• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[晶状体老化与白内障(作者译)]

[Aging of the lens and cataract (author's transl)].

作者信息

Hockwin O, Koch H R, Ohrloff C, Bours J

出版信息

Klin Monbl Augenheilkd. 1976 Aug;169(2):165-81.

PMID:979041
Abstract

Lens opacities in old patients are usually classified as "senile cataracts". Since there are very distinct morphologic types of opacities it is evident that we have to deal with different types of triggers in discussing the cataractogenesis. A great variety of risk factors might act as triggers for the development of opacities in aged people, and there is no doubt that among them age changes of lens metabolism are the most important. These age induced changes of lens metabolism do not only influence the energy level of lens metabolism (energy concept of lens transparency), the trigger may as well be located within the protein synthesizing system or the processes responsible for maintaining normal protein conformation, further, an exogenous intoxication may also occur. Lack of normal human lenses of all ages suited for metabolic research and an undefined classification for instance, coloration of the cataractous lens) makes biochemical research with respect to the pathogenesis of senile cataracts almost impossible. Animal models (naphthalene cataract, tryptophane-deficiency, X-irradiation) suited for the purpose may well support the basic research of this subject, even if we have to assume certain species differences of lens metabolism.

摘要

老年患者的晶状体混浊通常被归类为“老年性白内障”。由于存在非常明显的混浊形态类型,显然在讨论白内障的发生机制时我们必须应对不同类型的触发因素。多种风险因素可能作为老年人晶状体混浊发展的触发因素,毫无疑问,其中晶状体代谢的年龄变化是最重要的。这些年龄引起的晶状体代谢变化不仅会影响晶状体代谢的能量水平(晶状体透明度的能量概念),触发因素也可能位于蛋白质合成系统内或负责维持正常蛋白质构象的过程中,此外,还可能发生外源性中毒。缺乏适合进行代谢研究的各年龄段正常人类晶状体以及未明确的分类(例如,白内障晶状体的着色)使得关于老年性白内障发病机制的生化研究几乎无法进行。适合该目的的动物模型(萘性白内障、色氨酸缺乏、X射线照射)即使我们必须假定晶状体代谢存在某些物种差异,也可能很好地支持该主题的基础研究。

相似文献

1
[Aging of the lens and cataract (author's transl)].[晶状体老化与白内障(作者译)]
Klin Monbl Augenheilkd. 1976 Aug;169(2):165-81.
2
[What possibilities exist to modify cataract development on the basis of current biochemical knowledge? Where can drugs act?].基于当前的生化知识,改变白内障发展的可能性有哪些?药物作用于何处?
Klin Monbl Augenheilkd. 1985 Jun;186(6):455-61. doi: 10.1055/s-2008-1050959.
3
[Anything new concerning the human lens and senile cataract (author's transl)].关于人晶状体与老年性白内障的新进展(作者译)
J Fr Ophtalmol. 1981;4(5):359-73.
4
Protein oxidation and lens opacity in humans.人类中的蛋白质氧化与晶状体混浊
Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2461-5.
5
[X-ray-induced cataract as a model for investigating cataractogenesis (author's transl)].[X射线诱导的白内障作为研究白内障发生机制的模型(作者译)]
Klin Monbl Augenheilkd. 1982 Jan;180(1):13-6. doi: 10.1055/s-2008-1055003.
6
The Emory mouse cataract: increased accumulation of calcium during cataractogenesis.埃默里小鼠白内障:白内障形成过程中钙积累增加。
Lens Eye Toxic Res. 1989;6(4):853-62.
7
Characterization of water-insoluble proteins in normal and cataractous human lens.正常和白内障人晶状体中不溶性蛋白质的特性分析
Jpn J Ophthalmol. 1990;34(2):216-24.
8
Methylglyoxal-derived modifications in lens aging and cataract formation.甲基乙二醛衍生修饰在晶状体老化和白内障形成中的作用
Invest Ophthalmol Vis Sci. 1998 Nov;39(12):2355-64.
9
Cortical cataract development--an expression of primary damage to the lens epithelium.皮质性白内障的发展——晶状体上皮原发性损伤的一种表现。
Lens Eye Toxic Res. 1989;6(4):559-71.
10
Transition metal-catalyzed oxidation of ascorbate in human cataract extracts: possible role of advanced glycation end products.过渡金属催化人白内障提取物中抗坏血酸的氧化:晚期糖基化终产物的可能作用。
Invest Ophthalmol Vis Sci. 2000 May;41(6):1473-81.