Isogai S, Mogami K, Shiina N, Yoshino G
Second Department of Internal Medicine, Toho University School of Medicine, Tokyo, Japan.
Nephron. 1999 Sep;83(1):53-8. doi: 10.1159/000045473.
BACKGROUND/AIM: The present study was conducted to elucidate the mechanism(s) of the development of early diabetic nephropathy, examining ultrastructural changes employing electron microscopy, especially changes in pore size of the glomerular basement membrane (GBM) of streptozotocin (STZ)-induced diabetics rats.
Urinary albumin excretion rate (UAE), pore size of the lamina densa of the GBM visualized directly by the tissue negative staining method, and number of anionic sites (AS) in the corresponding portion of the lamina rara externa were determined for 6 weeks in diabetic rats without and with insulin treatment.
The UAE of the diabetic rats increased with time and was significantly greater than that of the nondiabetic control rats after 4 weeks (p < 0.01), while insulin treatment suppressed the increased UAE of diabetic rats. The median values in both short diameter and long dimension of the pores in the diabetic group were markedly increased at the 2nd week as compared with those in the nondiabetic control rats, whereas no significant change was found in the pore size of the diabetic rats with insulin treatment. Moreover, the number of AS in the GBM of the diabetic rats was significantly (p < 0.001) decreased from the 2nd week onward. Insulin treatment also prevented a decrease in AS number in diabetic rats.
It is suggested from these results that an impairment of barrier size selectivity occurs at a very early stage of STZ-induced diabetes in rats, which may enhance the abnormality of the charge-selective properties of the GBM. In addition, insulin treatment may protect this barrier system through normalizing blood glucose control in STZ-diabetic rats.
背景/目的:本研究旨在阐明早期糖尿病肾病的发病机制,采用电子显微镜检查超微结构变化,尤其是链脲佐菌素(STZ)诱导的糖尿病大鼠肾小球基底膜(GBM)孔径的变化。
在未接受胰岛素治疗和接受胰岛素治疗的糖尿病大鼠中,测定6周内的尿白蛋白排泄率(UAE)、通过组织负染法直接观察到的GBM致密层孔径以及相应的肾小球外疏松层中阴离子位点(AS)的数量。
糖尿病大鼠的UAE随时间增加,4周后显著高于非糖尿病对照大鼠(p<0.01),而胰岛素治疗可抑制糖尿病大鼠UAE的升高。与非糖尿病对照大鼠相比,糖尿病组在第2周时孔隙短径和长径的中位数均显著增加,而接受胰岛素治疗的糖尿病大鼠的孔径未发现显著变化。此外,糖尿病大鼠GBM中的AS数量从第2周起显著减少(p<0.001)。胰岛素治疗也可防止糖尿病大鼠AS数量的减少。
从这些结果可以看出,在STZ诱导的大鼠糖尿病的极早期就出现了屏障大小选择性的损害,这可能会增强GBM电荷选择性特性的异常。此外,胰岛素治疗可能通过使STZ糖尿病大鼠的血糖控制正常化来保护这种屏障系统。