Pritchard J B, Miller D S
Comparative Membrane Pharmacology Section, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709.
Am J Physiol. 1991 Dec;261(6 Pt 2):R1329-40. doi: 10.1152/ajpregu.1991.261.6.R1329.
Comparative models have played a major role in defining the mechanisms that enable vertebrate proximal tubules to transport organic anions and cations from the peritubular interstitium to the urine. The unique advantages of these models and their contributions to our understanding of organic anion and cation transport mechanisms are summarized here. Recent studies of the organic anion transport system suggest that transport is coupled to metabolic energy via indirect coupling to the sodium gradient. Organic anions enter the cell across the basolateral membrane in exchange for alpha-ketoglutarate (alpha-KG), and the alpha-KG is returned to the interior via Na-alpha-KG cotransport. Indirect coupling to Na has been demonstrated in both isolated membranes and intact renal epithelial cells of species ranging from marine crustaceans to mammals. This mechanism was shown to drive not only cellular accumulation but also secretory transepithelial fluxes of organic anions. Luminal exit of secreted organic anions appears to be carrier mediated but is, at present, poorly understood, with mediated potential-driven efflux and anion exchange-driven efflux implicated in some species. As for organic anions, the renal clearance of some organic cations approaches the renal plasma flow. Although there is considerable variation in the handling of specific substrates between species, the basic properties of organic cation transport include carrier-mediated potential-driven uptake at the basolateral membrane, intracellular sequestration that reduces the free concentration of the cation, and luminal exit by organic cation-proton exchange. Reabsorptive transport is also observed for some organic cations, but its mechanisms and driving forces are not well understood.
比较模型在确定脊椎动物近端小管将有机阴离子和阳离子从肾小管周围间质转运到尿液的机制方面发挥了重要作用。本文总结了这些模型的独特优势及其对我们理解有机阴离子和阳离子转运机制的贡献。最近对有机阴离子转运系统的研究表明,转运通过与钠梯度的间接偶联与代谢能量相偶联。有机阴离子通过与α-酮戊二酸(α-KG)交换穿过基底外侧膜进入细胞,然后α-KG通过Na-α-KG共转运返回细胞内部。从海洋甲壳类动物到哺乳动物等物种的分离膜和完整肾上皮细胞中均已证实与钠的间接偶联。该机制不仅驱动细胞内积累,还驱动有机阴离子的分泌性跨上皮通量。分泌的有机阴离子的管腔排出似乎是载体介导的,但目前了解甚少,在某些物种中涉及介导的电位驱动流出和阴离子交换驱动流出。至于有机阴离子,一些有机阳离子的肾清除率接近肾血浆流量。尽管不同物种对特定底物的处理存在很大差异,但有机阳离子转运的基本特性包括在基底外侧膜上由载体介导的电位驱动摄取、降低阳离子游离浓度的细胞内隔离以及通过有机阳离子-质子交换的管腔排出。一些有机阳离子也存在重吸收转运,但其机制和驱动力尚不清楚。