Abstract
Cyclic adenosine 3′,5′-monophosphate (cAMP) or the free catalytic subunit (C) of the cAMP-dependent protein kinase were pressure injected into single guinea pig ventricular cells. The following results were obtained:
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1.
Injection of cAMP prolonged the action potential and shifted the action potential plateau to a more positive level. Under voltage clamp, cAMP injection increased the amplitude of the slow inward calcium current (I si).
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2.
Injection of C permanently prolonged the action potential and enhanced the amplitude ofI si by a factor of 2–4, depending on the amount of injected C. In the current-voltage relations the potential of maximumI si and the apparent current reversal did not change.
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3.
After maximum prolongation of the action potential due to repeated injections of C, even high concentrations of adrenaline did not further change the configuration of the action potential.
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4.
In many experiments transient depolarizations appeared after the injection. Correspondingly, under voltage clamp transient inward currents occurred.
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5.
C injection increased both the time-dependent and time-independent potassium outward current.
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6.
In response to injection of the catalytic subunit, the isotonic contraction was larger in amplitude and relaxation was faster.
It is concluded that the cAMP-dependent protein kinase increases the slow inward calcium current in the heart, presumably by phosphorylation of some membrane proteins.
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This work was supported by the Deutsche Forschungsgemeinschaft SFB 38, Membranforschung, project G, and DFG Ho 579/6-1 and Fonds der Chemischen Industrie
Dr. Brum is a recipient of a fellowship from the Deutscher Akademischer Austauschdienst
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Brum, G., Flockerzi, V., Hofmann, F. et al. Injection of catalytic subunit of cAMP-dependent protein kinase into isolated cardiac myocytes. Pflugers Arch. 398, 147–154 (1983). https://doi.org/10.1007/BF00581064
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DOI: https://doi.org/10.1007/BF00581064