Juanbi Qianggu Formula Alleviates Rheumatoid Arthritis by Suppressing the TNF-α/NF-κB Signaling Pathway.

IF 3 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Guowei Qiu, Junjie Wen, Zheng Xiang, Wei Hu, Xinyu A, Chenxin Gao, Yanqing Bian, Xirui Xu, Lu Meng, Lianbo Xiao
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引用次数: 0

Abstract

Juanbi Qianggu Formula (JBQGF) is a traditional Chinese medicine prescription with demonstrated clinical efficacy in rheumatoid arthritis (RA), yet its pharmacological mechanisms remain unclear. This study investigated whether JBQGF attenuates RA-associated inflammation by inhibiting the TNF-α/NF-κB signaling pathway. In a collagen-induced arthritis (CIA) mouse model, JBQGF significantly ameliorated joint swelling, bone erosion, and systemic inflammation, with efficacy comparable to methotrexate, and reduced serum and synovial TNF-α levels. In LPS-stimulated RAW 264.7 macrophages, JBQGF-containing serum suppressed NF-κB p65 nuclear translocation and downregulated TNF-α, iNOS, and COX-2 expression. Transcriptomic profiling of synovial tissue, coupled with functional rescue assays, revealed that JBQGF directly suppresses TNFAIP2 expression via the primary NF-κB axis rather than secondary TNF-α depletion, thereby disrupting an NF-κB/TNFAIP2/ROS inflammatory cascade. These findings indicate that JBQGF targets the TNF-α/NF-κB pathway at multiple nodes to restore cellular inflammatory and redox balance, providing a mechanistic basis for its therapeutic effects in RA.

蠲痹强骨方通过抑制TNF-α/NF-κB信号通路缓解类风湿关节炎。
蠲痹强骨方(JBQGF)是治疗类风湿性关节炎(RA)临床疗效较好的中药方剂,其药理机制尚不清楚。本研究探讨JBQGF是否通过抑制TNF-α/NF-κB信号通路减轻ra相关炎症。在胶原诱导关节炎(CIA)小鼠模型中,JBQGF显著改善关节肿胀、骨质侵蚀和全身炎症,其疗效与甲氨蝶呤相当,并降低血清和滑膜TNF-α水平。在lps刺激的RAW 264.7巨噬细胞中,含jbqgf的血清抑制NF-κB p65核易位,下调TNF-α、iNOS和COX-2的表达。滑膜组织的转录组学分析,结合功能挽救试验,显示JBQGF通过主要的NF-κB轴而不是继发性的TNF-α耗尽直接抑制TNFAIP2的表达,从而破坏NF-κB/TNFAIP2/ROS炎症级联反应。上述结果提示JBQGF可通过多个节点的TNF-α/NF-κB通路恢复细胞炎症和氧化还原平衡,为其治疗RA的作用提供了机制基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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