Na+-H+ exchange in cardiac sarcolemmal vesicles
- PMID: 2992585
- DOI: 10.1016/0005-2736(85)90553-x
Na+-H+ exchange in cardiac sarcolemmal vesicles
Abstract
The transport of Na+ by a purified sarcolemmal vesicular preparation from canine ventricular tissue was studied as a function of both internal and external pH. The uptake of Na+ into sarcolemmal vesicles increased upon raising the extravesicular pH of the reaction medium. Half-maximal uptake of Na+ was observed at a pHo of about 8.1 and maximal uptake occurred at pH 8.6. The uptake of Na+ by sarcolemma was also dependent upon the intravesicular pH. Na+ uptake into sarcolemmal vesicles was greatly attenuated in the absence of a H+ gradient across the membrane. Transport of Na+ was potently inhibited by amiloride, a known blocker of Na+-H+ exchange. LiCl was also an effective inhibitor of Na+ transport. In the presence of optimal H+ gradients, Na+ uptake was linear for the first 5 seconds of the reaction and exhibited a Vmax of 290 nmol Na+/mg per min and a KNa of 3.5 mM. These experiments strongly indicate the presence of a Na+-H+ exchange system in cardiac sarcolemma. This activity appeared to be relatively specific for this membrane fraction. The identification of Na+-H+ exchange activity in a sarcolemmal vesicular fraction from the heart will permit extensive characterization of the regulation and kinetics of this antiporter in future investigations.
Similar articles
-
Demonstration of a Na+/H+ exchange activity in purified canine cardiac sarcolemmal vesicles.J Biol Chem. 1985 Apr 25;260(8):4869-76. J Biol Chem. 1985. PMID: 2985568
-
Sodium-lithium exchange and sodium-proton exchange are mediated by the same transport system in sarcolemmal vesicles from bovine superior mesenteric artery.Circ Res. 1989 Sep;65(3):818-28. doi: 10.1161/01.res.65.3.818. Circ Res. 1989. PMID: 2548766
-
Ion specificity of cardiac sarcolemmal Na+/H+ antiporter.J Biol Chem. 1990 Apr 15;265(11):6035-41. J Biol Chem. 1990. PMID: 2156838
-
The sodium/hydrogen exchange system in cardiac cells: its biochemical and pharmacological properties and its role in regulating internal concentrations of sodium and internal pH.J Mol Cell Cardiol. 1985 Nov;17(11):1029-42. doi: 10.1016/s0022-2828(85)80119-x. J Mol Cell Cardiol. 1985. PMID: 3001319 Review.
-
Regulation of cardiac sarcolemmal Na+/H+ exchanger activity by endogenous ligands. Relevance to ischemia.Ann N Y Acad Sci. 1999 Jun 30;874:335-45. doi: 10.1111/j.1749-6632.1999.tb09249.x. Ann N Y Acad Sci. 1999. PMID: 10415545 Review.
Cited by
-
Role for sulfur-containing groups in the Na+-Ca2+ exchange of cardiac sarcolemmal vesicles.J Membr Biol. 1986;94(3):217-25. doi: 10.1007/BF01869717. J Membr Biol. 1986. PMID: 3560203
-
Na+/H+ exchanger and reperfusion-induced ventricular arrhythmias in isolated perfused heart: possible role of amiloride.Mol Cell Biochem. 1993 Feb 17;119(1-2):151-7. doi: 10.1007/BF00926866. Mol Cell Biochem. 1993. PMID: 8384297
-
Enhanced Na+/H+ exchange during ischemia and reperfusion impairs mitochondrial bioenergetics and myocardial function.J Cardiovasc Pharmacol. 2008 Sep;52(3):236-44. doi: 10.1097/FJC.0b013e3181831337. J Cardiovasc Pharmacol. 2008. PMID: 18806604 Free PMC article.
-
Cationic interactions with Na+-H+ exchange and passive Na+ flux in cardiac sarcolemmal vesicles.Mol Cell Biochem. 1987 Nov;78(1):89-94. doi: 10.1007/BF00224428. Mol Cell Biochem. 1987. PMID: 3137451
-
The Remaining Conundrum of the Role of the Na+/H+ Exchanger Isoform 1 (NHE1) in Cardiac Physiology and Pathology: Can It Be Rectified?Rev Cardiovasc Med. 2022 Aug 15;23(8):284. doi: 10.31083/j.rcm2308284. eCollection 2022 Aug. Rev Cardiovasc Med. 2022. PMID: 39076631 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources