Literature DB >> 3217235

Contraluminal para-aminohippurate (PAH) transport in the proximal tubule of the rat kidney. IV. Specificity: mono- and polysubstituted benzene analogs.

K J Ullrich1, G Rumrich, S Klöss.   

Abstract

In order to study the specificities of the contraluminal anion transport systems, the inhibitory potency of substituted benzene analogs on influx of [3H]PAH, [14C]succinate, and [35S]sulfate from the interstitium into cortical tubular cells has been determined in situ: (1) Contraluminal [3H]PAH influx is moderately inhibited by benzene-carboxylate and benzene-sulfonate, and strongly by benzene-dicarboxylates, -disulfonates and carboxy-benzene-sulfonates, if the substituents are located at positions 1 and 3 or 1 and 4. The affinity of the PAH transporter to polysubstituted benzoates increases with increasing hydrophobicity, decreasing electron density at the carboxyl group and decreasing pKa. Similar dependencies are observed for phenols. Benzaldehydes which do not carry an ionic negative charge are accepted by the PAH-transporter, if they possess a second partially charged aldehyde or NO2-group. (2) Contraluminal [14C]succinate influx is inhibited by benzene 1,3- or 1,4-dicarboxylates, -disulfonates and 1,3- or 1,4-carboxybenzene-sulfonates. Monosubstituted benzoates do not interact with the dicarboxylate transporter, but NO2-polysubstituted benzoates do. Phenol itself and 2-substituted phenol interact weakly possibly due to oligomer formation. (3) The contraluminal sulfate transporter interacts only with compounds which show a negative group accumulation such as 3,5-dinitro- or 3,5-dichloro-substituted salicylates. The data are consistent with three separate anion transport systems in the contraluminal membrane: The PAH transporter interacts with hydrophobic molecules carrying one or two negative charges (-COO-, -SO3-) or two or more than two partial negative charges (-OH, -CHO, -SO2NH2, -NO2). The dicarboxylate transporter requires two electronegative ionic charges (-COO-, -SO3-) at 5-9 A distance or one ionic and several partial charges (-Cl, -NO2) at a favourable distance. The sulfate transporter interacts with molecules which have neighbouring electronegative charge accumulation.

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Year:  1988        PMID: 3217235     DOI: 10.1007/bf00582523

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  15 in total

1.  Anion transport through the contraluminal cell membrane of renal proximal tubule. The influence of hydrophobicity and molecular charge distribution on the inhibitory activity of organic anions.

Authors:  G Fritzsch; G Rumrich; K J Ullrich
Journal:  Biochim Biophys Acta       Date:  1989-01-30

2.  "Aromatic" substituent constants for structure-activity correlations.

Authors:  C Hansch; A Leo; S H Unger; K H Kim; D Nikaitani; E J Lien
Journal:  J Med Chem       Date:  1973-11       Impact factor: 7.446

3.  Sulphate-ion/sodium-ion co-transport by brush-border membrane vesicles isolated from rat kidney cortex.

Authors:  H Lücke; G Stange; H Murer
Journal:  Biochem J       Date:  1979-07-15       Impact factor: 3.857

4.  Contraluminal transport systems in the proximal renal tubule involved in secretion of organic anions.

Authors:  K J Ullrich; G Rumrich
Journal:  Am J Physiol       Date:  1988-04

5.  Contraluminal sulfate transport in the proximal tubule of the rat kidney. V. Specificity: phenolphthaleins, sulfonphthaleins, and other sulfo dyes, sulfamoyl-compounds and diphenylamine-2-carboxylates.

Authors:  K J Ullrich; G Rumrich; S Klöss; H J Lang
Journal:  Pflugers Arch       Date:  1985-08       Impact factor: 3.657

6.  Contraluminal sulfate transport in the proximal tubule of the rat kidney. III. Specificity: disulfonates, di- and tri-carboxylates and sulfocarboxylates.

Authors:  K J Ullrich; G Rumrich; S Klöss
Journal:  Pflugers Arch       Date:  1985-08       Impact factor: 3.657

7.  Specificity of the transport system for tricarboxylic acid cycle intermediates in renal brush borders.

Authors:  S H Wright; I Kippen; J R Klinenberg; E M Wright
Journal:  J Membr Biol       Date:  1980-11-15       Impact factor: 1.843

8.  A stopped flow capillary perfusion method to evaluate contraluminal transport parameters of methylsuccinate from interstitium into renal proximal tubular cells.

