Suppr超能文献

机械应力引起的软骨细胞功能障碍和软骨损伤可以通过薯蓣皂素激活 SIRT1/叉头框 O1 来减轻。

Mechanical stress-caused chondrocyte dysfunction and cartilage injury can be attenuated by dioscin via activating sirtuin1/forkhead box O1.

机构信息

Department of Orthopaedic Surgery, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University, Shanghai, China.

出版信息

J Biochem Mol Toxicol. 2022 Dec;36(12):e23212. doi: 10.1002/jbt.23212. Epub 2022 Sep 14.

Abstract

Sirtuin1 (Sirt1)/forkhead box O1 (FoxO1) axis has been reported as a crucial regulator involved in chondral homeostasis of healthy or osteoarthritis (OA) cartilage. In our study, the aim is to investigate whether dioscin functions as an activator of Sirt1/FoxO1 to protect against mechanical stress-induced chondrocyte dysfunction in vitro and in vivo models. HERB and PubChem databases were implemented to predict dioscin-related gene targets. Cell and mouse models of OA were established to determine the pharmacological value of dioscin, a steroidal saponin. Cartilage loss in the knee joint was detected by Safranin O staining. Phosphorylation and nucleocytoplasmic shuttling of FoxO1 was observed in mechanical stress-stimulated chondrocyte and anterior cruciate ligament transection-induced cartilage injury. However, dioscin treatment repressed FoxO1 phosphorylation and cytoplasmic transfer and elevated Sirt1 protein expression. Dioscin treatment reversed mechanical stress-induced growth inhibition and apoptosis of chondrocytes and improved cartilage degradation and bone loss in the epiphysis of the distal femur. Moreover, dioscin could maintain the normal phenotype of chondrocytes via mediating multiple gene expressions. Dioscin inhibited apoptosis and metabolic disorders in OA-like chondrocytes via maintaining the transcriptional activity of FoxO1 and enhancing Sirt1 expression. Dioscin might be a potential Sirt1 activator providing a novel therapeutic schedule for the treatment of OA.

摘要

Sirtuin1 (Sirt1)/forkhead box O1 (FoxO1) 轴已被报道为参与健康或骨关节炎 (OA) 软骨软骨内稳态的关键调节因子。在我们的研究中,目的是研究薯蓣皂苷是否作为 Sirt1/FoxO1 的激活剂,以防止体外和体内模型中机械应激诱导的软骨细胞功能障碍。HERB 和 PubChem 数据库被用来预测薯蓣皂苷的相关基因靶点。建立 OA 的细胞和小鼠模型,以确定薯蓣皂苷(一种甾体皂苷)的药理学价值。通过番红 O 染色检测膝关节软骨丢失。观察到机械应激刺激的软骨细胞和前交叉韧带横断诱导的软骨损伤中 FoxO1 的磷酸化和核质穿梭。然而,薯蓣皂苷处理抑制 FoxO1 磷酸化和细胞质转移,并提高 Sirt1 蛋白表达。薯蓣皂苷处理逆转了机械应激诱导的软骨细胞生长抑制和凋亡,并改善了远端股骨骨骺的软骨降解和骨丢失。此外,薯蓣皂苷可以通过调节多种基因表达来维持软骨细胞的正常表型。薯蓣皂苷通过维持 FoxO1 的转录活性和增强 Sirt1 表达来抑制 OA 样软骨细胞的凋亡和代谢紊乱。薯蓣皂苷可能是一种潜在的 Sirt1 激活剂,为 OA 的治疗提供了一种新的治疗方案。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验