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大鼠糖尿病发病过程中视网膜和大脑氧化还原状态的变化。

Changes in the redox state in the retina and brain during the onset of diabetes in rats.

作者信息

Salceda R, Vilchis C, Coffe V, Hernández-Muñoz R

机构信息

Departamento de Neurociencias, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, D.F.

出版信息

Neurochem Res. 1998 Jun;23(6):893-7. doi: 10.1023/a:1022467230259.

Abstract

Diabetic retinopathy is thought to result from chronic changes in the metabolic pathways of the retina. Hyperglycemia leads to increased intracellular glucose concentrations, alterations in glucose degradation and an increase in lactate/pyruvate ratio. We measured lactate content in retina and other ocular and non-ocular tissues from normal and diabetic rats in the early stages of streptozotocin-induced diabetes. The intracellular redox state was calculated from the cytoplasmic [lactate]/[pyruvate] ratio. Elevated lactate concentration were found in retina and cerebral cortex from diabetic rats. These concentrations led to a significant and progressive decrease in the NAD+/NADH ratio, suggesting that altered glucose metabolism is an initial step of retinopathy. It is thus possible that tissues such as cerebral cortex have mechanisms that prevent the damaging effect of lactate produced by hyperglycemia and/or alterations of the intracellular redox state.

摘要

糖尿病视网膜病变被认为是由视网膜代谢途径的慢性变化引起的。高血糖导致细胞内葡萄糖浓度升高、葡萄糖降解改变以及乳酸/丙酮酸比值增加。我们测量了链脲佐菌素诱导糖尿病早期正常和糖尿病大鼠视网膜及其他眼部和非眼部组织中的乳酸含量。细胞内氧化还原状态由细胞质中[乳酸]/[丙酮酸]比值计算得出。在糖尿病大鼠的视网膜和大脑皮层中发现乳酸浓度升高。这些浓度导致NAD+/NADH比值显著且逐渐降低,表明葡萄糖代谢改变是视网膜病变的初始步骤。因此,大脑皮层等组织可能具有防止高血糖产生的乳酸和/或细胞内氧化还原状态改变所造成损害作用的机制。

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