Polkowski C A, Grassl S M
Department of Pharmacology, State University of New York, Syracuse, NY 13210.
Biochim Biophys Acta. 1993 Feb 23;1146(1):145-52. doi: 10.1016/0005-2736(93)90349-5.
Pathways for urate transport across the basolateral membrane of rat proximal tubule cells were investigated using membrane vesicles isolated from rat renal cortex. The presence of an anion exchange mechanism(s) operative in the mode of alpha-keto-glutarate/urate; Cl-/urate and OH-(HCO3-)/urate as well as a mediated conductive mechanism was assessed from tracer flux measurements. In the presence of an inwardly directed Na+ gradient an alpha-ketoglutarate dependent concentrative accumulation of PAH but not urate was observed suggesting an absence of the mediated exchange of alpha-ketoglutarate for urate. The imposition of an outwardly directed Cl- gradient stimulated urate uptake in the absence but not the presence of conditions designed to minimize membrane potential development suggesting an indirect electrostatic coupling of urate uptake to a Cl- gradient-induced diffusion potential. Conditions favoring the development of an inside-positive K+ diffusion potential was observed to induce an inhibitor-sensitive, concentrative accumulation of urate in the absence of Cl-. The stimulation of urate uptake measured in the presence of an inside-alkaline pH gradient was not of sufficient magnitude to suggest the apparent conductive urate uptake was secondary to a membrane voltage induced, inside alkaline pH gradient and the operation of an OH-(HCO3-)/urate exchanger. The evidence obtained from the present investigation suggests rat basolateral membrane urate transport occurs by a mediated, conductive mechanism and is not coupled to Cl-, alpha-ketoglutarate or HCO3-.(ABSTRACT TRUNCATED AT 250 WORDS)
利用从大鼠肾皮质分离的膜囊泡,研究了尿酸盐跨大鼠近端小管细胞基底外侧膜的转运途径。通过示踪剂通量测量评估了以α-酮戊二酸/尿酸盐、Cl⁻/尿酸盐和OH⁻(HCO₃⁻)/尿酸盐模式运行的阴离子交换机制以及介导的传导机制的存在情况。在存在内向性Na⁺梯度的情况下,观察到PAH有α-酮戊二酸依赖性的浓缩积累,但尿酸盐没有,这表明不存在α-酮戊二酸与尿酸盐的介导交换。施加外向性Cl⁻梯度在不存在旨在最小化膜电位发展的条件下刺激了尿酸盐摄取,但在存在这些条件时则没有,这表明尿酸盐摄取与Cl⁻梯度诱导的扩散电位存在间接静电耦合。在不存在Cl⁻的情况下,观察到有利于产生内向正性K⁺扩散电位的条件会诱导尿酸盐的抑制剂敏感性浓缩积累。在存在内向碱性pH梯度的情况下测量的尿酸盐摄取刺激程度不足以表明明显的传导性尿酸盐摄取是继发于膜电压诱导的内向碱性pH梯度以及OH⁻(HCO₃⁻)/尿酸盐交换器的运作。本研究获得的证据表明,大鼠基底外侧膜尿酸盐转运通过介导的传导机制发生,并且与Cl⁻、α-酮戊二酸或HCO₃⁻无关。(摘要截短于250字)