Wang Hao, Jiang Zengxin, Pang Zhiying, Qi Guobin, Hua Bingxuan, Yan Zuoqin, Yuan Hengfeng
Department of Orthopaedic Surgery, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Department of Orthopaedic Surgery, Shanghai Sixth People's Hospital, Shanghai Jiaotong University, Shanghai, People's Republic of China.
J Inflamm Res. 2021 Mar 9;14:745-760. doi: 10.2147/JIR.S297166. eCollection 2021.
Osteoarthritis (OA) is a progressive disease characterized by pain and impaired joint functions. Engeletin is a natural compound with anti-inflammatory and antioxidant effects on other diseases, but the effect of engeletin on OA has not been evaluated. This study aimed to elucidate the protective effect of engeletin on cartilage and the underlying mechanisms.
Chondrocytes were isolated from rat knee cartilage, and TNF-α was used to simulate OA in vitro. After treatment with engeletin, the expression of extracellular matrix (ECM) components (collagen II and aggrecan) and matrix catabolic enzymes (MMP9 and MMP3) was determined by Western blotting and qPCR. Chondrocyte apoptosis was evaluated using Annexin V-FITC/PI and flow cytometry. Apoptosis-related proteins (Bax, Bcl-2, and cleaved caspase-3) were evaluated by Western blotting. The mitochondrial membrane potential of chondrocytes was measured with JC-1, and intracellular reactive oxygen species (ROS) levels were determined with DCFH-DA. Changes in signaling pathways (Nrf2, NF-κB and MAPK) were evaluated by Western blotting. In vivo, anterior cruciate ligament transection (ACLT) was used to induce the rat OA model, and engeletin was administered intraarticularly. The therapeutic effect of engeletin was analyzed by histopathological analysis.
Pretreatment with engeletin alleviated TNF-α-induced inhibition of ECM components (collagen II and aggrecan) and upregulation of matrix catabolic enzymes (MMP9 and MMP3). Engeletin ameliorated chondrocyte apoptosis by inhibiting Bax expression and upregulating Bcl-2 expression. Engeletin maintained the mitochondrial membrane potential of chondrocytes and scavenged intracellular ROS by activating the Nrf2 pathway. The NF-κB and MAPK pathways were inhibited by treatment with engeletin. In vivo, ACLT-induced knee OA in rats was alleviated by intraarticular injection of engeletin.
Engeletin ameliorated OA in vitro and in vivo. It may be a potential therapeutic drug for OA.
骨关节炎(OA)是一种以疼痛和关节功能受损为特征的进行性疾病。恩格letin是一种对其他疾病具有抗炎和抗氧化作用的天然化合物,但恩格letin对OA的作用尚未得到评估。本研究旨在阐明恩格letin对软骨的保护作用及其潜在机制。
从大鼠膝关节软骨中分离软骨细胞,并用肿瘤坏死因子-α(TNF-α)在体外模拟OA。用恩格letin处理后,通过蛋白质印迹法和定量聚合酶链反应(qPCR)测定细胞外基质(ECM)成分(胶原蛋白II和聚集蛋白聚糖)和基质分解代谢酶(基质金属蛋白酶9和基质金属蛋白酶3)的表达。使用膜联蛋白V-异硫氰酸荧光素/碘化丙啶(Annexin V-FITC/PI)和流式细胞术评估软骨细胞凋亡。通过蛋白质印迹法评估凋亡相关蛋白(Bax、Bcl-2和裂解的半胱天冬酶-3)。用JC-1测量软骨细胞的线粒体膜电位,并用2′,7′-二氯二氢荧光素二乙酸酯(DCFH-DA)测定细胞内活性氧(ROS)水平。通过蛋白质印迹法评估信号通路(核因子E2相关因子2、核因子κB和丝裂原活化蛋白激酶)的变化。在体内,采用前交叉韧带横断术(ACLT)诱导大鼠OA模型,并通过关节内注射给予恩格letin。通过组织病理学分析恩格letin的治疗效果。
恩格letin预处理减轻了TNF-α诱导的ECM成分(胶原蛋白II和聚集蛋白聚糖)的抑制以及基质分解代谢酶(基质金属蛋白酶9和基质金属蛋白酶3)的上调。恩格letin通过抑制Bax表达和上调Bcl-2表达改善软骨细胞凋亡。恩格letin通过激活核因子E2相关因子2途径维持软骨细胞的线粒体膜电位并清除细胞内ROS。恩格letin处理抑制了核因子κB和丝裂原活化蛋白激酶途径。在体内,关节内注射恩格letin减轻了ACLT诱导的大鼠膝关节OA。
恩格letin在体外和体内均改善了OA。它可能是一种潜在的OA治疗药物。