Levine S, Franki N, Hays R M
J Clin Invest. 1973 Aug;52(8):2083-6. doi: 10.1172/JCI107393.
The permeability of the toad bladder to a series of isotopically labeled nonelectrolytes was determined in the presence of 150 mM unlabeled acetamide. Under these conditions, overall bladder function was unimpaired, as shown by a normal response to vasopressin of short-circuit current and permeability coefficient of [(3)H]water,[(14)C]ethanol, and [(14)C]propionamide. The permeability of the bladder to isotopic acetamide and urea, however, was significantly depressed by unlabeled acetamide, in both the absence and presence of vasopressin. These experiments indicate a competition between unlabeled and isotopic species for binding sites, and show the existence of a saturable, vasopressin-sensitive carrier for urea and acetamide in the epithelial cell membrane.
在含有150 mM未标记乙酰胺的情况下,测定了蟾蜍膀胱对一系列同位素标记的非电解质的通透性。在这些条件下,膀胱的整体功能未受损害,这表现为对血管加压素的正常反应,即短路电流以及[³H]水、[¹⁴C]乙醇和[¹⁴C]丙酰胺的通透系数正常。然而,无论有无血管加压素,未标记的乙酰胺都会显著降低膀胱对同位素乙酰胺和尿素的通透性。这些实验表明未标记和同位素物质之间存在对结合位点的竞争,并表明上皮细胞膜中存在一种可饱和的、对血管加压素敏感的尿素和乙酰胺载体。