Knorr B A, Beck J C, Abramson R G
Department of Medicine, Mount Sinai School of Medicine, New York, New York.
Kidney Int. 1994 Mar;45(3):727-36. doi: 10.1038/ki.1994.97.
The precise mechanism by which urate is transported across rabbit renal proximal tubule luminal membranes has not been defined. To determine whether urate flux across this membrane represents simple diffusion or transport on specific carriers, urate uptake was examined in brush border membrane vesicles that were prepared by a Mg+(+)-aggregation technique and then exposed to CuCl2. Na(+)-independent, voltage sensitive urate transport was demonstrated in these Cu+(+)-exposed vesicles. Transport was trans-stimulated by urate and cis inhibited by pyrazinoic acid and oxonate. A small fraction of transported urate and urate in the extravesicular fluid was oxidized to allantoin. Kinetic analysis revealed the presence of two kinetically distinct transporters; a channel-like carrier that was inhibited by pyrazinoic acid and oxonate, and a high-affinity, classical, saturable carrier that was inhibited by higher concentrations of oxonate. These studies provide the first direct evidence for carrier-mediated urate transport in rabbit renal brush-border membranes and demonstrate that the rabbit transporter(s) share a number of properties with the urate uniporter in rat proximal tubule cell membranes.
尿酸盐跨兔肾近端小管管腔膜转运的确切机制尚未明确。为了确定尿酸盐跨此膜的通量是代表简单扩散还是通过特定载体转运,在通过Mg²⁺聚集技术制备并随后暴露于CuCl₂的刷状缘膜囊泡中检测尿酸盐摄取。在这些暴露于Cu²⁺的囊泡中证实了不依赖Na⁺、电压敏感的尿酸盐转运。转运受尿酸盐反式刺激,受吡嗪酸和氧嗪酸顺式抑制。一小部分转运的尿酸盐和囊泡外液中的尿酸盐被氧化为尿囊素。动力学分析显示存在两种动力学上不同的转运体;一种受吡嗪酸和氧嗪酸抑制的通道样载体,以及一种受较高浓度氧嗪酸抑制的高亲和力、经典、可饱和载体。这些研究为兔肾刷状缘膜中载体介导的尿酸盐转运提供了首个直接证据,并证明兔转运体与大鼠近端小管细胞膜中的尿酸盐单向转运体具有许多共同特性。