Division of Cardiology, Department of Medicine, Tri-Service General Hospital, Taiwan, ROC.
Eur J Pharmacol. 2010 Jun 25;636(1-3):181-8. doi: 10.1016/j.ejphar.2010.03.031. Epub 2010 Mar 31.
The pro-inflammatory cytokine interleukin-1 beta (IL-1 beta) plays critical roles in pathogenesis of osteoarthritis. Although estrogen is protective for cartilage in osteoarthritis patients, it also potentially increases the risk of stroke and cancer. Phytoestrogens acting as natural estrogen receptor modulators may serve as alternatives. This study aimed to identify medicinal phytoestrogens that preserve anti-inflammatory property and may function as potential chondro-protective compounds. Both human chondrocytes and chondrocytic cell line CHON-002 were used for this study. Protein concentrations or expressions were measured by ELISA or Western blot, respectively. The DNA-binding activity and transcriptional activity of transcription factors were evaluated by electrophoretic mobility shift assay and dual-luciferase reporter assay, respectively. Cell migration was analyzed by chemotaxis assays. We found that among screened phytoestrogens, bavachin could potently decrease IL-1 beta-induced nuclear factor-kappa B (NF-kappaB) but not activator protein-1 (AP-1) DNA-binding activity. Bavachin also inhibited I kappaB alpha degradation, increased nuclear translocation of p65 and p50 as well as decreased I kappaB alpha kinase (IKK) activity. Furthermore, bavachin inhibited IL-1 beta-induced chemokine production that resulted in reduced migration of THP-1 monocytic cells. Our results suggest that through decreasing IL-1 beta-induced activation of IKK-I kappaB alpha-NF-kappaB signaling pathway, bavachin potentially protects cartilage from inflammation-mediated damage in joints of osteoarthritis patients.
促炎细胞因子白细胞介素-1β(IL-1β)在骨关节炎发病机制中起关键作用。尽管雌激素对骨关节炎患者的软骨具有保护作用,但它也可能增加中风和癌症的风险。作为天然雌激素受体调节剂的植物雌激素可能是替代品。本研究旨在鉴定具有抗炎特性并可能作为潜在软骨保护化合物的药用植物雌激素。本研究使用人软骨细胞和软骨细胞系 CHON-002。通过 ELISA 或 Western blot 分别测量蛋白质浓度或表达。通过电泳迁移率变动分析和双荧光素酶报告基因分析分别评估转录因子的 DNA 结合活性和转录活性。通过趋化性测定分析细胞迁移。我们发现,在所筛选的植物雌激素中,补骨脂素可有效降低 IL-1β诱导的核因子-κB(NF-κB)但不激活蛋白-1(AP-1)DNA 结合活性。补骨脂素还抑制 IκBα降解,增加 p65 和 p50 的核易位,并降低 IκBα激酶(IKK)活性。此外,补骨脂素抑制 IL-1β诱导的趋化因子产生,从而减少单核细胞 THP-1 细胞的迁移。我们的研究结果表明,通过降低 IL-1β诱导的 IKK-IκBα-NF-κB 信号通路的激活,补骨脂素可能保护骨关节炎患者关节中的软骨免受炎症介导的损伤。