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毛蕊花糖苷对过氧化氢诱导的人角膜上皮细胞氧化损伤的保护作用。

Protective Effect of Acteoside against Hydrogen Peroxide-Induced Oxidative Damage in Human Corneal Epithelial Cells.

作者信息

Huang Y, Peng Q

机构信息

Hunan University of Chinese Medicine, Changsha, Hunan, China.

The First Affiliated Hospital of Hunan University of Chinese Medicine, Hunan, Changsha, Yuhua District, China.

出版信息

Bull Exp Biol Med. 2024 Dec;178(2):213-217. doi: 10.1007/s10517-025-06309-x. Epub 2025 Jan 7.

Abstract

We studied the effect of acteoside on a model of human corneal epithelial cells (HCEC) injury induced by HO. HCEC were divided into 4 groups and cultured for 24 h in normal medium (intact and control groups, respectively), or in a medium containing DMSO or 160 μM acteoside (DMSO and acteoside groups, respectively). Then, HO solution was added to HCEC for 4 h, except for intact cells. The cell viability was assessed by the CCK8 method to determine the working concentrations of acteoside and HO for further experiments. Quantitative PCR and Western blotting were used to determine the effect of acteoside and HO on the expression of nuclear factor erythroid 2-related factor 2 (Nrf2), heme oxygenase-1 (HO-1), NADPH:quinone oxidoreductase-1 (NQO-1), and cyclooxygenase-2 (COX-2). The effects of these agents on cell proliferation were assessed by staining with 5-ethynyl-2'-deoxyuridine (EdU). It was found that acteoside protected HCEC against HO-induced damage by inhibiting the expression of Nrf2, HO-1, NQO-1, and COX-2.

摘要

我们研究了毛蕊花糖苷对由血红素加氧酶(HO)诱导的人角膜上皮细胞(HCEC)损伤模型的影响。将HCEC分为4组,分别在正常培养基中(分别为完整组和对照组)培养24小时,或在含有二甲基亚砜(DMSO)或160μM毛蕊花糖苷的培养基中(分别为DMSO组和毛蕊花糖苷组)培养24小时。然后,除完整细胞外,向HCEC中加入HO溶液4小时。采用CCK8法评估细胞活力,以确定毛蕊花糖苷和HO用于进一步实验的工作浓度。运用定量聚合酶链反应(qPCR)和蛋白质免疫印迹法(Western blotting)来确定毛蕊花糖苷和HO对核因子E2相关因子2(Nrf2)、血红素加氧酶-1(HO-1)、NADPH:醌氧化还原酶-1(NQO-1)和环氧化酶-2(COX-2)表达的影响。通过5-乙炔基-2'-脱氧尿苷(EdU)染色评估这些药物对细胞增殖的影响。结果发现,毛蕊花糖苷通过抑制Nrf2、HO-1、NQO-1和COX-2的表达来保护HCEC免受HO诱导的损伤。

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