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Alterations of the force-frequency relationship in the failing human heart depend on the underlying cardiac disease

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Summary

We investigated the force-frequency relationship (0.5–3 Hz) in non-failing human myocardium and in end-stage failing human myocardium due to dilated cardiomyopathy or subacute myocarditis. In non-failing myocardium, force of contraction increased with increasing stimulation frequency. In end-stage heart failure, the force-frequency relationship was inverse in myocardium from dilated cardiomyopathy, but was similar to control in myocardium from subacute myocarditis. After increasing extracellular Ca2+-concentration from 2.5 to 7.2 mM, the shape of the force-frequency relationship was not changed in nonfailing myocardium. In dilated cardiomyopathy, the decline in force with increasing frequencies was even more pronounced at 7.2 mM compared to 2.5 mM extracellular Ca2+.In subacute myocarditis, at Ca2+ 7.2 mM, increasing frequencies increased force in the lower frequency range (< 1.75 Hz) only, whereas at higher stimulation rates force declined again. These results indicate that (1.) alterations of the force-frequency relationship in the failing human heart depend on the underlying cardiac disease and/or the time-course of the disease, and (2.) an increase in the extracellular Ca2+-concentration aggravates changes in the force-frequency relationship in the failing myocardium.

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© 1992 Dr. Dietrich Steinkopff Verlag GmbH & Co.KG, Darmstadt

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Pieske, B., Hasenfuss, G., Holubarsch, C., Schwinger, R., Böhm, M., Just, H. (1992). Alterations of the force-frequency relationship in the failing human heart depend on the underlying cardiac disease. In: Hasenfuss, G., Holubarsch, C., Just, H., Alpert, N.R. (eds) Cellular and Molecular Alterations in the Failing Human Heart. Steinkopff. https://doi.org/10.1007/978-3-642-72474-9_17

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  • DOI: https://doi.org/10.1007/978-3-642-72474-9_17

  • Publisher Name: Steinkopff

  • Print ISBN: 978-3-642-72476-3

  • Online ISBN: 978-3-642-72474-9

  • eBook Packages: Springer Book Archive

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