Mechanisms underlying the frequency dependence of contraction and [Ca2+]i transients in mouse ventricular myocytes

doi:10.1113/jphysiol.2002.025619

Mechanisms underlying the frequency dependence of contraction and [Ca²⁺]_i transients in mouse ventricular myocytes

Gudrun Antoons, Kanigula Mubagwa†, Ines Nevelsteen† and Karin R. Sipido*

*Laboratory of Experimental Cardiology and †Centre for Experimental Surgery and Anesthesiology, University of Leuven, Belgium

ABSTRACT

Top
Abstract
Introduction
Methods
Results
Discussion
References

In most mammalian species force of contraction of cardiac muscle increases with increasing rate of stimulation, i.e. a positive force-frequency relationship. In single mouse ventricular cells, both positive and negative relationships have been described and little is known about the underlying mechanisms. We studied enzymatically isolated single ventricular mouse myocytes, at 30 °C. During field stimulation, amplitude of unloaded cell shortening increased with increasing frequency of stimulation (0.04 ± 0.01 $Delta$ L/L₀ at 1 Hz to 0.07 ± 0.01 $Delta$ L/L₀ at 4 Hz, n = 12, P < 0.05). During whole cell voltage clamp with 50 µM [K5-fluo-3]_pip, both peak and baseline [Ca²⁺]_i increased at higher stimulation frequencies, but the net $Delta$ [Ca²⁺]_i increased only modestly from 1.59 ± 0.08 $Delta$ F/F₀ at 1 Hz, to 1.71 ± 0.11 $Delta$ F/F₀ at 4 Hz (n = 17, P < 0.05). When a 1 s pause was interposed during stimulation at 2 and 4 Hz, [Ca²⁺]_i transients were significantly larger (at 4 Hz, peak F/F₀ increased by 78 ± 2 %, n = 5). SR Ca²⁺ content assessed during caffeine application, significantly increased from 91 ± 24 µmol l^-1 at 1 Hz to 173 ± 20 µmol l^-1 at 4 Hz (n = 5, P < 0.05). Peak I_Ca,L decreased at higher frequencies (by 28 ± 6 % at 2 Hz, and 45 ± 8 % at 4 Hz), due to slow recovery from inactivation. This loss of I_Ca,L resulted in reduced fractional release. Thus, in mouse ventricular myocytes the [Ca²⁺]_i-frequency response depends on a balance between the increase in SR content and the loss of trigger I_Ca,L. Small changes in this balance may contribute to variability in frequency-dependent behaviour. In addition, there may be a regulation of the contractile response downstream of [Ca²⁺]_i.

(Resubmitted 30 May 2002; accepted 11 June 2002; first published online 5 July 2002)
Corresponding author K. R. Sipido: Laboratory of Experimental Cardiology, University of Leuven, Campus Gasthuisberg, Herestraat 49, B-3000 Leuven, Belgium. Email: karin.sipido{at}med.kuleuven.ac.be

INTRODUCTION

Top
Abstract
Introduction
Methods
Results
Discussion
References

The change in contractile force in response to a change in frequency of stimulation is a general property of cardiac muscle. For most species, including healthy humans, the relation is a positive one, i.e. force of contraction increases with increasing frequency of stimulation (e.g. Gwathmey et al. 1990 for human). This positive staircase results from larger [Ca²⁺]_i transients at higher frequencies, due to an increase in sarcoplasmic reticulum (SR) content with increasing stimulation frequency (reviewed in Bers, 2001). Frequency-dependent facilitation of I_Ca,L may also contribute to the positive staircase (Zygmunt & Maylie, 1990). For the rat the relation is negative in the lower range of frequencies (below 2 Hz, e.g. Henderson et al. 1974; but see also Layland & Kentish, 1999). It is thought that resting SR content in the rat is high and cannot be increased in this range of frequencies; incomplete recovery of the release channel during stimulation at higher frequencies would then result in a negative staircase (reviewed in Bers, 2001). The force-frequency relation is often used to describe the contractile state and can be altered by inotropic interventions, e.g. by drugs that increase [Na⁺]_i (Koch-Weser & Blinks, 1963; Mubagwa et al. 1997) or that affect SR Ca²⁺ uptake and release (Baudet et al. 1996; Bers & Christensen, 1990), and by disease states such as heart failure (Mulieri et al. 1992). Changes in the relation usually reflect alterations in one of the underlying mechanisms, e.g. the diminished capacity of the SR to increase its Ca²⁺ content, which has been implicated in the negative force-frequency of the failing human heart (Pieske et al. 1999).

Because of transgenic technology, the mouse has become a much-studied species for cardiovascular pathophysiology. The basic, normal physiology, may however be quite particular in this small animal with high in vivo heart rates. For the frequency response, experiments on trabeculae have shown a positive relation with an increase in force for increase in stimulation frequency from 1 to 4 Hz (Gao et al. 1998). The response in the amplitude of the Ca²⁺ transient was also positive, though less pronounced than for contraction. In vivo, the frequency response appears to be rather flat in the range from 500 to 850 beats min^-1 (Georgakopoulos & Kass, 2001). In some of the recent transgenic mouse models the frequency response was found to be altered, e.g. by changes in phospholamban, PLB, expression (Kadambi et al. 1999), or by knockout of Annexin VII (Herr et al. 2001). Yet the mechanisms determining the frequency response in the mouse, which may be particular to this species, have not been studied. We therefore examined the characteristics of the frequency response of contraction and of Ca²⁺ fluxes in single mouse ventricular myocytes. We found a prominent role for frequency-dependent reductions in I_Ca,L which offset the effect of an increase in SR Ca²⁺ content at higher frequencies. This interplay between factors promoting a positive frequency response and factors promoting a negative frequency response results in a rather flat [Ca²⁺]_i-frequency relation.

METHODS

Top
Abstract
Introduction
Methods
Results
Discussion
References

Cell isolation

Single ventricular myocytes were enzymatically dissociated from 3- to 4-month-old mice (strain 129/SV). Mice were killed by an overdose of pentobarbital (100 mg kg^-1 I.P.), and the heart quickly excised. After cannulation of the aorta, hearts were mounted to a Langendorff perfusion set. The heart was briefly rinsed with normal Tyrode solution, containing (mM): 137 NaCl, 5.4 KCl, 0.5 MgCl₂, 1 CaCl₂, 11.8 Hepes and 10 glucose, pH adjusted to 7.4 with NaOH. Subsequently it was perfused with a Ca²⁺-free solution for 8 min. The Ca²⁺-free Tyrode solution contained (mM): 130 NaCl, 5.4 KCl, 1.2 KH₂PO₄, 1.2 MgSO₄, 6 Hepes, 20 glucose, pH adjusted to 7.2 with NaOH. Collagenase A (0.6 mg ml^-1, Roche Diagnostics, GmbH, Mannheim, Germany) and protease (type XIV, 0.1 mg ml^-1, Sigma, St Louis, MO, USA), added to the Ca²⁺-free solution, were recirculated for 10 min. The enzymes were washed out with low Ca²⁺ solution, i.e. the Ca²⁺-free solution to which 0.18 mM CaCl₂ was added. The heart was then removed, the ventricles were cut into small pieces and further dissociated into single cells by gentle shaking. Cells were stored in low Ca²⁺ solution at room temperature and used within 8 h after isolation. All experimental procedures were approved by the Ethics Committee on Animal Use of the University of Leuven.

Measurements of contraction, [Ca²⁺]_i and membrane currents

The setup for combined [Ca²⁺]_i and membrane current recording was as described before (Sipido et al. 1997).

Cell shortening was measured with a video-edge detector (Crescent, Salt Lake City, UT, USA) at 240 Hz frame rate. Field stimulation was done with 5 ms square pulses of constant voltage, at 20 % above threshold. The absolute cell shortening is expressed as the fractional shortening, i.e. normalized to resting cell length, $Delta$ L/L₀.

[Ca²⁺]_i was measured with fluo-3, and is reported as the fluorescence normalized to baseline values, after background subtraction, F/F₀. For higher frequencies of stimulation the baseline fluorescence increased, and values were normalized to the value at rest, before the onset of stimulation, or 10 s after stopping stimulation. In a subset of voltage clamped cells we calibrated fluo-3 signals after obtaining the F_max, as described by Trafford et al. (1999). With this method we established that [Ca²⁺]_i of resting myocytes is 108 ± 10 nM (n = 8). To calibrate signals of field-stimulated cells, loaded with fluo-3-AM, we used the approach of Cheng et al. (1993) assuming a K_d of 800 nM and a resting [Ca²⁺]_i of 108 nM.

Membrane currents were sampled at 4 kHz and filtered at 1 kHz. For the global analysis of frequency dependence of Ca²⁺ release, we used a K⁺-based pipette solution (mM): 120 potassium aspartate, 20 KCl, 10 Hepes, 5 MgATP, 10 NaCl, 0.05 K5-fluo-3, pH adjusted to 7.2 using KOH, and Tyrode solution with 1 mM CaCl₂ as the external solution. For measurements of L-type Ca²⁺ current, we blocked K⁺ currents and Cl^- concentrations were set to have a reversal potential near 0 mV. For these experiments the pipette solution contained (mM): 130 CsCl, 10 Hepes, 0.5 MgCl₂, 4 MgATP (pH 7.2 with CsOH), and the external solution contained (mM): 130 NaCl, 10 CsCl, 11.8 Hepes, 0.5 MgCl₂, 1 CaCl₂, 10 glucose, with pH 7.4 with NaOH.

To determine SR Ca²⁺ content, we perfused the cell with 10 mM caffeine for 8 s to empty the stores and extrude Ca²⁺ via Na⁺-Ca²⁺ exchange. The Na⁺-Ca²⁺ exchange current was integrated and from the resulting charge we recalculated the amount of Ca²⁺ released from the SR (Varro et al. 1993). We applied a correction for Ca²⁺ removal by other pathways of 19 %. This value is based on measurements of the rate of decline of [Ca²⁺]_i in the presence of caffeine and with Na⁺-Ca²⁺ exchange blocked with NiCl₂ (Varro et al. 1993). The SR Ca²⁺ content is expressed as [Ca²⁺] per accessible cell volume, assuming a surface/volume (S/V) ratio of 7.47 pF pl^-1, and an accessible fraction of 0.65. The S/V is based on measurements of cell capacity and estimates of cell volume during confocal imaging as described by Satoh et al. (1996). The values are close to those reported for rat ventricular myocytes, a species which like the mouse has an extensive T-tubular network, and are consistent with morphology data from the literature (reviewed in Bers, 2001).

All experiments were done at 30 °C. Different frequencies were tested in random order to minimize time-dependent changes. For statistical analysis we used ANOVA for repeated measurements, with Bonferroni or Tukey post hoc testing; values of P < 0.05 were considered significant. Values are reported as mean ± S.E.M.

RESULTS

Top
Abstract
Introduction
Methods
Results
Discussion
References

Frequency dependence of contraction of unloaded myocytes

Figure 1 shows in the top panel original traces of cell shortening in a myocyte stimulated at 1, 2 and 4 Hz. The amplitude of shortening increased with increasing frequency, but the cell did not relax completely at 2 and 4 Hz. The lower panel summarizes the data for 12 cells. Only one cell has a frank negative response. A few cells have a very pronounced positive response. On average there is a significant increase in the amplitude of shortening at higher stimulation frequencies: $Delta$ L/L₀ increases from 0.040 ± 0.007 at 1 Hz, to 0.047 ± 0.005 at 2 Hz, and to 0.069 ± 0.009 at 4 Hz (P < 0.05).

