Hopfer U
Proc Natl Acad Sci U S A. 1975 Jun;72(6):2027-31. doi: 10.1073/pnas.72.6.2027.
Isolated, small intestinal microvillous membranes from normal and acutely diabetic rats were compared with respect to D-glucose transport. D-Glucose was accumulated to a greater extent by diabetic membrane vesicles when supplied with energy in the form of a NaC1 or a NaSCN gradient across the vesicle membrane. The difference appeared to be caused by an ability of the diabetic membranes to maintain a higher driving force for active D-glucose transport and not by changes in the glucose "carrier." Increasing the glucose-independent Na-+-conductance of the membrane with monactin or gramicidin D reduced the active accumulation of D-glucose by membrane preparations from both control and diabetic groups. Concentrations of monactin and gramicidin D in the incubation medium of membrane vesicles from diabetic animals could be adjusted so that their D-glucose transport became indistinguishable from that of membranes from normal animals not treated with ionophores. These observatins suggest the microvillous membranes as one site where changes occur in acute diabetes. In addition, the change in the transport properties of the isolated membranes offer a rational explanation for the simultaneous elevation of active intestinal sugar, amino acid, and bile salt transport observed for intact intestinal tissue.
对正常大鼠和急性糖尿病大鼠分离出的小肠微绒毛膜的D-葡萄糖转运进行了比较。当以跨囊泡膜的NaCl或NaSCN梯度形式提供能量时,糖尿病膜囊泡积累D-葡萄糖的程度更高。这种差异似乎是由糖尿病膜维持更高的D-葡萄糖主动转运驱动力的能力引起的,而不是由葡萄糖“载体”的变化引起的。用莫能菌素或短杆菌肽D增加膜的非葡萄糖依赖性Na⁺电导,会降低对照组和糖尿病组膜制剂对D-葡萄糖的主动积累。可以调节糖尿病动物膜囊泡孵育培养基中莫能菌素和短杆菌肽D的浓度,使它们的D-葡萄糖转运与未用离子载体处理的正常动物的膜转运没有区别。这些观察结果表明,微绒毛膜是急性糖尿病中发生变化的一个部位。此外,分离膜转运特性的变化为完整肠道组织中观察到的主动肠糖、氨基酸和胆盐转运同时升高提供了合理的解释。