Literature DB >> 13463272

Studies of the chloride transport in the gastric mucosa of the frog.

E HEINZ, R P DURBIN.   

Abstract

The unidirectional fluxes of Cl(-) and Na(+) across the frog gastric mucosa in vitro were investigated with radioactive isotopes, and related to the secretory and electrical properties of the normal, and metabolically inhibited, mucosa. The flux of Cl(-) from nutrient to secretory surface of the mucosa was observed to rise sharply with increasing acid secretion, while the corresponding flux of Na(+) did not change appreciably. Lowering [NaCl] in the secretory solution caused a proportional drop in the fluxes from secretory to nutrient surface, of both Cl(-) and Na(+). Under the same conditions, the flux of Cl(-) from nutrient to secretory surface fell by nearly the same amount as did the flux of Cl(-) in the opposite direction, while the flux of Na(+) from nutrient to secretory surface remained essentially unchanged. Electrical and hydrodynamic causes for this observation could be excluded. Metabolic inhibitors, including cyanide, azide, DNP, and anaerobiosis depressed Cl(-) flux in both directions distinctly below the corresponding values observed with the normal, non-secreting mucosa. At the same time, a decrease in electrical potential difference and conductance was observed under inhibition. The flux of Na(+) was little changed by metabolic inhibition. The relationship between fluxes and conductance of Cl(-) during metabolic inhibition differs markedly from that observed under normal conditions, and is consistent with the view that during metabolic inhibition most of the Cl(-) moving across the mucosa does so as a free ion. From the above data it is concluded that Cl(-) is normally transported across the mucosa in combination with a carrier, the supply of which is impaired under metabolic inhibition. According to the behavior of the Na(+) flux, the passive permeability of the mucosa appeared to be little affected by the metabolic inhibition applied, but seemed to rise considerably after death of the mucosa, probably due to structural damage.

Entities:  

Keywords:  CHLORIDES/metabolism; STOMACH/physiology

Mesh:

Substances:

Year:  1957        PMID: 13463272      PMCID: PMC2194816          DOI: 10.1085/jgp.41.1.101

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  6 in total

1.  Active transport of chloride by isolated frog gastric epithelium; origin of the gastric mucosal potential.

Authors:  C A HOGBEN
Journal:  Am J Physiol       Date:  1955-03

2.  Acid formation and acidity control in the stomach.

Authors:  E HEINZ; K J OBRINK
Journal:  Physiol Rev       Date:  1954-10       Impact factor: 37.312

3.  The secretion of halogens into the gastric juice.

Authors:  E HEINZ; K J OBRINK
Journal:  Gastroenterology       Date:  1954-07       Impact factor: 22.682

4.  The influence of the corticotropic hormone from ox on the active salt uptake in the axolotl.

Authors:  V K JOHNSEN; H H USSING
Journal:  Acta Physiol Scand       Date:  1949-01-31

5.  The chloride transport system of the gastric mucosa.

Authors:  C A M HOGBEN
Journal:  Proc Natl Acad Sci U S A       Date:  1951-07       Impact factor: 11.205

6.  Water flow through frog gastric mucosa.

Authors:  R P DURBIN; H FRANK; A K SOLOMON
Journal:  J Gen Physiol       Date:  1956-03-20       Impact factor: 4.086

  6 in total
  17 in total

1.  Transport and electrical phenomena in resting and secreting piglet gastric mucosa.

Authors:  J G Forte; T E Machen
Journal:  J Physiol       Date:  1975-01       Impact factor: 5.182

2.  PERMEABILITY OF THE HUMAN RED CELL TO LABELLED GLUCOSE.

Authors:  H G BRITTON
Journal:  J Physiol       Date:  1964-01       Impact factor: 5.182

3.  Ion transport in single cell populations.

Authors:  A K SOLOMON
Journal:  Biophys J       Date:  1962-03       Impact factor: 4.033

4.  Physiochemical aspects of hydrochloric acid formation.

Authors:  C A HOGBEN
Journal:  Am J Dig Dis       Date:  1959-03

5.  Na(+)-coupled Cl- transport in the gastric mucosa of the guinea pig.

Authors:  G Klemperer; S Lelchuk; S R Caplan
Journal:  J Bioenerg Biomembr       Date:  1983-06       Impact factor: 2.945

6.  On the meaning of effects of substrate structure on biological transport.

Authors:  H N Christensen
Journal:  J Bioenerg       Date:  1973-01

7.  Transport of methionine and proline by rat liver slices and the effect of certain hormones.

Authors:  J C Crawhall; P Purkiss
Journal:  Biochem J       Date:  1973-09       Impact factor: 3.857

Review 8.  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

9.  Transport of sodium and chloride across rat gastric mucosa in vitro.

Authors:  M J Jackson; S H Norris
Journal:  J Physiol       Date:  1985-03       Impact factor: 5.182

10.  Characteristics of sodium flux from serosa to mucosa in rabbit ileum.

Authors:  J F Desjeux; Y H Tai; P F Curran
Journal:  J Gen Physiol       Date:  1974-09       Impact factor: 4.086

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