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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Heart Rhythm. Author manuscript; available in PMC 2011 January 1.
Published in final edited form as:
PMCID: PMC2824242
NIHMSID: NIHMS169285

Yin and Yang of the cardiac pacemaker clock system in health and disease

Cardiac arrhythmias in general, and atrial fibrillation (AF), in particular, are important global health problems. Despite extensive studies, arrhythmia mechanisms remain unclear. The problem is complicated because heart function is affected by a complex integration of numerous biochemical and biophysical processes within and among cardiac cells. Interactions within SA node, the primary hearts' pacemaker that initiates and regulates the cardiac rhythm, results in one such critical unsolved complexity. Joung et al. 1 have recently applied a method of simultaneous recording of intracellular Ca2+ and membrane potential to approach the riddle of complex/intimate interactions between electrophysiology and intracellular Ca2+ signaling within cells comprising SA node. In this issue of HeartRhythm, Joung et al. 2 combined their method with measurements of expression of Ca2+ cycling proteins to explore the mechanisms of SA node dysfunction in AF.

Voltage-gated sarcolemmal ion currents are the proximal cause of an action potential (AP) as originally described by Hodgkin and Huxley based on voltage clamp data. In silico, the ensemble, or system, of the sarcolemmal electrogenic molecules (ion channels and transporters) of cardiac pacemaker cell can generate rhythmic APs, e.g. in 12 SA node cell (SANC) numerical models 3). Therefore, this system of ion currents can be envisioned as a membrane voltage oscillator or “membrane clock” (M clock). The classical perspective on cardiac pacemaker cell function is that the M clock is the ultimate cardiac pacemaker clock, i.e. its function is not only necessary, but also sufficient to drive normal automaticity. However, in addition to an M clock, cardiac pacemaker cells have another intrinsic oscillatory subsystem that resides within the cell: the sarcoplasmic reticulum (SR) pumps and periodically releases Ca2+ 4. While a potential role of the Ca cycling in normal function of cardiac pacemaker cells had been envisioned 5,6 and experimentally demonstrated r-10 long ago, recent extensive studies (during last decade) have discovered the spatiotemporal characteristics of the SR Ca2+ cycling and its interactions with the M clock (review 11). Confocal measurements in isolated pacemaker cells detect Localized submembrane Ca2+ Releases (LCR's) generated by the SR via ryanodine receptors (RyRs) during the late diastolic depolarization (DD) 12,13. The integrated Ca2+ signal of these multiple LCRs during DD represents diastolic Ca2+ release (Fig.3 in 14) that was observed by Joung et al. 1 as Late Diastolic Ca2+ elevation (LDCAE) in the primary region (i.e. impulse initiating part) of the isolated intact dog SA node. The spontaneous Ca2+ releases are referred to as an intracellular “Ca2+ clock” because their occurrence is periodic during voltage clamp 15, in detergent-permeabilized SANC 16, and in silico (when membrane currents set to zero) 17. In nature, i.e., in spontaneously firing SANC, in contrast to in silico or skinned or voltage-clamped cells, Ca2+ and M clocks do not exist in isolation of each other: Numerous and complex interactions via membrane voltage, submembrane Ca2+, and protein phosphorylation occur between the two subsystem clocks (M clock and Ca2+ clock), and the subsystems become mutually entrained forming the full pacemaker cell SYSTEM or the master pacemaker clock (reviews 11,18). The two interacting clock subsystems do not just simply coexist within the pacemaker system but their interaction confers robustness and flexibility to the cardiac pacemaker function as discussed in a recent review 11 and demonstrated in a numerical study that predicts LDCAE 17. Specifically, the presence of Ca2+ clock extends the fail-safe variations of membrane clock parameters, such as L-type Ca2+ current (ICaL) conductance and, vice versa, the presence of some membrane components, such as funny current (If), increases the fail-safe variations of Ca2+ clock parameters, such as Ca2+ pumping rate11.

In the context of the concept of a coupled clock system, the finding of Joung et al study 2 that RyR2 are down regulated, and LDCAE are absent in their experimental AF model, can be interpreted to indicate that the Ca2+ clock subsystem is impaired in AF, resulting probably in decreased robustness and flexibility of the pacemaker system. In other words, the impairment of diastolic Ca2+ releases shifts the operation of SANC likely towards less safe (i.e. susceptible to arrhythmia) operation.

