Literature DB >> 240439

Some features of hydrogen (ion) secretion by the frog skin.

T Machen, D Erlij.   

Abstract

We have studied the movements of H+ from the in vitro frog skin into the outside solution because it has been suggested that the movement of sodium from the outside solution into the skin may result from the forced exchange of Na+ by H+. Our main observations can be summarized as follows: (a) Hydrogen moves from the skin into the outside solution at a rate of 0.04 muequiv-cm-2-h-1 while Na+ influx had a value of 0.49 muequiv-cm-2-h-1. (b) The rate of H+ secretion is not significantly affected by substituting the Na+ in the outside solution by K+ nor by inhibiting Na+ influx with amiloride (5-10(-5) M). (c) Acetazolamide (5-10(-3) M) blocked H+ secretion without altering the potential difference across the skin. (d) The rate of H+ production is not underestimated because it may have been neutralized by HCO3- secreted into the outside solution in exchange for Cl-. Substituting all the Cl- by SO4(2-) in the outside solutions does not result in an increase in the rate of H+ production. (e) The steady-state rate of H+ secretion is not affected by large changes in electrochemical potential gradients for H+. Neither abolishing the potential difference across the skin nor a 10-fold change in H+ concentration in the outside solution affected significantly the steady-state rate of H+ secretion. (f) The H+ secretion was abolished by the metabolic inhibitors dinitrophenol (1-10(-4) M) and Antimycin A (1.5-10(-6) M) which also markedly reduced the potential difference across the skin. Observations (a), (b), and (c) suggest that H+ and Na+ movements across the outer border of the isolated frog skin are not coupled. The ratio of Na+ to H+ movements is very different from unity and Na+ movements can be abolished without any effects on H+ secretion and conversely H+ movements can be abolished without interruption of Na+ uptake. A second conclusion suggested by these results is that the H+ secretion does not result from movement of H+ following its electrochemical potential gradient since that rate of secretion is not affected by marked changes in either potential or [H+]. Furthermore, the effects of metabolic inhibitors suggest that H+ secretion requires the expenditure of energy by the cell.

Entities:  

Mesh:

Substances:

Year:  1975        PMID: 240439     DOI: 10.1016/0005-2736(75)90047-4

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  5 in total

1.  Electrogenic active proton pump in Rana esculenta skin and its role in sodium ion transport.

Authors:  J Ehrenfeld; F Garcia-Romeu; B J Harvey
Journal:  J Physiol       Date:  1985-02       Impact factor: 5.182

2.  Proton pump activity of mitochondria-rich cells. The interpretation of external proton-concentration gradients.

Authors:  L J Jensen; J N Sørensen; E H Larsen; N J Willumsen
Journal:  J Gen Physiol       Date:  1997-01       Impact factor: 4.086

3.  Tissue kinetics, ion transport, and recruitment of mitochondria-rich cells in the skin of the toad (Bufo bufo) in response to exposure to distilled water.

Authors:  P E Budtz; B C Christoffersen; J S Johansen; I Spies; N J Willumsen
Journal:  Cell Tissue Res       Date:  1995-04       Impact factor: 5.249

4.  Role of proton pump of mitochondria-rich cells for active transport of chloride ions in toad skin epithelium.

Authors:  E H Larsen; N J Willumsen; B C Christoffersen
Journal:  J Physiol       Date:  1992-05       Impact factor: 5.182

5.  Intracellular ion concentrations in the isolated frog skin epithelium: evidence for different types of mitochondria-rich cells.

Authors:  R Rick
Journal:  J Membr Biol       Date:  1992-05       Impact factor: 1.843

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.