophages via Inhibiting NF-κB/MAPK Signaling Pathways

被引:26
作者
Jayasinghe, Arachchige Maheshika Kumari [1 ]
Kirindage, Kirinde Gedara Isuru Sandanuwan [1 ]
Fernando, Ilekuttige Priyan Shanura [2 ]
Kim, Kil-Nam [3 ]
Oh, Jae-Young [4 ]
Ahn, Ginnae [1 ,5 ]
机构
[1] Chonnam Natl Univ, Dept Food Technol & Nutr, Yeosu 59626, South Korea
[2] Univ Alberta, Dept Agr Food & Nutr Sci, 4-10 Ag Bldg, Edmonton, AB T6G 2P5, Canada
[3] Korea Basic Sci Inst KBSI, Chuncheon Ctr, Chunchon 24341, South Korea
[4] Natl Inst Fisheries Sci, Food Safety & Proc Res Div, Busan 46083, South Korea
[5] Chonnam Natl Univ, Dept Marine Biofood Sci, Yeosu 59626, South Korea
关键词
Sargassum siliquastrum; low molecular weight fucoidan; RAW; 264.7; macrophages; anti-inflammation; NF-kappa B/MAPK signaling; BROWN SEAWEED SARGASSUM; SULFATED POLYSACCHARIDES; ECKLONIA-CAVA; INFLAMMATION; HORNERI;
D O I
10.3390/md21060347
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Brown seaweed is a rich source of fucoidan, which exhibits a variety of biological activities. The present study discloses the protective effect of low molecular weight fucoidan (FSSQ) isolated from an edible brown alga, Sargassum siliquastrum, on lipopolysaccharide (LPS)-stimulated inflammatory responses in RAW 264.7 macrophages. The findings of the study revealed that FSSQ increases cell viability while decreasing intracellular reactive oxygen species production in LPS-stimulated RAW 264.7 macrophages dose-dependently. FSSQ reduced the iNOS and COX-2 expression, inhibiting the NO and prostaglandin E-2 production. Furthermore, mRNA expression of L-1 beta, IL-6, and TNF-alpha was downregulated by FSSQ via modulating MAPK and NF-kappa B signaling. The NLRP3 inflammasome protein complex, including NLRP3, ASC, and caspase-1, as well as the subsequent release of pro-inflammatory cytokines, such as IL-1 beta and IL-18, release in LPS-stimulated RAW 264.7 macrophages was inhibited by FSSQ. The cytoprotective effect of FSSQ is indicated via Nrf2/HO-1 signaling activation, which is considerably reduced upon suppression of HO-1 activity by ZnPP. Collectively, the study revealed the therapeutic potential of FSSQ against inflammatory responses in LPS-stimulated RAW 264.7 macrophages. Moreover, the study suggests further investigations on commercially viable methods for fucoidan isolation.
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页数:16
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