Literature DB >> 1887903

Basolateral tetraethylammonium transport in intact tubules: specificity and trans-stimulation.

W H Dantzler1, S H Wright, V Chatsudthipong, O H Brokl.   

Abstract

To examine the specificity of proximal renal basolateral organic cation transport, the effects of unlabeled organic cation substrates in the bathing medium on the rate of uptake [14C]tetraethylammonium ([14C]TEA) by intact nonperfused proximal tubules and isolated basolateral membrane vesicles (BLMV) from rabbit kidneys were explored. The pattern of inhibition of transport by a battery of unlabeled organic cations was similar in intact tubules and BLMV. To determine if trans-stimulation could be demonstrated across the basolateral membrane of intact tubules, the effects of preloading tubules with unlabeled substrates on the rate of uptake of [14C]TEA and the effects of unlabeled substrates in the bathing medium on the rate of efflux of [14C]TEA from tubules preloaded with this labeled substrate were examined. Trans-stimulation was clearly demonstrated for the first time in intact tubules. However, of the compounds that significantly inhibited [14C]TEA uptake (TEA, amiloride, tetrapropylammonium, mepiperphenidol, isopropyl pyridinium, and choline), only TEA itself and choline produced a trans-stimulation of [14C]TEA uptake. Moreover, choline appeared to be at least as effective as TEA itself as a counter ion for TEA transport. Such trans-stimulation could play a physiological role in the net reabsorption of choline and the net secretion of most other organic cations.

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Year:  1991        PMID: 1887903     DOI: 10.1152/ajprenal.1991.261.3.F386

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  7 in total

1.  Twelve transmembrane helices form the functional core of mammalian MATE1 (multidrug and toxin extruder 1) protein.

Authors:  Xiaohong Zhang; Xiao He; Joseph Baker; Florence Tama; Geoffrey Chang; Stephen H Wright
Journal:  J Biol Chem       Date:  2012-06-21       Impact factor: 5.157

2.  Kinetic analysis of tetraethylammonium transport in the kidney epithelial cell line, LLC-PK1.

Authors:  Y Tomita; Y Otsuki; Y Hashimoto; K Inui
Journal:  Pharm Res       Date:  1997-09       Impact factor: 4.200

3.  Distinct characteristics of organic cation transporters, OCT1 and OCT2, in the basolateral membrane of renal tubules.

Authors:  Y Urakami; M Okuda; S Masuda; M Akazawa; H Saito; K Inui
Journal:  Pharm Res       Date:  2001-11       Impact factor: 4.200

4.  Precision-cut dog renal cortical slices in dynamic organ culture for the study of cisplatin nephrotoxicity.

Authors:  H J Toutain; J P Sarsat; A Bouant; D Hoet; D Leroy; V Moronvalle-Halley
Journal:  Cell Biol Toxicol       Date:  1996-12       Impact factor: 6.691

5.  pH-dependent transport of procainamide in cultured renal epithelial monolayers of OK cells: consistent with nonionic diffusion.

Authors:  A J Dudley; C D Brown
Journal:  Br J Pharmacol       Date:  1995-09       Impact factor: 8.739

6.  Luminal transport system for H+/organic cations in the rat proximal tubule. Kinetics, dependence on pH; specificity as compared with the contraluminal organic cation-transport system.

Authors:  C David; G Rumrich; K J Ullrich
Journal:  Pflugers Arch       Date:  1995-08       Impact factor: 3.657

Review 7.  Molecular and cellular physiology of organic cation transporter 2.

Authors:  Stephen H Wright
Journal:  Am J Physiol Renal Physiol       Date:  2019-11-04
  7 in total

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