A wogonin-rich-fraction of Scutellaria baicalensis root extract exerts chondroprotective effects by suppressing IL-1β-induced activation of AP-1 in human OA chondrocytes

被引:35
作者
Khan, Nazir M. [1 ]
Haseeb, Abdul [1 ,2 ]
Ansari, Mohammad Y. [1 ]
Haqqi, Tariq M. [1 ]
机构
[1] Northeast Ohio Med Univ, Dept Anat & Neurobiol, 4209 St Rt 44, Rootstown, OH 44272 USA
[2] Cleveland Clin, Dept Cellular & Mol Med, Lerner Res Inst, 9500 Euclid Ave, Cleveland, OH 44195 USA
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
NF-KAPPA-B; NITRIC-OXIDE SYNTHASE; SELECTIVE-INHIBITION; GENE-EXPRESSION; MAP KINASES; OSTEOARTHRITIS; MANAGEMENT; ARTHRITIS; STRESS; MODELS;
D O I
10.1038/srep43789
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Osteoarthritis (OA) is a common joint disorder with varying degrees of inflammation and sustained oxidative stress. The root extract of Scutellaria baicalensis (SBE) has been used for the treatment of inflammatory and other diseases. Here, we performed activity-guided HPLC-fractionation of SBE, identified the active ingredient(s) and investigated its chondroprotective potential. We found that the Wogonin containing fraction-4 (F4) was the most potent fraction based on its ability to inhibit ROS production and the suppression of catabolic markers including IL-6, COX-2, iNOS, MMP-3, MMP-9, MMP-13 and ADAMTS-4 in IL-1 beta-treated OA chondrocytes. OA chondrocytes treated with F4 in the presence of IL-1 beta showed significantly enhanced expression of anabolic genes ACAN and COL2A1. In an in vitro model of cartilage degradation treatment with F4 inhibited s-GAG release from IL-1 beta-treated human cartilage explants. The inhibitory effect of F4 was not mediated through the inhibition of MAPKs and NF-kappa B activation but was mediated through the suppression of c-Fos/AP-1 activity at transcriptional and post transcriptional levels in OA chondrocytes. Purified Wogonin mimicked the effects of F4 in IL-1 beta-stimulated OA chondrocytes. Our data demonstrates that a Wogonin-rich fraction of SBE exert chondroprotective effects through the suppression of c-Fos/AP-1 expression and activity in OA chondrocytes under pathological conditions.
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页数:14
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