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使用泛硫乙胺和WR-77913延缓或抑制大鼠晶状体混浊

Delay or inhibition of rat lens opacification using pantethine and WR-77913.

作者信息

Clark J I, Livesey J C, Steele J E

机构信息

Department of Biological Structure, University of Washington, Seattle 98195, USA.

出版信息

Exp Eye Res. 1996 Jan;62(1):75-84. doi: 10.1006/exer.1996.0009.

Abstract

Pantethine and the amino phosphorothioate, WR-77913, protected lenses against increased light scattering and opacification during cataract formation in five animal models: (1) radiation, (2) selenite, (3) galactose, (4) streptozotocin and (5) Royal College of Surgeons. In the radiation or selenite models, each test reagent was administered 15 to 30 min prior to initiation of cataract by a single injection of Na2SeO3 or a single exposure to 15 Gy (gray) gamma radiation. In the galactose, streptozotocin and Royal College of Surgeons models where the cataractogenic insult was continuous, repeated administrations of pantethine and WR-77913 were necessary. The results suggested that protein aggregation and lens opacification associated with a variety of physiological and biochemical mechanisms can be delayed or inhibited using a systemic administration of pantethine or WR-77913.

摘要

泛硫乙胺和氨基硫代磷酸酯WR-77913可在五种动物白内障形成模型中保护晶状体,防止其在白内障形成过程中出现光散射增加和浑浊:(1)辐射;(2)亚硒酸盐;(3)半乳糖;(4)链脲佐菌素;(5)皇家外科学院模型。在辐射或亚硒酸盐模型中,每种测试试剂在通过单次注射亚硒酸钠或单次暴露于15戈瑞(Gy)γ射线引发白内障前15至30分钟给药。在半乳糖、链脲佐菌素和皇家外科学院模型中,致白内障损伤是持续性的,因此需要重复给予泛硫乙胺和WR-77913。结果表明,通过全身给予泛硫乙胺或WR-77913,与多种生理和生化机制相关的蛋白质聚集和晶状体浑浊可被延迟或抑制。

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