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糖尿病肾病:由正反馈回路驱动的疾病进展及针对致病途径的治疗策略

Diabetic Kidney Disease: Disease Progression Driven by Positive Feedback Loops and Therapeutic Strategies Targeting Pathogenic Pathways.

作者信息

Mo Gaozhi P, Zhu Yao, You Yue, Chen Hui, Zhang Jiahao, Ku Bunhav, Yu Haichuan, Peng Zhiyong

机构信息

Department of Critical Care Medicine, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, People's Republic of China.

Hubei Clinical Research Center for Critical Care Medicine, Wuhan, Hubei, People's Republic of China.

出版信息

Diabetes Metab Syndr Obes. 2025 Apr 9;18:1073-1085. doi: 10.2147/DMSO.S513080. eCollection 2025.

DOI:10.2147/DMSO.S513080
PMID:40226441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11994106/
Abstract

Diabetic kidney disease (DKD) is a major complication of diabetes mellitus, with its pathogenesis intricately regulated by dynamic feedback mechanisms. This comprehensive review systematically analyzes the hierarchical feedback networks driving DKD progression, spanning from systemic interactions to molecular cross-talks. We reveal that self-amplifying positive feedback loops dominate the disease process, manifested through three key dimensions: (1) The systemic triad of hyperglycemia-hypertension-proteinuria establishes a vicious cycle accelerating renal dysfunction; (2) Cellular homeostasis collapse through cross-amplified cell death modalities (apoptosis, pyroptosis, ferroptosis) and cell cycle dysregulation; (3) Molecular cascades centered on AGE/RAGE signaling that fuel chronic inflammation and fibrotic transformation. Collectively, these form a major positive feedback loop where PKC activation, oxidative stress propagation, and TGF-β-mediated fibrosis induced by hyperglycemia lead to progressive renal deterioration and fibrosis. Therapeutically, we propose a dual intervention strategy targeting both the acute phase through AGE/RAGE axis inhibition, coupled with chronic phase via precision modulation of fibrotic pathways. These findings redefine DKD progression as a self-reinforcing network disorder, providing a roadmap for developing multi-target therapies that disrupt pathological feedback loops while preserving renal repair mechanisms.

摘要

糖尿病肾病(DKD)是糖尿病的一种主要并发症,其发病机制由动态反馈机制复杂调控。这篇综述系统地分析了驱动DKD进展的分级反馈网络,涵盖从全身相互作用到分子间相互作用。我们发现自我放大的正反馈回路主导疾病过程,体现在三个关键维度:(1)高血糖 - 高血压 - 蛋白尿的全身三联征建立了加速肾功能障碍的恶性循环;(2)细胞内稳态通过交叉放大的细胞死亡方式(细胞凋亡、焦亡、铁死亡)和细胞周期失调而崩溃;(3)以AGE/RAGE信号为中心的分子级联反应引发慢性炎症和纤维化转变。总体而言,这些形成了一个主要的正反馈回路,其中高血糖诱导的PKC激活、氧化应激传播和TGF-β介导的纤维化导致进行性肾脏恶化和纤维化。在治疗方面,我们提出一种双重干预策略,即急性期通过抑制AGE/RAGE轴,慢性期通过精确调节纤维化途径。这些发现将DKD进展重新定义为一种自我强化的网络紊乱,为开发多靶点疗法提供了路线图,这种疗法在保留肾脏修复机制的同时破坏病理反馈回路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca0/11994106/e619fd757ab5/DMSO-18-1073-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca0/11994106/16c268c746f8/DMSO-18-1073-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca0/11994106/9ceea152a456/DMSO-18-1073-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca0/11994106/e619fd757ab5/DMSO-18-1073-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca0/11994106/16c268c746f8/DMSO-18-1073-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca0/11994106/9ceea152a456/DMSO-18-1073-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca0/11994106/e619fd757ab5/DMSO-18-1073-g0004.jpg

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本文引用的文献

1
Research Progress of Pyroptosis in Diabetic Kidney Disease.糖尿病肾病中细胞焦亡的研究进展。
Int J Mol Sci. 2024 Jun 28;25(13):7130. doi: 10.3390/ijms25137130.
2
Oxidative Stress: A Culprit in the Progression of Diabetic Kidney Disease.氧化应激:糖尿病肾病进展的罪魁祸首。
Antioxidants (Basel). 2024 Apr 12;13(4):455. doi: 10.3390/antiox13040455.
3
Simvastatin mitigates diabetic nephropathy by upregulating farnesoid X receptor and Nrf2/HO-1 signaling and attenuating oxidative stress and inflammation in rats.辛伐他汀通过上调法尼酯X受体和Nrf2/HO-1信号通路、减轻大鼠氧化应激和炎症来减轻糖尿病肾病。
Life Sci. 2024 Mar 1;340:122445. doi: 10.1016/j.lfs.2024.122445. Epub 2024 Jan 24.
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The Role of Autophagy in Type 2 Diabetic Kidney Disease Management.自噬在 2 型糖尿病肾病管理中的作用。
Cells. 2023 Nov 23;12(23):2691. doi: 10.3390/cells12232691.
5
Non-steroidal mineralocorticoid receptor antagonist finerenone ameliorates mitochondrial dysfunction via PI3K/Akt/eNOS signaling pathway in diabetic tubulopathy.非甾体类盐皮质激素受体拮抗剂非奈利酮通过 PI3K/Akt/eNOS 信号通路改善糖尿病肾小管病变中的线粒体功能障碍。
Redox Biol. 2023 Dec;68:102946. doi: 10.1016/j.redox.2023.102946. Epub 2023 Oct 24.
6
Research progress on multiple cell death pathways of podocytes in diabetic kidney disease.糖尿病肾病中足细胞多种细胞死亡通路的研究进展。
Mol Med. 2023 Oct 12;29(1):135. doi: 10.1186/s10020-023-00732-4.
7
The role of the mesangium in glomerular function.系膜在肾小球功能中的作用。
Acta Physiol (Oxf). 2023 Oct;239(2):e14045. doi: 10.1111/apha.14045. Epub 2023 Sep 1.
8
JAK/STAT signaling in diabetic kidney disease.糖尿病肾病中的JAK/STAT信号通路
Front Cell Dev Biol. 2023 Aug 11;11:1233259. doi: 10.3389/fcell.2023.1233259. eCollection 2023.
9
Tubular injury in diabetic kidney disease: molecular mechanisms and potential therapeutic perspectives.糖尿病肾病中的管状损伤:分子机制和潜在的治疗前景。
Front Endocrinol (Lausanne). 2023 Aug 2;14:1238927. doi: 10.3389/fendo.2023.1238927. eCollection 2023.
10
Protein kinase C: A potential therapeutic target for endothelial dysfunction in diabetes.蛋白激酶 C:糖尿病内皮功能障碍的潜在治疗靶点。
J Diabetes Complications. 2023 Sep;37(9):108565. doi: 10.1016/j.jdiacomp.2023.108565. Epub 2023 Jul 28.