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. 1963 Jan 1;46(3):491–503. doi: 10.1085/jgp.46.3.491

The Electrical Characteristics of Active Sodium Transport in the Toad Bladder

Howard S Frazier 1, Alexander Leaf 1
PMCID: PMC2195270  PMID: 13959378

Abstract

The mechanism responsible for active sodium transport in the urinary bladder of the toad appears to be located at the serosal boundary of the epithelial cell layer of the bladder. Studies of the potential step observed at the serosal boundary in the open-circuited state were undertaken in an attempt to define the factors responsible for its production. Glass micropipettes were used to measure the serosal potential step in bladders exposed on the serosal side to solutions of high potassium or of high potassium and low chloride concentration. Observed potentials exceed the maximum values which would have been expected if the serosal potential step were a potassium or chloride diffusion potential. Measurements of net cation flux exclude the possibility of a diffusion potential at this border due to the passive movement of any anionic species. The observed independence of transbladder potential and short-circuit current from the pH of the serosal medium over a wide range of pH makes it unlikely that the observed serosal potential step is a hydrogen ion diffusion potential. We conclude that the active sodium transport mechanism in toad bladder is "electrogenic."

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. CALDWELL P. C., HODGKIN A. L., KEYNES R. D., SHAW T. L. The effects of injecting 'energy-rich' phosphate compounds on the active transport of ions in the giant axons of Loligo. J Physiol. 1960 Jul;152:561–590. doi: 10.1113/jphysiol.1960.sp006509. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. FRAZIER H. S., DEMPSEY E. F., LEAF A. Movement of sodium across the mucosal surface of the isolated toad bladder and its modification by vasopressin. J Gen Physiol. 1962 Jan;45:529–543. doi: 10.1085/jgp.45.3.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. HAYS R. M., LEAF A. Studies on the movement of water through the isolated toad bladder and its modification by vasopressin. J Gen Physiol. 1962 May;45:905–919. doi: 10.1085/jgp.45.5.905. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. HAYS R. M., LEAF A. The problem of clinical vasopressin resistance: in vitro studies. Ann Intern Med. 1961 Apr;54:700–709. doi: 10.7326/0003-4819-54-4-700. [DOI] [PubMed] [Google Scholar]
  5. LEAF A., ANDERSON J., PAGE L. B. Active sodium transport by the isolated toad bladder. J Gen Physiol. 1958 Mar 20;41(4):657–668. doi: 10.1085/jgp.41.4.657. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. LEAF A., HAYS R. M. Permeability of the isolated toad bladder to solutes and its modification by vasopressin. J Gen Physiol. 1962 May;45:921–932. doi: 10.1085/jgp.45.5.921. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. LEIBMAN J., GOTCH F. A., EDELMAN I. S. Tritium assay by liquid scintillation spectrometry. Comparison of tritium and deuterium oxides as tracers for body water. Circ Res. 1960 Sep;8:907–912. doi: 10.1161/01.res.8.5.907. [DOI] [PubMed] [Google Scholar]
  8. USSING H. H., ZERAHN K. Active transport of sodium as the source of electric current in the short-circuited isolated frog skin. Acta Physiol Scand. 1951 Aug 25;23(2-3):110–127. doi: 10.1111/j.1748-1716.1951.tb00800.x. [DOI] [PubMed] [Google Scholar]

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