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在白内障形成早期抑制晶状体混浊。

Inhibition of lens opacification during the early stages of cataract formation.

作者信息

Hiraoka T, Clark J I

机构信息

Department of Biological Structure, University of Washington School of Medicine, Seattle 98195-7420, USA.

出版信息

Invest Ophthalmol Vis Sci. 1995 Nov;36(12):2550-5.

PMID:7591646
Abstract

PURPOSE

To characterize the time period during cataract formation in which administration of pantethine inhibits lens cell opacification in the selenite model for cataract.

METHODS

Pantethine was administered to neonatal rat pups at selected time points from -0.5 to 17 hours with respect to injection of selenite at time = 0. The injection dose of pantethine was 820 mg/kg (1.5 mmol/kg) diluted in water at 410 mg/ml concentration. The injection dose of selenite was 3.28 mg/kg (19 mumol/kg) diluted in saline at 1.8 mg/ml concentration. Opacification was observed using a slit lamp microscope at selected time points over a 14-day period. Cataracts were staged using a classification of opacity from 0 (normal) to 6 (mature).

RESULTS

The effect of pantethine was characterized by three different time periods: administration -0.5 to 6 hours with respect to selenite injection provided highly significant protection, P < 0.001; administration 8 hours after selenite provided significant protection, P < 0.005; administration 10 to 17 hours after selenite was not protective.

CONCLUSIONS

The metabolite pantethine inhibited lens opacification during cataract formation in the selenite model. Even when pantethine was injected several hours after the administration of selenite, opacification was inhibited. Advanced stages of opacification were unresponsive to the administration of pantethine. The inhibitory effect of pantethine was statistically significant when administered during the earliest stage of opacification in the selenite model for cataract.

摘要

目的

确定在亚硒酸盐诱导的白内障模型中,泛硫乙胺给药抑制晶状体细胞浑浊形成的时间段。

方法

在亚硒酸盐注射时间(时间=0)的-0.5至17小时的选定时间点,对新生大鼠幼崽给予泛硫乙胺。泛硫乙胺的注射剂量为820mg/kg(1.5mmol/kg),以410mg/ml的浓度用水稀释。亚硒酸盐的注射剂量为3.28mg/kg(19μmol/kg),以1.8mg/ml的浓度用盐水稀释。在14天的时间段内,于选定时间点使用裂隙灯显微镜观察浑浊情况。白内障分期采用从0(正常)到6(成熟)的浑浊分类。

结果

泛硫乙胺的作用表现为三个不同时间段:相对于亚硒酸盐注射,在给药后-0.5至6小时给予泛硫乙胺提供了高度显著的保护作用,P<0.001;在亚硒酸盐注射后8小时给药提供了显著的保护作用,P<0.005;在亚硒酸盐注射后10至17小时给药没有保护作用。

结论

在亚硒酸盐模型中,代谢产物泛硫乙胺在白内障形成过程中抑制晶状体浑浊。即使在给予亚硒酸盐数小时后注射泛硫乙胺,浑浊仍被抑制。浑浊的晚期阶段对泛硫乙胺给药无反应。在亚硒酸盐诱导的白内障模型中,在浑浊形成的最早阶段给予泛硫乙胺,其抑制作用具有统计学意义。

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