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白内障形成建模中的不同实验方法:大鼠亚硒酸盐诱导核性白内障概述

Different experimental approaches in modelling cataractogenesis: An overview of selenite-induced nuclear cataract in rats.

作者信息

Kyselova Zuzana

机构信息

Institute of Experimental Pharmacology & Toxicology, Slovak Academy of Sciences, SK-84104 Bratislava, Slovakia.

出版信息

Interdiscip Toxicol. 2010 Mar;3(1):3-14. doi: 10.2478/v10102-010-0005-3. Epub 2010 Mar 29.

Abstract

Cataract, the opacification of eye lens, is the leading cause of blindness worldwide. At present, the only remedy is surgical removal of the cataractous lens and substitution with a lens made of synthetic polymers. However, besides significant costs of operation and possible complications, an artificial lens just does not have the overall optical qualities of a normal one. Hence it remains a significant public health problem, and biochemical solutions or pharmacological interventions that will maintain the transparency of the lens are highly required. Naturally, there is a persistent demand for suitable biological models. The ocular lens would appear to be an ideal organ for maintaining culture conditions because of lacking blood vessels and nerves. The lens in vivo obtains its nutrients and eliminates waste products via diffusion with the surrounding fluids. Lens opacification observed in vivo can be mimicked in vitro by addition of the cataractogenic agent sodium selenite (Na(2)SeO(3)) to the culture medium. Moreover, since an overdose of sodium selenite induces also cataract in young rats, it became an extremely rapid and convenient model of nuclear cataract in vivo. The main focus of this review will be on selenium (Se) and its salt sodium selenite, their toxicological characteristics and safety data in relevance of modelling cataractogenesis, either under in vivo or in vitro conditions. The studies revealing the mechanisms of lens opacification induced by selenite are highlighted, the representatives from screening for potential anti-cataract agents are listed.

摘要

白内障,即眼球晶状体的浑浊,是全球失明的主要原因。目前,唯一的治疗方法是手术摘除白内障晶状体并用合成聚合物制成的晶状体进行替代。然而,除了手术成本高昂以及可能出现并发症外,人工晶状体并不具备正常晶状体的整体光学品质。因此,这仍然是一个重大的公共卫生问题,迫切需要能够维持晶状体透明度的生化解决方案或药物干预措施。自然而然地,对合适的生物学模型一直有需求。由于缺乏血管和神经,眼球晶状体似乎是维持培养条件的理想器官。晶状体在体内通过与周围液体的扩散获取营养并排出废物。在培养基中添加致白内障剂亚硒酸钠(Na₂SeO₃)可在体外模拟体内观察到的晶状体浑浊。此外,由于过量的亚硒酸钠也会在幼鼠中诱发白内障,它成为了一种极其快速且便捷的体内核性白内障模型。本综述的主要重点将是硒(Se)及其盐亚硒酸钠,它们在体内或体外模拟白内障形成过程中的毒理学特征和安全数据。重点介绍了揭示亚硒酸盐诱导晶状体浑浊机制的研究,并列出了筛选潜在抗白内障药物的代表。

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