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高丽槐素通过调节 NLRP3 通路抑制骨关节炎。

Curculigoside inhibits osteoarthritis <em>via</em> the regulation of NLRP3 pathway.

机构信息

Department of Clinical Laboratory, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan; Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan.

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan; Department of Rehabilitation, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan.

出版信息

Eur J Histochem. 2023 Dec 13;67(4):3896. doi: 10.4081/ejh.2023.3896.

Abstract

Osteoarthritis (OA) is characterized by degenerative articular cartilage. Nucleotide-binding oligomerization domain-like receptor containing pyrin domain 3 (NLRP3) plays an important role in inflammation. This study aims to investigate whether protective effects of curculigoside on OA are medicated by the regulation of NLRP3 pathway. Destabilization of the medial meniscus (DMM) was performed to build an OA mouse model. After surgery, OA mice were treated with curculigoside. Immunohistochemistry was conducted to evaluate OA cartilage. In addition, human chondrocytes were isolated and treated with curculigoside. The mRNA and protein expression of iNOS, MMP-9, NLRP3 was detected by PCR and Western blot analysis. Curculigoside inhibited mRNA and protein levels of iNOS and MMP-9 induced by DMM surgery in a dose-dependent manner. Furthermore, the expression of NLRP3, NF-κB and PKR was downregulated after curculigoside administration. Moreover, curculigoside reversed the effects of IL-1β on MMP-9, iNOS and type II collagen expression at mRNA and protein levels in human chondrocytes in a dose-dependent manner. In conclusion, curculigoside exhibits beneficial effect on cartilage via the inhibition of NLRP3 pathway.

摘要

骨关节炎(OA)的特征是退行性关节软骨。核苷酸结合寡聚化结构域样受体包含 pyrin 域 3(NLRP3)在炎症中起重要作用。本研究旨在探讨卷曲糖苷对 OA 的保护作用是否通过 NLRP3 途径的调节来介导。内侧半月板不稳定(DMM)用于构建 OA 小鼠模型。手术后,OA 小鼠用卷曲糖苷治疗。免疫组织化学用于评估 OA 软骨。此外,分离并用人软骨细胞卷曲糖苷处理。通过 PCR 和 Western blot 分析检测 iNOS、MMP-9、NLRP3 的 mRNA 和蛋白表达。卷曲糖苷以剂量依赖性方式抑制 DMM 手术诱导的 iNOS 和 MMP-9 的 mRNA 和蛋白水平。此外,卷曲糖苷给药后 NLRP3、NF-κB 和 PKR 的表达下调。此外,卷曲糖苷以剂量依赖性方式逆转 IL-1β 对人软骨细胞中 MMP-9、iNOS 和 II 型胶原表达的影响。总之,卷曲糖苷通过抑制 NLRP3 通路对软骨表现出有益的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24fb/10773194/ae05c70fec5d/ejh-67-4-3896-g001.jpg

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