Sodium/proton antiport in brush-border-membrane vesicles isolated from rat small intestine and kidney
- PMID: 942389
- PMCID: PMC1172760
Sodium/proton antiport in brush-border-membrane vesicles isolated from rat small intestine and kidney
Abstract
Studies on proton and Na+ transport by isolated intestinal and renal brush-border-membrane vesicles were carried out to test for the presence of an Na+/H+-exchange system. Proton transport was evaluated as proton transfer from the intravesicular space to the incubation medium by monitoring pH changes in the membrane suspension induced by sudden addition of cations. Na+ transport was determined as Na+ uptake into the vesicles by filtration technique. A sudden addition of sodium salts (but not choline) to the membrane suspension provokes an acidification of the incubation medium which is abolished by the addition of 0.5% Triton X-100. Pretreatment of the membranes with Triton X-100 prevents the acidification. The acidification is also not observed if the [K+] and proton conductance of the membranes have been increased by the simultaneous addition of valinomycin and carbonyl cyanide p-trifluoromethoxyphenylhydrazone to the K+-rich incubation medium. Either valinomycin or carbonyl cyanide p-trifluoromethoxyphenylhydrazone when added alone do not alter the response of the membranes to the addition of Na+. Na+ uptake by brush-border microvilli is enhanced in the presence of a proton gradient directed from the intravesicular space to the incubation medium. Under these conditions a transient accumulation of Na+ inside the vesicles is observed. It is concluded that intestinal and renal brush-border membranes contain a NA+/H+ antiport system which catalyses an electroneutral exchange of Na+ against protons and consequently can produce a proton gradient in the presence of a concentration difference for Na+. This system might be involved in the active proton secretion of the small intestine and the proximal tubule of the kidney.
Similar articles
-
Comparison of Na+/H+ and Cl-/OH- exchange in rat jejunal brush border membrane vesicles: studies with acridine orange.Boll Soc Ital Biol Sper. 1984 May 30;60 Suppl 4:143-7. Boll Soc Ital Biol Sper. 1984. PMID: 6087849
-
Active alanine transport in isolated brush border membranes.J Biol Chem. 1975 Jul 25;250(14):5674-80. J Biol Chem. 1975. PMID: 1141245
-
Sodium gradient-dependent phosphate transport in renal brush border membrane vesicles. Effect of an intravesicular greater than extravesicular proton gradient.J Biol Chem. 1981 Aug 10;256(15):8080-4. J Biol Chem. 1981. PMID: 7263641
-
Is intestinal peptide transport energized by a proton gradient?Am J Physiol. 1985 Aug;249(2 Pt 1):G153-60. doi: 10.1152/ajpgi.1985.249.2.G153. Am J Physiol. 1985. PMID: 2992286 Review.
-
Electrophysiology of plasma membrane vesicles.Am J Physiol. 1984 Apr;246(4 Pt 2):F363-72. doi: 10.1152/ajprenal.1984.246.4.F363. Am J Physiol. 1984. PMID: 6372509 Review.
Cited by
-
Electrogenic 2 Na+/1 H+ exchange in crustaceans.J Membr Biol. 1990 Jul;116(3):215-26. doi: 10.1007/BF01868461. J Membr Biol. 1990. PMID: 2167376
-
Sodium-hydrogen ion exchange in rabbit renal cortical slices incubated in acetate media.J Physiol. 1988 Apr;398:523-41. doi: 10.1113/jphysiol.1988.sp017055. J Physiol. 1988. PMID: 2839675 Free PMC article.
-
Evidence from renal proximal tubules that HCO3- and solute reabsorption are acutely regulated not by pH but by basolateral HCO3- and CO2.Proc Natl Acad Sci U S A. 2005 Mar 8;102(10):3875-80. doi: 10.1073/pnas.0500423102. Epub 2005 Feb 22. Proc Natl Acad Sci U S A. 2005. PMID: 15728388 Free PMC article.
-
Acid-base transport systems in gastrointestinal epithelia.Gut. 1992 Aug;33(8):1134-45. doi: 10.1136/gut.33.8.1134. Gut. 1992. PMID: 1398242 Free PMC article. Review. No abstract available.
-
pH regulation in HT29 colon carcinoma cells.Pflugers Arch. 1994 Sep;428(2):179-85. doi: 10.1007/BF00374856. Pflugers Arch. 1994. PMID: 7971175
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources