Biochemical properties of membranes isolated from calcium-depleted rabbit hearts.
- 1 March 1984
- journal article
- research article
- Published by Wolters Kluwer Health in Circulation Research
- Vol. 54 (3) , 217-226
- https://doi.org/10.1161/01.res.54.3.217
Abstract
The purpose of this study was to define the biochemical properties of sarcolemma from the calcium-depleted rabbit heart. Calcium repletion after calcium-free perfusion results in irreversible damage to the heart (calcium paradox). No difference was found in specific activity of the Na+ -Ca++ antiporter in a crude preparation of sarcolemmal vesicles that was isolated from calcium-depleted hearts, compared with control perfused hearts. Likewise, the passive calcium efflux from sarcolemmal vesicles, preloaded with calcium via the Na+ -Ca++ antiporter, showed rates that were identical with control values. This indicates that the sarcolemma calcium permeability is not affected by calcium-free perfusion of the heart. Na+,K+ -ATPase activity in sarcolemma isolated from calcium-depleted hearts was reduced by 75% (P less than 0.005) compared with the control activity. Sarcolemmal phosphoproteins, whether produced by endogenous cyclic AMP- or calcium-calmodulin-dependent protein kinase, were not altered by calcium-free perfusion of the heart. The content of an important calcium-binding site in the myocardial cell, the sialic acid residues, was also estimated. Only a long period (60 minutes) of calcium-free perfusion resulted in a significant decrease (by 68%, P less than 0.025) of sialic acid content in the homogenate but not in the sarcolemma preparation. In hearts that were reperfused for 15 minutes with a normal calcium concentration (1.3 mM), sarcolemmal Na+,K+ -ATPase remained depressed and calcium permeability was still unchanged. It is possible that the sarcolemma isolation method selected a distinct part of the sarcolemma from the calcium-depleted and repleted heart that had no modified glycocalyx and permeability barriers to calcium ions, and that another part of the sarcolemma with altered properties was lost during the isolation procedure. Another possibility is that reconstitution processes during isolation affected membrane permeability properties. The results of the Na+,K+ -ATPase measurements provide evidence that the net calcium gain of the cells after calcium repletion may be associated, in part, with a loss in ability of the sarcolemma to remove calcium from the cytosol.This publication has 48 references indexed in Scilit:
- Isolation of cardiac membrane proteolipids by high pressure liquid chromatography. A comparison of reticular and sarcolemmal proteolipids, phospholamban and calciductinBiochimica et Biophysica Acta (BBA) - Biomembranes, 1983
- Ca2+-free perfusion of rat heart reveals a (Na+ + K+) ATPase form highly sensitive to ouabainNature, 1982
- Phosphorylation of troponin I and phospholamban during catecholamine stimulation of rabbit heartNature, 1982
- Partial purification of an intercalated disc-containing cardiac plasma membrane fractionBiochimica et Biophysica Acta (BBA) - Biomembranes, 1982
- (Na+ + K+)-ATPase activity of newborn rabbit cardiac muscleBiochemical Medicine, 1981
- On the role of cyclic AMP and Ca2+—calmodulin‐dependent phosphorylation in the control of (Ca2+ + Mg2+)‐ATPase of cardiac sarcolemmaFEBS Letters, 1981
- Membrane localization of myocardial type II cyclic amp-dependent protein kinase activityBiochimica et Biophysica Acta (BBA) - Biomembranes, 1981
- An electrogenic Na+/Ca2+ antiporter in addition to the Ca2+ pump in cardiac sarcolemmaBiochimica et Biophysica Acta (BBA) - Biomembranes, 1981
- Defective calcium pump in the sarcoplasmic reticulum of the hypertrophied rabbit heartLife Sciences, 1979
- ATP-induced stimulation of calcium binding to cardiac sarcolemmaBiochemical and Biophysical Research Communications, 1979