PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
October 1, 1993Acta Physiologica Scandinavica72 citationsOpen Access

Potassium currents in isolated human atrial and ventricular cardiocytes

View Full Paper
AVAndrás VarróPNPéter P. NánásiDLDavid A. Lathrop

Key Result

In isolated human cardiocytes, the K+ inward rectifier current (IK1) was three times larger in ventricular than atrial cells, while a pacemaker-like current (If) was observed only in atrial cells.

Key Points

  • The aim is to compare potassium ion currents between isolated human ventricular and atrial cardiocytes.
  • Applied whole-cell patch-clamp technique on isolated human cardiocytes.
  • Measured inward rectifier current (IK1) and transient outward current (Ito) at various potentials.
  • Analyzed inactivation kinetics and steady-state inactivation of currents.
  • IK1 was three times larger in ventricular cardiocytes (p<0.01) than in atrial cells.
  • Inactivation kinetics of IK1 were slower in ventricular cells (p<0.05).
  • A time-dependent inward current resembling pacemaker current (If) was observed in 4 of 12 atrial cells, with a time constant of activation of 240 +/- 21 ms.

Structured PICO

P
Population
Single ventricular and atrial cardiocytes isolated from human myocardium
I
Intervention
Whole-cell configuration of the patch-clamp technique
C
Comparator
Comparison between ventricular and atrial cardiocytes
O
Outcome
Characteristics of ion currents (K+ inward rectifier current IK1, transient outward current Ito, K+ delayed rectifier current IK, pacemaker current If)surrogate

Human ventricular cardiocytes exhibit a three-fold larger K+ inward rectifier current with slower inactivation kinetics compared to atrial cardiocytes, highlighting distinct electrophysiological properties between the two cell types.

Abstract

The whole-cell configuration of the patch-clamp technique was applied to study and compare ion currents in single ventricular and atrial cardiocytes isolated from human myocardium. In ventricular cardiocytes the K+ inward rectifier current (IK1) was three times larger than in atrial cardiocytes, while its inactivation kinetics were twice as slow when measured at -140 mV. The magnitude of these variables depended on the test potential but was independent of changes in holding potential. A transient outward current (I(to)) was observed in both ventricular and atrial cardiocytes. The amplitude of the inactivating component of Ito was not significantly different in atrial and ventricular cells, but the time course of inactivation was significantly longer in atrial than in ventricular cardiocytes. Steady-state inactivation of Ito in atrial cells was well described by a two-state Boltzmann function having a midpoint potential of -41.4 mV and a slope factor of 6.9 mV-1. No discernible K+ delayed rectifier current (IK) was observed in either cell type. In four of the 12 atrial cells studied, a time dependent inward current was observed at negative test potentials having a 240 +/- 21 ms time constant for activation and an amplitude of 101 +/- 28 pA. This current, which resembled the pacemaker current (I(f)), was not observed in any of the ventricular cells examined.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Varró et al. (1993) studied Isolated human myocardium. Patch-clamp technique vs. Ventricular vs atrial cardiocytes was evaluated on Ion currents (IK1, Ito, IK, If). In isolated human cardiocytes, the K+ inward rectifier current (IK1) was three times larger in ventricular than atrial cells, while a pacemaker-like current (If) was observed only in atrial cells.

synapsesocial.com/papers/6a15b0b915658026c082ab19https://doi.org/10.1111/j.1748-1716.1993.tb09605.x
Ask AI
Helpful
Bookmark
Share
View Full Paper