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Tetrandrine Inhibits the Wnt/β-Catenin Signalling Pathway and Alleviates Osteoarthritis: An In Vitro and In Vivo Study

机译:粉防己碱抑制Wnt /β-Catenin信号传导途径并减轻骨关节炎:一项体内和体外研究

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摘要

There is currently no effective drug treatment for the early phase of osteoarthritis (OA), one of the most common senile diseases. The goal of this study was to investigate the protective effect of the tetrandrine (Tet) on OA, in vitro and in vivo. In an in vitro experiment, quantitative real-time polymerase chain reaction (qRT-PCR) was used to investigate changes in gene expression upon the addition of Tet in chondrocytes processed with IL-1β; changes in protein profiles were assessed by Western blotting. In vivo, to determine whether Tet has the protective effects on articular cartilage, a rabbit anterior cruciate ligament transaction model of OA was established. Expression of matrix metalloproteinase and β-catenin genes increased significantly, while that of tissue inhibitor of metalloproteinase-1 decreased significantly in the OA group both in vivo and in chondrocytes. However, the changes of expression were reversed by Tet, and there was less cartilage degradation in vivo compared with the OA group, as assessed by histological and macroscopic observations. Thus, Tet may play a useful role in the treatment of OA through the Wnt/β-catenin signalling pathway and has potential for the treatment of OA.
机译:目前,骨关节炎(OA)是最常见的老年性疾病之一,目前尚无有效的药物治疗方法。这项研究的目的是在体外和体内研究粉防己碱(Tet)对OA的保护作用。在体外实验中,实时定量聚合酶链反应(qRT-PCR)用于研究IL-1β处理的软骨细胞中添加Tet后基因表达的变化。通过蛋白质印迹评估蛋白质谱的变化。在体内,为了确定Tet是否对关节软骨具有保护作用,建立了兔前交叉韧带OA交易模型。在OA组中,体内和软骨细胞中基质金属蛋白酶和β-catenin基因的表达显着增加,而金属蛋白酶-1的组织抑制剂的表达显着降低。然而,如通过组织学和宏观观察所评估的,Tet逆转了表达的变化,并且与OA组相比,体内软骨降解较少。因此,Tet可能通过Wnt /β-catenin信号通路在OA的治疗中发挥有用的作用,并具有治疗OA的潜力。

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