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小白菊内酯和β-谷甾醇具有协同作用,能缓解胶原诱导性关节炎。

Imperatorin and β-sitosterol have synergistic activities in alleviating collagen-induced arthritis.

机构信息

Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, China.

Law Sau Fai Institute for Advancing Translational Medicine in Bone & Joint Diseases, School of Chinese Medicine, Hong Kong Baptist University, Hong Kong, China.

出版信息

J Leukoc Biol. 2020 Aug;108(2):509-517. doi: 10.1002/JLB.3MA0320-440RR. Epub 2020 May 11.

DOI:10.1002/JLB.3MA0320-440RR
PMID:32392637
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7496114/
Abstract

Rheumatoid arthritis (RA) is a chronic disease with complex molecular network of pathophysiology, single drug is usually not full satisfactory because it is almost impossible to target the whole molecular network of the disease. Drug combinations that act synergistically with each another is an effective strategy in RA therapy. In this study, we aimed to establish a new strategy to search effective synergized compounds from Chinese herbal medicine (CHM) used in RA. Based on multi-information integrative approaches, imperatorin (IMP) and β-sitosterol (STO) were predicted as the most effective pair for RA therapy. Further animal experiments demonstrated that IMP+STO treatment ameliorated arthritis severity of collagen-induced arthritis (CIA) rats in a synergistic manner, whereas IMP or STO administration separately had no such effect. RNA sequencing and IPA analysis revealed that the synergistic mechanism of IMP+STO treatment was related to its regulatory effect on 5 canonical signaling pathways, which were not found when IMP or STO used alone. Moreover, LTA, CD83, and SREBF1 were 3 important targets for synergistic mechanism of IMP+STO treatment. The levels of these 3 genes were significantly up-regulated in IMP+STO group compared to model group, whereas IMP or STO administration separately had no effect on them. In conclusion, this study found that IMP and STO were 2 synergistic compounds from the CHM in RA therapy, whose synergistic mechanism was closely related to regulate the levels of LTA, CD83, and SREBF1.

摘要

类风湿关节炎(RA)是一种慢性疾病,其病理生理学具有复杂的分子网络,单一药物通常不能完全令人满意,因为几乎不可能针对疾病的整个分子网络。具有协同作用的药物联合是 RA 治疗的有效策略。在这项研究中,我们旨在建立一种从用于 RA 的中药中寻找有效协同化合物的新策略。基于多信息综合方法,预测欧前胡素(IMP)和β-谷甾醇(STO)是治疗 RA 的最有效组合。进一步的动物实验表明,IMP+STO 治疗以协同方式改善胶原诱导性关节炎(CIA)大鼠的关节炎严重程度,而单独给予 IMP 或 STO 则没有这种作用。RNA 测序和 IPA 分析表明,IMP+STO 治疗的协同机制与其对 5 个经典信号通路的调节作用有关,而单独使用 IMP 或 STO 则没有这种作用。此外,LTA、CD83 和 SREBF1 是 IMP+STO 治疗协同机制的 3 个重要靶点。与模型组相比,IMP+STO 组这 3 个基因的水平明显上调,而单独给予 IMP 或 STO 则没有影响。总之,这项研究发现,IMP 和 STO 是 RA 治疗中来自中药的 2 种协同化合物,其协同机制与调节 LTA、CD83 和 SREBF1 的水平密切相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff31/7496114/f327ce297372/JLB-108-509-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff31/7496114/632b00f1196a/JLB-108-509-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff31/7496114/fed75456d254/JLB-108-509-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff31/7496114/bbd417d2d4cd/JLB-108-509-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff31/7496114/d5dde1f05162/JLB-108-509-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff31/7496114/f327ce297372/JLB-108-509-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff31/7496114/632b00f1196a/JLB-108-509-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff31/7496114/fed75456d254/JLB-108-509-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff31/7496114/bbd417d2d4cd/JLB-108-509-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff31/7496114/d5dde1f05162/JLB-108-509-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff31/7496114/f327ce297372/JLB-108-509-g005.jpg

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