View larger version
[in this window]
[in a new window]

Figure 1. Frequency dependence of cell shortening in mouse myocytes
A, example of cell shortening measurements in an unloaded cell, externally stimulated at 1, 2 and 4 Hz, showing a positive frequency response. B, frequency response of amplitude of cell shortening ( $Delta$ L), normalized to resting cell length (L₀) of individual cells, represented by thin lines, one cell showed a negative response. Average data show an increase in amplitude with increasing stimulation frequency (mean ± S.E.M., n = 12, * P < 0.05 vs. 1 Hz).

Frequency dependence of [Ca²⁺]_i transients

We further studied the underlying mechanisms of the frequency response in whole cell voltage clamp mode. The mouse action potential is very brief and in current clamp mode we found that at 25 ms the membrane had repolarized to values below -50 mV (n = 8, data not shown). In the voltage clamp mode we thus used 25 ms depolarizing steps from -70 to +20 mV. Figure 2A shows in the top panel a typical example of [Ca²⁺]_i transients during this protocol. The peak [Ca²⁺]_i increases with frequency, and so does the baseline [Ca²⁺]_i. The data for all cells is summarized in Fig. 2B. Baseline [Ca²⁺]_i, expressed as F/F₀, increases from 1.03 ± 0.01 at 1 Hz to 1.25 ± 0.06 at 2 Hz, and to 1.60 ± 0.10 at 4 Hz; peak [Ca²⁺]_i increases from 2.58 ± 0.08 at 1 Hz to 2.94 ± 0.11 at 2 Hz, and to 3.31 ± 0.08 at 4 Hz (n = 17, P < 0.05). In panel C, the average data for the amplitude of the [Ca²⁺]_i transients, i.e. peak - baseline, is shown. On average there is a small increase in the amplitude: $Delta$ F/F₀ increases from 1.56 ± 0.08 at 1 Hz to 1.70 ± 0.11 at 2 Hz and 1.71 ± 0.11 at 4 Hz (n = 17, P < 0.05 for 4 Hz only). This change in amplitude is modest, suggesting there is little increase in SR Ca²⁺ release.

View larger version
[in this window]
[in a new window]

Figure 2. Frequency dependence of [Ca²⁺]_i transients
A, original current traces, I, and [Ca²⁺]_i transients, F/F₀, recorded in a voltage clamped cell during steady-state stimulation with 25 ms depolarizing steps from -70 to +20 mV at the indicated frequencies. B, individual data for frequency dependence of [Ca²⁺]_i transients, F/F₀, showing peak values (continuous lines) and baseline values (dashed lines) of 17 cells. Pooled data show an increase in peak [Ca²⁺]_i ( small square ) and baseline [Ca²⁺]_i ( filled square ) at higher stimulation frequencies (mean ± S.E.M., * P < 0.05 vs. 1 Hz). C, amplitude of the [Ca²⁺]_i transients, $Delta$ F/F₀, with increasing stimulation rate (mean ± S.E.M., * P < 0.05 vs. 1 Hz).

We checked that this was not due to the rather short pulses. In three cells, we compared the frequency response with 25 ms pulses to the response with 100 ms pulses. The absolute [Ca²⁺]_i values were larger for the 100 ms pulses, consistent with higher SR content for longer pulse duration (Terracciano et al. 1997), but the relative change with frequency was the same (data not shown).

The lack of significant increase in Ca²⁺ release at higher frequencies could be the result of a lack of increase in SR Ca²⁺ content, and/or of a decrease in fractional release due to a decrease in (trigger) Ca²⁺ current and/or opening of the Ca²⁺ release channel, the ryanodine receptor, RyR. In the first case, introducing a longer pause during the stimulation will not increase SR Ca²⁺ release, but in the second case a pause will increase SR Ca²⁺ release, as it may relieve inactivation of I_Ca,L and/or RyR. We thus tested these hypotheses in the experiment illustrated in Fig. 3A. Following a train of pulses at 2 and 4 Hz, we introduced a 1 s pause before the next depolarizing test step. The [Ca²⁺]_i transients with this test step, t, were compared to the last [Ca²⁺]_i transient of the conditioning step, c. In the example it can be seen that the [Ca²⁺]_i transients for t are significantly larger than for c at 2 Hz and at 4 Hz, suggesting there is a decrease in I_Ca,L and/or ryanodine receptor availability. Average data are shown in Fig. 3B, and the differences between test and conditioning pulses are significant (# P < 0.05, n = 5). In this same experiment we also compared the test steps at 2 and 4 Hz with the steady-state at 1 Hz. This analysis shows that for t there is a large increase with frequency (* P < 0.05), suggesting that there is an increase in SR Ca²⁺ content during the conditioning pulses.

