Literature DB >> 3009455

Phosphonocarboxylic acids as specific inhibitors of Na+-dependent transport of phosphate across renal brush border membrane.

M Szczepanska-Konkel, A N Yusufi, M VanScoy, S K Webster, T P Dousa.   

Abstract

We investigated interactions of phosphonoformic acid (PFA), phosphonoacetic acid (PAA), and other phosphonyl derivatives with the Na+ gradient [Na+ extravesicular greater than Na+ intravesicular; Nao+ greater than Na+i]-dependent transport system for phosphate (Pi) in renal cortical brush border membrane vesicles (BBMV). PFA and PAA inhibited in a dose-dependent manner the Na+ gradient [Na+o greater than Na+i]-dependent uptake of Pi by rat kidney BBMV. PFA was a more potent inhibitor than PAA while phosphonopropionic acid, hydroxymethylphosphonic acid, and phenylphosphonic acid had no effect on Pi transport. The inhibitory effect of PFA was competitive (Ki approximately equal to 4.6 X 10(-4) M) and reversible upon dilution. The uptake of Pi by BBMV in the absence of Na+ gradient [Nao+ = Na+i] was also inhibited by PFA. The PFA had no effect on uptake of L-[3H]proline, D-[3H]glucose, or 22Na+ by BBMV nor did it alter intravesicular volume of BBMV. The relative (%) extent of inhibition by PFA was not altered by changes in the extravesicular pH or changes in the steepness of the Na+ gradient [Nao+ greater than Na+i]. The inhibition of PFA was analogous in renal BBMV from rats, mice, rabbits, or dogs. Unlike other known inhibitors of brush border membrane (BBM) transport of Pi, e.g. arsenate, NAD, and ethane-1-hydroxy-1,1-diphosphonate, PFA and PAA had no inhibitory effect on BBM-bound or solubilized alkaline phosphatase. Also, PFA did not interfere with the activity of renal cortical (Na-K)ATPase. Administration of PFA (0.5 g/kg/day, intraperitoneally) to thyroparathyroidectomized rats fed a low Pi diet elicited an increase in urinary excretion of Pi, but did not change the excretion of Na+, K, and Ca2+. The results show that the PFA, and to a lesser degree PAA, are specific competitive inhibitors of the Na+-Pi cotransport in renal cortical BBM and are suitable probes for studies of this transport system.

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Year:  1986        PMID: 3009455

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  29 in total

1.  Reconstitution and characterization of a Na+/Pi co-transporter protein from rabbit kidney brush-border membranes.

Authors:  H Debiec; R Lorenc; P M Ronco
Journal:  Biochem J       Date:  1992-08-15       Impact factor: 3.857

Review 2.  The emergence of phosphate as a specific signaling molecule in bone and other cell types in mammals.

Authors:  Solmaz Khoshniat; Annabelle Bourgine; Marion Julien; Pierre Weiss; Jérôme Guicheux; Laurent Beck
Journal:  Cell Mol Life Sci       Date:  2010-09-17       Impact factor: 9.261

3.  Reconstitution of the renal brush-border membrane sodium/phosphate co-transporter.

Authors:  V Vachon; M C Delisle; R Laprade; R Béliveau
Journal:  Biochem J       Date:  1991-09-01       Impact factor: 3.857

4.  Preparation and characterization of basolateral plasma-membrane vesicles from sheep parotid glands. Mechanisms of phosphate and D-glucose transport.

Authors:  S Vayro; R Kemp; R B Beechey; S Shirazi-Beechey
Journal:  Biochem J       Date:  1991-11-01       Impact factor: 3.857

Review 5.  Phosphate transport processes in eukaryotic cells.

Authors:  J P Wehrle; P L Pedersen
Journal:  J Membr Biol       Date:  1989-11       Impact factor: 1.843

6.  Acute parathyroid hormone differentially regulates renal brush border membrane phosphate cotransporters.

Authors:  Nicolas Picard; Paola Capuano; Gerti Stange; Marija Mihailova; Brigitte Kaissling; Heini Murer; Jürg Biber; Carsten A Wagner
Journal:  Pflugers Arch       Date:  2010-06-05       Impact factor: 3.657

7.  Elevated phosphate activates N-ras and promotes cell transformation and skin tumorigenesis.

Authors:  Corinne E Camalier; Matthew R Young; Gerd Bobe; Christine M Perella; Nancy H Colburn; George R Beck
Journal:  Cancer Prev Res (Phila)       Date:  2010-02-09

8.  Effect of low-phosphate diet on sodium/phosphate cotransport mRNA and protein content and on oocyte expression of phosphate transport.

Authors:  J Biber; G Caderas; G Stange; A Werner; H Murer
Journal:  Pediatr Nephrol       Date:  1993-12       Impact factor: 3.714

9.  The Na+-Pi cotransporter PiT-2 (SLC20A2) is expressed in the apical membrane of rat renal proximal tubules and regulated by dietary Pi.

Authors:  Ricardo Villa-Bellosta; Silvia Ravera; Victor Sorribas; Gerti Stange; Moshe Levi; Heini Murer; Jürg Biber; Ian C Forster
Journal:  Am J Physiol Renal Physiol       Date:  2008-12-10

10.  PF-06869206 is a selective inhibitor of renal Pi transport: evidence from in vitro and in vivo studies.

Authors:  Linto Thomas; Jianxiang Xue; Viktor N Tomilin; Oleh M Pochynyuk; Jessica A Dominguez Rieg; Timo Rieg
Journal:  Am J Physiol Renal Physiol       Date:  2020-08-03
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