Kuck J F, Kuck K D
Department of Ophthalmology, Emory University, Atlanta, Georgia.
J Ocul Pharmacol. 1988 Fall;4(3):243-51. doi: 10.1089/jop.1988.4.243.
The Emory mouse develops a late-onset hereditary cataract bearing some resemblances to human senile cataract. It was used as a model system for testing the effects of several drugs expected to have anticataractogenic potential. A low level of added dietary alpha-tocopherol had only a marginal effect. Penicillamine increased lens soluble protein, a good index of lens viability. Triethylenetetramine was too toxic to permit satisfactory treatment. Mercaptopropionylglycine produced several positive effects including a retardation of cataract at 6 months of age; parameters which increased under drug treatment were lens weight, soluble protein content and protein sulfhydryl, but not glutathione. There was no effect on the total calcium concentration.
埃默里小鼠会患上一种迟发性遗传性白内障,与人类老年性白内障有一些相似之处。它被用作一个模型系统,以测试几种有望具有抗白内障潜力的药物的效果。低水平添加到饮食中的α-生育酚只有轻微的效果。青霉胺增加了晶状体可溶性蛋白,这是晶状体活力的一个良好指标。三亚乙基四胺毒性太大,无法进行令人满意的治疗。巯基丙酰甘氨酸产生了几个积极效果,包括在6个月大时延缓白内障的发生;在药物治疗下增加的参数有晶状体重量、可溶性蛋白含量和蛋白质巯基,但不包括谷胱甘肽。对总钙浓度没有影响。