白藜芦醇和虾青素保护在气液界面培养的人鼻上皮细胞免受急性氧化剂暴露。

Ayaho Yamamoto, Peter D Sly, Nelufa Begum, Abrey J Yeo, Emmanuelle Fantino
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引用次数: 2

摘要

气道上皮氧化应激(OS)与细胞损伤、炎症和线粒体功能障碍相关,可引发或加重呼吸道疾病。然而,外源性抗氧化剂是否能保护气道上皮免受OS的侵害尚不清楚。白藜芦醇和虾青素是营养化合物,在各种情况下显示出多种益处,包括防止OS和炎症。本研究的目的是研究白藜芦醇和虾青素预处理的效用,以防止氧化暴露的负面影响,并恢复由原代人鼻上皮细胞(NECs)在气液界面生长的良好分化上皮的氧化还原稳态。将完全分化的NECs用抗氧化剂预处理24小时,然后将培养的上皮细胞暴露于过氧化氢(H2O2)中1小时以诱导急性OS。测量的反应包括线粒体活性氧(mtROS)生成、氧化还原状态(GSH/GSSG比率)、细胞ATP和信号通路(SIRT1、FOXO3、p21、PINK1、PARKIN、NRF2)。H2O2暴露后,与对照组相比,mtROS产量增加了4倍(pp2O2暴露降低了GSH/GSSG比率,这种下降可以通过抗氧化剂预处理来防止。H2O2暴露导致p21 mRNA表达量较对照增加2.5倍(p . 442)
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Resveratrol and Astaxanthin Protect Primary Human Nasal Epithelial Cells Cultured at an Air-liquid Interface from an Acute Oxidant Exposure.

Oxidative stress (OS) in the airway epithelium is associated with cell damage, inflammation, and mitochondrial dysfunction that may initiate or worsen respiratory disease. However, it is unclear whether exogenous antioxidants can provide protection to the airway epithelium from OS. Resveratrol and astaxanthin are nutritional compounds that have shown diverse benefits including protection against OS and inflammation in various situations. The aim of this study was to examine the utility of pre-treatment with resveratrol and astaxanthin to prevent the negative effects of oxidant exposure and restore redox homeostasis in a well-differentiated epithelium grown from primary human nasal epithelial cells (NECs) at the air-liquid interface. Fully differentiated NECs were pretreated with the antioxidants for 24 hours and the cultured epithelia was subsequently exposed to hydrogen peroxide (H2O2) for 1 hour to induce an acute OS. Responses measured included mitochondrial reactive oxygen species (mtROS) generation, redox status (GSH/GSSG ratio), cellular ATP, and signaling pathways (SIRT1, FOXO3, p21, PINK1, PARKIN, NRF2). Following H2O2 exposure, mtROS production increased by 4-fold compared with control (p<0.01) and pre-treatment with resveratrol or astaxanthin reduced this by 50% (p<0.05). H2O2 exposure reduced GSH/GSSG ratio and this decline was prevented by antioxidants pre-treatment. H2O2 exposure caused 2.5-fold increase in p21 mRNA expression compared with control (p<0.05), while a slight decrease in p21 mRNA expression was observed when cells were pre-treated with resveratrol or astaxanthin. Our results demonstrate that antioxidants, resveratrol, and astaxanthin were able to protect cells from an acute OS. These agents show promise that encourages further research.

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