诺沃乔宁通过调节氧化还原信号和钙振荡减轻炎性骨溶解和胶原诱导的关节炎

IF 5.3
Haojue Wang, Tao Yuan, Xiao Yu, Yi Wang, Changxing Liu, Ziqing Li, Shui Sun
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引用次数: 0

摘要

黄芩苷是从黄芩中提取的黄酮类化合物。然而,其在类风湿关节炎(RA)中的潜在机制尚不清楚。本研究探讨诺沃戈宁在ra相关炎症性骨溶解中的具体作用和相关靶点。采用网络药理学方法分析Norwogonin在RA中的核心作用靶点和信号通路。通过体外实验探讨Norwogonin对破骨细胞行为的实际影响及其信号传导机制。体内研究进一步验证了诺沃戈蛋白对胶原诱导关节炎(CIA)小鼠的治疗作用。网络药理学分析确定了Norwogonin和RA之间的18个共同靶点,表明与炎症反应和氧化还原酶活性有关。体外实验结果显示,160 μM的Norwogonin抑制lps驱动的破骨细胞分化和功能。qPCR和Western blot分析也显示,由于Norwogonin治疗,破骨细胞标记基因和蛋白的变化持续减少,包括破骨细胞分化(Traf6, Tnfrsf11a和Nfatc1),融合(Atp6v0d2, Dcstamp和Ocstamp)和功能(Mmp9, Ctsk和Acp5)。进一步的机制研究表明,Norwogonin抑制lps驱动的ROS生成和钙(Ca2+)振荡。此外,每隔一天腹腔注射30 mg/kg诺沃戈宁成功地减轻了CIA模型的临床关节炎进展和骨破坏。我们的研究探讨了Norwogonin治疗RA的前景,并阐明了其在lps诱导的破骨细胞生成和CIA小鼠中的抑制作用和潜在机制,为Norwogonin治疗RA相关炎症性溶骨的进一步转化研究提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Norwogonin Attenuates Inflammatory Osteolysis and Collagen-Induced Arthritis via Modulating Redox Signalling and Calcium Oscillations

Norwogonin Attenuates Inflammatory Osteolysis and Collagen-Induced Arthritis via Modulating Redox Signalling and Calcium Oscillations

Norwogonin is a flavonoid extraction derived from Scutellaria baicalensis. However, its potential mechanisms in the context of rheumatoid arthritis (RA) are unclear. This study investigates the specific effects and associated targets of Norwogonin in RA-related inflammatory osteolysis. Network pharmacology was conducted to analyse the core targets and signalling pathways of Norwogonin in RA. In vitro experiments were carried out to explore the actual effects of Norwogonin on osteoclast behaviours and related signalling mechanisms. In vivo studies further validated the therapeutic effect of Norwogonin in collagen-induced arthritis (CIA) mice. The network pharmacological analysis identified 18 shared targets between Norwogonin and RA, indicating a connection with inflammatory response and oxidoreductase activity. For biological validations, the results of in vitro experiments revealed 160 μM of Norwogonin inhibited LPS-driven osteoclast differentiation and function. The qPCR assay and Western blot analysis also disclosed consistently diminished changes to osteoclastic marker genes and proteins due to Norwogonin treatment, including those for osteoclast differentiation (Traf6, Tnfrsf11a and Nfatc1), fusion (Atp6v0d2, Dcstamp and Ocstamp) and function (Mmp9, Ctsk and Acp5). Further mechanism study revealed Norwogonin suppressed LPS-driven ROS production and calcium (Ca2+) oscillations. Also, intraperitoneal injection of 30 mg/kg Norwogonin every other day successfully mitigated clinical arthritis progression and attenuated bone destruction in the CIA model. Our study scrutinises Norwogonin's therapeutic prospects in treating RA and illustrates its inhibitory effects and potential mechanism within LPS-induced osteoclastogenesis and CIA mice, providing a basis for further translational research on Norwogonin in the treatment of RA-related inflammatory osteolysis.

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来源期刊
CiteScore
11.50
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0.00%
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期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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