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August 1, 1993Circulation Research236 citationsOpen Access

Characteristics of transient outward current in human ventricular myocytes from patients with terminal heart failure.

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MNMichael NäbauerDBDirk J. BeuckelmannEEErland Erdmann

Key Result

A large Ca2+-independent transient outward K+ current is present in human ventricular myocytes from patients with terminal heart failure, exhibiting monoexponential inactivation.

Key Points

  • This research aims to determine the existence and electrophysiological properties of transient outward currents in human ventricular myocardium.
  • Current recordings from enzymatically isolated human ventricular myocytes of 22 patients with terminal heart failure
  • Investigated characteristics including half-maximal activation and inactivation
  • Assessed frequency-dependent reduction and pharmacological sensitivity using 4-aminopyridine
  • A transient outward current was recorded in almost all myocytes on depolarization, masking the Ca2+ current.
  • Inactivation was monoexponential with a time constant of 54.8 +/- 3.7 ms at +40 mV, indicating rapid recovery from inactivation.
  • The current was sensitive to 4-aminopyridine, with an IC50 of 1.15 mM.

Structured PICO

P
Population
Enzymatically isolated human ventricular myocytes obtained from explanted hearts of 22 patients with terminal heart failure.
E
Exposure
Electrophysiological characterization (depolarization, application of 4-aminopyridine)
O
Outcome
Presence and basic electrophysiological properties of transient outward currentsurrogate

A large Ca2+-independent transient outward K+ current exists in human ventricular myocytes from terminal heart failure patients, representing a potential site for pharmacological intervention.

Abstract

A variety of outward currents exists in ventricular myocardium of different species influencing action potential duration and electrical activity. Transient outward currents have been reported in ventricular tissue of some animals but are small or absent in others. This study was conducted to investigate whether a transient outward current exists in human ventricular myocardium and to characterize its basic electrophysiological properties. Currents were recorded from enzymatically isolated human ventricular myocytes obtained from explanted hearts of 22 patients with terminal heart failure. In almost all cells studied, a transient outward current could be recorded on depolarization to between -20 and +80 mV. The size of the transient outward current was usually large enough to mask the Ca2+ current. It could be recorded under conditions in which Ca2+ influx and intracellular Ca2+ transients were suppressed. Basic current characteristics were similar to transient outward currents observed in other species. Inactivation of the transient outward current was monoexponential, with a time constant of 54.8 +/- 3.7 milliseconds at +40 mV. Half-maximal activation occurred at 16.7 +/- 1.6 mV; half-maximal steady-state inactivation occurred at -34.5 +/- 2.3 mV. Frequency-dependent reduction of peak transient outward current was 29.8 +/- 1.4% at 2 Hz compared with resting conditions. Recovery from inactivation was voltage dependent and had a biexponential time course; the faster time constant (41.0 +/- 6.5 milliseconds at -80 mV) accounted for 86.0 +/- 5.2% of total current. The transient outward current was sensitive to 4-aminopyridine (IC50, 1.15 mM). These results indicate that a large Ca(2+)-independent transient outward K+ current is present in human ventricular myocytes that might be regulated by physiological or pathological events and is a potential site for pharmacological intervention.

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Cite This Study

Näbauer et al. (1993) studied Terminal heart failure (n=22). Electrophysiological characterization of transient outward current was evaluated on Presence and characteristics of transient outward current. A large Ca2+-independent transient outward K+ current is present in human ventricular myocytes from patients with terminal heart failure, exhibiting monoexponential inactivation.

synapsesocial.com/papers/6a21fce63081c2f8f8e2265ehttps://doi.org/10.1161/01.res.73.2.386
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