But what about SANC M clock changes in AF? A recent study by Yeh et al. 19 has identified that major electrophysiological changes of SANC in experimentally induced AF in dogs include a 50% reduction in If conductance and a 33% reduction in slow delayed rectifier K+ current (IKs). Their numerical simulations showed that IKs change had almost no effect on SANC rhythm (less than 1% cycle length change) and the If change resulted in a cycle length increase of ~9%. But a change of this magnitude seems to be a relatively moderate effect, i.e. far from trouble. However, taking into account that the robustness of coupled clock system had been compromised by Ca2+ clock impairment identified by Joung et al 2 and discussed above, is it possible that this If change could be critical for SANC function? We believe that the answer to this question is not trivial, and presently can be approached only by numerical integration of changes of both Ca2+ and M clocks. Accordingly, we used our recently developed prototype model of interacting Ca2+ clock and M clock in rabbit SANC 17 and performed numerical simulations to illustrate that it is indeed possible, at least at the level of a single pacemaker cell (Fig.1). The 50% reduction in If conductance produced a moderate rate reduction of the simulated AP firing rate (i.e. similar to numerical modeling by Yeh et al. 19). The absence of Ca2+ release, with If remaining intact, however, substantially slowed the rate by ~40%, but AP firing still remained rhythmic (Fig.1C). However when the “impaired” Ca2+ release was combined with the “impaired” If function, the spontaneous beating became irregular.

Figure 1
The combined impairment of M clock and Ca2+ clock in AF can result in generation of irregular action potentials by SA node cells. Simulations by a recent numerical model of rabbit SANC 17 illustrate spontaneous action potentials (top traces), funny current ...

These simple “first order” estimates illustrate that:

  1. interactions of subsystem clocks are crucial to the generation of spontaneous APs of a normal rate and rhythm, and
  2. when both M clock and Ca clock are impaired in AF (or in any other experimental or pathological conditions), uncoupling of M clock and Ca clock can push the master pacemaker clock towards its limits of fail safe operation.

Specific, detailed mechanisms of the system changes in AF and their numerical integration, specifically in canine SANC and SA node (and, ultimately, in human SA node), however, merit further studies. These additional mechanisms include characterization and integration of components of PKA and CaMKII-dependent phosphorylation (e.g. phosphorylation of phospholamban, SERCA, RyR, L-type Ca2+ channels), sarcolemmal ion exchangers (e.g. Na+/Ca2+ exchanger and Na+/K+ pump), ion channel kinetics, intracellular contacts (e.g. via connexins), and mechanical factor, i.e. strain. An additional important requirement is a further improvement of both selectivity and spatiotemporal resolution of LDCAE recording within SA node. Such improvements will permit a determination of whether LDCAE exists during basal beating in large animals like canines as the case for rabbit and mouse, as well as whether LDCAE can propagate within the SA node. An intriguing question is also how expression of sarcolemmal electrogenic molecules (ion channels and transporters) and Ca2+ cycling proteins (especially RyR as found by Joung et al. 2) is regulated, the nature and kinetics of the molecular dysregulation in AF, and whether, in particular, changes in RyRs and AF are concomitantly reversed by cessation of chronic pacing.

In summary, the study by Joung et al. 2 in this issue of Heart Rhythm suggests that rhythm disturbances in canine experimental AF are caused, at least in part, by a failure of Ca2+ clock function, specifically its release from SR via RyR2. However, the extent to which this mechanism contributes to AF requires further studies aimed to integration of changes in Ca2+ cycling proteins, their phosphorylation status, and changes in sarcolemmal electrogenic molecules. We believe that an important lesson from the recent papers by Joung et al. 1,2 and Yeh et al. 19 and our simple simulations (Fig.1) is that to be informative, future studies of cardiac pacemaker function, either normal or abnormal, must include integration of the two mutually entrained subsystems, Ca2+ clock and membrane clock, the Yin and Yang of the cardiac pacemaker cell function.

Acknowledgments

This research was supported by the Intramural Research Program of the National Institutes of Health, National Institute on Aging.

Footnotes

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