首页|基于铁死亡的糖尿病肾病发病机制及中药干预的研究进展

基于铁死亡的糖尿病肾病发病机制及中药干预的研究进展

Research Progress on Pathogenesis of Diabetic Kidney Disease Based on Ferroptosis and Intervention of Traditional Chinese Medicine

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糖尿病肾病(diabetic kidney disease,DKD)是全球终末期肾病的主要原因,是糖尿病的主要微血管并发症之一.DKD的发病机制是多因素的,其病理过程涉及多种途径.铁死亡是一种以铁依赖性脂质过氧化为特征的调节性细胞死亡.近几年,越来越多的研究表明铁死亡是DKD发生发展的关键驱动因素,在各种肾脏疾病的发生、发展和治疗中起着至关重要的作用.中药以其多成分、多靶点、多途径的作用特点,在防治和延缓DKD进程方面具有独特优势.该文重点总结铁死亡关键调节因子和信号途径对DKD病理过程的影响,以及中药调控铁死亡关键因子与通路防治DKD的研究进展,以期为DKD的临床治疗和中药新药的研发提供新思路.
Diabetic kidney disease(DKD)is the leading cause of end-stage renal disease worldwide and one of the major microvascular complications of diabetes.The pathogenesis of DKD is multifactorial,and its pathological process involves multiple pathways.Ferroptosis is a regulatory cell death characterized by iron dependent lipid peroxidation.Recently,an increasing number of studies have shown that ferroptosis is a key driving factor for the occurrence and development of DKD and has been identified to play a crucial role in the occurrence,development,and treatment of various kidney diseases.Traditional Chinese medicine has unique advantages in preventing and delaying the progression of DKD due to the characteristics of multi-component,multi-target,and multi-pathway.This article focuses on summarizing the impact of key regulatory factors and signaling pathways of ferroptosis on the pathological process of DKD,as well as the research progress of traditional Chinese medicine in regulating ferroptosis key factors and pathways for preventing and treating DKD.The aim of this study is to provide new ideas for the clinical treatment of DKD and the development of new traditional Chinese medicine drugs.

Ferroptosisdiabetic kidney diseasemechanismtraditional Chinese medicine formulaactive ingredients

樊俐慧、王志刚、杨霞、张坤、梅小龙

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甘肃中医药大学中医临床学院,甘肃 兰州 730000

天水市中医医院,甘肃 天水 741000

铁死亡 糖尿病肾病 作用机制 中药复方 活性成分

甘肃省中医药科研课题天水市科技支撑计划甘肃省产业支撑计划甘肃省中医药综合防治重大疑难疾病科技攻关计划

GZKP-2021-462020-SHFZKJK-42072021CYZC-03GZKZD-2018-01

2024

中药新药与临床药理
广州中医药大学

中药新药与临床药理

CSTPCD北大核心
影响因子:0.908
ISSN:1003-9783
年,卷(期):2024.35(6)
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