Literature DB >> 155742

Transport of organic ions in renal cortical luminal and antiluminal membrane vesicles.

J L Kinsella, P D Holohan, N I Pessah, C R Ross.   

Abstract

Based upon saturability, kinetic analysis and specific inhibition, specific transport for the organic anion, p-aminohippurate was found in isolated luminal and antiluminal membrane vesicles from dog kidney cortex. The transport for organic anions in the two membranes differed from one another on the basis of kinetic parameters ((Km, Vmax and Ki for probenecid) and counterflow phenomenon (only the antiluminal membrane displayed the capacity to accelerate the exchange of p-aminohippurate). Also described is specific transport for the organic cation N1 methylnicotinamide in each membrane. The luminal and antiluminal transport of N1-methylnicotinamide are distinguished from one another by kinetic parameters (Km, Vmax and Ki for Darstine) and counterflow data (counterflow of N1-methylnicotinamide was observed only in the luminal membrane). The results are discussed in view of a proposed model to explain transepithelial transport of these organic ions.

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Year:  1979        PMID: 155742

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


  26 in total

Review 1.  Saturable pharmacokinetics in the renal excretion of drugs.

Authors:  C A van Ginneken; F G Russel
Journal:  Clin Pharmacokinet       Date:  1989-01       Impact factor: 6.447

Review 2.  Drug interactions at the renal level. Implications for drug development.

Authors:  P L Bonate; K Reith; S Weir
Journal:  Clin Pharmacokinet       Date:  1998-05       Impact factor: 6.447

Review 3.  Renal transport of drugs: an overview of methodology with application to cimetidine.

Authors:  K M Giacomini; P H Hsyu; L G Gisclon
Journal:  Pharm Res       Date:  1988-08       Impact factor: 4.200

4.  A physiological function for multidrug-resistant membrane glycoproteins: a hypothesis regarding the renal organic cation-secretory system.

Authors:  J A Nelson
Journal:  Cancer Chemother Pharmacol       Date:  1988       Impact factor: 3.333

5.  Simultaneous kinetic modelling of plasma levels and urinary excretion of salicyluric acid, and the influence of probenecid.

Authors:  P Hekman; C A van Ginneken
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1983 Jul-Sep       Impact factor: 2.441

6.  Contraluminal para-aminohippurate (PAH) transport in the proximal tubule of the rat kidney. I. Kinetics, influence of cations, anions, and capillary preperfusion.

Authors:  K J Ullrich; G Rumrich; G Fritzsch; S Klöss
Journal:  Pflugers Arch       Date:  1987-07       Impact factor: 3.657

7.  p-Aminohippurate/2-oxoglutarate exchange in bovine renal brush-border and basolateral membrane vesicles.

Authors:  C Schmitt; G Burckhardt
Journal:  Pflugers Arch       Date:  1993-05       Impact factor: 3.657

8.  Correlation between renal membrane binding and nephrotoxicity of aminoglycosides.

Authors:  P D Williams; D B Bennett; C R Gleason; G H Hottendorf
Journal:  Antimicrob Agents Chemother       Date:  1987-04       Impact factor: 5.191

9.  Uptake of 3H-catecholamines by rat liver cells occurs mainly through a system which is distinct from uptake1 or uptake2.

Authors:  F Martel; I Azevedo; W Osswald
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1994-08       Impact factor: 3.000

10.  Effects of cysteine derivatives of styrene on the transport of p-aminohippurate ion in renal plasma membrane vesicles.

Authors:  S Chakrabarti; D D Vu; M G Côté
Journal:  Arch Toxicol       Date:  1991       Impact factor: 5.153

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