Nuclear factor erythroid 2-related factor-mediated signaling alleviates ferroptosis during cerebral ischemia-reperfusion injury

IF 6.9 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Zheng Li, Jihong Xing
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引用次数: 0

Abstract

Cardiac arrest (CA) is a significant challenge for emergency physicians worldwide and leads to increased morbidity and mortality rates. The poor prognosis of CA primarily stems from the complexity and irreversibility of cerebral ischemia-reperfusion injury (CIRI). Ferroptosis, a form of programmed cell death characterized by iron overload and lipid peroxidation, plays a crucial role in the progression and treatment of CIRI. In this review, we highlight the mechanisms of ferroptosis within the context of CIRI, focusing on its role as a key contributor to neuronal damage and dysfunction post-CA. We explore the crucial involvement of the nuclear factor erythroid 2-related factor (Nrf2)-mediated signaling pathway in modulating ferroptosis-associated processes during CIRI. Through comprehensive analysis of the regulatory role of Nrf2 in the cellular responses to oxidative stress, we highlight its potential as a therapeutic target for mitigating ferroptotic cell death and improving the neurological prognosis of patients experiencing CA. Furthermore, we discuss interventions targeting the Kelch-like ECH-associated protein 1/Nrf2/antioxidant response element pathway, including the use of traditional Chinese medicine and Western medicine, which demonstrate potential for attenuating ferroptosis and preserving neuronal function in CIRI. Owing to the limitations in the safety, specificity, and effectiveness of Nrf2-targeted drugs, as well as the technical difficulties and ethical constraints in obtaining the results related to the brain pathological examination of patients, most of the studies focusing on Nrf2-related regulation of ferroptosis in CIRI are still in the basic research stage. Overall, this review aims to provide a comprehensive understanding of the mechanisms underlying ferroptosis in CIRI, offering insights into novel therapeutics aimed at enhancing the clinical outcomes of patients with CA.
核因子红细胞 2 相关因子介导的信号传导缓解了脑缺血再灌注损伤过程中的铁蛋白沉积症
心脏骤停(CA)是全世界急诊医生面临的重大挑战,会导致发病率和死亡率上升。心脏骤停的预后不良主要源于脑缺血再灌注损伤(CIRI)的复杂性和不可逆性。铁变态反应是一种以铁超载和脂质过氧化为特征的程序性细胞死亡,在 CIRI 的进展和治疗中起着至关重要的作用。在这篇综述中,我们将着重介绍 CIRI 背景下的铁蜕变机制,重点是铁蜕变作为导致脑梗死后神经元损伤和功能障碍的关键因素的作用。我们探讨了核因子红细胞 2 相关因子(Nrf2)介导的信号通路在调控 CIRI 期间铁蜕变相关过程中的关键作用。通过全面分析 Nrf2 在细胞对氧化应激反应中的调控作用,我们强调了 Nrf2 作为治疗靶点的潜力,可减轻铁沉着细胞死亡,改善 CA 患者的神经系统预后。此外,我们还讨论了针对 Kelch-like ECH-associated protein 1/Nrf2/antioxidant response element 通路的干预措施,包括使用传统中药和西药,这些措施在减轻铁凋亡和保护 CIRI 神经元功能方面具有潜力。由于 Nrf2 靶向药物在安全性、特异性和有效性方面的局限性,以及获得与患者脑部病理检查相关结果的技术难度和伦理限制,大多数关注 Nrf2 相关调控 CIRI 中铁细胞减少的研究仍处于基础研究阶段。总之,本综述旨在提供对 CIRI 中铁细胞减少机制的全面理解,为旨在提高 CA 患者临床疗效的新型疗法提供见解。
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来源期刊
CiteScore
11.90
自引率
2.70%
发文量
1621
审稿时长
48 days
期刊介绍: Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.
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