Department of Orthopaedics, China-Japan Union Hospital of Jilin University, Changchun 130033, Jilin, China.
Department of Orthopaedics, Heze Municipal Hospital, Heze 274031, Shandong, China.
Int Immunopharmacol. 2019 Apr;69:373-381. doi: 10.1016/j.intimp.2019.02.014. Epub 2019 Feb 15.
Kaempferol is a kind of bioflavonoid exerts diverse pharmacological activities, including anti-apoptotic and anti-inflammatory activities. Kaempferol has been recognized as an effective agent for alleviating the clinical symptoms of osteoarthritis (OA). This study aimed to provide evidence that Kaempferol has potential in the management of OA. Lipopolysaccharide (LPS) stimulation induced a significant cell death and inflammatory injury in ATDC5 cells, as evidenced by the decreased cell viability, the induced apoptosis, the activated caspase-3, and the excessive production of IL-6, IL-8 and TNF-α. Precondition of cells with Kaempferol prevented apoptosis and the release of proinflammatory cytokines triggered by LPS. miR-146a was down-regulated by Kaempferol treatment, and Decorin was up-regulated by miR-146a overexpression. Consistently, both silence of miR-146a and Decorin exhibited Kaempferol-like effects towards ATDC5 cells stimulated by LPS. Moreover, Decorin silence activated PI3K/AKT/mTOR signaling pathway. In rat model of OA, the expression of miR-146a and Decorin in cartilage tissues was repressed by Kaempferol. Also, the activated PI3K/AKT/mTOR signaling pathway in OA animal model was enhanced by Kaempferol administration. These data suggested that Kaempferol exerted potential anti-OA effects through down-regulation of miR-146a, and thus repressing the expression of Decorin.
山奈酚是一种生物类黄酮,具有多种药理活性,包括抗凋亡和抗炎活性。山奈酚已被认为是缓解骨关节炎(OA)临床症状的有效药物。本研究旨在为山奈酚在 OA 管理中的应用提供证据。脂多糖(LPS)刺激可诱导 ATDC5 细胞发生显著的细胞死亡和炎症损伤,这表现在细胞活力降低、诱导的细胞凋亡、激活的 caspase-3 以及过量产生的 IL-6、IL-8 和 TNF-α。用山奈酚预处理细胞可预防 LPS 引发的细胞凋亡和促炎细胞因子的释放。山奈酚处理可下调 miR-146a,上调 Decorin。miR-146a 沉默和 Decorin 过表达对 LPS 刺激的 ATDC5 细胞具有与山奈酚相似的作用。此外,沉默 Decorin 可激活 PI3K/AKT/mTOR 信号通路。在 OA 大鼠模型中,山奈酚抑制软骨组织中 miR-146a 和 Decorin 的表达。此外,山奈酚给药可增强 OA 动物模型中激活的 PI3K/AKT/mTOR 信号通路。这些数据表明,山奈酚通过下调 miR-146a 发挥潜在的抗 OA 作用,从而抑制 Decorin 的表达。