scholarly journals Electrogenicity of phosphate transport by renal brush-border membranes

1988 ◽  
Vol 252 (3) ◽  
pp. 801-806 ◽  
Author(s):  
R Béliveau ◽  
H Ibnoul-Khatib

Phosphate uptake by rat renal brush-border membrane vesicles was studied under experimental conditions where transmembrane electrical potential (delta psi) could be manipulated. Experiments were performed under initial rate conditions to avoid complications associated with the dissipation of ion gradients. First, phosphate uptake was shown to be strongly affected by the nature of Na+ co-anions, the highest rates of uptake being observed with 100 mM-NaSCN (1.010 +/- 0.086 pmol/5 s per micrograms of protein) and the lowest with 50 mM-Na2SO4 (0.331 +/- 0.046 pmol/5 s per micrograms of protein). Anion substitution studies showed that potency of the effect of the co-anions was in the order thiocyanate greater than nitrate greater than chloride greater than isethionate greater than gluconate greater than sulphate, which correlates with the known permeability of the membrane to these anions and thus to the generation of transmembrane electrical potentials of decreasing magnitude (inside negative). The stimulation by ion-diffusion-induced potential was observed from pH 6.5 to 8.5, indicating that the transport of both monovalent and divalent phosphate was affected. In addition, inside-negative membrane potentials were generated by valinomycin-induced diffusion of K+ from K+-loaded vesicles and showed a 57% stimulation of phosphate uptake, at pH 7.5. Similar experiments with H+-loaded vesicles, in the presence of carbonyl cyanide m-chlorophenylhydrazone gave a 50% stimulation compared with controls. Inside-positive membrane potentials were also induced by reversal of the K+ gradient (outside greater than inside) in the presence of valinomycin and gave 58% inhibition of phosphate uptake. The membrane-potential dependency of phosphate uptake was finally analysed under thermodynamic equilibrium, and a stimulation by inside-negative potential was observed. The transport of phosphate was thus driven against a concentration gradient by a membrane potential, implicating the net transfer of a positive charge during the translocation process. These results indicate a major contribution of electrical potential to phosphate uptake in renal brush-border membranes.

1990 ◽  
Vol 258 (5) ◽  
pp. F1145-F1153 ◽  
Author(s):  
F. Martinez ◽  
M. Manganel ◽  
C. Montrose-Rafizadeh ◽  
D. Werner ◽  
F. Roch-Ramel

The mechanisms involved in urate and p-aminohippurate (PAH) transport in the rabbit renal brush-border membrane were investigated through study of membrane vesicles. Transport of [14C]urate and [3H]PAH was measured by a rapid filtration method. As previously reported by others, no OH(-)-PAH exchanger could be demonstrated by imposing an outwardly directed OH- gradient (pHin 7.4, pHout 6). In contrast, an OH(-)-lactate exchanger (or H(+)-lactate cotransport) was demonstrated. In the presence of valinomycin and an inwardly directed K+ gradient, both [14C]urate and [3H]PAH vesicle uptake were stimulated, demonstrating a potential-driven transport of these two anions. Probenecid, PAH, or cold urate decreased potential-driven urate uptake, suggesting that this transport was facilitated by a specific transport mechanism. The potential-driven urate transport described here may play a role in the second step of urate secretion in rabbits, because rate (or PAH) is transported across the brush-border membrane from the negative interior of the cell to the more positive omen.


1984 ◽  
Vol 18 ◽  
pp. 366A-366A
Author(s):  
Eddie S Moore ◽  
Eunice G John ◽  
Lawrence Rufr ◽  
Christine S Mooers ◽  
Nochik Park ◽  
...  

1982 ◽  
Vol 685 (3) ◽  
pp. 260-272 ◽  
Author(s):  
C. Burnham ◽  
C. Munzesheimer ◽  
E. Rabon ◽  
G. Sachs

1984 ◽  
Vol 18 ◽  
pp. 366A-366A
Author(s):  
Lawrence Rufer ◽  
Eddie S Moore ◽  
Christine S Mooers ◽  
Nochik Park

1984 ◽  
Vol 246 (4) ◽  
pp. F363-F372
Author(s):  
E. M. Wright

In both renal and gastrointestinal physiology, it has become popular to study epithelial transport phenomena using vesicles isolated from the apical and basolateral cell membranes. Transport in vesicle preparations is usually monitored with radioactive tracers, but more recently attention has been directed to electrophysiological methods. As it is impossible to measure the electrical properties of membranes in small vesicles (less than 500 nm diam) with classical electrophysiological techniques, indirect methods have to be employed. In this review I focus on the application of voltage-sensitive optical probes to measure membrane potentials in brush border membrane vesicles. Optical signals are calibrated with diffusion potentials generated with known ion gradients in the presence of ionophores, e.g., EKS with K gradients in the presence of valinomycin. Membrane potential measurements can be used 1) to illustrate the specificity and kinetics of sugar-, amino acid-, and carboxylic acid-Na cotransport systems in brush border membranes, and 2) to determine the ion permeability of brush border membranes. All organic solutes known to be transported by Na cotransport across brush border membranes depolarize the membrane in a Na-dependent, saturable manner. The results agree, both qualitatively and quantitatively, with electrophysiological data obtained in the intact renal tubule and with tracer uptake in vesicles. Bi-ionic potential measurements demonstrate that brush border membranes are permselective to anions and cations, but there are indications that the permeabilities are somewhat dependent on the method of vesicle preparation and the experimental conditions. However, electrical potential measurements provide insight into the mechanisms of ion transport in vesicle preparations, and the application of patch-clamp techniques should provide further gains in the future.


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