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首页> 外文期刊>Investigative ophthalmology & visual science >Protection of the Retina by Rapid Diffusion of Hydrogen: Administration of Hydrogen-Loaded Eye Drops in Retinal Ischemiaa??Reperfusion Injury
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Protection of the Retina by Rapid Diffusion of Hydrogen: Administration of Hydrogen-Loaded Eye Drops in Retinal Ischemiaa??Reperfusion Injury

机译:氢的快速扩散对视网膜的保护:视网膜缺血再灌注损伤中载氢滴眼液的给药

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摘要

Purpose.: Retinal ischemia-reperfusion (I/R) injury by transient elevation of intraocular pressure (IOP) is known to induce neuronal damage through the generation of reactive oxygen species. Study results have indicated that molecular hydrogen (H2) is an efficient antioxidant gas that selectively reduces the hydroxyl radical (?· OH) and suppresses oxidative stress-induced injury in several organs. This study was conducted to explore the neuroprotective effect of H2-loaded eye drops on retinal I/R injury. Methods.: Retinal ischemia was induced in rats by raising IOP for 60 minutes. H2-loaded eye drops were prepared by dissolving H2 gas into a saline to saturated level and administered to the ocular surface continuously during the ischemia and/or reperfusion periods. One day after I/R injury, apoptotic cells in the retina were quantified, and oxidative stress was evaluated by markers such as 4-hydroxynonenal and 8-hydroxy-2-deoxyguanosine. Seven days after I/R injury, retinal damage was quantified by measuring the thickness of the retina. Results.: When H2-loaded eye drops were continuously administered, H2 concentration in the vitreous body immediately increased and I/R-induced ?· OH level decreased. The drops reduced the number of retinal apoptotic and oxidative stress markera??positive cells and prevented retinal thinning with an accompanying activation of M??ller glia, astrocytes, and microglia. The drops improved the recovery of retinal thickness by 70%. Conclusions.: H2 has no known toxic effects on the human body. Thus, the results suggest that H2-loaded eye drops are a highly useful neuroprotective and antioxidative therapeutic treatment for acute retinal I/R injury.
机译:目的:通过短暂升高眼内压(IOP)引起的视网膜缺血再灌注(I / R)损伤可通过产生活性氧来诱导神经元损伤。研究结果表明,分子氢(H2)是一种有效的抗氧化剂气体,可以选择性地还原羟基自由基(α·OH)并抑制氧化应激在多个器官中引起的损伤。进行该研究以探讨负载H2的滴眼液对视网膜I / R损伤的神经保护作用。方法:通过升高IOP 60分钟诱导大鼠视网膜缺血。通过将H 2气体溶解在盐水中至饱和水平来制备装载有H 2的滴眼剂,并在缺血和/或再灌注期间将其连续施用至眼表。 I / R损伤后一天,对视网膜中的凋亡细胞进行定量,并通过诸如4-羟基壬烯醛和8-羟基-2-脱氧鸟苷等标记物评估氧化应激。 I / R损伤后7天,通过测量视网膜厚度来量化视网膜损伤。结果:当连续服用含H2的眼药水时,玻璃体内的H2浓度立即升高,而I / R诱导的α·OH水平降低。滴剂减少了视网膜细胞凋亡和氧化应激标记物阳性细胞的数量,并防止了视网膜变薄,并伴随着MΔller胶质细胞,星形胶质细胞和小胶质细胞的活化。滴剂使视网膜厚度的恢复提高了> 70%。结论:H2对人体没有已知的毒性作用。因此,结果表明,装载H2的眼药水对于急性视网膜I / R损伤是高度有用的神经保护和抗氧化治疗方法。

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