Protection against Oxidative Stress by Coenzyme Q10 in a Porcine Retinal Degeneration Model

被引:1
|
作者
Deppe, Leonie [1 ]
Mueller-Buehl, Ana M. [1 ]
Tsai, Teresa [1 ]
Erb, Carl [2 ]
Dick, H. Burkhard [1 ]
Joachim, Stephanie C. [1 ]
机构
[1] Ruhr Univ Bochum, Expt Eye Res Inst, Univ Eye Hosp, Schornau 23-25, D-44892 Bochum, Germany
[2] Eye Clin Wittenbergplatz, Private Inst Appl Ophthalmol, D-10787 Berlin, Germany
来源
JOURNAL OF PERSONALIZED MEDICINE | 2024年 / 14卷 / 04期
关键词
glaucoma; coenzyme Q10; oxidative stress; neuroprotection; porcine organ culture; NORMAL-TENSION GLAUCOMA; BINDING PROTEIN; GANGLION-CELLS; MICROGLIA; MECHANISMS; APOPTOSIS; CULTURE; TARGET; FUTURE; DEATH;
D O I
10.3390/jpm14040437
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Oxidative stress plays an important role in neurodegenerative diseases, including glaucoma. Therefore, we analyzed if the antioxidant coenzyme Q10 (CoQ10), which is also commercially available, can prevent retinal degeneration induced by hydrogen peroxide (H2O2) in a porcine organ culture model. Retinal explants were cultivated for eight days, and H2O2 (500 mu M, 3 h) induced the oxidative damage. CoQ10 therapy was applied (700 mu M, 48 h). Retinal ganglion cells (RGCs) and microglia were examined immunohistologically in all groups (control, H2O2, H2O2 + CoQ10). Cellular, oxidative, and inflammatory genes were quantified via RT-qPCR. Strong RGC loss was observed with H2O2 (p <= 0.001). CoQ10 elicited RGC protection compared to the damaged group at a histological (p <= 0.001) and mRNA level. We detected more microglia cells with H2O2, but CoQ10 reduced this effect (p = 0.004). Cellular protection genes (NRF2) against oxidative stress were stimulated by CoQ10 (p <= 0.001). Furthermore, mitochondrial oxidative stress (SOD2) increased through H2O2 (p = 0.038), and CoQ10 reduced it to control level. Our novel results indicate neuroprotection via CoQ10 in porcine retina organ cultures. In particular, CoQ10 appears to protect RGCs by potentially inhibiting apoptosis-related pathways, activating intracellular protection and reducing mitochondrial stress.
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页数:16
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