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Rosmarinic acid down‐regulates NO and PGE2 expression via MAPK pathway in rat chondrocytes
by
Hu, Peng‐Fei
, Jin, Guo‐Jun
, Bao, Jia‐Peng
, Chen, We‐Ping
, Xiong, Yan
, Wu, Li‐Dong
in
chondrocyte
/ interleukin‐1β
/ matrix metalloproteinase
/ nitric oxide
/ osteoarthritis
/ prostaglandin E2
/ rosmarinic acid
2018
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Rosmarinic acid down‐regulates NO and PGE2 expression via MAPK pathway in rat chondrocytes
by
Hu, Peng‐Fei
, Jin, Guo‐Jun
, Bao, Jia‐Peng
, Chen, We‐Ping
, Xiong, Yan
, Wu, Li‐Dong
in
chondrocyte
/ interleukin‐1β
/ matrix metalloproteinase
/ nitric oxide
/ osteoarthritis
/ prostaglandin E2
/ rosmarinic acid
2018
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Do you wish to request the book?
Rosmarinic acid down‐regulates NO and PGE2 expression via MAPK pathway in rat chondrocytes
by
Hu, Peng‐Fei
, Jin, Guo‐Jun
, Bao, Jia‐Peng
, Chen, We‐Ping
, Xiong, Yan
, Wu, Li‐Dong
in
chondrocyte
/ interleukin‐1β
/ matrix metalloproteinase
/ nitric oxide
/ osteoarthritis
/ prostaglandin E2
/ rosmarinic acid
2018
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Rosmarinic acid down‐regulates NO and PGE2 expression via MAPK pathway in rat chondrocytes
Journal Article
Rosmarinic acid down‐regulates NO and PGE2 expression via MAPK pathway in rat chondrocytes
2018
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Overview
Rosmarinic acid (RosA) is a water‐soluble polyphenol, which can be isolated from many herbs such as orthosiphon diffuses and rosmarinus officinalis. Previous studies have shown that RosA possesses various biological properties. In this study, we investigate the anti‐osteoarthritic effects of RosA in rat articular chondrocytes. Chondrocytes were pre‐treated with RosA, followed by the stimulation of IL‐1β. Real‐time PCR and Western blot were performed to detect the expression of matrix metalloproteinase (MMP)‐1, MMP‐3 and MMP‐13. Nitric oxide and PGE2 production were measured by Griess reagent and enzyme‐linked immunosorbent assay (ELISA). The expression of mitogen‐activated protein kinase (MAPK) and nuclear factor‐κB (NF‐κB) was also investigated by Western blot analysis. We found that RosA down‐regulated the MMPs expression as well as nitric oxide and PGE2 production in IL‐1β‐induced chondrocytes. In addition, RosA inhibited p38 and JNK phosphorylation as well as p65 translocation. The results suggest that RosA may be considered a possible agent in the treatment of OA.
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