The objective of this project is to investigate the stoichiometry and voltage dependence of the sodium pump of squid giant axons using simultaneous measurements of isotopic 22Na efflux or 42K influx and electrogenic pump current. The electrogenic pump current is measured by the change in holding current that occurs upon addition of the reversible pump toxin dihydrodigitoxigenin (H2DTG) or of the irreversible (in squid) toxin ouabain. The toxin-sensitive change in holding current is measured using a stable, low-noise voltage-clamp apparatus. The composition of the intracellular axoplasm is controlled by the technique of internal dialysis. This method also permits the use of radioactive tracers for the measurement of both influx and efflux. By steepening the normal ionic gradients for Na+ and K+, the pump can be made to run backwards. Experiments will be done to determine the effect of changes in nucleotide and ionic composition on the magnitude of the pump current and the stoichiometry of the pump cycle. Experiments have been done that demonstrate that the backward-running sodium pump produces an electrical current in the reverse direction. The magnitude of the reverse pump current is decreased by hyperpolarization corresponding to a region of negative slope conductance in the current-voltage relationship of the reverse pump. Experiments have also shown that both the forward pump current and flux are inhibited by hyperpolarization. These results suggest that membrane voltage may be an important factor in the regulation of pump activity. The validity of the pump-clamp technique has been verified by the demonstration that H2DTG and ouabain have no effect on passive membrane conductance and that measurements of Na+-channel or K+-channel mediated flux and current are in agreement under experimental conditions that allow only a unidirectional ion flow. Future experiments will focus on the determination of the current-voltage relationship of both the forward and reverse modes of pump operation and the determination of whether the stoichiometry of the pump is fixed or variable. These studies have mechanistic implications for the operation of the sodium pump which is important in the regulation of cell volume and in establishing and maintaining the electrochemical gradient for sodium-coupled transport processes in a wide variety of animal and plant cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
2R01NS022979-02
Application #
3405873
Study Section
Physiology Study Section (PHY)
Project Start
1985-05-01
Project End
1989-04-30
Budget Start
1986-05-01
Budget End
1987-04-30
Support Year
2
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Rosalind Franklin University of Medicine & Sci
Department
Type
Schools of Medicine
DUNS #
069501252
City
North Chicago
State
IL
Country
United States
Zip Code
60064
Potvin, Olivier; Dieumegarde, Louis; Duchesne, Simon et al. (2017) Freesurfer cortical normative data for adults using Desikan-Killiany-Tourville and ex vivo protocols. Neuroimage 156:43-64
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Ding, Yanli; Rakowski, Robert F (2010) The effect of holding potential on charge translocation by the Na+/K +-ATPase in the absence of potassium. J Membr Biol 236:203-14
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Rakowski, Robert F; Kaya, Savas; Fonseca, James (2005) Electro-Chemical Modeling Challenges of Biological Ion Pumps. J Comput Electron 4:189-193
Vasilyev, A; Khater, K; Rakowski, R F (2004) Effect of extracellular pH on presteady-state and steady-state current mediated by the Na+/K+ pump. J Membr Biol 198:65-76
Vasilyev, A; Indyk, E; Rakowski, R F (2002) Properties of a sodium channel (Na(x)) activated by strong depolarization of Xenopus oocytes. J Membr Biol 185:237-47

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