Wogonin通过调节PPARα、AKT和NRF2减轻急性肺损伤的炎症和氧化应激。

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY Naunyn-Schmiedeberg's archives of pharmacology Pub Date : 2025-08-01 Epub Date: 2025-02-17 DOI:10.1007/s00210-025-03889-3
Hui Yang, Yunran Hu, Long Cheng, Yuan Xiong, Yuan Xu, Changxing Gao, Ming Qian, Lin Zhou
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引用次数: 0

摘要

本研究旨在阐明沃戈宁(WOG)对急性肺损伤(ALI)的治疗作用及其机制。建立脂多糖诱导的ALI小鼠体内模型和体外RAW264.7细胞模型。H&E染色观察肺组织病理变化。采用H&E染色及流式细胞术检测肺组织及支气管肺泡灌洗液(BALF)炎症细胞浸润情况。对炎症因子、活性氧(ROS)和抗氧化介质进行定量分析。通过生物信息学和网络药理学鉴定WOG的潜在靶点,并通过Western blotting进一步验证。WOG处理(10 mg/kg、20 mg/kg、40 mg/kg)通过改善肺组织中炎症细胞的浸润和BALF,抑制炎症因子,提高抗氧化介质水平,减轻肺水肿,减轻ALI小鼠肺损伤。在RAW264.7细胞中,WOG (10 μM、20 μM、40 μM)处理也能抑制炎症反应和氧化应激。通过整合网络药理学数据库和GSE1871数据集,预测过氧化物酶体增殖物激活受体α (PPARα)、蛋白激酶B (AKT)和核因子红系2相关因子2 (NRF2)是WOG抗ALI的靶点。有趣的是,WOG在体内和体外均能显著促进PPARα和NRF2的表达和激活,抑制AKT的表达和磷酸化。我们全面研究了WOG通过调节PPARα、AKT和NRF2改善炎症和氧化应激对ALI的治疗作用。
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Wogonin attenuates inflammation and oxidative stress in acute lung injury via regulating PPARα, AKT, and NRF2.

The study aims to clarify the therapeutic effect and underlying mechanisms of wogonin (WOG) against acute lung injury (ALI). Lipopolysaccharide-induced in vivo ALI mice model and in vitro RAW264.7 cell model were established. Lung histopathologic changes were assessed by H&E staining. Inflammatory cell infiltration in lung tissues and bronchoalveolar lavage fluid (BALF) was determined using H&E staining and flow cytometry. Inflammatory cytokines, reactive oxygen species (ROS), and antioxidant mediators were quantified. Potential targets of WOG were identified by bioinformatics and network pharmacology and further verified by Western blotting. WOG treatment (10 mg/kg, 20 mg/kg, 40 mg/kg) alleviated lung injury of ALI mice by ameliorating infiltration of inflammatory cells in lung tissues and BALF, inhibiting inflammatory cytokines, elevating antioxidant mediator levels, and attenuating lung edema. In RAW264.7 cells, WOG treatment (10 μM, 20 μM, 40 μM) also suppressed inflammatory response and oxidative stress. Peroxisome proliferator-activated receptor α (PPARα), protein kinase B (AKT), and nuclear factor erythroid 2-related factor 2 (NRF2) were predicted to be the targets of WOG against ALI by integrating the network pharmacology database and the GSE1871 dataset. Interestingly, WOG markedly promoted the expression and activation of PPARα and NRF2, while it inhibited the expression and phosphorylation of AKT both in vivo and in vitro. We provided a comprehensive insight into investigating the therapeutic effect of WOG against ALI via ameliorating inflammation and oxidative stress through regulating PPARα, AKT, and NRF2.

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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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