Husted R F, Steinmetz P R
J Clin Invest. 1982 Oct;70(4):832-4. doi: 10.1172/jci110679.
Transepithelial K(+) movement was studied in vitro in the short-circuited turtle bladder by increasing luminal K(+) permeability and by inhibiting the basolateral Na/K pump. Luminal addition of amphotericin B caused net K(+) secretion (180+/-52 nmol/h) compared with net K(+) absorption (42+/-6 nmol/h) in control bladders. Serosal ouabain and luminal amiloride abolished K(+) secretion in amphotericin-treated bladders; ouabain restored net absorption (45+/-16 nmol/h). The direction and rate of net K(+) transport are controlled by the relative K(+) permeabilities and the Na/K pump sites at the two cell membranes of the epithelium.
通过增加管腔钾离子通透性和抑制基底外侧钠钾泵,在体外对短路龟膀胱的跨上皮钾离子转运进行了研究。与对照膀胱中的钾离子净吸收(42±6 nmol/h)相比,管腔添加两性霉素B导致钾离子净分泌(180±52 nmol/h)。在两性霉素处理的膀胱中,浆膜侧哇巴因和管腔侧阿米洛利消除了钾离子分泌;哇巴因恢复了净吸收(45±16 nmol/h)。上皮细胞两层细胞膜处的相对钾离子通透性和钠钾泵位点控制着钾离子净转运的方向和速率。