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Effects of neomycin on galactose absorption across rat jejunum.

机译:新霉素对大鼠空肠半乳糖吸收的影响。

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摘要

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.
机译:已经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(-3)M)增加了体内吸收活性成分的最大转运量(Jmax)。吸收的表观Kt不受影响。抗生素在体外测得的跨粘膜(Vm)的电位差引起剂量依赖性的增加,在10(-4)M的浓度下效果最大。此外,新霉素(10(-4)M)增强了向粘膜液中添加半乳糖(4 mM)诱导的去极化强度。在不存在和存在抗生素的情况下,Phlohizin(10(-4)M)都消除了半乳糖诱导的去极化作用。结论是,新霉素增加了Na +耦合的半乳糖进入肠细胞的过程中Na +的电驱动力。

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