中药调控铁死亡干预糖尿病肾病的研究进展
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1.甘肃中医药大学;2.天水市中医院;3.甘肃省肿瘤医院

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]甘肃省级中医药管理局项目(GZKZ-2024-39);甘肃中医药大学校院协同创新重点项目(HXLH-XTCX15);甘肃省级科技计划项(22JR5RA611)


Advancements in research on the modulation of ferroptosis by traditional chinese medicine for treating diabetic nephropathy
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1.甘肃中医药大学;2.Gansu University of Chinese Medicine;3.17789395527;4.18794755660;5.Tianshui City Hospital of Traditional Chinese Medicine;6.Gansu Cancer Hospita Lanzhou

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    摘要:

    糖尿病肾病(DKD)是糖尿病严重的微血管并发症,它已成为糖尿病和终末期肾病患者死亡的主要原因。铁死亡是一种以铁依赖性脂质过氧化物过度累积为特征的新型细胞程序性死亡方式,在DKD的发生与发展中扮演关键驱动角色。近年来的多种研究表明,DKD在发生与发展过程中通过诱发铁代谢紊乱、抑制System Xc?/GPX4/GSH抗氧化通路、导致脂质过氧化爆发等机制,促进肾脏固有细胞(包括肾小管上皮细胞、足细胞及系膜细胞)的铁死亡,进而导致了肾损伤进程加快。而中医药在防治DKD方面具有多成分、多靶点的整体调节优势。本文系统综述了中药复方(如参芪地黄汤、芪蒡糖肾方等)及活性成分(如黄芪甲苷、马齿苋多糖、红景天苷等)通过调控铁死亡相关通路(如Fe2+Nrf2/GPX4等),抑制脂质过氧化、调节铁稳态、缓解氧化应激与炎症反应,从而延缓DKD进展的作用机制。现有研究突显了中医药靶向铁死亡在DKD治疗中的巨大潜力,为开发新的肾脏保护策略提供了重要理论依据与研究方向。

    Abstract:

    Diabetic kidney disease (DKD) is a major microvascular complication of diabetes and has become the leading cause of mortality among individuals with diabetes and end-stage renal disease. Ferroptosis is a novel form of programmed cell death characterized by the excessive accumulation of iron-dependent lipid peroxides, playing a key driving role in the occurrence and progression of DKD. Recent studies have shown that during the onset and progression of DKD, mechanisms such as inducing iron metabolism disorder, inhibiting the System Xc?/GPX4/GSH antioxidant pathway, and triggering lipid peroxidation bursts promote ferroptosis in intrinsic kidney cells (including renal tubular epithelial cells, podocytes, and mesangial cells), thereby accelerating the process of kidney injury. Traditional Chinese medicine (TCM) has the advantage of multi-component and multi-target holistic regulation in the prevention and treatment of DKD. This article systematically reviews how TCM formulas (such as Shenqi Dihuang Decoction, Qibang Tangshen Decoction, etc.) and active ingredients (such as astragaloside IV, Portulaca polysaccharides, salidroside, etc.) delay the progression of DKD by regulating ferroptosis-related pathways (such as Fe2+, Nrf2/GPX4), inhibiting lipid peroxidation, modulating iron homeostasis, and alleviating oxidative stress and inflammatory responses. Existing research highlights the great potential of traditional Chinese medicine targeting ferroptosis in the treatment of DKD, providing an important theoretical basis and research direction for developing new kidney protection strategies.

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  • 收稿日期:2025-10-21
  • 最后修改日期:2025-12-06
  • 录用日期:2026-03-09
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