基于1H-NMR的代谢组学分析中药促进间充质干细胞归巢对威尔逊氏病小鼠模型肝纤维化的干预作用

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Ying Ma, Yuancheng Bao, Han Wang, Huaizhou Jiang, Lei Zhou, Bo Yang, Xiaofeng Huang, Wenming Yang, Daojun Xie, Juan Zhang
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引用次数: 0

摘要

研究背景我们将藿香正气水(BSHXHZF)和骨髓间充质干细胞(BMSCs)移植到Wilson病(WD)相关肝纤维化小鼠体内,以评估该方剂的保肝机制:方法:将小鼠随机分为不同的治疗组,观察其组织病理学变化和肝细胞凋亡程度。测定肝脏羟脯氨酸(Hyp)、转化生长因子-β1(TGF-β1)和骨形态发生蛋白-7(BMP-7)的 mRNA 和蛋白。利用液相色谱-质谱联用技术(LC-MS/MS)对BSHXHZF提取物进行化学分析,并利用代谢组学揭示其抗纤维化机制:结果:中药+BMSC组肝脏表现出较少的炎症细胞。结果:中药+BMSC组肝脏中炎症细胞较少,TUNEL显示模型对照组有大量棕色凋亡细胞,而中药+BMSC组肝细胞蓝阴性表达显著增加。毒奶(TX)小鼠组的 Hyp 明显低于模型对照组(MG)。与 MG 组相比,TGF-β1 的表达明显低于其他各组,而 BMP-7 的表达则明显高于其他各组。代谢分析发现了20个潜在的生物标志物和10个关键通路,表明BSHXHZF+BMSC干预对这些小分子物质的代谢紊乱有明显的调节作用:结论:BSHXHZF联合BMSCs可通过改善相关代谢紊乱抑制肝纤维化和肝细胞凋亡,对WD相关肝纤维化有治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
1H-NMR-based metabolomics to dissect the traditional Chinese medicine promotes mesenchymal stem cell homing as intervention in liver fibrosis in mouse model of Wilson's disease.

Background: We administered Bushen Huoxue Huazhuo Formula (BSHXHZF) and transplanted bone marrow mesenchymal stem cells (BMSCs) into mice with Wilson's disease (WD)-related liver fibrosis to evaluate the liver-protecting mechanism of this prescription.

Methods: Mice, randomly divided into different treatment groups, showed histopathological changes and degree of hepatocyte apoptosis. For hepatic hydroxyproline (Hyp) determination, transforming growth factor-β1 (TGF-β1) and bone morphogenetic protein-7 (BMP-7) mRNA and protein were measured. Chemical profiling of the extract of BSHXHZF using The liquid chromatography-mass spectrometry (LC-MS/MS) and revealing its antifibrosis mechanism using metabolomics.

Results: TCM+BMSC group livers exhibited few inflammatory cells. TUNEL revealed abundant brown apoptotic cells in model control groups, while the TCM+BMSC groups showed a significant increase in blue negative expression of liver cells. Hyp in toxic milk (TX) mice groups was significantly lower than that in model control groups (MG). Compared with MG, TGF-β1 expression was significantly lower than all other groups, while BMP-7 expression was significantly higher. Metabolic analysis identified 20 potential biomarkers and 10 key pathways, indicating that BSHXHZF+BMSC intervention has a significant regulatory effect on metabolic disorders of these small molecule substances.

Conclusion: BSHXHZF combined with BMSCs can inhibit liver fibrosis and hepatocyte apoptosis by improving related metabolic disorders, and achieving therapeutic effects in WD-related liver fibrosis.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
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