Literature DB >> 1735148

Contractile properties and Ca2+ release activity of the sarcoplasmic reticulum in dilated cardiomyopathy.

A D'Agnolo1, G B Luciani, A Mazzucco, V Gallucci, G Salviati.   

Abstract

BACKGROUND: We performed a comparative study on Ca2+ release activity of the sarcoplasmic reticulum and calcium sensitivity of contractile apparatus of chemically skinned myocardial fibers obtained from four nonfailing human hearts and 13 excised hearts from patients with idiopathic dilated cardiomyopathy. METHODS AND
RESULTS: Ca2+ sensitivity of contractile apparatus was studied by following the isometric tension developed by chemically skinned myocardial fibers challenged with solutions of decreasing pCa. Ca2+ release from sarcoplasmic reticulum was monitored indirectly by measurement of the isometric tension developed by skinned fibers challenged with caffeine. We observed no significant difference of Ca2+ sensitivity and cooperativity between normal myocardium (pCa50 = 6.00 +/- 0.05; Hill coefficient, nHill = 2.07 +/- 0.10) and dilated cardiomyopathy (pCa50 = 6.03 +/- 0.07; nHill = 2.72 +/- 0.30) when the fibers were stretched to 130% of the resting length. We also found that both in normal myocardium and dilated cardiomyopathy, stretching to 150% of the resting length increased the Ca2+ sensitivity of the contractile system; pCa50 = 6.21 +/- 0.01 and 6.13 +/- 0.04 in normal and dilated cardiomyopathy, respectively, whereas in dilated cardiomyopathy there was a decrease of Hill coefficient with stretching that was not observed in the control group. The caffeine threshold in idiopathic dilated cardiomyopathy was markedly increased compared with the control group, 1.94 +/- 0.27 mmol/l and 0.29 +/- 0.04 mmol/l caffeine, respectively, whereas there were no significant differences in the extent and rate of caffeine-induced Ca2+ release.
CONCLUSIONS: These results indicate that in idiopathic dilated cardiomyopathy there is no alteration of contractile and regulatory proteins; on the contrary, the gating mechanism of the Ca2+ release channel of sarcoplasmic reticulum is abnormal, suggesting a possible involvement of the excitation-contraction coupling in the pathogenesis of this disease. It should also be taken into account, however, that the increased caffeine threshold in dilated cardiomyopathy would be a result of the enhanced resistance to the skinning procedure secondary to the modification of lipid species and/or content in sarcoplasmic reticulum membrane.

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Year:  1992        PMID: 1735148     DOI: 10.1161/01.cir.85.2.518

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  14 in total

1.  Intracellular calcium and the relationship to contractility in an avian model of heart failure.

Authors:  C S Kim; A J Davidoff; T M Maki; A A Doye; J K Gwathmey
Journal:  J Comp Physiol B       Date:  2000-06       Impact factor: 2.200

2.  Diminished post-rest potentiation of contractile force in human dilated cardiomyopathy. Functional evidence for alterations in intracellular Ca2+ handling.

Authors:  B Pieske; M Sütterlin; S Schmidt-Schweda; K Minami; M Meyer; M Olschewski; C Holubarsch; H Just; G Hasenfuss
Journal:  J Clin Invest       Date:  1996-08-01       Impact factor: 14.808

3.  Myofibrillar calcium sensitivity of isometric tension is increased in human dilated cardiomyopathies: role of altered beta-adrenergically mediated protein phosphorylation.

Authors:  M R Wolff; S H Buck; S W Stoker; M L Greaser; R M Mentzer
Journal:  J Clin Invest       Date:  1996-07-01       Impact factor: 14.808

4.  Myocardial region (right or left ventricle) and aetiology of heart failure can influence the inotropic effect of ouabain in failing human myocardium.

Authors:  R Padrini; M Panfili; G Magnolfi; D Piovan; D Casarotto; M Ferrari
Journal:  Br J Clin Pharmacol       Date:  1999-11       Impact factor: 4.335

5.  Unaltered ryanodine receptor protein levels in ischemic cardiomyopathy.

Authors:  W Schillinger; M Meyer; G Kuwajima; K Mikoshiba; H Just; G Hasenfuss
Journal:  Mol Cell Biochem       Date:  1996 Jul-Aug       Impact factor: 3.396

6.  Evaluation of the regional responsivity to ryanodine of human myocardium from patients with idiopathic dilated cardiomyopathy and secondary cardiomyopathies.

Authors:  R Padrini; M Panfili; L Testolin; F Pesarin; D Piovan; G Magnolfi; U Livi; D Casarotto; S Dalla Volta
Journal:  Basic Res Cardiol       Date:  1996 Sep-Oct       Impact factor: 17.165

Review 7.  Myocardial phenotype changes in heart failure: cellular and subcellular adaptations and their functional significance.

Authors:  G Hasenfuss; H Just
Journal:  Br Heart J       Date:  1994-08

8.  The ryanodine binding sarcoplasmic reticulum calcium release channel in nonfailing and in failing human myocardium.

Authors:  C Schumacher; B Konigs; M Sigmund; B Kohne; F Schondube; M Vob; B Stein; J Weil; P Hanrath
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1995-12       Impact factor: 3.000

9.  Reduced troponin I phosphorylation and increased Ca(2+)-dependent ATP-consumption in triton X-skinned fiber preparations from Galphaq overexpressor mice.

Authors:  C Pott; L Willkomm; S Grafweg; B Bölck; G W Dorn; R H G Schwinger; K Brixius
Journal:  Mol Cell Biochem       Date:  2008-05-13       Impact factor: 3.396

Review 10.  Is contractility depressed in the failing human heart?

Authors:  J K Gwathmey; R Liao; P A Helm; G Thaiyananthan; R J Hajjar
Journal:  Cardiovasc Drugs Ther       Date:  1995-08       Impact factor: 3.727

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