Literature DB >> 1325933

Excitation-contraction coupling in the heart: the state of the question.

M D Stern1, E G Lakatta.   

Abstract

Recent developments have led to great progress toward determining the mechanism by which calcium is released from the sarcoplasmic reticulum in the heart. The data support the notion of calcium-induced calcium release via a calcium-sensitive release channel. Calcium release channels have been isolated and cloned. This situation creates a paradox, as it has also been found that calcium release is smoothly graded and closely responsive to sarcolemmal membrane potential, properties that would not be expected of calcium-induced calcium release, which has intrinsic positive feedback. There is, therefore, no quantitative understanding of how the properties of the calcium release channel can lead to the macroscopic physiology of the whole cell. This problem could, in principle, be solved by various schemes involving heterogeneity at the ultrastructural level. The simplest of these require only that the sarcolemmal calcium channel be located in close proximity to one or more sarcoplasmic reticulum release channels. Theoretical modeling shows that such arrangements can, in fact, resolve the positive feedback paradox. An agenda is proposed for future studies required in order to reach a specific, quantitative understanding of the functioning of calcium-induced calcium release.

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Year:  1992        PMID: 1325933     DOI: 10.1096/fasebj.6.12.1325933

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  35 in total

1.  The role of luminal Ca2+ in the generation of Ca2+ waves in rat ventricular myocytes.

Authors:  V Lukyanenko; S Subramanian; I Gyorke; T F Wiesner; S Gyorke
Journal:  J Physiol       Date:  1999-07-01       Impact factor: 5.182

2.  Ca2+ sparks and Ca2+ waves in saponin-permeabilized rat ventricular myocytes.

Authors:  V Lukyanenko; S Gyorke
Journal:  J Physiol       Date:  1999-12-15       Impact factor: 5.182

3.  Location of ryanodine and dihydropyridine receptors in frog myocardium.

Authors:  Pierre Tijskens; Gerhard Meissner; Clara Franzini-Armstrong
Journal:  Biophys J       Date:  2003-02       Impact factor: 4.033

4.  Deformation of the Bowditch staircase in Ca(2+)-overloaded mammalian cardiac tissue--a calcium phenomenon?

Authors:  M Löhn; G Szymanski; F Markwardt
Journal:  Mol Cell Biochem       Date:  1996 Jul-Aug       Impact factor: 3.396

5.  Influence of glycosylation inhibitors on dihydropyridine binding to cardiac cells.

Authors:  U Henning; G Wallukat; M Holtzhauer
Journal:  Mol Cell Biochem       Date:  1996 Jul-Aug       Impact factor: 3.396

6.  Purification and characterization of ryanotoxin, a peptide with actions similar to those of ryanodine.

Authors:  J Morrissette; M Beurg; M Sukhareva; R Coronado
Journal:  Biophys J       Date:  1996-08       Impact factor: 4.033

7.  Regulation of the cardiac ryanodine receptor channel by luminal Ca2+ involves luminal Ca2+ sensing sites.

Authors:  I Györke; S Györke
Journal:  Biophys J       Date:  1998-12       Impact factor: 4.033

8.  Termination of Ca2+ release during Ca2+ sparks in rat ventricular myocytes.

Authors:  V Lukyanenko; T F Wiesner; S Gyorke
Journal:  J Physiol       Date:  1998-03-15       Impact factor: 5.182

9.  Influence of ryanodine on the mechanical restitution and on the post-extrasystolic potentiation of the guinea-pig ventricular myocardium.

Authors:  G Oblonczek; G Szymanski
Journal:  Mol Cell Biochem       Date:  1997-10       Impact factor: 3.396

10.  Alteration by lipopolysaccharide of the relationship between intracellular calcium levels and contraction in rat mesenteric artery.

Authors:  M C Martínez; B Muller; J C Stoclet; R Andriantsitohaina
Journal:  Br J Pharmacol       Date:  1996-07       Impact factor: 8.739

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