Debnam E S, Thompson C S
Br J Pharmacol. 1984 Jul;82(3):673-7. doi: 10.1111/j.1476-5381.1984.tb10806.x.
The effects of neomycin sulphate on galactose absorption have been studied using in vivo and in vitro preparations of rat small intestine. Neomycin (10(-3)M) produced an increase in the maximum transport capacity (Jmax) for the active component of absorption in vivo. The apparent Kt for absorption was unaffected. The antibiotic caused a dose-dependent increase in the potential difference across the mucosal membrane (Vm) measured in vitro, a maximal effect being seen at a concentration of 10(-4)M. Furthermore, the magnitude of the depolarization induced by the addition of galactose (4 mM) to the mucosal fluid was enhanced by neomycin (10(-4)M). Phlorhizin (10(-4)M) abolished the galactose-induced depolarization in both the absence and presence of the antibiotic. It is concluded that neomycin increases the electrical driving force for Na+ during Na+-coupled galactose entry into the enterocyte.
已使用大鼠小肠的体内和体外制剂研究了硫酸新霉素对半乳糖吸收的影响。新霉素(10⁻³M)使体内吸收活性成分的最大转运能力(Jmax)增加。吸收的表观Kt未受影响。该抗生素导致体外测量的跨粘膜膜电位差(Vm)呈剂量依赖性增加,在10⁻⁴M浓度时观察到最大效应。此外,新霉素(10⁻⁴M)增强了向粘膜液中添加半乳糖(4 mM)所诱导的去极化幅度。无论有无抗生素,根皮苷(10⁻⁴M)都消除了半乳糖诱导的去极化。结论是新霉素在Na⁺偶联的半乳糖进入肠细胞过程中增加了Na⁺的电驱动力。