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首页> 外文期刊>Journal of ocular pharmacology and therapeutics: The official journal of the Association for Ocular Pharmacology and Therapeutics >Resveratrol mitigates rat retinal ischemic injury: The roles of matrix metalloproteinase-9, inducible nitric oxide, and heme oxygenase-1
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Resveratrol mitigates rat retinal ischemic injury: The roles of matrix metalloproteinase-9, inducible nitric oxide, and heme oxygenase-1

机译:白藜芦醇减轻大鼠视网膜缺血性损伤:基质金属蛋白酶9,诱导型一氧化氮和血红素加氧酶1的作用

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Purpose: Retinal ischemia-associated ocular disorders, such as retinal occlusive disorders, neovascular age-related macular degeneration, proliferative diabetic retinopathy, and glaucoma are vision-threatening. In this study, we examined whether and by what mechanisms resveratrol, a polyphenol found in red wine, is able to protect against retinal ischemia/reperfusion injury. Methods: In vivo rat retinal ischemia was induced by high intraocular pressure (HIOP), namely, 120 mmHg for 60 min. The mechanism and management was evaluated by electroretinogram (ERG) b-wave amplitudes measurement, immunohistochemistry, and real-time polymerase chain reaction. Results: The HIOP-induced retinal ischemic changes were characterized by a decrease in ERG b-wave amplitudes, a loss of choline acetyltransferase immunolabeling of amacrine cell bodieseuronal processes, and increased vimentin immunoreactivity, which is a marker of Müller cells, together with upregulation of matrix metalloproteinase-9 (MMP-9), heme oxygenase-1 (HO-1), and inducible nitric oxide (iNOS), and downregulation of Thy-1, both at the mRNA level. The detrimental effects due to the ischemia were concentration-dependent (weaker effect at 0.05 nmole) and/or significantly (at 0.5 nmole) altered when resveratrol was applied 15 min before or after retina ischemia. Conclusion: This study supports the hypothesis that resveratrol may be able to protect the retina against ischemia by downregulation of MMP-9 and iNOS, and upregulation of HO-1.
机译:目的:视网膜缺血相关的眼部疾病,例如视网膜闭塞性疾病,新血管性年龄相关的黄斑变性,增生性糖尿病性视网膜病和青光眼,会威胁视力。在这项研究中,我们检查了白藜芦醇(一种在红酒中发现的多酚)是否能够以及通过什么机制能够预防视网膜缺血/再灌注损伤。方法:以120 mmHg的高眼压(HIOP)诱导60分钟,体内诱导大鼠视网膜缺血。通过视网膜电图(ERG)的b波幅度测量,免疫组织化学和实时聚合酶链反应来评估其机制和管理。结果:HIOP诱导的视网膜缺血性改变的特征是ERG b波振幅降低,无长突细胞体/神经元过程的胆碱乙酰基转移酶免疫标记丧失以及波形蛋白免疫反应性增加,波形蛋白免疫反应性是Müller细胞的标志,在mRNA水平上,基质金属蛋白酶9(MMP-9),血红素加氧酶1(HO-1)和诱导型一氧化氮(iNOS)的上调以及Thy-1的下调。由于缺血引起的有害作用是浓度依赖性的(在0.05 nmole处减弱),和/或在视网膜缺血之前或之后15分钟施用白藜芦醇时,其变化显着(在0.5 nmole下)。结论:本研究支持白藜芦醇可能通过下调MMP-9和iNOS以及上调HO-1来保护视网膜免受缺血的假说。

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