Yorek M A, Dunlap J A, Ginsberg B H
Veterans Administration Medical Center, Department of Internal Medicine, Iowa City, IA 52240.
J Neurochem. 1988 Aug;51(2):605-10. doi: 10.1111/j.1471-4159.1988.tb01081.x.
Neuroblastoma cells were used to analyze the effect of elevated glucose levels on myo-inositol metabolism and Na+/K+-pump activity. The activity of the Na+/K+ pump in neuroblastoma cells is almost totally sensitive to ouabain inhibition. Culturing neuroblastoma cells in 30 mM glucose caused a significant decrease in Na+/K+-pump activity, myo-inositol metabolism, and myo-inositol content, compared to cells grown in the presence of 30 mM fructose. Glucose supplementation also caused a large intracellular accumulation of sorbitol. The aldose reductase inhibitor sorbinil prevented the abnormalities in myo-inositol metabolism and partially restored Na+/K+-pump activity in neuroblastoma cells cultured in the presence of elevated glucose levels. These results suggest that the accumulation of sorbitol by neuroblastoma cells exposed to elevated concentrations of extracellular glucose causes a decrease in myo-inositol metabolism and these abnormalities are associated with a reduction in Na+/K+-pump activity.
神经母细胞瘤细胞被用于分析葡萄糖水平升高对肌醇代谢和钠钾泵活性的影响。神经母细胞瘤细胞中钠钾泵的活性几乎完全对哇巴因抑制敏感。与在30 mM果糖存在下生长的细胞相比,在30 mM葡萄糖中培养神经母细胞瘤细胞会导致钠钾泵活性、肌醇代谢和肌醇含量显著降低。补充葡萄糖还会导致细胞内山梨醇大量积累。醛糖还原酶抑制剂索比尼尔可预防肌醇代谢异常,并部分恢复在高葡萄糖水平下培养的神经母细胞瘤细胞中的钠钾泵活性。这些结果表明,暴露于细胞外葡萄糖浓度升高的神经母细胞瘤细胞中积累的山梨醇会导致肌醇代谢降低,并且这些异常与钠钾泵活性降低有关。