Department of Chemistry, Tamkang University, 151, Yingzhuan Road, Danshui Dist., New Taipei City 25137, Taiwan.
Molecules. 2013 Feb 5;18(2):2052-60. doi: 10.3390/molecules18022052.
The aim of this study was to investigate novel chalcones with potent anti-inflammatory activities in vivo. Chalcone and two chalcone analogues (compound 5 and 9) were evaluated using a caudal fin-wounded transgenic zebrafish line "Tg(mpx:gfp)" to visualize the effect of neutrophil recruitment dynamically. Results showed that treatment with compound 9 not only affected wound-induced neutrophil recruitment, but also affected Mpx enzymatic activity. Moreover, protein expression levels of pro-inflammatory factors (Mpx, NFκB, and TNFα) were also regulated by compound 9. Taken together, our results provide in vivo evidence of the anti-inflammatory effects of synthesized chalcone analogues on wound-induced inflammation.
本研究旨在探索具有体内抗炎活性的新型查尔酮。使用尾鳍受伤的转基因斑马鱼系“Tg(mpx:gfp)”来动态观察中性粒细胞募集的效果,评估了查尔酮和两种查尔酮类似物(化合物 5 和 9)。结果表明,化合物 9 的处理不仅影响了伤口诱导的中性粒细胞募集,还影响了 Mpx 酶活性。此外,促炎因子(Mpx、NFκB 和 TNFα)的蛋白表达水平也受到化合物 9 的调节。综上所述,我们的结果为合成查尔酮类似物对伤口诱导的炎症的抗炎作用提供了体内证据。