Schäli C, Roch-Ramel F
Am J Physiol. 1980 Sep;239(3):F222-7. doi: 10.1152/ajprenal.1980.239.3.F222.
Segments of rabbit proximal tubules (S1, S2, and S3) were incubated (30 min, 37 degrees C, pH 7.4) in Ringer solution (under O2) containing [14C]urate or [3H]PAH and probenecid, pyrazinoic acid (PZA), urate, or PAH, all at 1 mM. The ratio [14C]urate (counts/min per nanoliter of tubular cell water)/(counts/min per nanoliter of incubation medium) (T/M) reached 2.92 +/- 0.31 (mean +/- SE; n = 15), 6.08 +/- 0.42 (n = 42), and 1.72 +/- 0.31 (n = 14) for S1, S2, and S3 segments, respectively. In these segments the uptake of [3H]PAH was 22.7 +/- 4.6 (n = 19), 133 +/- 18.9 (n = 24), and 66.2 +/- 15.3 (n =0). The accumulation of [14C]urate was saturated at 2 x 10(-4) M in the medium, and that of [3H]PAH at 7 x 10(-5) M in the medium. Secretory transport was saturated at the same bath PAH concentration in perfused tubules. Urate and PAH transports inhibited each other, thus suggesting a common transport mechanism mainly located in the S2 segment. Probenecid was a strong and PZA a weak inhibitor of this transport system.
将兔近端肾小管节段(S1、S2和S3)在含有[14C]尿酸盐或[3H]对氨基马尿酸(PAH)以及丙磺舒、吡嗪酸(PZA)、尿酸盐或PAH的林格溶液(在O2条件下)中孵育(30分钟,37℃,pH 7.4),所有物质浓度均为1 mM。S1、S2和S3节段的[14C]尿酸盐比率(每纳升肾小管细胞水的计数/分钟)/(每纳升孵育培养基的计数/分钟)(T/M)分别达到2.92±0.31(平均值±标准误;n = 15)、6.08±0.42(n = 42)和1.72±0.31(n = 14)。在这些节段中,[3H]PAH的摄取量分别为22.7±4.6(n = 19)、133±18.9(n = 24)和66.2±15.3(n = 0)。培养基中[14C]尿酸盐的积累在2×10−4 M时达到饱和,[3H]PAH在7×10−5 M时达到饱和。在灌注的肾小管中,分泌转运在相同的浴中PAH浓度下达到饱和。尿酸盐和PAH转运相互抑制,因此提示主要位于S2节段的共同转运机制。丙磺舒是该转运系统的强抑制剂,吡嗪酸是弱抑制剂。