类黄酮可保护视网膜神经节细胞免受氧化应激诱导的死亡。

Flavonoids protect retinal ganglion cells from oxidative stress-induced death.

作者信息

Maher Pamela, Hanneken Anne

机构信息

Salk Institute, La Jolla, California 92037, USA.

出版信息

Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4796-803. doi: 10.1167/iovs.05-0397.

Abstract

PURPOSE

Mounting evidence suggests that oxidative stress contributes to the pathogenesis of many ocular diseases, including glaucoma and diabetic retinopathy. No treatments are available to prevent the neuronal degeneration that occurs in these disorders. The purpose of this study was to determine whether flavonoids, natural products that are abundant in fruits and vegetables, can protect retinal ganglion cells from oxidative stress-induced death.

METHODS

The ability of flavonoids to protect an immortalized retinal ganglion cell line, RGC-5 cells, was tested using three model systems of oxidative stress-induced cell death: glutathione (GSH) depletion, t-butyl peroxide (t-BOOH) treatment, and hydrogen peroxide (H2O2) treatment.

RESULTS

GSH depletion causes retinal ganglion cell death by a pathway involving the production of endogenous reactive oxygen species (ROS), whereas the other two treatments use exogenous sources of ROS. It was found that specific flavonoids could protect retinal ganglion cells from cell death initiated by all three of the inducers of oxidative stress with high levels of potency and low toxicity. In the case of GSH depletion, different flavonoids could be shown to act at distinct steps in the cell death pathway. Several of the protective flavonoids also induced the synthesis of the transcription factor NF-E2-related factor 2 and phase 2 antioxidant enzymes such as heme oxygenase 1, markers for the activation of the antioxidant response element.

CONCLUSIONS

These results suggest that certain flavonoids can function as potent and effective neuroprotective agents for retinal ganglion cells.

摘要

目的

越来越多的证据表明,氧化应激在包括青光眼和糖尿病视网膜病变在内的许多眼部疾病的发病机制中起作用。目前尚无治疗方法可预防这些疾病中发生的神经元变性。本研究的目的是确定水果和蔬菜中丰富的天然产物类黄酮是否能保护视网膜神经节细胞免受氧化应激诱导的死亡。

方法

使用氧化应激诱导细胞死亡的三种模型系统:谷胱甘肽(GSH)耗竭、叔丁基过氧化氢(t-BOOH)处理和过氧化氢(H2O2)处理,测试类黄酮保护永生化视网膜神经节细胞系RGC-5细胞的能力。

结果

GSH耗竭通过涉及内源性活性氧(ROS)产生的途径导致视网膜神经节细胞死亡,而其他两种处理使用外源性ROS来源。研究发现,特定的类黄酮可以保护视网膜神经节细胞免受所有三种氧化应激诱导剂引发的细胞死亡,效力高且毒性低。在GSH耗竭的情况下,不同的类黄酮可显示在细胞死亡途径的不同步骤起作用。几种具有保护作用的类黄酮还诱导了转录因子NF-E2相关因子2和第二阶段抗氧化酶如血红素加氧酶1的合成,这些是抗氧化反应元件激活的标志物。

结论

这些结果表明,某些类黄酮可作为视网膜神经节细胞有效的神经保护剂发挥作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索