Department of Pediatrics, Section of Neonatology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
Laboratory of Toxicology, University of Crete, Medical School, Voutes, Heraklion 71409, Crete, Greece.
Food Chem Toxicol. 2018 Apr;114:23-33. doi: 10.1016/j.fct.2018.02.026. Epub 2018 Feb 9.
Quercetin (QU) is one of the most common flavonoids that are present in a wide variety of fruits, vegetables, and beverages. This compound possesses potent anti-inflammatory and anti-oxidant properties. Supplemental oxygen is routinely administered to premature infants with pulmonary insufficiency. However, hyperoxia is one of the major risk factors for the development of bronchopulmonary dysplasia (BPD), which is also termed chronic lung disease in premature infants. Currently, no preventive approaches have been reported against BPD. The treatment of BPD is notably limited to oxygen administration, ventilatory support, and steroids. Since QU has been shown to be effective in reducing inflammation and oxidative stress in various disease models, we hypothesized that the postnatal QU treatment of newborn mice will protect against hyperoxic lung injury by the upregulation of the phase I (CYP1A/B) and/or phase II, NADPH quinone reductase enzymes. Newborn C57BL/6J mice within 24 h of birth with the nursing dams were exposed to either 21% O (air) and/or 85% O (hyperoxia) for 7 days. The mice were treated, intraperitoneally (i.p.) once every other day with quercetin, at a concentration of 20 mg/kg, or saline alone from postnatal day (PND) 2-6. The mice were sacrificed on day 7, and lung and liver tissues were collected. The expression levels of CYP1A1, CYP1B1, NQO1 proteins and mRNA as well as the levels of MDA-protein adducts were analyzed in lung and liver tissues. The findings indicated that QU attenuated hyperoxia-mediated lung injury by reducing inflammation and improving alveolarization with decreased number of neutrophil and macrophage infiltration. The attenuation of this lung injury correlated with the upregulation of CYP1A1/CYP1B1/NQO1 mRNA, proteins and the down regulation of NF-kB levels and MDA-protein adducts in lung and liver tissues. The present study demonstrated the potential therapeutic value of quercetin in the prevention and/or treatment of BPD.
槲皮素(QU)是一种最常见的类黄酮,存在于各种水果、蔬菜和饮料中。这种化合物具有强大的抗炎和抗氧化特性。氧气补充是肺功能不全的早产儿的常规治疗方法。然而,高氧是支气管肺发育不良(BPD)发展的主要危险因素之一,早产儿的 BPD 也称为慢性肺病。目前,尚无针对 BPD 的预防方法。BPD 的治疗主要限于吸氧、通气支持和类固醇。由于 QU 已被证明在各种疾病模型中有效减轻炎症和氧化应激,我们假设新生小鼠的产后 QU 治疗将通过上调 I 相(CYP1A/B)和/或 II 相、NADPH 醌还原酶来预防高氧肺损伤。出生后 24 小时内的新生 C57BL/6J 小鼠与哺乳母鼠一起,在出生后第 2-6 天,每隔一天腹膜内(i.p.)用 20mg/kg 的浓度接受一次 QU 或单独生理盐水治疗,接受 21% O(空气)和/或 85% O(高氧)处理 7 天。第 7 天处死小鼠,收集肺和肝组织。分析肺和肝组织中 CYP1A1、CYP1B1、NQO1 蛋白和 mRNA 的表达水平以及 MDA-蛋白加合物的水平。结果表明,QU 通过减少炎症和改善肺泡化来减轻高氧介导的肺损伤,减少中性粒细胞和巨噬细胞浸润的数量。这种肺损伤的减轻与 CYP1A1/CYP1B1/NQO1 mRNA、蛋白的上调以及肺和肝组织中 NF-kB 水平和 MDA-蛋白加合物的下调相关。本研究表明,槲皮素在预防和/或治疗 BPD 方面具有潜在的治疗价值。