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May 1, 1990Journal of Clinical Investigation276 citationsOpen Access

Role of intracellular calcium handling in force-interval relationships of human ventricular myocardium.

JGJudith K. GwathmeyMSMara SlawskyRHRoger J. Hajjar

Structured PICO

How do changes in stimulation rate and pattern affect intracellular calcium handling and force in human myopathic ventricular myocardium compared to controls?

P
Population
Human working myocardium (control and myopathic muscles)
I
Intervention
Changes in stimulation rate and pattern
C
Comparator
Control muscles
O
Outcome
Peak isometric force and intracellular calcium transientsurrogate

Abnormalities in contractile function of myopathic muscles during frequency-related force potentiation are likely due to differences in myofibrillar calcium responsiveness rather than decreased availability of intracellular calcium.

Abstract

Experiments were performed in human working myocardium to investigate the relationship of intracellular calcium handling and availability to alterations in the strength of contraction produced by changes in stimulation rate and pattern. Both control and myopathic muscles exhibited potentiation of peak isometric force during the postextrasystolic contraction which was associated with an increase in the peak intracellular calcium transient. Frequency-related force potentiation was attenuated in myopathic muscles compared to controls. This occurred despite an increase in resting intracellular calcium and in the peak amplitude of the calcium transient as detected with aequorin. Therefore, abnormalities in contractile function of myopathic muscles during frequency-related force potentiation are not due to decreased availability of intracellular calcium, but more likely reflect differences in myofibrillar calcium responsiveness. Sarcolemmal calcium influx may also contribute to frequency-related changes in contractile force in myopathic muscles as suggested by a decrease in action potential duration with increasing stimulation frequency which is associated with fluctuations in peak calcium transient amplitude.

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Cite This Study

Gwathmey et al. (1990) studied this question.

synapsesocial.com/papers/6a1ba526ab6181c407abb11ehttps://doi.org/10.1172/jci114611
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Postextrasystolic Potentiation of Contraction in Cardiac Muscle1956 · 166 citations
  2. 2Inactivation of calcium channels in mammalian heart cells: joint dependence on membrane potential and intracellular calcium.1985 · 476 citations
  3. 3Intracellular calcium transients underlying the short‐term force‐interval relationship in ferret ventricular myocardium.1986 · 269 citations
  4. 4Calcium Transients During Excitation-Contraction Coupling in Mammalian Heart: Aequorin Signals of Canine Purkinje Fibers1980 · 102 citations
  5. 5Postextrasystolic potentiation of the isolated canine left ventricle. Relationship to mechanical restitution.1985 · 116 citations