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原发性开角型青光眼氧化应激、免疫反应和细胞凋亡的推定生物标志物评估。

Evaluation of presumptive biomarkers of oxidative stress, immune response and apoptosis in primary open-angle glaucoma.

机构信息

Ophthalmic Research Unit Santiago Grisolia, Valencia, Spain.

出版信息

Curr Opin Pharmacol. 2013 Feb;13(1):98-107. doi: 10.1016/j.coph.2012.10.007. Epub 2012 Nov 8.

Abstract

There is growing interest on the correlation among oxidative stress, inflammation, apoptosis and primary open-angle glaucoma initiation and progression. Reactive oxygen species are formed in the eyes following a wide variety of stressors, and are largely implicated in glaucoma pathogenesis. Immune-inflammatory response mediators have recently become a target of ophthalmologic concern, including glaucoma. Much attention has been derived to the role of specific pro and anti-apoptotic molecules in glaucoma. This article reviews the early evidence suggesting that reactive oxygen species, immune inflammatory response mediators, and apoptogenic molecules are engaged in glaucoma disease. Moreover, further research concerning the functions, effectors and signaling pathways of the above molecules and their interactions, may lead to specifically develop targeted screening tools based on presumptive biomarkers and surrogate endpoints against primary open-angle glaucoma progression and blindness.

摘要

目前,人们对于氧化应激、炎症、细胞凋亡与原发性开角型青光眼发生和进展之间的相关性产生了浓厚的兴趣。在受到各种应激源的刺激后,眼睛内会产生大量的活性氧,这些活性氧在青光眼的发病机制中起着重要作用。免疫炎症反应介质最近成为眼科关注的焦点,包括青光眼。人们越来越关注特定的促凋亡和抗凋亡分子在青光眼发病机制中的作用。本文综述了早期的研究证据,表明活性氧、免疫炎症反应介质和促凋亡分子参与了青光眼疾病的发生。此外,对这些分子的功能、效应器和信号通路及其相互作用的进一步研究,可能会导致针对原发性开角型青光眼进展和失明的特定靶向筛查工具的开发,这些工具基于假设的生物标志物和替代终点。

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