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Nrf2 与铁死亡:缺血性脑卒中的新研究方向。

Nrf2 and Ferroptosis: A New Research Direction for Ischemic Stroke.

机构信息

Department of Acupuncture and Rehabilitation, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210029, Jiangsu Province, China.

Henan University of Chinese Medicine, Zhengzhou, 450000, Henan Province, China.

出版信息

Cell Mol Neurobiol. 2023 Nov;43(8):3885-3896. doi: 10.1007/s10571-023-01411-y. Epub 2023 Sep 20.

Abstract

Ischemic stroke (IS) is one of the leading causes of death and morbidity worldwide. As a novel form of cell death, ferroptosis is an important mechanism of ischemic stroke. Nuclear factor E2-related factor 2 (Nrf2) is the primary regulator of cellular antioxidant response. In addition to alleviating ischemic stroke nerve damage by reducing oxidative stress, Nrf2 regulates genes associated with ferroptosis, suggesting that Nrf2 may inhibit ferroptosis after ischemic stroke. However, the specific pathway of Nrf2 on ferroptosis in the field of ischemic stroke remains unclear. Therefore, this paper provides a concise overview of the mechanisms underlying ferroptosis, with a particular focus on the regulatory role of Nrf2. The discussion highlights the potential connections between Nrf2 and the mitigation of oxidative stress, regulation of iron metabolism, modulation of the interplay between ferroptosis and inflammation, as well as apoptosis. This paper focuses on the specific pathway of Nrf2 regulation of ferroptosis after ischemic stroke, providing scientific research ideas for further research on the treatment of ischemic stroke.

摘要

缺血性脑卒中(IS)是全球范围内主要的死亡和发病原因之一。作为一种新型的细胞死亡形式,铁死亡是缺血性脑卒中的重要机制。核因子 E2 相关因子 2(Nrf2)是细胞抗氧化反应的主要调节因子。Nrf2 通过降低氧化应激来减轻缺血性脑卒中神经损伤,同时调节与铁死亡相关的基因,这表明 Nrf2 可能在缺血性脑卒中后抑制铁死亡。然而,Nrf2 在缺血性脑卒中领域对铁死亡的具体途径仍不清楚。因此,本文简要概述了铁死亡的发生机制,并特别关注了 Nrf2 的调节作用。讨论强调了 Nrf2 与氧化应激缓解、铁代谢调节、铁死亡与炎症相互作用的调节以及细胞凋亡之间的潜在联系。本文重点关注缺血性脑卒中后 Nrf2 调节铁死亡的具体途径,为缺血性脑卒中治疗的进一步研究提供了科学研究思路。

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