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December 1, 1997The Journal of Physiology74 citationsOpen Access

Ionic currents during sustained pacemaker activity in rabbit sino‐atrial myocytes

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AZAntonio ZazaMMMaria Vittoria MichelettiABAngelica Brioschi

Structured PICO

P
Population
Rabbit sino-atrial myocytes
I
Intervention
Action potential clamp technique with specific channel blockers (dihydropyridines, 2 mM Cs+, E-4031)
O
Outcome
Contribution of various ionic currents to diastolic depolarization (DD)surrogate

This study elucidates the complex interplay of ionic currents, including ICa,L, I(f), and IK,r, during diastolic depolarization in rabbit sinoatrial node cells.

Abstract

The contribution of various ionic currents to diastolic depolarization (DD) in rabbit sinoatrial myocytes was evaluated by the action potential clamp technique. Individual currents were identified, during sustained pacemaking activity reproduced under voltage clamp conditions, according to their sensitivity to specific channel blockers. 2. The current sensitive to dihydropyridines (DHPs), blockers of L-type Ca2+ current (ICa,L), was small and outward during most of DD. Diastolic DHP-sensitive current was affected by changes in the driving force for K+, but it was insensitive to E-4031, which blocks the current termed IK,r; it was abolished by cell dialysis with a Ca2+ chelator. 3. The current sensitive to 2 mM Cs+ (ICs), a blocker of hyperpolarization-activated current (I(f)), was inward during the whole DD and it was substantially larger than the net inward current flowing during this phase. However, diastolic IK,r, identified in the same cells as the current sensitive to the blocker E-4031, exceeded ICs 2-fold. 4. These findings suggest that: (a) Ca2+ influx during the pacemaker cycle increases a K+ conductance, thus inverting the direction of the net current generated by L-type Ca2+ channel activity during DD; (b) the magnitude of I(f) would be adequate to account fully for DD; however, the coexistence of a larger IK,r suggests that other channels besides I(f) contribute inward current during this phase.

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Cite This Study

Zaza et al. (1997) studied this question.

synapsesocial.com/papers/6a222a553081c2f8f8e24c84https://doi.org/10.1111/j.1469-7793.1997.677ba.x
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Also Consider

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

  1. 1Role of rapidly activating delayed rectifier K+ current in sinoatrial node pacemaker activity1995 · 106 citations
  2. 2Inactivation of calcium channels in mammalian heart cells: joint dependence on membrane potential and intracellular calcium.1985 · 476 citations
  3. 3Subcellular mechanism for Ca(2+)-dependent enhancement of delayed rectifier K+ current in isolated membrane patches of guinea pig ventricular myocytes.1994 · 80 citations
  4. 4Block and activation of the pace‐maker channel in calf Purkinje fibres: effects of potassium, caesium and rubidium1982 · 182 citations
  5. 5Properties and modulation of If in newborn versus adult cardiac SA node1997 · 62 citations