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一种新型查尔酮衍生物(化合物27)通过PI3K/AKT/Nrf2-Keap1信号通路作用于上皮细胞,减轻小鼠内毒素诱导的急性肺损伤的证据。

Evidence that a Novel Chalcone Derivative, Compound 27, Acts on the Epithelium Via the PI3K/AKT/Nrf2-Keap1 Signaling Pathway, to Mitigate LPS-Induced Acute Lung Injury in Mice.

作者信息

Zhou Liqin, Lin Yuting, Zhou Tengfei, Xue Yincong, Bellusci Saverio, Shen Mengya, Chen Chengshui, Chen Chaolei

机构信息

Zhejiang Provincial Key Laboratory of Interventional Pulmonology, Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.

Department of Physiology, Zhejiang University School of Medicine, Hangzhou, 310058, Zhejiang, China.

出版信息

Inflammation. 2025 Apr;48(2):590-606. doi: 10.1007/s10753-024-02051-0. Epub 2024 May 24.

Abstract

Acute lung injury (ALI) is a highly heterogeneous clinical syndrome and an important cause of mortality in critically ill patients, with limited treatment options currently available. Chalcone, an essential secondary metabolite found in edible or medicinal plants, exhibits good antioxidant activity and simple structure for easy synthesis. In our study, we synthesized a novel chalcone derivative, compound 27 (C27). We hypothesized that C27 could be a potential treatment for acute respiratory distress syndrome (ARDS). Therefore, the protective effects of C27 on lung epithelial cells during ALI and the underlying molecular mechanisms were investigated. In vivo, Intratracheal instillation of LPS (10 mg/kg) was used to induce acute lung injury in mice. In vitro, the bronchial epithelial cell line (Beas-2b) was treated with 30 μM tert-butyl hydroperoxide (t-BHP) to simulate oxidative stress. Our findings demonstrate that pretreatment with C27 reduces LPS-induced oxidative destruction and cellular apoptosis in lung tissues of mice. Furthermore, it significantly attenuates t-BHP-induced cellular reactive oxygen species (ROS) generation, mitochondrial damage, and apoptosis in vitro. Mechanistically, the signaling pathway involving Nrf2-Keap1 and the downstream antioxidative proteins were activated by C27 in vivo. Additionally, PI3K inhibitor LY294002 and Nrf2 inhibitor ML385 abolished the effect of C27 in vitro, indicating that the protective effect of C27 is mediated via the PI3K/AKT/Nrf2-Keap1 pathway. Our study provides evidence that C27 protects against LPS-induced ALI by mitigating oxidative stress via activation of the PI3K/AKT/Nrf2-Keap1 signaling pathway. Therefore, we hypothesize that C27 represents a viable alternative for ALI therapy.

摘要

急性肺损伤(ALI)是一种高度异质性的临床综合征,是危重症患者死亡的重要原因,目前治疗选择有限。查尔酮是一种存在于食用或药用植物中的重要次生代谢产物,具有良好的抗氧化活性且结构简单易于合成。在我们的研究中,我们合成了一种新型查尔酮衍生物,化合物27(C27)。我们假设C27可能是急性呼吸窘迫综合征(ARDS)的一种潜在治疗方法。因此,研究了C27在ALI期间对肺上皮细胞的保护作用及其潜在的分子机制。在体内,通过气管内滴注脂多糖(LPS,10 mg/kg)诱导小鼠急性肺损伤。在体外,用30 μM叔丁基过氧化氢(t-BHP)处理支气管上皮细胞系(Beas-2b)以模拟氧化应激。我们的研究结果表明,C27预处理可减少LPS诱导的小鼠肺组织氧化破坏和细胞凋亡。此外,它在体外显著减轻了t-BHP诱导的细胞活性氧(ROS)生成、线粒体损伤和细胞凋亡。机制上,C27在体内激活了涉及Nrf2-Keap1的信号通路和下游抗氧化蛋白。此外,PI3K抑制剂LY294002和Nrf2抑制剂ML385消除了C27在体外的作用,表明C27的保护作用是通过PI3K/AKT/Nrf2-Keap1途径介导的。我们的研究提供了证据,表明C27通过激活PI3K/AKT/Nrf2-Keap1信号通路减轻氧化应激,从而预防LPS诱导的ALI。因此,我们假设C27是ALI治疗的一种可行替代方案。

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