Literature DB >> 1822544

Heterogeneity in the effects of membrane potentials on pantothenate and glucose uptakes by rabbit renal apical membranes.

B Barbarat1, R Chambrey, R A Podevin.   

Abstract

1. Previous studies using renal brush-border membrane vesicles have established that both the pantothenate and the low Km (Michaelis-Menten constant), low Vmax (maximal rate) D-glucose systems have a stoichiometry of 2 Na+: 1 organic molecule. In this study, we compared the mechanisms by which the membrane potential energizes pantothenate and D-glucose uptakes by brush-border membrane vesicles isolated from the whole cortex of rabbit kidney. 2. In the absence of Na+, varying the membrane potential from +60 to -60 mV decreased pantothenate uptake, whereas D-glucose uptake was increased in a linear manner. These results suggested the existence of a conductive pathway for pantothenate in these membranes. They also suggested that the pantothenate free carrier is electroneutral, while the glucose free carrier is negatively charged. 3. In the presence of an inwardly directed Na+ gradient, varying the membrane potential from +60 to -60 mV increased Na(+)-dependent pantothenate influx linearly. In contrast, a shift from +60 to +40 mV in the membrane potential had no influence on Na(+)-dependent D-glucose influx, whereas influx was a linear function of the membrane potential from +40 to -60 mV, indicating that there is a threshold membrane potential required for membrane potential-dependent D-glucose movement to occur. 4. Kinetic studies revealed that the effect of membrane potential on pantothenate uptake is through changes in the Km, while Vmax was unchanged. On the other hand, the membrane potential exerted its effect on D-glucose transport solely on the Vmax. 5. Finally, binding studies revealed that membrane potential, both in the presence and absence of a Na+ gradient, elicited effects on phlorizin binding qualitatively similar to those observed for D-glucose transport. 6. Implications of these findings for tubular regulation of these electrogenic secondary active transport systems are discussed.

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Year:  1991        PMID: 1822544      PMCID: PMC1179831          DOI: 10.1113/jphysiol.1991.sp018823

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  16 in total

Review 1.  Biochemistry of the Na+, D-glucose cotransporter of the small-intestinal brush-border membrane. The state of the art in 1984.

Authors:  G Semenza; M Kessler; M Hosang; J Weber; U Schmidt
Journal:  Biochim Biophys Acta       Date:  1984-09-03

Review 2.  The small-intestinal Na+, D-glucose cotransporter: an asymmetric gated channel (or pore) responsive to delta psi.

Authors:  M Kessler; G Semenza
Journal:  J Membr Biol       Date:  1983       Impact factor: 1.843

3.  Potential-dependent D-glucose uptake by renal brush border membrane vesicles in the absence of sodium.

Authors:  S Hilden; B Sacktor
Journal:  Am J Physiol       Date:  1982-04

4.  Kinetics of sodium succinate cotransport across renal brush-border membranes.

Authors:  S H Wright; B Hirayama; J D Kaunitz; I Kippen; E M Wright
Journal:  J Biol Chem       Date:  1983-05-10       Impact factor: 5.157

5.  Na+-coupled sugar transport: membrane potential-dependent Km and Ki for Na+.

Authors:  G A Kimmich; J Randles
Journal:  Am J Physiol       Date:  1988-10

6.  Energy-dependence of phlorizin binding to isolated renal microvillus membranes. Evidence concerning the mechanism of coupling between the electrochemical Na+ gradient the sugar transport.

Authors:  P S Aronson
Journal:  J Membr Biol       Date:  1978-07-21       Impact factor: 1.843

7.  Pantothenate-sodium cotransport in renal brush-border membranes.

Authors:  B Barbarat; R A Podevin
Journal:  J Biol Chem       Date:  1986-11-05       Impact factor: 5.157

8.  Phlorizin as a probe of the small-intestinal Na+,D-glucose cotransporter. A model.

Authors:  G Toggenburger; M Kessler; G Semenza
Journal:  Biochim Biophys Acta       Date:  1982-06-14

9.  Further studies of proximal tubular brush border membrane D-glucose transport heterogeneity.

Authors:  R J Turner; A Moran
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

10.  Biotin uptake mechanisms in brush-border and basolateral membrane vesicles isolated from rabbit kidney cortex.

Authors:  R A Podevin; B Barbarat
Journal:  Biochim Biophys Acta       Date:  1986-04-25
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