Literature DB >> 2778796

Characterization of sodium and pyruvate interactions of the two carrier systems specific of mono- and di- or tricarboxylic acids by renal brush-border membrane vesicles.

R Mengual1, M H Claude-Schlageter, J C Poiree, M Yagello, P Sudaka.   

Abstract

The experiments reported in this paper aim at characterizing the carboxylic acid transport, the interactions of pyruvate and citrate with their transport sites and specificity. The study of these carriers was performed using isotopic solutes for the influx measurements in brush-border membrane vesicles under zero trans conditions where the membrane potential was abolished with KCl preloading with valinomycin or equilibrium exchange conditions and delta psi = 0. Under zero trans condition and delta psi = 0, the influence of pyruvate concentrations on its initial rates of transport revealed the existence of two families of pyruvate transport sites, one with a high affinity for pyruvate (Kt = 88 microM) and a low affinity for sodium (Kt = 57.7 mM) (site I), the second one with a low affinity for pyruvate (Kt = 6.1 mM) and a high affinity for sodium (Kt = 23.9 mM) (site II). The coupling factor [Na]/[pyruvate] stoichiometry were determined at 0.25 mM and 8 mM pyruvate and estimated at 1.8 for site I, and 3 when the first and the second sites transport simultaneously. Under chemical equilibrium (delta psi congruent to 0) single isotopic labeling, transport kinetics of pyruvate carrier systems have shown a double interaction of pyruvate with the transporter; the sodium/pyruvate stoichiometry also expressed according to a Hill plot representation was n = 1.7. The direct method of measuring Na+/pyruvate stoichiometry from double labeling kinetics and isotopic exchange, for a time course, gives a n = 1.67. Studies of transport specificity, indicate that the absence of inhibition of lactate transport by citrate and the existence of competitive inhibition of lactate and citrate transports by pyruvate leads to the conclusion that the low pyruvate affinity site can be attributed to the citrate carrier (tricarboxylate) and the high pyruvate affinity site to the lactate carrier (monocarboxylate).

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2778796     DOI: 10.1007/BF01871734

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  22 in total

1.  Transport of tricarboxylic acid cycle intermediates by membrane vesicles from renal brush border.

Authors:  I Kippen; B Hirayama; J R Klinenberg; E M Wright
Journal:  Proc Natl Acad Sci U S A       Date:  1979-07       Impact factor: 11.205

2.  The interaction of sodium and potassium with the sodium pump in red cells.

Authors:  R P Garay; P J Garrahan
Journal:  J Physiol       Date:  1973-06       Impact factor: 5.182

Review 3.  Transport studies in plasma membrane vesicles isolated from renal cortex.

Authors:  H Murer; P Gmaj
Journal:  Kidney Int       Date:  1986-08       Impact factor: 10.612

4.  Stoichiometry of Na+-succinate cotransport in renal brush-border membranes.

Authors:  S H Wright; I Kippen; E M Wright
Journal:  J Biol Chem       Date:  1982-02-25       Impact factor: 5.157

5.  The mechanism of Na+-dependent D-glucose transport.

Authors:  U Hopfer; R Groseclose
Journal:  J Biol Chem       Date:  1980-05-25       Impact factor: 5.157

6.  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

7.  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

8.  Sodium ion/L-lactate co-transport in rabbit small-intestinal brush-border-membrane vesicles.

Authors:  B Hildmann; C Storelli; W Haase; M Barac-Nieto; H Murer
Journal:  Biochem J       Date:  1980-01-15       Impact factor: 3.857

9.  Glucose transport by horse kidney brush borders. I.--Transport properties of brush border membrane closed vesicles.

Authors:  J C Poirée; C Vannier; P Sudaka; M Fehlmann
Journal:  Biochimie       Date:  1978-09-29       Impact factor: 4.079

10.  Pathways for carboxylic acid transport by rabbit renal brush border membrane vesicles.

Authors:  E Nord; S H Wright; I Kippen; E M Wright
Journal:  Am J Physiol       Date:  1982-11
View more
  3 in total

1.  Sodium-coupled and electrogenic transport of B-complex vitamin nicotinic acid by slc5a8, a member of the Na/glucose co-transporter gene family.

Authors:  Elangovan Gopal; You-Jun Fei; Seiji Miyauchi; Lina Zhuang; Puttur D Prasad; Vadivel Ganapathy
Journal:  Biochem J       Date:  2005-05-15       Impact factor: 3.857

2.  Cloning and functional identification of slc5a12 as a sodium-coupled low-affinity transporter for monocarboxylates (SMCT2).

Authors:  Sonne R Srinivas; Elangovan Gopal; Lina Zhuang; Shirou Itagaki; Pamela M Martin; You-Jun Fei; Vadivel Ganapathy; Puttur D Prasad
Journal:  Biochem J       Date:  2005-12-15       Impact factor: 3.857

3.  The drug of abuse gamma-hydroxybutyrate is a substrate for sodium-coupled monocarboxylate transporter (SMCT) 1 (SLC5A8): characterization of SMCT-mediated uptake and inhibition.

Authors:  Dapeng Cui; Marilyn E Morris
Journal:  Drug Metab Dispos       Date:  2009-04-23       Impact factor: 3.922

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.