Yueyue Li, Yanqiu Gu, Yuhuan Shi, Bin Zhang, Shu Pan, Yifeng Chai, Xiaofei Chen, Yongfang Yuan
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Among them, 8 components retained well on both CMC columns. We further validate the pharmacological activity of 5-O-methylvisammioside, 3'-O-angeloylhamaudol, imperatorin, phellopterin and anomalin. They could efficiently target both inflammatory macrophages and fibroblast synovial cells, reduce the release of inflammatory factors, inhibit abnormal cell proliferation, and promote cell apoptosis. 5-O-methylvisammioside, which exhibited the best pharmacological ability on both target cells, inhibited the NF-κB pathway. Our results showed that the dual channel MPTS modified 2D CMC system is a practical method for rapid screening the active components in TCM binding on multiple target cells' membrane protein of a disease. 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引用次数: 0
摘要
菝葜(SD)是一种常用的治疗类风湿性关节炎的中药。然而,其抗ra的活性成分和作用机制尚不清楚。靶向类风湿性关节炎-成纤维细胞滑膜(RA- fls)和滑膜巨噬细胞是治疗RA的有前途的策略,其膜受体是抗RA活性物质的重要靶点。建立了一种双通道3-巯基丙基三甲氧基硅烷(MPTS)修饰的二维细胞膜色谱(CMC)体系,以表征SD双细胞膜结合活性成分。筛选出RAW-CMC柱上残留的9个组分和FLS-CMC柱上残留的8个组分。其中8个组分在两个CMC柱上均保持良好。我们进一步验证了5- o -甲基维沙米苷、3'-O-angeloylhamaudol、欧前胡素、黄檗碱和反常素的药理活性。它们能有效靶向炎性巨噬细胞和成纤维滑膜细胞,减少炎性因子的释放,抑制细胞异常增殖,促进细胞凋亡。5- o -甲基维沙米苷对两种靶细胞均表现出最佳的药理作用,抑制NF-κB通路。结果表明,双通道MPTS修饰的二维CMC系统是一种快速筛选中药与疾病多靶细胞膜蛋白结合活性成分的实用方法。该方法适用于阐明多组分、多靶点中药的作用机理和先导化合物的快速筛选。
Application of a dual channel MPTS-modified two-dimensional cell membrane chromatography system for rapid screening of effective ingredients in Saposhnikovia divaricata targeting inflammatory macrophages and fibroblast synovial cells in the treatment of rheumatoid arthritis.
Saposhnikovia divaricata (SD) is a traditional Chinese medicine (TCM) which has been commonly used for the treatment of rheumatoid arthritis (RA). However, its active components and mechanism of anti-RA are still unclear. Targeting rheumatoid arthritis-fibroblastoid synovial (RA-FLS) and synovial macrophages are promising strategies for RA treatment, and their membrane receptors are important targets for anti-RA active substances. A dual channel 3-mercaptopropyltrimethoxysilane (MPTS) modified 2D cell membrane chromatography (CMC) system was established to characterize dual-cell membrane binding active components in SD. Nine components retained on RAW-CMC column and 8 components retained on FLS-CMC column were screened out. Among them, 8 components retained well on both CMC columns. We further validate the pharmacological activity of 5-O-methylvisammioside, 3'-O-angeloylhamaudol, imperatorin, phellopterin and anomalin. They could efficiently target both inflammatory macrophages and fibroblast synovial cells, reduce the release of inflammatory factors, inhibit abnormal cell proliferation, and promote cell apoptosis. 5-O-methylvisammioside, which exhibited the best pharmacological ability on both target cells, inhibited the NF-κB pathway. Our results showed that the dual channel MPTS modified 2D CMC system is a practical method for rapid screening the active components in TCM binding on multiple target cells' membrane protein of a disease. The method is very suitable for elucidating the mechanism of TCM with multiple-components and targets, and rapid screening of lead compounds.
期刊介绍:
This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome.
Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.