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线粒体自噬在脊髓缺血再灌注损伤中的作用

Role of mitophagy in spinal cord ischemia-reperfusion injury.

作者信息

Duan Yanni, Yang Fengguang, Zhang Yibao, Zhang Mingtao, Shi Yujun, Lang Yun, Sun Hongli, Wang Xin, Jin Hongyun, Kang Xuewen

机构信息

Department of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou, Gansu Province, China.

The Second Clinical Medical School, Lanzhou University, Lanzhou, Gansu Province, China.

出版信息

Neural Regen Res. 2026 Feb 1;21(2):598-611. doi: 10.4103/NRR.NRR-D-24-00668. Epub 2024 Dec 7.

Abstract

Spinal cord ischemia-reperfusion injury, a severe form of spinal cord damage, can lead to sensory and motor dysfunction. This injury often occurs after traumatic events, spinal cord surgeries, or thoracoabdominal aortic surgeries. The unpredictable nature of this condition, combined with limited treatment options, poses a significant burden on patients, their families, and society. Spinal cord ischemia-reperfusion injury leads to reduced neuronal regenerative capacity and complex pathological processes. In contrast, mitophagy is crucial for degrading damaged mitochondria, thereby supporting neuronal metabolism and energy supply. However, while moderate mitophagy can be beneficial in the context of spinal cord ischemia-reperfusion injury, excessive mitophagy may be detrimental. Therefore, this review aims to investigate the potential mechanisms and regulators of mitophagy involved in the pathological processes of spinal cord ischemia-reperfusion injury. The goal is to provide a comprehensive understanding of recent advancements in mitophagy related to spinal cord ischemia-reperfusion injury and clarify its potential clinical applications.

摘要

脊髓缺血再灌注损伤是脊髓损伤的一种严重形式,可导致感觉和运动功能障碍。这种损伤常发生在创伤事件、脊髓手术或胸腹主动脉手术后。这种情况的不可预测性,加上治疗选择有限,给患者及其家庭和社会带来了沉重负担。脊髓缺血再灌注损伤会导致神经元再生能力下降和复杂的病理过程。相比之下,线粒体自噬对于降解受损线粒体至关重要,从而支持神经元代谢和能量供应。然而,虽然适度的线粒体自噬在脊髓缺血再灌注损伤的情况下可能有益,但过度的线粒体自噬可能有害。因此,本综述旨在研究参与脊髓缺血再灌注损伤病理过程的线粒体自噬的潜在机制和调节因子。目的是全面了解与脊髓缺血再灌注损伤相关的线粒体自噬的最新进展,并阐明其潜在的临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25ef/12220710/bb8a39fe0557/NRR-21-598-g001.jpg

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