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Effect ofAngelica sinensisPolysaccharides on OsteoarthritisIn VivoandIn Vitro: A Possible Mechanism to Promote Proteoglycans Synthesis
Author(s) -
Jun Qin,
Yansong Liu,
Jun Liu,
Jing Li,
Yang Tan,
Xiaojun Li,
Jacques Magdalou,
Qibing Mei,
Hui Wang,
Liaobin Chen
Publication year - 2013
Publication title -
evidence-based complementary and alternative medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.552
H-Index - 90
eISSN - 1741-4288
pISSN - 1741-427X
DOI - 10.1155/2013/794761
Subject(s) - aggrecan , in vivo , in vitro , osteoarthritis , chemistry , cartilage , gene expression , microbiology and biotechnology , biochemistry , biology , medicine , gene , pathology , anatomy , articular cartilage , alternative medicine
This study investigated the effect of Angelica sinensis polysaccharides (APS-3c) on rat osteoarthritis (OA) model in vivo and rat interleukin-1-beta- (IL-1 β -) stimulated chondrocytes in vitro . APS-3c was administrated into rat OA knee joints and had protective effects on rat OA cartilage in vivo . Primary rat articular chondrocytes were cotreated with APS-3c and IL-1 β    in vitro . 2~50  μ g/mL APS-3c had no effect on chondrocytes viability, whereas it increased the proteoglycans (PGs) synthesis inhibited by IL-1 β . Microarray analysis showed that the significant changes were concentrated in the genes which were involved in PGs synthesis. RT-PCR confirmed that treatment with APS-3c increased the mRNA expression of aggrecan and glycosyltransferases (GTs) inhibited by IL-1 β but did not affect the mRNA expression of matrix-degrading enzymes. These results indicate that APS-3c can improve PGs synthesis of chondrocytes on rat OA model in vivo and IL-1 β -stimulated chondrocytes in vitro , which is due to the promotion of the expression of aggrecan and GTs involved in PGs synthesis but not the inhibition of the expression of matrix-degrading enzymes. Our findings suggest the clinical relevance of APS-3c in the prospective of future alternative medical treatment for OA.

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