Literature DB >> 1750557

Comparative insights into the mechanisms of renal organic anion and cation secretion.

J B Pritchard1, D S Miller.   

Abstract

Comparative models have played a major role in defining the mechanisms that enable vertebrate proximal tubules to transport organic anions and cations from the peritubular interstitium to the urine. The unique advantages of these models and their contributions to our understanding of organic anion and cation transport mechanisms are summarized here. Recent studies of the organic anion transport system suggest that transport is coupled to metabolic energy via indirect coupling to the sodium gradient. Organic anions enter the cell across the basolateral membrane in exchange for alpha-ketoglutarate (alpha-KG), and the alpha-KG is returned to the interior via Na-alpha-KG cotransport. Indirect coupling to Na has been demonstrated in both isolated membranes and intact renal epithelial cells of species ranging from marine crustaceans to mammals. This mechanism was shown to drive not only cellular accumulation but also secretory transepithelial fluxes of organic anions. Luminal exit of secreted organic anions appears to be carrier mediated but is, at present, poorly understood, with mediated potential-driven efflux and anion exchange-driven efflux implicated in some species. As for organic anions, the renal clearance of some organic cations approaches the renal plasma flow. Although there is considerable variation in the handling of specific substrates between species, the basic properties of organic cation transport include carrier-mediated potential-driven uptake at the basolateral membrane, intracellular sequestration that reduces the free concentration of the cation, and luminal exit by organic cation-proton exchange. Reabsorptive transport is also observed for some organic cations, but its mechanisms and driving forces are not well understood.

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Year:  1991        PMID: 1750557     DOI: 10.1152/ajpregu.1991.261.6.R1329

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


  8 in total

Review 1.  Relationships between the renal handling of DMPS and DMSA and the renal handling of mercury.

Authors:  Rudolfs K Zalups; Christy C Bridges
Journal:  Chem Res Toxicol       Date:  2012-06-15       Impact factor: 3.739

2.  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

Review 3.  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

4.  Epithelial transport of anthelmintic ivermectin in a novel model of isolated proximal kidney tubules.

Authors:  G Fricker; H Gutmann; A Droulle; J Drewe; D S Miller
Journal:  Pharm Res       Date:  1999-10       Impact factor: 4.200

5.  P-glycoprotein- and mrp2-mediated octreotide transport in renal proximal tubule.

Authors:  H Gutmann; D S Miller; A Droulle; J Drewe; A Fahr; G Fricker
Journal:  Br J Pharmacol       Date:  2000-01       Impact factor: 8.739

Review 6.  Aquatic toxicology: past, present, and prospects.

Authors:  J B Pritchard
Journal:  Environ Health Perspect       Date:  1993-04       Impact factor: 9.031

Review 7.  Introduction of Organic Anion Transporters (SLC22A) and a Regulatory Mechanism by Caveolins.

Authors:  Woon Kyu Lee; Sun-Mi Jung; Jin-Oh Kwak; Seok Ho Cha
Journal:  Electrolyte Blood Press       Date:  2006-03

8.  Effect of t-butylhydroperoxide on p-aminohippurat uptake in rabbit renal cortical slices.

Authors:  S S Choi; K D Huh; J S Woo; Y K Kim
Journal:  Korean J Intern Med       Date:  1994-07       Impact factor: 2.884

  8 in total

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