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有效提取雪通素及其通过靶向滑膜细胞迁移和凋亡预防 RA 滑膜过度增生的作用。

Effective extraction of Xuetongsu and its role in preventing RA synovial hyperplasia by targeting synovial cell migration and apoptosis.

机构信息

TCM and Ethnomedicine Innovation & Development International Laboratory, Innovative Materia Medica Research Institute, School of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, China.

出版信息

Sci Rep. 2024 Oct 7;14(1):23345. doi: 10.1038/s41598-024-73471-z.

DOI:10.1038/s41598-024-73471-z
PMID:39375373
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11458764/
Abstract

Kadsura heteroclita (Roxb) Craib also named Xuetong in Tujia ethnomedicine in China, has been traditionally employed in rheumatoid arthritis (RA) treatment. Our preceding investigations have elucidated that Xuetongsu (XTS), a triterpenoid compound predominant in Xuetong, showed excellent anti-RA-fibroblast-like synoviocytes (RAFLS) proliferation effect. However, XTS belongs to the trace components of the Xuetong plant, which poses certain limitations to the research. In this study, we designed a method that enhanced the extraction yield of XTS and explored the mechanism of its inhibition of RAFLS cell proliferation and migration in the treatment of RA. The results displayed that XTS reduced RAFLS cell proliferation, with an IC value of 4.68 ± 0.65 µM. A series of experimental techniques were utilized to show that XTS induce apoptosis in RAFLS cells at concentrations ranging from 4.5 to 18 µM, including wound healing assay, flow cytometry, and western blot analysis. Moreover, XTS at dosages of 0.42-0.84 mg/kg markedly attenuated paw swelling and synovial hyperplasia in arthritic rats, primarily through the inhibition of RAFLS migration and promotion of RAFLS apoptosis via High mobility group box 1 (HMGB-1)/Matrix metalloproteinase-9 (MMP-9)/MMP-13 signaling pathway and Bcl-2/Bax/Caspase-3 signaling pathway, respectively.

摘要

中国土家族医学中的异型南五味子(Roxb)Craib 也被称为雪藤,传统上用于治疗类风湿关节炎(RA)。我们之前的研究已经阐明,雪藤中的主要三萜化合物雪藤素(XTS)对 RA 成纤维样滑膜细胞(RAFLS)增殖具有极好的抑制作用。然而,XTS 属于雪藤植物的痕量成分,这对研究有一定的限制。在这项研究中,我们设计了一种方法来提高 XTS 的提取产率,并探讨了其抑制 RAFLS 细胞增殖和迁移从而治疗 RA 的机制。结果显示,XTS 降低 RAFLS 细胞的增殖,IC 值为 4.68±0.65 µM。一系列实验技术表明,XTS 在 4.5 至 18 µM 的浓度范围内诱导 RAFLS 细胞凋亡,包括划痕愈合试验、流式细胞术和 Western blot 分析。此外,XTS 在 0.42-0.84 mg/kg 的剂量下显著减轻关节炎大鼠的足肿胀和滑膜增生,主要通过抑制 RAFLS 迁移和促进 RAFLS 凋亡,分别通过高迁移率族蛋白 1(HMGB-1)/基质金属蛋白酶-9(MMP-9)/基质金属蛋白酶-13(MMP-13)信号通路和 Bcl-2/Bax/Caspase-3 信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5249/11458764/6bc35dc72e8a/41598_2024_73471_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5249/11458764/33a478aa51c9/41598_2024_73471_Sch1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5249/11458764/1fc20be637e9/41598_2024_73471_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5249/11458764/6bc35dc72e8a/41598_2024_73471_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5249/11458764/33a478aa51c9/41598_2024_73471_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5249/11458764/2380e8730806/41598_2024_73471_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5249/11458764/c2feac516209/41598_2024_73471_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5249/11458764/84315c9ec739/41598_2024_73471_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5249/11458764/e8c533d957fc/41598_2024_73471_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5249/11458764/1fc20be637e9/41598_2024_73471_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5249/11458764/6bc35dc72e8a/41598_2024_73471_Fig6_HTML.jpg

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The synovial microenvironment suppresses chondrocyte hypertrophy and promotes articular chondrocyte differentiation.滑膜微环境抑制软骨细胞肥大并促进关节软骨细胞分化。
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