Literature DB >> 3688235

Transport of tetraethylammonium by rabbit renal brush-border and basolateral membrane vesicles.

S H Wright1, T M Wunz.   

Abstract

Brush-border and basolateral membrane vesicles (BBMV and BLMV, respectively) from rabbit renal cortex were used to study transport of the organic cation, tetraethylammonium (TEA). Outwardly directed proton gradients stimulated uptake of TEA into BBMV and supported concentrative accumulation. Furthermore, an inwardly directed H+ gradient accelerated TEA efflux from BBMV. These data suggest that TEA transport in BBMV involved exchange with H+. The Jmax and Kt for TEA transport into BBMV under pH equilibrium conditions (pH 7.5) were 2.1 nmol.mg-1.min-1 and 0.15 mM, respectively. Under pH gradient conditions (6.0in:7.5out), Jmax increased by 270% with no effect on Kt. Uptake of TEA into BBMV was stimulated by an inside-positive electrical potential difference (PD), although exchange of TEA for H+ appeared to be one for one. In BLMV, H+ gradients had little effect on TEA uptake and were incapable of supporting concentrative transport. The Jmax and Kt for TEA transport in BLMV were 0.33 nmol.mg-1.min-1 and 0.37 mM, respectively. Inside-negative PDs stimulated this uptake, suggesting that it involved an electrically conductive pathway. TEA transport in BBMV and BLMV was inhibited by amiloride and cimetidine, although p-aminohippuric acid was without effect. Thus, secretion of TEA involves carrier-mediated transport steps at both the luminal and peritubular membranes, although an active step is not evident in isolated BLMV.

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Year:  1987        PMID: 3688235     DOI: 10.1152/ajprenal.1987.253.5.F1040

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


  18 in total

1.  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

2.  A choline transporter in renal brush-border membrane vesicles: energetics and structural specificity.

Authors:  S H Wright; T M Wunz; T P Wunz
Journal:  J Membr Biol       Date:  1992-02       Impact factor: 1.843

3.  Transport of small organic cations in the rat liver. The role of the organic cation transporter OCT1.

Authors:  F Martel; T Vetter; H Russ; D Gründemann; I Azevedo; H Koepsell; E Schömig
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1996 Aug-Sep       Impact factor: 3.000

4.  Molecular cloning, functional characterization and tissue distribution of rat H+/organic cation antiporter MATE1.

Authors:  Tomohiro Terada; Satohiro Masuda; Jun-Ichi Asaka; Masahiro Tsuda; Toshiya Katsura; Ken-ichi Inui
Journal:  Pharm Res       Date:  2006-08       Impact factor: 4.200

5.  MATE1 has an external COOH terminus, consistent with a 13-helix topology.

Authors:  Xiaohong Zhang; Stephen H Wright
Journal:  Am J Physiol Renal Physiol       Date:  2009-06-10

6.  Tetraethylammonium transport by snake renal brush-border membrane vesicles.

Authors:  W H Dantzler; S H Wright; O H Brokl
Journal:  Pflugers Arch       Date:  1991-05       Impact factor: 3.657

7.  Expression of renal organic cation transporter in Xenopus laevis oocytes.

Authors:  R Hori; M Hirai; T Katsura; M Takano; M Yasuhara; S Kaneko; M Satoh
Journal:  Biochem J       Date:  1992-04-15       Impact factor: 3.857

8.  Membrane transporters in drug disposition.

Authors:  K M Giacomini
Journal:  J Pharmacokinet Biopharm       Date:  1997-12

9.  Structure and interaction of inhibitors with the TEA/H+ exchanger of rabbit renal brush border membranes.

Authors:  S H Wright; T M Wunz; T P Wunz
Journal:  Pflugers Arch       Date:  1995-01       Impact factor: 3.657

10.  Stereoselective interactions of organic cations with the organic cation transporter in OK cells.

Authors:  R J Ott; K M Giacomini
Journal:  Pharm Res       Date:  1993-08       Impact factor: 4.200

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