Kim K R, Park Y S
Department of Physiology, Kosin Medical College, Pusan, Korea.
Toxicol Appl Pharmacol. 1995 Aug;133(2):244-8. doi: 10.1006/taap.1995.1148.
The effect of cadmium injection on the high-affinity phlorizin binding to renal outer cortical brush-border membranes was studied in rabbits. Animals received subcutaneous injections of CdCl2 at a dose of 3 mg Cd/kg.day for about 3 weeks. Brush-border membranes were isolated from renal outer cortex by Percoll gradient centrifugation and magnesium precipitation. Cadmium injection resulted in a marked increase in membrane cadmium content and decrease in Na(+)-dependent phlorizin binding. The latter effect was attributed to a reduction in the number of binding sites (N0) and not to changes in the dissociation constant (Kd). Similar results were observed in normal membrane vesicles directly exposed to cadmium in vitro. These results suggest that one mechanism of the cadmium-induced glycosuria is a loss of active Na(+)-glucose cotransport carrier in the proximal tubular brush-border membrane by direct interaction with free cadmium.
研究了给兔子注射镉对高亲和力根皮苷与肾外皮质刷状缘膜结合的影响。动物接受皮下注射氯化镉,剂量为3毫克镉/千克·天,持续约3周。通过Percoll梯度离心和镁沉淀从肾外皮质分离刷状缘膜。注射镉导致膜镉含量显著增加,且钠依赖性根皮苷结合减少。后一种效应归因于结合位点数量(N0)的减少,而非解离常数(Kd)的变化。在体外直接暴露于镉的正常膜囊泡中也观察到了类似结果。这些结果表明,镉诱导糖尿的一种机制是近端肾小管刷状缘膜中的活性钠-葡萄糖共转运载体通过与游离镉直接相互作用而丧失。