Literature DB >> 7235017

Basis for heterogeneity of para-aminohippurate secretion in rabbit proximal tubules.

A Shimomura, A M Chonko, J J Grantham.   

Abstract

Para-aminohippurate (PAH) is secreted at different rates in S1, S2, and S3 segments of isolated perfused proximal tubules of rabbit kidney. To characterize PAH transport we determined the maximal rate of secretion (Vmax) and the apparent Michaelis constant (Km) for each segment by examining the relationship between bath concentration of PAH and net PAH secretion (Jb leads to lPAH) transposed for Lineweaver-Burk analysis. The passive component of secretion for all segments was estimated by slope analysis at relatively high concentrations of PAH, by the component of PAH secretion insensitive to inhibition by probenecid, and, additionally, in S2 segments, from PAH efflux from lumen to bath. Subtraction of the passive component from Jb leads to lPAH (probenecid method) gave Vmax values for S1, S2, and S3 segments of 1,097 +/- 336 (n = 6), 7,430 +/- 1,338 (n = 6), 1,647 +/- 138 (n = 8) X 10(-15) mol.min-1.mm-1 (+/- SE) and apparent Km values of 139 +/- 37 (n = 6), 195 +/- 37 (n = 6), and 113 +/- 16 (n = 6) X 10(-6) M, respectively. Thus, Vmax for S2 greater than S3 congruent to S1, whereas apparent Km was not consistently different among the segments. On the basis of these results we suggest that axial heterogeneity of PAH secretion may reflect an increased basolateral membrane density of PAH transporters of common affinity in the S2 segment of the proximal tubule.

Entities:  

Mesh:

Substances:

Year:  1981        PMID: 7235017     DOI: 10.1152/ajprenal.1981.240.5.F430

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

Review 2.  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

3.  Recombinant human insulin-like growth factor-I accelerates recovery and reduces catabolism in rats with ischemic acute renal failure.

Authors:  H Ding; J D Kopple; A Cohen; R Hirschberg
Journal:  J Clin Invest       Date:  1993-05       Impact factor: 14.808

Review 4.  Molecular and ionic mimicry and the transport of toxic metals.

Authors:  Christy C Bridges; Rudolfs K Zalups
Journal:  Toxicol Appl Pharmacol       Date:  2005-05-01       Impact factor: 4.219

5.  A physiological model for renal drug metabolism: enalapril esterolysis to enalaprilat in the isolated perfused rat kidney.

Authors:  I A de Lannoy; H Hirayama; K S Pang
Journal:  J Pharmacokinet Biopharm       Date:  1990-12

6.  Pyrazinoate transport in the isolated perfused rabbit proximal tubule.

Authors:  K Besseghir; F Roch-Ramel
Journal:  Pflugers Arch       Date:  1986-12       Impact factor: 3.657

7.  Excretion of para-aminohippurate in the isolated perfused rat kidney: net secretion and net reabsorption.

Authors:  M L MacDougall; T B Wiegmann
Journal:  J Physiol       Date:  1988-03       Impact factor: 5.182

Review 8.  Chronic Kidney Disease and Exposure to Nephrotoxic Metals.

Authors:  Sarah E Orr; Christy C Bridges
Journal:  Int J Mol Sci       Date:  2017-05-12       Impact factor: 5.923

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.