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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.

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/fca0/11994106/16c268c746f8/DMSO-18-1073-g0001.jpg

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