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阿魏酸(FA)可保护人视网膜色素上皮细胞免受 H2O2 诱导的氧化损伤。

Ferulic acid (FA) protects human retinal pigment epithelial cells from H O -induced oxidative injuries.

机构信息

Department of Ophthalmology, the First Affiliated Hospital of Zhengzhou University, Henan Province Eye Hospital, Henan International Joint Research Laboratory for Ocular Immunology and Retinal Injury Repair, Zhengzhou, China.

出版信息

J Cell Mol Med. 2020 Nov;24(22):13454-13462. doi: 10.1111/jcmm.15970. Epub 2020 Oct 20.

Abstract

The aim of present study is to investigate whether Ferulic acid (FA), a natural polyphenol antioxidant, was able to protect ARPE-19 cells from hydrogen peroxide (H O )-induced damage, and elucidate the underlying mechanisms. Our results revealed that FA pre-treatment for 24 hours can reverse cell loss of H O -induced ARPE-19 cells via the promotion of cell proliferation and prevention of apoptosis, as evidenced by 5-ethynyl-2'-deoxyuridine (EdU) incorporation and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labelling (TUNEL) assay, respectively. Moreover, the addition of FA (5 mM) can decrease Bax and cleaved caspase-3 protein expression, but increase Bcl-2 protein expression in ARPE-19 cells. Furthermore, H O -induced oxidative stress in ARPE-19 cells was significantly alleviated by FA, illustrated by reduced levels of ROS and MDA. In addition, the attenuated antioxidant enzymes activities of (SOD, CAT and GPX) and GSH level were reversed almost to the normal base level by the pre-addition of FA for 24 hours. In all assays, FA itself did not exert any effect on the change of the above parameters. These novel findings indicated that FA effectively protected human ARPE-19 cells from H O -induced oxidative damage through its pro-proliferation, anti-apoptosis and antioxidant activity, suggesting that FA has a therapeutic potential in the prevention and treatment of AMD.

摘要

本研究旨在探讨是否可以通过天然多酚抗氧化剂阿魏酸(FA)来保护 ARPE-19 细胞免受过氧化氢(H O )诱导的损伤,并阐明其潜在机制。我们的结果表明,FA 预处理 24 小时可以通过促进细胞增殖和防止细胞凋亡来逆转 H O 诱导的 ARPE-19 细胞的损失,这一点可以通过 5-乙炔基-2'-脱氧尿苷(EdU)掺入和末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记(TUNEL)测定来证明。此外,添加 FA(5mM)可以降低 Bax 和 cleaved caspase-3 蛋白表达,但增加 ARPE-19 细胞中的 Bcl-2 蛋白表达。此外,FA 还可以显著减轻 H O 诱导的 ARPE-19 细胞中的氧化应激,表现为 ROS 和 MDA 水平降低。此外,FA 的预处理几乎可以将抗氧化酶活性(SOD、CAT 和 GPX)和 GSH 水平的减弱恢复到正常基础水平。在所有试验中,FA 本身对上述参数变化没有任何影响。这些新发现表明,FA 通过其促增殖、抗凋亡和抗氧化活性有效保护人 ARPE-19 细胞免受 H O 诱导的氧化损伤,表明 FA 在预防和治疗 AMD 方面具有治疗潜力。

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