Literature DB >> 6321053

Biochemical properties of membranes isolated from calcium-depleted rabbit hearts.

J M Lamers, J T Stinis, T J Ruigrok.   

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.

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Year:  1984        PMID: 6321053     DOI: 10.1161/01.res.54.3.217

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  11 in total

1.  No evidence of oxygen free radicals-mediated damage during the calcium paradox.

Authors:  R Ferrari; C Ceconi; S Curello; A Cargnoni; T J Ruigrok
Journal:  Basic Res Cardiol       Date:  1989 Jul-Aug       Impact factor: 17.165

2.  Prevention by 7-oxo-prostacyclin of the calcium paradox in rat heart: role of the sarcolemmal (Na,K)-ATPase.

Authors:  A Ziegelhöffer; T Ravingerová; A Dzurba; N Tribulová; J Slezák; A Breier; L Szekeres
Journal:  Mol Cell Biochem       Date:  1996 Jul-Aug       Impact factor: 3.396

3.  Beta-adrenergic receptors and enzymes in rat myocardial membranes: implications of fractionation procedures and beta-adrenoceptor antagonists.

Authors:  E Schrader; M Inczédy-Marcsek; H Grobecker
Journal:  Cell Mol Neurobiol       Date:  1988-06       Impact factor: 5.046

4.  Alterations in cardiac function and subcellular membrane activities after hypervitaminosis D3.

Authors:  S Takeo; R Tanonaka; K Tanonaka; K Miyake; H Hisayama; N Ueda; K Kawakami; H Tsumura; S Katsushika; Y Taniguchi
Journal:  Mol Cell Biochem       Date:  1991-10-16       Impact factor: 3.396

5.  The effect of hypothermia during the period of calcium repletion on the calcium paradox.

Authors:  T J Ruigrok; D de Moes; P van der Meer
Journal:  Basic Res Cardiol       Date:  1986 Jul-Aug       Impact factor: 17.165

6.  Polyamines mediate uncontrolled calcium entry and cell damage in rat heart in the calcium paradox.

Authors:  H Koenig; A D Goldstone; J J Trout; C Y Lu
Journal:  J Clin Invest       Date:  1987-11       Impact factor: 14.808

7.  L-leucine transport in rat heart under normal conditions and effects of a simulated hypoxia.

Authors:  N King; M S Suleiman
Journal:  Mol Cell Biochem       Date:  2001-05       Impact factor: 3.396

8.  Modification of heart sarcolemmal Na+/K+-ATPase activity during development of the calcium paradox.

Authors:  L E Alto; V Elimban; A Lukas; N S Dhalla
Journal:  Mol Cell Biochem       Date:  2000-04       Impact factor: 3.396

9.  Suppression of cellular injury during the calcium paradox in rat heart by factors which reduce calcium uptake by mitochondria.

Authors:  P Busselen
Journal:  Pflugers Arch       Date:  1985-05       Impact factor: 3.657

10.  Modification of caffeine-induced injury in Ca2+-free perfused rat hearts. Relationship to the calcium paradox.

Authors:  R S Vander Heide; R A Altschuld; K G Lamka; C E Ganote
Journal:  Am J Pathol       Date:  1986-05       Impact factor: 4.307

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