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中野小鼠的遗传性白内障。

Hereditary cataract of the Nakano mouse.

作者信息

Takehana M

机构信息

Department of Biophysical Chemistry, Faculty of Pharmaceutical Sciences, Meijo University, Nagoya, Japan.

出版信息

Exp Eye Res. 1990 Jun;50(6):671-6. doi: 10.1016/0014-4835(90)90112-8.

Abstract

The Nakano mouse is a hereditary cataract model whose most characteristic change is a deficiency in lens Na+,K(+)-ATPase. Consequently, there is a change in lenticular sodium and potassium ion levels just before cataract formation. The amounts of calcium ion also change suddenly in the lens, with accumulated levels higher than any other type of cataract. Other biochemical changes coincide with the development of lens opacity, including decreases in the levels of reduced glutathione, ATP, biosynthetic activity of proteoglycans in epithelial cells, and the permeability of gap junction channels in fiber cells. The decrease in the activity of Na+,K(+)-ATPase results in changes in a number of key metabolic parameters, resulting in the eventual opacification of the Nakano mouse lens at approximately 30 days of age.

摘要

中野小鼠是一种遗传性白内障模型,其最典型的变化是晶状体钠钾ATP酶缺乏。因此,在白内障形成前,晶状体中的钠和钾离子水平会发生变化。晶状体中的钙离子含量也会突然改变,其累积水平高于其他任何类型的白内障。其他生化变化与晶状体混浊的发展同时发生,包括还原型谷胱甘肽、ATP水平的降低,上皮细胞中蛋白聚糖生物合成活性的降低,以及纤维细胞中缝隙连接通道通透性的降低。钠钾ATP酶活性的降低导致许多关键代谢参数的变化,最终导致中野小鼠晶状体在大约30日龄时发生混浊。

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