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首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Adverse effects of excessive nitric oxide on cytochrome c oxidase in lenses of hereditary cataract UPL rats.
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Adverse effects of excessive nitric oxide on cytochrome c oxidase in lenses of hereditary cataract UPL rats.

机译:一氧化氮过多对遗传性白内障UPL大鼠晶状体中细胞色素c氧化酶的不利影响。

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The UPL rat is a newly developed hereditary cataract model. We previously found that the ATP content in UPL rat lenses decreases during cataract development, and the decrease in ATP content causes Ca(2+)-ATPase dysfunction resulting in an elevation in Ca(2+) and cataract development. In addition, we reported that the oral administration of disulfiram and aminoguanidine ameliorates the decrease in ATP content and the elevation in Ca(2+) content in UPL rat lenses. In this study, we demonstrate the effect of nitric oxide (NO) on the expression and activity of cytochrome c oxidase (CCO) in normal and UPL rat lenses during cataract development. We also determined the effects of the oral administration of disulfiram and aminoguanidine on the mRNA expression and activity of CCO and NO production in UPL rat lenses. The expression of CCO-1 mRNA in UPL rat lenses, determined by a quantitative real-time RT-PCR method, decreased during cataract development. CCO activity in UPL rat lenses also decreased with aging.On the other hand, the oral administration of disulfiram and aminoguanidine attenuated the decrease in CCO-1 mRNA expression and CCO activity. These results suggest that excessive NO causes the decrease in CCO-1 mRNA expression and CCO activity, and that the decrease in CCO may cause the decrease in ATP production in UPL rat lenses. Disulfiram and aminoguanidine may attenuate the decrease in ATP production, resulting in a delay in cataract development.
机译:UPL大鼠是一种新近开发的遗传性白内障模型。我们先前发现,UPL大鼠晶状体中的ATP含量在白内障发展过程中降低,而ATP含量的下降导致Ca(2 +)-ATPase功能障碍,导致Ca(2+)和白内障发展。此外,我们报道口服双硫仑和氨基胍改善了UPL大鼠晶状体中ATP含量的降低和Ca(2+)含量的升高。在这项研究中,我们证明了一氧化氮(NO)对白内障发展过程中正常和UPL大鼠晶状体中细胞色素c氧化酶(CCO)的表达和活性的影响。我们还确定了口服双硫仑和氨基胍对UPL大鼠晶状体mRNA表达,CCO活性和NO产生的影响。通过定量实时RT-PCR方法确定的UPL大鼠晶状体中CCO-1 mRNA的表达在白内障发展过程中下降。 UPL大鼠晶状体的CCO活性也随着年龄的增长而降低;另一方面,口服双硫仑和氨基胍可减轻CCO-1 mRNA表达和CCO活性的下降。这些结果表明,过量的NO会导致UPL大鼠晶状体中CCO-1 mRNA表达和CCO活性下降,而CCO的下降可能会导致ATP产生的下降。双硫仑和氨基胍可能会减弱ATP产生的减少,从而导致白内障发展延迟。

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