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Experimental research on the influence of cinnamic aldehyde on the proliferation, apoptosis and cell cycle of fibroblast-like synovial cells
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DOI   10.11656/j.issn.1672-1519.2017.01.13
Key Words   osteoarthritis;cinnamic aldehyde;fibroblast-like synovial cell;proliferation;flow cytometry
Author NameAffiliationE-mail
WANG Huan Beijing University of Chinese Medicine, Beijing 100029, China  
WANG Qing-fu The Third Affiliated Hospital of Beijing University of Chinese Medicine, Beijing 100029, China qingpu-wang@sohu.com 
YANG Li-li Beijing University of Chinese Medicine, Beijing 100029, China  
ZHANG Dong Beijing University of Chinese Medicine, Beijing 100029, China  
WANG Wei-li Beijing University of Chinese Medicine, Beijing 100029, China  
DING Hao-bin Beijing University of Chinese Medicine, Beijing 100029, China  
GUO Yu-ru Beijing University of Chinese Medicine, Beijing 100029, China  
DU Wang-yang Beijing University of Chinese Medicine, Beijing 100029, China  
XU Ming-kang Beijing University of Chinese Medicine, Beijing 100029, China  
GAN Wen Beijing University of Chinese Medicine, Beijing 100029, China  
Abstract
    [Objective] To investigate the influence of different concentrations of cinnamic aldehyde (CA) on the proliferation, apoptosis and cell cycle of fibroblast-like synovial cells(FLS), and then explore the regulatory mechanism of CA to the synovial inflammation in osteoarthritis.[Methods] Different concentrations of CA were intervened on LPS-induced FLS respectively, and the proliferation, apoptosis and cell cycle were measured through Methylthiazolyldiphenyl-tetrazolium bromide assay (MTT) and flow cytometry(FCM).[Results] Low concentration of CA could promote the growth of FLS mildly, while high concentration of CA could significantly reduce the survival rate (P<0.05) in concentration-dependent manner. LPS could reduce the apoptosis rate of FLS, shorten the G1 phase and extend the S phase, it meant that the inflammatory model was successfully established. Compared with the control group, both high and low concentration of CA groups could obviously increase the ratio of cells in the areas of Q2 and Q4 (P<0.05), and extend the G1 phase and S phase (P<0.05) to induct the apoptosis and inhibit the proliferation of FLS, especially the effect of high concentration of CA group was more significant.[Conclusion] Different concentrations of CA has certain inhibition for the growth of FLS, and the high concentration of CA group has stronger inhibitory effect, which may be the potential mechanism of CA's anti-inflammatory effects.

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