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甘迪胶囊通过SIRT1/AMPK/HNF4A通路改善糖尿病肾病小鼠的足细胞脂质代谢

Gandi Capsule Improved Podocyte Lipid Metabolism of Diabetic Nephropathy Mice through SIRT1/AMPK/HNF4A Pathway.

作者信息

Zhang Ying, Yao Huijuan, Li Chao, Sun Wei, Chen Xiaofei, Cao Yan, Liu Yue, Liu Yan, Chen Jihui, Qi Jia, Zhang Qiqiang, Zhang Hai, Xu Ajing, Zhang Jian

机构信息

Department of Clinical Pharmacy, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.

Innovation Research Institute of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

出版信息

Oxid Med Cell Longev. 2022 Apr 18;2022:6275505. doi: 10.1155/2022/6275505. eCollection 2022.

Abstract

Podocyte lipid accumulation is a potential therapeutic target for diabetic nephropathy (DN). This study was aimed at clarifying the mechanism of Gandi capsule (GDC) ameliorating DN by regulating the lipid metabolism of podocytes. Network pharmacology methods were performed to screen the key molecules and potential targets of GDC for constructing the molecular-protein interaction network of GDC and conducting signal pathway enrichment analysis. GDC was predicted to ameliorate DN through SIRT1/AMPK/HNF4A pathway. Our results showed that GDC improved renal function in db/db mice. Besides, GDC exhibited effectiveness in relieving kidney tissue damage and renal lipid accumulation in db/db mice, and same effects were present in GDC-active ingredient baicalin. We further proved the new role of HNF4A in the lipid metabolism of DN mediated by SIRT1 and AMPK signaling pathways. The results suggested decreased expression of SIRT1 and p-AMPK in the kidney tissue and increased expression of HNF4A of db/db mice compared with the control group. GDC and baicalin could reverse these expression changes. Furthermore, similar expression changes were observed in the murine podocyte cell line (MPC-5) treated with different concentrations of GDC and baicalin. Our research suggested that GDC and its active ingredient baicalin could alleviate the abnormal lipid metabolism in the kidney of db/db mice and might exert renal protection through the SIRT1/AMPK/HNF4A pathway.

摘要

足细胞脂质蓄积是糖尿病肾病(DN)的一个潜在治疗靶点。本研究旨在阐明甘迪胶囊(GDC)通过调节足细胞脂质代谢改善DN的机制。运用网络药理学方法筛选GDC的关键分子和潜在靶点,构建GDC的分子-蛋白质相互作用网络并进行信号通路富集分析。预测GDC通过SIRT1/AMPK/HNF4A通路改善DN。我们的结果表明,GDC改善了db/db小鼠的肾功能。此外,GDC在减轻db/db小鼠肾组织损伤和肾脂质蓄积方面显示出有效性,GDC的活性成分黄芩苷也有同样的效果。我们进一步证实了HNF4A在由SIRT1和AMPK信号通路介导的DN脂质代谢中的新作用。结果显示,与对照组相比,db/db小鼠肾组织中SIRT1和p-AMPK的表达降低,HNF4A的表达增加。GDC和黄芩苷可以逆转这些表达变化。此外,在用不同浓度的GDC和黄芩苷处理的小鼠足细胞系(MPC-5)中也观察到了类似的表达变化。我们的研究表明,GDC及其活性成分黄芩苷可以减轻db/db小鼠肾脏中异常的脂质代谢,并可能通过SIRT1/AMPK/HNF4A通路发挥肾脏保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9622/9038418/7885a54b9eec/OMCL2022-6275505.001.jpg

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