Literature DB >> 6450281

Mechanisms of organic cation transport in kidney plasma membrane vesicles: 1. Countertransport studies.

P D Holohan, C R Ross.   

Abstract

Transport for organic cations has been described in both luminal and antiluminal membranes. The two transport systems difer from one another on the basis of kinetic parameters and countertransport. By using N1-[3H]methylnicotinamide as the indication cation, a series of organic cations (which were known to be secreted) were tested for their capacity to stimulate countertransport. The phenomenon of countertransport was symmetrical in that it was observed for both influx and efflux in both membranes. However, under appropriate conditions, certain organic cations were effective in producing "uphill" transport of N1-[3H]methylnicotinamide in the luminal membrane and the effect was limited to that membrane exclusively. Detailed analysis of countertransport in the luminal membrane showed quantitative differences in the maximal stimulation produced by the various cations: giving rise to the relationship that the concentration of organic cation which gave one-half maximal N1-[3H]methylnicotinamide countertransport approximated its affinity constant. The data were interpreted to suggest that all the members of the organic cation series tested are translocated across the luminal membrane by the same carrier but that they are moved at different rates.

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Year:  1980        PMID: 6450281

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  14 in total

1.  Assessment of Substrate-Dependent Ligand Interactions at the Organic Cation Transporter OCT2 Using Six Model Substrates.

Authors:  Philip J Sandoval; Kimberley M Zorn; Alex M Clark; Sean Ekins; Stephen H Wright
Journal:  Mol Pharmacol       Date:  2018-06-08       Impact factor: 4.436

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.  Competitive inhibition of p-aminohippurate transport by quinapril in rabbit renal basolateral membrane vesicles.

Authors:  W Akarawut; D E Smith
Journal:  J Pharmacokinet Biopharm       Date:  1998-06

4.  Molecular determinants of ligand selectivity for the human multidrug and toxin extruder proteins MATE1 and MATE2-K.

Authors:  Bethzaida Astorga; Sean Ekins; Mark Morales; Stephen H Wright
Journal:  J Pharmacol Exp Ther       Date:  2012-03-14       Impact factor: 4.030

5.  Characterization of guanidine transport in human renal brush border membranes.

Authors:  J K Chun; L Zhang; M Piquette-Miller; E Lau; L Q Tong; K M Giacomini
Journal:  Pharm Res       Date:  1997-07       Impact factor: 4.200

6.  Characteristics of tetraethylammonium transport in rabbit renal plasma-membrane vesicles.

Authors:  J S Jung; Y K Kim; S H Lee
Journal:  Biochem J       Date:  1989-04-15       Impact factor: 3.857

7.  Novobiocin is a potent inhibitor for human organic anion transporters.

Authors:  Peng Duan; Guofeng You
Journal:  Drug Metab Dispos       Date:  2009-03-12       Impact factor: 3.922

8.  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

9.  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

10.  Contraluminal transport of organic cations in the proximal tubule of the rat kidney. I. Kinetics of N1-methylnicotinamide and tetraethylammonium, influence of K+, HCO3-, pH; inhibition by aliphatic primary, secondary and tertiary amines and mono- and bisquaternary compounds.

Authors:  K J Ullrich; F Papavassiliou; C David; G Rumrich; G Fritzsch
Journal:  Pflugers Arch       Date:  1991-08       Impact factor: 3.657

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