Literature DB >> 6859260

Citrate uptake by basolateral and luminal membrane vesicles from rabbit kidney cortex.

K E Jørgensen, U Kragh-Hansen, H Røigaard-Petersen, M I Sheikh.   

Abstract

The mechanisms of tubular transport of citrate in renal basolateral and luminal membrane vesicles were studied under various experimental conditions. Both membrane preparations take up citrate by a Na+-dependent transport system, although with different characteristics. The uptake of citrate by basolateral membrane vesicles was insensitive to changes in membrane potential, which is indicative of electroneutral transport of the anion. The Na+-dependent uptake of citrate by luminal membrane vesicles was influenced by the presence of Na+salt anions of different permeabilities in the order: chloride greater than sulfate greater than gluconate. Furthermore, addition of citrate to membrane vesicle-potential-sensitive dye suspensions resulted in optical changes of the dye, indicative of electrogenic transfer of this compound. The apparent affinity of the citrate transport system located in luminal membrane vesicles, in contrast to basolateral membrane vesicles, was sensitive to changes in medium pH and was higher than that of basolateral membrane vesicles in the pH range studied. On the basis of these results a model for the transport of citrate by rabbit kidney proximal tubule is proposed.

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Year:  1983        PMID: 6859260     DOI: 10.1152/ajprenal.1983.244.6.F686

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


  10 in total

1.  Localization of the calcium-regulated citrate transport process in proximal tubule cells.

Authors:  Kathleen S Hering-Smith; Weibo Mao; Faith R Schiro; Joycelynn Coleman-Barnett; Ana M Pajor; L Lee Hamm
Journal:  Urolithiasis       Date:  2014-03-21       Impact factor: 3.436

2.  Sodium-gradient-driven, high-affinity, uphill transport of succinate in human placental brush-border membrane vesicles.

Authors:  V Ganapathy; M E Ganapathy; C Tiruppathi; Y Miyamoto; V B Mahesh; F H Leibach
Journal:  Biochem J       Date:  1988-01-01       Impact factor: 3.857

3.  Calcium sensitivity of dicarboxylate transport in cultured proximal tubule cells.

Authors:  Kathleen S Hering-Smith; Faith R Schiro; Ana M Pajor; L Lee Hamm
Journal:  Am J Physiol Renal Physiol       Date:  2010-12-01

4.  Renal transport of monocarboxylic acids. Heterogeneity of lactate-transport systems along the proximal tubule.

Authors:  K E Jørgensen; M I Sheikh
Journal:  Biochem J       Date:  1984-11-01       Impact factor: 3.857

5.  Renal transport of neutral amino acids. Tubular localization of Na+-dependent phenylalanine- and glucose-transport systems.

Authors:  U Kragh-Hansen; H Røigaard-Petersen; C Jacobsen; M I Sheikh
Journal:  Biochem J       Date:  1984-05-15       Impact factor: 3.857

6.  Renal transport of neutral amino acids. Demonstration of Na+-independent and Na+-dependent electrogenic uptake of L-proline, hydroxy-L-proline and 5-oxo-L-proline by luminal-membrane vesicles.

Authors:  H Røigaard-Petersen; M I Sheikh
Journal:  Biochem J       Date:  1984-05-15       Impact factor: 3.857

7.  Electrophysiology of succinate transport across rabbit renal brush border membranes.

Authors:  R E Schell; E M Wright
Journal:  J Physiol       Date:  1985-03       Impact factor: 5.182

8.  Expression of a rat renal sodium-dependent dicarboxylate transporter in Xenopus oocytes.

Authors:  J Steffgen; S Kienle; F Scheyerl; H E Franz
Journal:  Biochem J       Date:  1994-01-01       Impact factor: 3.857

9.  Sodium-dependent dicarboxylate transport in rat renal basolateral membrane vesicles.

Authors:  G Burckhardt
Journal:  Pflugers Arch       Date:  1984-07       Impact factor: 3.657

10.  Hypocitraturia: pathophysiology and medical management.

Authors:  Jack M Zuckerman; Dean G Assimos
Journal:  Rev Urol       Date:  2009
  10 in total

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