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脊髓损伤中Nrf2驱动的发病机制及治疗靶点的机制性见解。

Mechanistic insights into Nrf2-driven pathogenesis and therapeutic targeting in spinal cord injury.

作者信息

Xie Tao, Xu Jiyu, Liu Xinyu, Yu Yaquan, Lu Yang, Wang Tao, Gao Feng, Yuan Hui

机构信息

School of Basic Medical Sciences, Mudanjiang Medical University, Mudanjiang, China.

School of Clinical Medicine, Jiamusi University, Jiamusi, China.

出版信息

Front Immunol. 2025 Jul 10;16:1574834. doi: 10.3389/fimmu.2025.1574834. eCollection 2025.

DOI:10.3389/fimmu.2025.1574834
PMID:40709178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12287063/
Abstract

Spinal cord injury (SCI) is a traumatic disease of the central nervous system that can result in significant tissue damage and neurological dysfunction. The pathophysiological process of SCI encompasses both primary and secondary injuries, involving various pathological mechanisms such as oxidative stress, inflammation, autophagy, ferroptosis, and mitochondrial dysfunction. Nuclear factor erythroid 2-related factor 2 (Nrf2) is a neuroprotective transcription factor intricately linked to these pathological processes. Upon exposure to external stimuli, Nrf2 undergoes increased nuclear transcription, regulating the expression of various antioxidant genes and directly modulating genes associated with the aforementioned pathological mechanisms to counteract the resultant alterations. Substantial evidence suggests that Nrf2 may be a potential therapeutic target for SCI. Activation of the Nrf2-related signaling pathway effectively inhibits neuronal death following SCI and promotes the recovery of multiple neurological functions. This review provides an overview of recent research on SCI, examines the physiological roles and mechanisms of Nrf2 in SCI, and explores therapeutic strategies targeting this signaling pathway, including non-coding RNAs, natural and synthetic compounds, and other treatments for SCI.

摘要

脊髓损伤(SCI)是一种中枢神经系统创伤性疾病,可导致显著的组织损伤和神经功能障碍。SCI的病理生理过程包括原发性和继发性损伤,涉及多种病理机制,如氧化应激、炎症、自噬、铁死亡和线粒体功能障碍。核因子红细胞2相关因子2(Nrf2)是一种与这些病理过程密切相关的神经保护转录因子。在受到外部刺激时,Nrf2的核转录增加,调节各种抗氧化基因的表达,并直接调节与上述病理机制相关的基因,以对抗由此产生的改变。大量证据表明,Nrf2可能是SCI的一个潜在治疗靶点。Nrf2相关信号通路的激活可有效抑制SCI后的神经元死亡,并促进多种神经功能的恢复。本综述概述了SCI近期的研究,探讨了Nrf2在SCI中的生理作用和机制,并探索了针对该信号通路的治疗策略,包括非编码RNA、天然和合成化合物以及其他SCI治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ee/12287063/37fcca4265c6/fimmu-16-1574834-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ee/12287063/0a3b3a203497/fimmu-16-1574834-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ee/12287063/e07a316c06d6/fimmu-16-1574834-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ee/12287063/37fcca4265c6/fimmu-16-1574834-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ee/12287063/0a3b3a203497/fimmu-16-1574834-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ee/12287063/e07a316c06d6/fimmu-16-1574834-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ee/12287063/37fcca4265c6/fimmu-16-1574834-g003.jpg

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本文引用的文献

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Stem Cell Res Ther. 2025 Apr 17;16(1):182. doi: 10.1186/s13287-025-04296-4.
2
Neurons Are Not All the Same: Diversity in Neuronal Populations and Their Intrinsic Responses to Spinal Cord Injury.神经元并非千篇一律:神经元群体的多样性及其对脊髓损伤的内在反应
ASN Neuro. 2025;17(1):2440299. doi: 10.1080/17590914.2024.2440299. Epub 2025 Jan 16.
3
The NFATC2/Nrf2 cascade regulates spinal cord ischemia-reperfusion injury by controlling inflammation, apoptosis and oxidative stress.
NFATC2/Nrf2 级联反应通过控制炎症、细胞凋亡和氧化应激来调节脊髓缺血再灌注损伤。
Regen Ther. 2024 Dec 7;28:126-133. doi: 10.1016/j.reth.2024.11.014. eCollection 2025 Mar.
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Unveiling vital biomarkers and immune infiltration profiles in endoplasmic reticulum stress following spinal cord injury.揭示脊髓损伤后内质网应激中的关键生物标志物和免疫浸润特征。
Sci Rep. 2024 Dec 2;14(1):29981. doi: 10.1038/s41598-024-81844-7.
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Representation of non-coding RNA-mediated regulation of gene expression using the Gene Ontology.使用基因本体论表示非编码 RNA 介导的基因表达调控。
RNA Biol. 2024 Jan;21(1):36-48. doi: 10.1080/15476286.2024.2408523. Epub 2024 Oct 7.
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Bibliometric analysis of the inflammation expression after spinal cord injury: current research status and emerging frontiers.脊髓损伤后炎症表达的文献计量分析:当前研究现状与新兴前沿
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