Melnik E, Latorre R, Hall J E, Tosteson D C
J Gen Physiol. 1977 Feb;69(2):243-57. doi: 10.1085/jgp.69.2.243.
Phloretin, the aglucone derivative of phlorizin, increases cation conductance and decreases anion conductance in lipid bilayer membranes. In this paper we present evidence that phloretin acts almost exclusively by altering the permeability of the membrane interior and not by modifying the partition of the permanent species between the membrane and the bulk aqueous phases. We base our conclusion on an analysis of the current responses to a senylborate, and the cation complex, peptide PV-K+. These results are consistent with the hypothesis that phloretin decreases the intrinsic positive internal membrane potential but does not modify to a great extent the potential energy minima at the membrane interfaces. Phloretin increases the conductance for the nonactin-K+ complex, but above 10(-5) M the steady-state nonactin-K+ voltage-current curve changes from superlinear to sublinear. These results imply that, above 10(-5) M phloretin, the nonactin-5+ transport across the membrane becomes interfacially limited.
根皮素是根皮苷的糖苷配基衍生物,它可增加脂质双分子层膜中的阳离子电导并降低阴离子电导。在本文中,我们提供证据表明,根皮素几乎完全通过改变膜内部的通透性起作用,而不是通过改变永久性物质在膜与本体水相之间的分配起作用。我们的结论基于对苯硼酸酯和阳离子复合物肽PV-K+的电流响应分析。这些结果与根皮素降低膜内固有正电位但在很大程度上不改变膜界面处势能最小值的假设一致。根皮素增加了缬氨霉素-K+复合物的电导,但在浓度高于10^(-5) M时,稳态缬氨霉素-K+电压-电流曲线从超线性变为亚线性。这些结果表明,在根皮素浓度高于10^(-5) M时,缬氨霉素-K+跨膜转运受到界面限制。