Department of Orthopaedic Surgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Department of Orthopaedic Surgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Int Immunopharmacol. 2017 Nov;52:218-226. doi: 10.1016/j.intimp.2017.09.017. Epub 2017 Sep 22.
Osteoarthritis (OA) is a degenerative joint disease with an inflammatory component that drives the degradation of cartilage extracellular matrix. Baicalin, a predominant flavonoid isolated from the dry root of Scutellaria baicalensis Georgi, has been reported to have anti-inflammatory effects. However, the anti-inflammatory effects of baicalin on OA have not been reported. Our study aimed to investigate the effect of baicalin on OA both in vitro and in vivo. In vitro, human OA chondrocytes were pretreated with baicalin (10, 50, 100μM) for 2h and subsequently stimulated with IL-1β for 24h. Production of NO and PGE2 were evaluated by the Griess reaction and ELISAs. The mRNA expression of COX-2, iNOS, MMP-3, MMP-13, ADAMTS-5, aggrecan and collagen-II were measured by real-time PCR. The protein expression of COX-2, iNOS, MMP-3, MMP-13, ADAMTS-5, p65, p-p65, IκBα and p-IκBα was detected by Western blot. The protein expression of collagen-II was evaluated by immunofluorescence. Luciferase activity assay was used to assess the relative activity of NF-kB. In vivo, the severity of OA was determined by histological analysis. We found that baicalin significantly inhibited the IL-1β-induced production of NO and PGE2, expression of COX-2, iNOS, MMP-3, MMP-13 and ADAMTS-5 and degradation of aggrecan and collagen-II. Furthermore, baicalin dramatically suppressed IL-1β-stimulated NF-κB activation. In vivo, treatment of baicalin not only prevented the destruction of cartilage but also relieved synovitis in mice OA models. Taken together, these results suggest that baicalin may be a potential agent in the treatment of OA.
骨关节炎(OA)是一种具有炎症成分的退行性关节疾病,可导致软骨细胞外基质降解。黄芩苷是从黄芩的干燥根中分离得到的主要黄酮类化合物,已被报道具有抗炎作用。然而,黄芩苷对 OA 的抗炎作用尚未见报道。本研究旨在探讨黄芩苷在体外和体内对 OA 的作用。在体外,用人 OA 软骨细胞用黄芩苷(10、50、100μM)预处理 2h,然后用 IL-1β刺激 24h。通过 Griess 反应和 ELISA 评估 NO 和 PGE2 的产生。通过实时 PCR 测量 COX-2、iNOS、MMP-3、MMP-13、ADAMTS-5、聚集蛋白聚糖和胶原-II 的 mRNA 表达。通过 Western blot 检测 COX-2、iNOS、MMP-3、MMP-13、ADAMTS-5、p65、p-p65、IκBα 和 p-IκBα 的蛋白表达。通过免疫荧光评估胶原-II 的蛋白表达。通过荧光素酶活性测定评估 NF-κB 的相对活性。在体内,通过组织学分析确定 OA 的严重程度。我们发现黄芩苷显著抑制了 IL-1β诱导的 NO 和 PGE2 的产生、COX-2、iNOS、MMP-3、MMP-13 和 ADAMTS-5 的表达以及聚集蛋白聚糖和胶原-II 的降解。此外,黄芩苷显著抑制了 IL-1β刺激的 NF-κB 激活。在体内,黄芩苷的治疗不仅防止了软骨的破坏,而且缓解了小鼠 OA 模型中的滑膜炎。综上所述,这些结果表明黄芩苷可能是治疗 OA 的潜在药物。