Krill Oil Attenuates Inflammation in Monosodium Iodoacetate-Induced Osteoarthritic Rats, SW982 Synovial Cell Line, and Primary Chondrocytes

被引:5
|
作者
Kim, Ok-Kyung [1 ]
Kim, Dakyung [2 ]
Lee, Minhee [2 ]
Park, Seong-Hoo [2 ]
Jung, Jaeeun [2 ]
Lee, Jeongmin [2 ,3 ]
机构
[1] Chonnam Natl Univ, Human Ecol Res Inst, Div Food & Nutr, Gwangju, South Korea
[2] Kyung Hee Univ, Dept Med Nutr, Yongin 17104, Gyeonggi, South Korea
[3] Kyung Hee Univ, Res Inst Clin Nutr, Seoul, South Korea
关键词
chondrocytes; krill oil; osteoarthritis; KNEE OSTEOARTHRITIS; OMEGA-3-FATTY-ACIDS; DEGRADATION;
D O I
10.1089/jmf.2021.K.0152
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The aim of this study was to investigate the effects of krill oil (FJH-KO) in monoiodoacetate (MIA)-induced osteoarthritis in rat models, and H2O2- or lipopolysaccharide (LPS)-treated primary chondrocytes and the SW982 synovial cell line. We found that 150 mg/kg b.w. FJH-KO supplementation increased running speed, stride, and foot pressure in MIA-induced osteoarthritic rats. In the H2O2-treated SW982 synovial cell line and primary chondrocytes, FJH-KO treatment prevented cell death and suppressed matrix degradation by increasing the levels of anabolic factors of cartilage tissue, including aggrecan, collagen type I, collagen type II, tissue inhibitors of metalloproteinase (TIMP)-1, and TIMP-3, and decreasing those of catabolic factors of cartilage tissue, including phosphorylation of Smad, MMP-3, and MMP-13. In addition, FJH-KO treatment suppressed the activation of inflammation and apoptosis pathways in the LPS-treated SW982 synovial cell line and primary chondrocytes. We suggest that FJH-KO supplementation may help prevent osteoarthritis progression because of its direct effects on inflammation and apoptosis of chondrocytes.
引用
收藏
页码:239 / 250
页数:12
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