Shpun S, Evans K K, Dantzler W H
Department of Physiology, College of Medicine, University of Arizona, Tucson 85724, USA.
Am J Physiol. 1995 Jun;268(6 Pt 2):F1109-16. doi: 10.1152/ajprenal.1995.268.6.F1109.
To understand the basolateral p-aminohippurate (PAH) transporter in the S3 segment of rabbit proximal tubules and its relationship to the transporter in the S2 segment, we measured the 30-s uptake and efflux of PAH across the basolateral membrane of single isolated S3 segments at 37 degrees C in bicarbonate-buffered media. Kinetic analysis of uptake data revealed a concentration of PAH at one-half Jmax of approximately 107 microM (same as in the S2 segment) but a Jmax of 600 fmol.min-1.nl-1 (one-tenth that of S2 segment). The coefficient for efflux across the basolateral membrane was also only one-sixth to one-tenth of that in the S2 segment. These data suggest that the basolateral PAH transporter is the same in both segments but that there are fewer transporters in the S3 than in the S2 segment. However, the apparent inhibitor constant values for cis-inhibition by probenecid (approximately 29 microM in S3, approximately 15 microM in S2) and by alpha-ketoglutarate (alpha-KG) in the presence of LiCl (approximately 40 microM in S3, approximately 160 microM in S2) suggest that the transporters may not be identical in the two segments. In bicarbonate-buffered medium, preloading the tubules with 100 microM alpha-KG did not trans-stimulate PAH uptake across the basolateral membrane, whereas preloading with 1.0 microM alpha-KG caused a significant stimulation of 43%. However, in N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid-buffered medium, preloading the tubules with 100 microM alpha-KG caused a twofold increase in PAH uptake.(ABSTRACT TRUNCATED AT 250 WORDS)
为了解兔近端小管S3段基底外侧对氨基马尿酸(PAH)转运体及其与S2段转运体的关系,我们在37℃的碳酸氢盐缓冲介质中,测量了单个分离的S3段基底外侧膜对PAH的30秒摄取和流出情况。摄取数据的动力学分析显示,PAH浓度在Jmax的一半时约为107微摩尔(与S2段相同),但Jmax为600飞摩尔·分钟-1·纳升-1(为S2段的十分之一)。基底外侧膜的流出系数也仅为S2段的六分之一到十分之一。这些数据表明,两个段的基底外侧PAH转运体相同,但S3段的转运体比S2段少。然而,丙磺舒顺式抑制(S3段约为29微摩尔,S2段约为15微摩尔)和在LiCl存在下α-酮戊二酸(α-KG)的表观抑制常数(S3段约为40微摩尔,S2段约为160微摩尔)表明,两个段的转运体可能并不相同。在碳酸氢盐缓冲介质中,用100微摩尔α-KG预加载小管不会反式刺激PAH跨基底外侧膜的摄取,而用1.0微摩尔α-KG预加载则会导致43%的显著刺激。然而,在N-2-羟乙基哌嗪-N'-2-乙磺酸缓冲介质中,用100微摩尔α-KG预加载小管会使PAH摄取增加两倍。(摘要截短于250字)