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肥胖型哮喘患者气道上皮细胞对氧磷酶 2

Airway epithelial Paraoxonase-2 in obese asthma.

机构信息

Department of Medicine, Division of Pulmonary Science and Critical Care, School of Medicine, University of Colorado, Aurora, Colorado, United States of America.

出版信息

PLoS One. 2022 Mar 14;17(3):e0261504. doi: 10.1371/journal.pone.0261504. eCollection 2022.

Abstract

BACKGROUND

Obesity in asthmatics has been associated with higher airway oxidative stress in which dysfunctional mitochondria are a potential contributing source of excess free radicals. Paraoxonase 2 (PON2) plays an important role in reducing mitochondrial-derived oxidative stress and could, therefore, have therapeutic potential in these patients.

OBJECTIVES

We used primary human bronchial epithelial cells (HBECs) from asthmatics and healthy controls to evaluate: a) protein levels of Paraoxonase 2 and b) to test the potential protective effect of quercetin supplementation in cells under oxidative stress conditions.

RESULTS

Compared to lean controls, obese asthmatics had significantly lower PON2 airway epithelial levels (respectively, 1.08 vs. 0.47 relative units normalized by GAPDH) (p-value < 0.006). Treating HBECs in vitro for 24 hrs. with 25μM quercetin significantly increased PON2 protein levels: 15.5 treated cells vs. 9.8 untreated cells (relative units normalized by GAPDH) (p value = 0.004). Notably, compared to untreated cells, quercetin supplementation reduces mitochondrial superoxide and hydrogen peroxide production on HBECs cells exposed to different oxidative stress triggers such as 1-2 Naphthoquinone (1-2 NQ) and hydrogen peroxide, suggesting that PON2 might play a protective role ameliorating oxidative injury on human airway epithelium.

CONCLUSION

Compared to lean controls, obese asthmatics have significantly reduced PON2 levels in airway epithelial cells. Treatment with quercetin in vitro increased PON2 protein levels and prevented oxidative stress from different types of stimuli. Hence, quercetin supplementation may be a potential therapeutic strategy to prevent obesity-mediated airway oxidative stress in obese asthmatics.

摘要

背景

哮喘患者的肥胖与更高的气道氧化应激有关,其中功能失调的线粒体是产生过多自由基的潜在来源。对氧磷酶 2(PON2)在减少线粒体衍生的氧化应激方面起着重要作用,因此在这些患者中可能具有治疗潜力。

目的

我们使用来自哮喘患者和健康对照者的原代人支气管上皮细胞(HBEC)来评估:a)对氧磷酶 2 的蛋白水平,以及 b)在氧化应激条件下测试槲皮素补充对细胞的潜在保护作用。

结果

与瘦对照组相比,肥胖哮喘患者的气道上皮 PON2 水平明显降低(分别为 1.08 与 0.47,用 GAPDH 归一化的相对单位)(p 值<0.006)。在体外用 25μM 槲皮素处理 HBEC 24 小时,明显增加了 PON2 蛋白水平:15.5 处理细胞与 9.8 未处理细胞(用 GAPDH 归一化的相对单位)(p 值=0.004)。值得注意的是,与未处理细胞相比,槲皮素补充可减少暴露于不同氧化应激触发物(如 1-2 萘醌(1-2 NQ)和过氧化氢)的 HBEC 细胞中的线粒体超氧化物和过氧化氢的产生,表明 PON2 可能在人类气道上皮细胞中发挥保护作用,减轻氧化损伤。

结论

与瘦对照组相比,肥胖哮喘患者的气道上皮细胞中的 PON2 水平明显降低。体外用槲皮素处理可增加 PON2 蛋白水平,并防止不同类型刺激引起的氧化应激。因此,槲皮素补充可能是预防肥胖介导的肥胖哮喘患者气道氧化应激的潜在治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee4b/8920196/323eb61e447a/pone.0261504.g001.jpg

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