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组织中毒性缺氧状态下兔角膜的吡啶核苷酸:化学分析、无创荧光测定法及生理相关性

Pyridine nucleotides of rabbit cornea with histotoxic anoxia: chemical analysis, non-invasive fluorometry and physiological correlates.

作者信息

Masters B R, Riley M V, Fischbarg J, Chance B

出版信息

Exp Eye Res. 1983 Jul;37(1):1-9. doi: 10.1016/0014-4835(83)90144-6.

Abstract

The pyridine nucleotides from both the epithelium and the endothelium of rabbit cornea were measured by the cycling assay. Sodium azide (10 mM) applied for 1 hr to induce histotoxic anoxia decreased the endothelial NAD+/NADH ratio from 4.62 to 1.49 and decreased the epithelial NAD+/NADH ratio from 2.56 to 1.08. The larger NAD+/NADH ratio for the endothelium as compared to the epithelium corresponds to a more oxidized state. The corresponding ratios for NADP+/NADPH were 1.2 for the endothelium and 0.70 for the epithelium. Sodium azide had no effect on the NADP+/NADPH ratio for the endothelium, but decreased the epithelial ratio to 0.62. Pyridine nucleotide fluorescence was measured with a difference corneal fluorometer on the perfused whole cornea preparation and the perfused everted corneal preparation. Sodium azide (10 mM) for 30 min resulted in a 19.4 +/- 0.7% increase in the pyridine nucleotide fluorescence from the whole corneal preparation and a 4.5 +/- 0.6% increase from the everted endothelial preparation. Corneal anoxia induced by stopping the perfusion on the endothelial side resulted in a 18.7 +/- 0.6% increase in pyridine nucleotide fluorescence for the whole corneal preparation. Sodium azide (10 mM) resulted in a 35% decrease in the transendothelial potential difference and a 76% decrease in the rate of transendothelial fluid transport. A comparison is made between invasive chemical analysis and real time, non-invasive fluorometry to measure histotoxic corneal anoxia.

摘要

采用循环分析法测定了兔角膜上皮和内皮中的吡啶核苷酸。施加10 mM叠氮化钠1小时以诱导组织中毒性缺氧,使内皮细胞的NAD⁺/NADH比值从4.62降至1.49,上皮细胞的NAD⁺/NADH比值从2.56降至1.08。与上皮细胞相比,内皮细胞的NAD⁺/NADH比值更大,这对应于更氧化的状态。内皮细胞和上皮细胞的NADP⁺/NADPH相应比值分别为1.2和0.70。叠氮化钠对内皮细胞的NADP⁺/NADPH比值没有影响,但使上皮细胞的该比值降至0.62。使用差分角膜荧光计在灌注的全角膜标本和灌注的外翻角膜标本上测量吡啶核苷酸荧光。10 mM叠氮化钠作用30分钟后,全角膜标本的吡啶核苷酸荧光增加了19.4±0.7%,外翻内皮标本的荧光增加了4.5±0.6%。通过停止内皮侧灌注诱导的角膜缺氧使全角膜标本的吡啶核苷酸荧光增加了18.7±0.6%。10 mM叠氮化钠使跨内皮电位差降低了35%,跨内皮液体运输速率降低了76%。对用于测量组织中毒性角膜缺氧的侵入性化学分析和实时非侵入性荧光测定法进行了比较。

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