Suppr超能文献

亚低温通过Keap1/GSK3β/Nrf2/GPX4信号通路抑制过度炎症和氧化应激诱导的铁死亡,从而减轻脓毒症相关急性肺损伤。

Moderate Hypothermia Alleviates Sepsis-Associated Acute Lung Injury by Suppressing Ferroptosis Induced by Excessive Inflammation and Oxidative Stress via the Keap1/GSK3β/Nrf2/GPX4 Signaling Pathway.

作者信息

Xu Jie, Tao Liujun, Jiang Liangyan, Lai Jie, Hu Juntao, Tang Zhanhong

机构信息

Department of Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.

Department of Critical Care Medicine, Suining Central Hospital, Suining, Sichuan, 629000, People's Republic of China.

出版信息

J Inflamm Res. 2024 Oct 25;17:7687-7704. doi: 10.2147/JIR.S491885. eCollection 2024.

Abstract

PURPOSE

Sepsis-associated acute lung injury (SA-ALI) is a common complication in patients with sepsis, contributing to high morbidity and mortality. Excessive inflammation and oxidative stress are crucial contributors to lung injury in sepsis. This study aims to examine the protective effects of moderate hypothermia on SA-ALI and explore the underlying mechanisms.

METHODS

Sepsis was induced in rats through cecal ligation and puncture followed by intervention with moderate hypothermia (32-33.9°C). Blood, bronchoalveolar lavage fluid, and lung tissues were collected 12 hours post-surgery. Inflammatory responses, oxidative injury, SA-ALI-related pathophysiological processes, and Keap1/GSK3β/Nrf2/GPX4 signaling in septic rats were observed by ELISA, lung W/D ratio, immunohistochemistry, immunofluorescence, histological staining, Western blotting, RT-qPCR, and TEM assays.

RESULTS

Moderate hypothermia treatment alleviated lung injury in septic rats, reflected in amelioration of pathological changes in lung structure and improved pulmonary function. Further, moderate hypothermia reduced arterial blood lactate production and suppressed the expression of inflammatory factors IL-1β, IL-6, and TNF-α; downregulated ROS, MDA, and redox-active iron levels; and restored GSH and SOD content. TEM results demonstrated that moderate hypothermia could mitigate ferroptosis in PMVECs within lung tissue. The underlying mechanism may involve regulation of the Keap1/Nrf2/SLC7A11/GPX4 signaling pathway, with the insulin pathway PI3K/Akt/GSK3β also playing a partial role.

CONCLUSION

Collectively, we illustrated a novel potential therapeutic mechanism in which moderate hypothermia could alleviate ferroptosis induced by excessive inflammation and oxidative stress via the regulation of Keap1/GSK3β/Nrf2/GPX4 expression, hence ameliorating acute lung injury in sepsis.

摘要

目的

脓毒症相关急性肺损伤(SA-ALI)是脓毒症患者常见的并发症,导致高发病率和死亡率。过度炎症和氧化应激是脓毒症肺损伤的关键因素。本研究旨在探讨中度低温对SA-ALI的保护作用并探索其潜在机制。

方法

通过盲肠结扎和穿刺诱导大鼠脓毒症,随后进行中度低温(32-33.9°C)干预。术后12小时收集血液、支气管肺泡灌洗液和肺组织。通过ELISA、肺湿干重比、免疫组织化学、免疫荧光、组织学染色、蛋白质免疫印迹法、逆转录定量聚合酶链反应和透射电镜检测观察脓毒症大鼠的炎症反应、氧化损伤、SA-ALI相关病理生理过程以及Keap1/GSK3β/Nrf2/GPX4信号通路。

结果

中度低温治疗减轻了脓毒症大鼠的肺损伤,表现为肺结构病理变化的改善和肺功能的提高。此外,中度低温降低了动脉血乳酸生成,抑制了炎症因子IL-1β、IL-6和TNF-α的表达;下调了活性氧、丙二醛和氧化还原活性铁水平;并恢复了谷胱甘肽和超氧化物歧化酶含量。透射电镜结果表明,中度低温可减轻肺组织内肺微血管内皮细胞的铁死亡。潜在机制可能涉及对Keap1/Nrf2/SLC7A11/GPX4信号通路的调节,胰岛素通路PI3K/Akt/GSK3β也发挥了部分作用。

结论

总体而言,我们阐明了一种新的潜在治疗机制,即中度低温可通过调节Keap1/GSK3β/Nrf2/GPX4表达减轻过度炎症和氧化应激诱导的铁死亡,从而改善脓毒症中的急性肺损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd77/11533192/9f30321bbbf7/JIR-17-7687-g0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验