非西汀
白杨素
HEK 293细胞
肿瘤坏死因子α
化学
磷酸化
山奈酚
药理学
槲皮素
生物化学
类黄酮
生物
基因
免疫学
抗氧化剂
作者
Soohyoung Rain Lee,Young-Jin Kim,Sanghoon Kwon,Young‐Hee Lee,Soo-Young Choi,Jinseu Park,Hyung‐Joo Kwon
标识
DOI:10.5483/bmbrep.2009.42.5.265
摘要
Due to their multiple biological activities, flavonoids have gained attention as potentially useful therapeutics for a variety of diseases including cancer, cardiovascular diseases, and autoimmune diseases. In this study, we demonstrated that several flavonoids, including kaempferol, quercetin, fisetin, and chrysin block TNF-alpha induced IL-8 promoter activation and gene expression in HEK 293 cells. In addition, phosphorylation and degradation of IkappaBalpha and translocation of NF-kappaB p65 were inhibited by these flavonoids in TNF-alpha-stimulated HEK 293 cells. Furthermore, generation of reactive oxygen species (ROS) in response to TNF-alpha was reduced by the flavonoids. Moreover, although pretreatment with fisetin, quercetin, or chrysin decreased cell viability, kaempferol did not. Taken together, these findings suggest that kaempferol would be useful for the treatment of TNF-alpha-induced inflammatory diseases.
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