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Gewählte Publikation:

Lehnart, SE; Schillinger, W; Pieske, B; Prestle, J; Just, H; Hasenfuss, G.
Sarcoplasmic reticulum proteins in heart failure.
Ann N Y Acad Sci. 1998; 853(4):220-230 Doi: 10.1111/j.1749-6632.1998.tb08270.x
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Co-Autor*innen der Med Uni Graz
Pieske Burkert Mathias
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Abstract:
Altered calcium homeostasis may play a key role in the pathophysiology of human heart failure. Levels of sarcoplasmic reticulum (SR) proteins and sarcolemmal Na(+)-Ca2+ exchanger were analyzed by Western blot in failing and nonfailing human myocardium and related to myocardial function. Levels of the SR calcium release channel and of calcium storage proteins (calsequestrin and calreticulin) were not different in nonfailing and failing hearts. However, proteins involved in calcium removal were significantly altered in the failing human heart: (1) SR-Ca(2+)-ATPase levels and the ratio of SR-Ca(2+)-ATPase to its inhibitory protein phospholamban were significantly decreased, and (2) Na(+)-Ca2+ exchanger levels and the ratio of Na(+)-Ca2+ exchanger to SR-Ca(2+)-ATPase were significantly increased. SR-Ca(2+)-ATPase levels were closely correlated to systolic function as evaluated by frequency potentiation of contractile force. The frequency-dependent rise of diastolic force was inversely correlated with protein levels of Na(+)-Ca2+ exchanger. These findings indicate that altered expression of SR-Ca(2+)-ATPase and Na(+)-Ca2+ exchanger is relevant for altered systolic and diastolic function in human heart failure.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Calcium - metabolism
Calcium-Binding Proteins - metabolism
Calcium-Transporting ATPases - metabolism
Calreticulin - metabolism
Calsequestrin - metabolism
Cardiomyopathy, Dilated - physiopathology
Heart Failure, Congestive - physiopathology
Humans - physiopathology
Myocardial Contraction - physiology
Ribonucleoproteins - metabolism
Ryanodine Receptor Calcium Release Channel - physiology
Sarcoplasmic Reticulum - physiology
Sodium-Calcium Exchanger - metabolism

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