Groves C E, Evans K K, Dantzler W H, Wright S H
Department of Physiology, College of Medicine, University of Arizona, Tucson 85724.
Am J Physiol. 1994 Mar;266(3 Pt 2):F450-8. doi: 10.1152/ajprenal.1994.266.3.F450.
The physiological characteristics of peritubular organic cation transport were examined by measuring the transport of the organic cation tetraethylammonium (TEA) in rabbit renal proximal tubule suspensions and isolated nonperfused rabbit renal proximal tubules. Peritubular organic cation transport in both single S2 segments and suspensions of isolated renal proximal tubules was found to be a high-capacity, high-affinity, carrier-mediated process. For tubule suspensions, the maximal capacity of the carrier for TEA (Jmax) and the concentration of TEA at 1/2 Jmax (Kt) (1.49 +/- 0.21 nmol.min-1.mg dry wt-1 and 131 +/- 16 microM, respectively), did not differ significantly from those measured in single S2 segments (Jmax, 1.16 +/- 0.075 nmol.min-1.mg dry wt-1; Kt, 108 +/- 10 microM). In addition, the pattern of inhibition of peritubular TEA transport by long-chain n-tetraalkylammonium compounds (n = 1-5) was both qualitatively and quantitatively similar in single S2 segments and tubule suspensions, exhibiting an increase in inhibitory potency with increasing alkyl chain length. For example, in tubule suspensions, apparent Michaelis constants for inhibition of TEA uptake ranged from 1.3 mM for tetramethylammonium (TMA) to 0.8 microM for tetrapentylammonium (TPeA). To determine whether these compounds were substrates for the peritubular organic cation transporter, their effect on the efflux of [14C]TEA from tubule suspensions was examined. A concentration of 0.5 mM of the short-chain tetraalkyls TMA or TEA increased the efflux of [14C]TEA (i.e., trans-stimulated) from tubules in suspension. The longer-chain tetraalkyls tetrapropylammonium, tetrabutylammonium, and TPeA all decreased the efflux of [14C]TEA from tubules in suspension; TPeA completely blocked efflux.(ABSTRACT TRUNCATED AT 250 WORDS)
通过测量有机阳离子四乙铵(TEA)在兔肾近端小管悬浮液和分离的未灌注兔肾近端小管中的转运,研究了肾小管周围有机阳离子转运的生理特性。发现单个S2节段和分离的肾近端小管悬浮液中的肾小管周围有机阳离子转运是一个高容量、高亲和力、载体介导的过程。对于小管悬浮液,载体对TEA的最大转运能力(Jmax)和TEA浓度在1/2 Jmax时(Kt)(分别为1.49±0.21 nmol·min-1·mg干重-1和131±16 μM),与在单个S2节段中测得的值(Jmax,1.16±0.075 nmol·min-1·mg干重-1;Kt,108±10 μM)无显著差异。此外,长链正四烷基铵化合物(n = 1 - 5)对肾小管周围TEA转运的抑制模式在单个S2节段和小管悬浮液中在定性和定量上均相似,随着烷基链长度增加抑制效力增强。例如,在小管悬浮液中,抑制TEA摄取的表观米氏常数范围从四甲基铵(TMA)的1.3 mM到四戊基铵(TPeA)的0.8 μM。为了确定这些化合物是否是肾小管周围有机阳离子转运体的底物,研究了它们对[14C]TEA从小管悬浮液中流出的影响。0.5 mM浓度的短链四烷基铵TMA或TEA增加了[14C]TEA从小管悬浮液中的流出(即反式刺激)。较长链的四烷基铵四丙基铵、四丁基铵和TPeA均降低了[14C]TEA从小管悬浮液中的流出;TPeA完全阻断了流出。(摘要截短于250字)