千石合剂调节脂质代谢重编程及抑制氧化应激损伤治疗糖尿病肾病

IF 4.2
Jian Liu, Boning Liu, Enzhi Fan, Han Zhang, Zhonglai Yin, Shuquan Lv, Weibo Wen, Feitian Min, Zhongyong Zhang, Huantian Cui
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引用次数: 0

摘要

糖尿病肾病(DN)是糖尿病的主要并发症,可发展为终末期肾脏疾病,构成重大的健康风险。千石合剂(QSM)显示出治疗DN的潜力;然而,其药理机制尚不清楚。我们在小鼠中建立了DN模型,并给予QSM作为干预。为了评价中药的疗效,我们测量了肾功能相关生化指标,并检查了肾脏病理变化。然后,我们应用转录组学和非靶向代谢组学来探索QSM对DN小鼠肾组织中基因表达和代谢产物的影响。基于我们的多组学分析,western blot证实了QSM对肾组织脂质代谢相关蛋白表达的影响。此外,我们通过测量氧化应激指标来评估QSM的抗氧化和抗凋亡特性。QSM干预可改善DN小鼠的高血糖和蛋白尿。它还减少了肾功能障碍的关键标志物,同时减轻了肾组织的病理变化。通过转录组学和代谢组学分析,我们发现QSM影响了参与脂质代谢途径的基因和代谢物。值得注意的是,差异表达的基因包括Ces2h、Ces1f和Alox5,而代谢物如EPA、9-Oxo-ODE和LPC(20:3)发生了改变。进一步的验证表明,QSM增加了CES2H和CES1F的蛋白水平,同时降低了FABP1、CD36、ALOX15和ALOX5的表达。此外,QSM降低了氧化应激标志物。QSM对肾组织氧化应激和细胞凋亡均有抑制作用。QSM可能通过调节脂质代谢和减轻氧化应激损伤来保护DN患者的肾组织。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Qianshi Mixture Treats Diabetic Nephropathy by Regulating Lipid Metabolism Reprogramming and Inhibiting Oxidative Stress Damage

Qianshi Mixture Treats Diabetic Nephropathy by Regulating Lipid Metabolism Reprogramming and Inhibiting Oxidative Stress Damage

Diabetic nephropathy (DN) is a major complication of diabetes that can advance to end-stage renal disease, posing a substantial health risk. The Qianshi Mixture (QSM) has shown therapeutic potential for DN; however, its pharmacological mechanisms remain insufficiently understood. We developed a DN model in mice and administered QSM as an intervention. To assess QSM's therapeutic effects, we measured the renal-function-related biochemical indicators and examined kidney pathological changes. We then applied transcriptomics and non-targeted metabolomics to explore QSM's impact on gene expression and metabolic products within DN mice renal tissues. Based on our multi-omics analysis, the effect of QSM on lipid-metabolism-related protein expression was confirmed by western blot in kidney tissue. Additionally, we evaluated the antioxidant and anti-apoptotic properties of QSM by measuring oxidative stress indicators. QSM intervention improved hyperglycemia and proteinuria in DN mice. It also reduced key markers of renal dysfunction whilst alleviating pathological changes in kidney tissue. Through transcriptomic and metabolomic analyses, we identified that QSM affected genes and metabolites involved in lipid metabolism pathways. Notably, differentially expressed genes included Ces2h, Ces1f and Alox5, whilst metabolites such as EPA, 9-Oxo-ODE and LPC (20:3) were altered. Further validation revealed that QSM increased the protein levels of CES2H and CES1F whilst decreasing the expression of FABP1, CD36, ALOX15 and ALOX5. Additionally, QSM reduced oxidative stress markers. QSM inhibited both oxidative stress and apoptosis in kidney tissues. QSM protects renal tissues in DN, likely through the regulation of lipid metabolism and the mitigation of oxidative stress damage.

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CiteScore
11.50
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0.00%
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期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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