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靶向AMPK/Nrf2信号通路:急性肺损伤的一种新型治疗方法。

Targeting the AMPK/Nrf2 Pathway: A Novel Therapeutic Approach for Acute Lung Injury.

作者信息

Huang Qianxia, Ren Yingcong, Yuan Ping, Huang Ma, Liu Guoyue, Shi Yuanzhi, Jia Guiyang, Chen Miao

机构信息

Department of Critical Care Medicine, Affiliated Hospital of Zunyi Medical University, Zunyi City, Gui Zhou, People's Republic of China.

出版信息

J Inflamm Res. 2024 Jul 15;17:4683-4700. doi: 10.2147/JIR.S467882. eCollection 2024.

Abstract

ALI(acute lung injury) is a severe respiratory dysfunction caused by various intrapulmonary and extrapulmonary factors. It is primarily characterized by oxidative stress and affects the integrity of the pulmonary barrier. In severe cases, ALI can progress to ARDS(acute respiratory distress syndrome), a condition that poses a serious threat to the lives of affected patients. To date, the etiological mechanisms underlying ALI remain elusive, and available therapeutic options are quite limited. AMPK(AMP-activated protein kinase), an essential serine/threonine protein kinase, performs a pivotal function in the regulation of cellular energy levels and cellular regulatory mechanisms, including the detection of redox signals and mitigating oxidative stress. Meanwhile, Nrf2(nuclear factor erythroid 2-related factor 2), a critical transcription factor, alleviates inflammation and oxidative responses by interacting with multiple signaling pathways and contributing to the modulation of oxidative enzymes associated with inflammation and programmed cell death. Indeed, AMPK induces the dissociation of Nrf2 from Keap1(kelch-like ECH-associated protein-1) and facilitates its translocation into the nucleus to trigger the transcription of downstream antioxidant genes, ultimately suppressing the expression of inflammatory cells in the lungs. Given their roles, AMPK and Nrf2 hold promise as novel treatment targets for ALI. This study aimed to summarise the current status of research on the AMPK/Nrf2 signaling pathway in ALI, encompassing recently reported natural compounds and drugs that can activate the AMPK/Nrf2 signaling pathway to alleviate lung injury, and provide a theoretical reference for early intervention in lung injury and future research on lung protection.

摘要

急性肺损伤(ALI)是由多种肺内和肺外因素引起的严重呼吸功能障碍。其主要特征为氧化应激,并影响肺屏障的完整性。在严重情况下,ALI可进展为急性呼吸窘迫综合征(ARDS),这一病症对受影响患者的生命构成严重威胁。迄今为止,ALI的病因机制仍不清楚,可用的治疗选择也非常有限。AMP激活的蛋白激酶(AMPK)是一种重要的丝氨酸/苏氨酸蛋白激酶,在调节细胞能量水平和细胞调节机制中发挥关键作用,包括检测氧化还原信号和减轻氧化应激。同时,核因子红细胞2相关因子2(Nrf2)是一种关键的转录因子,它通过与多种信号通路相互作用,并参与调节与炎症和程序性细胞死亡相关的氧化酶,从而减轻炎症和氧化反应。事实上,AMPK诱导Nrf2与kelch样ECH相关蛋白1(Keap1)解离,并促进其易位至细胞核以触发下游抗氧化基因的转录,最终抑制肺内炎症细胞的表达。鉴于它们的作用,AMPK和Nrf2有望成为ALI的新型治疗靶点。本研究旨在总结ALI中AMPK/Nrf2信号通路的研究现状,包括最近报道的可激活AMPK/Nrf2信号通路以减轻肺损伤的天然化合物和药物,并为肺损伤的早期干预和未来的肺保护研究提供理论参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5a/11268519/0f6baaed9a20/JIR-17-4683-g0001.jpg

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