Authors:  G Fritzsch; W Haase; G Rumrich; H Fasold; K J Ullrich
Journal:  Pflugers Arch       Date:  1984-03       Impact factor: 3.657

9.  Contraluminal para-aminohippurate (PAH) transport in the proximal tubule of the rat kidney. II. Specificity: aliphatic dicarboxylic acids.

Authors:  K J Ullrich; G Rumrich; G Fritzsch; S Klöss
Journal:  Pflugers Arch       Date:  1987-01       Impact factor: 3.657

10.  Indirect coupling to Na+ of p-aminohippuric acid uptake into rat renal basolateral membrane vesicles.

Authors:  H Shimada; B Moewes; G Burckhardt
Journal:  Am J Physiol       Date:  1987-11
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  11 in total

1.  Effect of substituted benzoates on p-aminohippurate transport in dog renal membrane vesicles.

Authors:  F G Russel; M Heijn; R C de Laet; C A van Ginneken
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1991-01       Impact factor: 3.000

2.  Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members.

Authors:  Gregory Kaler; David M Truong; Akash Khandelwal; Megha Nagle; Satish A Eraly; Peter W Swaan; Sanjay K Nigam
Journal:  J Biol Chem       Date:  2007-06-05       Impact factor: 5.157

Review 3.  Renal transport mechanisms for xenobiotics: chemicals and drugs.

Authors:  K J Ullrich; G Rumrich
Journal:  Clin Investig       Date:  1993-10

4.  Bisubstrates: substances that interact with both, renal contraluminal organic anion and organic cation transport systems. II. Zwitterionic substrates: dipeptides, cephalosporins, quinolone-carboxylate gyrase inhibitors and phosphamide thiazine carboxylates; nonionizable substrates: steroid hormones and cyclophosphamides.

Authors:  K J Ullrich; G Rumrich; C David; G Fritzsch
Journal:  Pflugers Arch       Date:  1993-11       Impact factor: 3.657

5.  Bisubstrates: substances that interact with renal contraluminal organic anion and organic cation transport systems. I. Amines, piperidines, piperazines, azepines, pyridines, quinolines, imidazoles, thiazoles, guanidines and hydrazines.

Authors:  K J Ullrich; G Rumrich; C David; G Fritzsch
Journal:  Pflugers Arch       Date:  1993-11       Impact factor: 3.657

6.  Renal contraluminal transport systems for organic anions (paraaminohippurate, PAH) and organic cations (N1-methyl-nicotinamide, NMeN) do not see the degree of substrate ionization.

Authors:  K J Ullrich; G Rumrich
Journal:  Pflugers Arch       Date:  1992-06       Impact factor: 3.657

7.  Contraluminal p-aminohippurate transport in the proximal tubule of the rat kidney. VII. Specificity: cyclic nucleotides, eicosanoids.

Authors:  K J Ullrich; G Rumrich; F Papavassiliou; S Klöss; G Fritzsch
Journal:  Pflugers Arch       Date:  1991-05       Impact factor: 3.657

8.  Effect of substituted benzoylglycines (hippurates) and phenylacetylglycines on p-aminohippurate transport in dog renal membrane vesicles.

Authors:  F G Russel; W G Vermeulen
Journal:  Pharm Res       Date:  1994-12       Impact factor: 4.200

9.  Contraluminal transport of organic cations in the proximal tubule of the rat kidney. II. Specificity: anilines, phenylalkylamines (catecholamines), heterocyclic compounds (pyridines, quinolines, acridines).

Authors:  K J Ullrich; G Rumrich; K Neiteler; G Fritzsch
Journal:  Pflugers Arch       Date:  1992-01       Impact factor: 3.657

10.  Contraluminal p-aminohippurate transport in the proximal tubule of the rat kidney. VIII. Transport of corticosteroids.

Authors:  K J Ullrich; G Rumrich; F Papavassiliou; K Hierholzer
Journal:  Pflugers Arch       Date:  1991-05       Impact factor: 3.657

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