Yorek M A, Dunlap J A, Leeney E M
Veterans Administration Medical Center, Iowa City, IA 52240.
Diabetes. 1989 Aug;38(8):996-1004. doi: 10.2337/diab.38.8.996.
Neuroblastoma cells were used to analyze the effect of galactose supplementation on myo-inositol metabolism, polyol accumulation, and Na+-K+ pump activity. Culturing cells in 30 mM galactose for a minimum of 1 wk led to a large accumulation of intracellular galactitol and a greater than 50% decrease in myo-inositol content. The effect of galactose on the intracellular content of galactitol and myo-inositol was concentration dependent. Extracellular myo-inositol accumulation and incorporation into phospholipid decreased by 20-30% in cells grown in 30 mM galactose. The decrease in myo-inositol accumulation is apparently due to a noncompetitive inhibition of high-affinity myo-inositol uptake. Treatment of the galactose-containing media with 0.4 mM sorbinil partially prevented the galactose-mediated decreases in myo-inositol metabolism and content. The galactitol content of the sorbinil-treated cells was significantly reduced compared with the galactitol levels in cells cultured in 30 mM galactose; however, galactitol levels remained significantly elevated over control cells. Exposing neuroblastoma cells to 30 mM galactose causes a decrease in the levels of phosphatidylinositol that is partially restored by the addition of sorbinil. The activity of the Na+-K+ pump was decreased by 20% in cells cultured in 30 mM galactose and was partially protected by sorbinil treatment. The effects of long-term galactose supplementation on myo-inositol metabolism, polyol accumulation, and Na+-K+-ATPase transport activity in cultured neuroblastoma cells are similar to the effects of high concentrations of glucose. These results provide additional evidence that the accumulation of polyol by neuroblastoma cells is partially responsible for alterations in myo-inositol metabolism and decreases in Na+-K+-ATPase transport activity.
神经母细胞瘤细胞被用于分析补充半乳糖对肌醇代谢、多元醇积累和钠钾泵活性的影响。将细胞在30 mM半乳糖中培养至少1周会导致细胞内半乳糖醇大量积累,肌醇含量降低超过50%。半乳糖对细胞内半乳糖醇和肌醇含量的影响呈浓度依赖性。在30 mM半乳糖中生长的细胞,细胞外肌醇积累及掺入磷脂的量减少了20 - 30%。肌醇积累的减少显然是由于高亲和力肌醇摄取受到非竞争性抑制。用0.4 mM索比尼尔处理含半乳糖的培养基可部分防止半乳糖介导的肌醇代谢和含量降低。与在30 mM半乳糖中培养的细胞相比,经索比尼尔处理的细胞中半乳糖醇含量显著降低;然而,与对照细胞相比,半乳糖醇水平仍显著升高。将神经母细胞瘤细胞暴露于30 mM半乳糖会导致磷脂酰肌醇水平降低,添加索比尼尔可部分恢复该水平。在30 mM半乳糖中培养的细胞,钠钾泵活性降低了20%,索比尼尔处理可部分保护该活性。长期补充半乳糖对培养的神经母细胞瘤细胞中肌醇代谢、多元醇积累和钠钾ATP酶转运活性的影响与高浓度葡萄糖的影响相似。这些结果提供了额外的证据,表明神经母细胞瘤细胞中多元醇的积累部分导致了肌醇代谢的改变和钠钾ATP酶转运活性的降低。