Lutein-stevioside nanoparticle attenuates H2O2-induced oxidative damage in ARPE cells
文献类型: 外文期刊
第一作者: Dai, Zhuqing
作者: Dai, Zhuqing;Nie, Meimei;Chen, Ye;Song, Jiangfeng;Xu, Yayuan;Zhang, Zhongyuan;Li, Dajing;Zhang, Zhongyuan;Zhang, Guodong;Zhang, Xing;Yan, Shumo
作者机构:
关键词: Lutein; Stevioside; Antioxidant; Human retinal pigment epithelial cell; Mechanism
期刊名称:FOOD SCIENCE AND HUMAN WELLNESS ( 影响因子:7.0; 五年影响因子:8.3 )
ISSN:
年卷期: 2024 年 13 卷 3 期
页码:
收录情况: SCI
摘要: In order to improve the bioavailability of lutein (LUT), a novel lutein-stevioside nanoparticle (LUT-STE) were prepared previously, but the information about LUT-STE on protecting of eye health was limited. This study investigated the effect of LUT-STE on antioxidant activity of H2O2-induced human retinal pigment epithelial (ARPE) cells. LUT and LUT-STE (final concentration of 5 mu g/mL) significantly enhanced cell viability from (74.84 +/- 5.10)% to (81.92 +/- 10.01)% (LUT) and (89.33 +/- 4.34)% (LUT-STE), and inhibited the cell apoptosis (P < 0.05). After pretreatment with LUT-STE in ARPE cells, the levels of superoxide dismutase (SOD), catalase (CAT) and glutathion peroxidase (GSH-Px) in ARPE cells were significantly increased (P < 0.05), the contents of reactive oxygen species (ROS) and malondialdehyde (MDA) were decreased. In addition, the vascular endothelial growth factor (VEGF) levels were inhibited by 13.61% and 17.39%, respectively, pretreatment with LUT and LUT-STE. Western blotting results showed that the pretreatment with LUT-STE inhibited the expression of caspase-9 and caspase-3 and up-regulated Bcl-2/Bax pathway to inhibit H2O2-induced apoptosis. In summary, the novel delivery LUT-STE had more pronounced inhibitory effect on H2O2-induced damage in human ARPE cells. (c) 2024 Beijing Academy of Food Sciences. Publishing services by Tsinghua University Press. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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