刺蒺藜总皂苷通过抑制 MAPK 信号通路,促进成纤维细胞样滑膜细胞凋亡并减轻炎症,从而减轻类风湿性关节炎。

IF 2.9 4区 医学 Q2 Medicine Clinical and Experimental Pharmacology and Physiology Pub Date : 2024-10-24 DOI:10.1111/1440-1681.13925
Xinghai Cheng, Yuantao Su, Ningzheng Dong, Meng Liu, Mengting Wang, Tiantian Zhou, Haibin Zhou
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引用次数: 0

摘要

在治疗类风湿性关节炎(RA)的众多方法中,促进滑膜细胞凋亡和抑制炎症被认为是最有效的方法。然而,从草本植物刺蒺藜中提取的天然皂甙--刺蒺藜总皂苷(GSTT)--对类风湿性关节炎成纤维细胞样滑膜细胞(RA-FLSs)的潜在促凋亡作用及其基本分子机制仍不清楚。本研究的目的是利用各种检测方法,包括细胞计数试剂盒-8(CCK-8)、反转录聚合酶链反应(RT-PCR)、酶联免疫吸附试验(ELISA)、流式细胞术、末端脱氧核苷酸转移酶 dUTP 缺口标记(TUNEL)和免疫印迹分析,研究不同浓度的 GSTT 对 RA-FLS 的影响。进行这些评估是为了评价细胞活力、炎症细胞因子水平的变化、细胞凋亡率以及与此相关的蛋白质表达变化。在体内,采用关节炎临床评分、血涂片和伊红(HE)染色以及酶联免疫吸附试验来评估爪部炎症、组织病理学和血清炎性细胞因子的变化。我们的研究结果表明,GSTT 大大促进了 RA-FLS 的凋亡,并降低了促炎细胞因子的水平。GSTT 还降低了 Bcl-2/Bax 比率,抑制了 JNK 和 p38 磷酸化。此外,GSTT 还能改善临床评分,减少滑膜炎症浸润,降低血清促炎细胞因子水平,从而对 RA 产生积极影响。因此,通过抑制 MAPK 信号通路促进 RA-FLS 的凋亡和抑制炎症,GSTT 是一种很有前景的 RA 治疗干预药物。
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Gross saponins of Tribulus terrestris attenuate rheumatoid arthritis by promoting apoptosis of fibroblast-like synoviocytes and reducing inflammation by inhibiting MAPK signalling pathway

Among the numerous treatment options for rheumatoid arthritis (RA), the promotion of synoviocyte apoptosis and inhibition of inflammation are considered the most effective. However, the potential pro-apoptotic effects of gross saponins of Tribulus terrestris (GSTT), which are natural saponins derived from the herb Tribulus terrestris L., on rheumatoid arthritis fibroblast-like synoviocytes (RA-FLSs) and their essential molecular mechanisms remain unclear. The aim of the present study was to investigate the influence of different concentrations of GSTT on RA-FLSs using various assays, including cell counting kit-8 (CCK-8), reverse transcription polymerase chain reaction (RT-PCR), enzyme-linked immunosorbent assay (ELISA), flow cytometry, terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL) and western blot analysis. These assessments were conducted to evaluate the cell viability, changes in the levels of inflammatory cytokines, apoptosis rates and alterations in protein expression related to this process. In vivo, arthritis clinical score, haematoxylin and eosin (HE) staining and ELISA were used to assess paw inflammation, histopathology and serum inflammatory cytokine changes. Our findings demonstrated that GSTT substantially promotes the apoptosis of RA-FLSs and reduces pro-inflammatory cytokine levels. GSTT also reduced the Bcl-2/Bax ratio and inhibited JNK and p38 phosphorylation. Furthermore, GSTT exhibits positive effects on RA by improving clinical scores, reducing synovial inflammatory infiltration and lowering serum pro-inflammatory cytokine levels. Therefore, by promoting the apoptosis of RA-FLSs and suppressing inflammation through the inhibition of the MAPK signalling pathway, GSTT is a promising therapeutic intervention for RA.

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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
128
审稿时长
6 months
期刊介绍: Clinical and Experimental Pharmacology and Physiology is an international journal founded in 1974 by Mike Rand, Austin Doyle, John Coghlan and Paul Korner. Our focus is new frontiers in physiology and pharmacology, emphasizing the translation of basic research to clinical practice. We publish original articles, invited reviews and our exciting, cutting-edge Frontiers-in-Research series’.
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