el-Seifi S, Freiberg J M, Kinsella J, Cheng L, Sacktor B
Am J Physiol. 1987 Jan;252(1 Pt 2):R40-7. doi: 10.1152/ajpregu.1987.252.1.R40.
The streptozotocin-induced diabetic rat was used to test the hypothesis that Na+-H+ exchange activity in the proximal tubule luminal membrane would be increased in association with renal hypertrophy, altered glomerular hemodynamics, enhanced filtered load and tubular reabsorption of Na+, and stimulated Na+ pump activity in the basolateral membrane, previously reported characteristics of this experimental animal model. Amiloride-sensitive H+ gradient-dependent Na+ uptake and Na+ gradient-dependent H+ flux were increased in brush-border membrane vesicles from the streptozotocin-treated animals. Na+ gradient-dependent uptakes of phosphate, D-glucose, L-proline, and myoinositol were decreased in the drug-induced diabetic animals. These membrane transport alterations were not found when the streptozotocin-diabetic animals were treated with insulin.
近端小管管腔膜中的Na⁺-H⁺交换活性会随着肾肥大、肾小球血流动力学改变、滤过负荷增加以及Na⁺的肾小管重吸收增强而增加,并且基底外侧膜中的Na⁺泵活性会受到刺激,这些都是此前报道的该实验动物模型的特征。在经链脲佐菌素处理的动物的刷状缘膜囊泡中,氨氯地平敏感的H⁺梯度依赖性Na⁺摄取和Na⁺梯度依赖性H⁺通量增加。在药物诱导的糖尿病动物中,磷酸盐、D-葡萄糖、L-脯氨酸和肌醇的Na⁺梯度依赖性摄取减少。当链脲佐菌素诱导的糖尿病动物接受胰岛素治疗时,未发现这些膜转运改变。