View larger version
[in this window]
[in a new window]

Figure 3. [Ca²⁺]_i transients following 1 s pause after different stimulation frequencies
A, typical example of [Ca²⁺]_i transients, F/F₀, elicited by a 25 ms depolarizing pulse from -70 to +20 mV following 1 s interval (test pulse, t) after stimulation with 10 conditioning pulses (conditioning, c) at different frequencies of 1, 2 and 4 Hz. B, pooled data of peak [Ca²⁺]_i, F/F₀, of the test pulse ( small square ) and of the last conditioning pulse ( filled square ) as a function of increasing stimulation frequency (# P < 0.05 for t vs. c, * P < 0.05 for 2 and 4 Hz vs. 1 Hz, mean ± S.E.M., n = 5).

SR Ca²⁺ content at different frequencies of stimulation

The SR content was measured by emptying the SR with a fast application of 10 mM caffeine following conditioning pulses to the different frequencies. A typical example is shown in Fig. 4A, with [Ca²⁺]_i transients shown as F/F₀ and the membrane current shown as the running integral. Average values are given in panels B and C. Peak of caffeine-induced transients increases with increasing frequency of stimulation (peak F/F₀ from 4.86 ± 0.34 at 1 Hz, to 5.86 ± 0.30 at 2 Hz and to 6.75 ± 0.40 at 4 Hz (n = 5, P < 0.05). SR Ca²⁺ content, calculated from I_Na,Ca as described in Methods, increases from 91 ± 24 µmM at 1 Hz to 132 ± 17 at 2 Hz and 173 ± 20 µM at 4 Hz (n = 5, P < 0.05).

View larger version
[in this window]
[in a new window]

Figure 4. Frequency dependence of SR Ca²⁺ content
A, typical example of integrated Na⁺-Ca²⁺ exchange current, shown as the running integral, and [Ca²⁺]_i transients, F/F₀, induced by 8 s application of 10 mM caffeine following a 1 s pause after stimulation with 10 conditioning pulses at the indicated frequency (1, 2 and 4 Hz). B, peak of caffeine-induced transients, F/F₀, with increasing frequency of stimulation (mean ± S.E.M., n = 5, P < 0.05). C, SR Ca²⁺ content, calculated from integrating I_Na,Ca, and normalized to accessible cell volume, as described in the Methods section (mean ± S.E.M., n = 5, P < 0.05).

In Fig. 5A, we compared the amplitude of the stimulation-induced [Ca²⁺]_i transient to the amplitude of the caffeine-induced [Ca²⁺]_i transient, as a rough approximation of fractional release during stimulation at 1, 2 and 4 Hz. For this we divided the amplitude of the last [Ca²⁺]_i transient of the conditioning train, $Delta$ F/F₀ of c, by the amplitude of the caffeine transient, $Delta$ F/F₀ of caffeine, evoked at the end of the train. This value decreases from 49 ± 5 % at 1 Hz, to 41 ± 4 % at 2 Hz and to 31 ± 5 % at 4 Hz (n = 5, P < 0.05). In Fig. 5B, we have plotted the ratio of the amplitude of the last [Ca²⁺]_i transient of the conditioning train, $Delta$ F/F₀ of c, over the amplitude of the test pulse transient, $Delta$ F/F₀ of t (data from Fig. 3). This ratio decreases with frequency, in a manner very similar to the ratio with the caffeine-induced [Ca²⁺]_i transient. These data are consistent with the hypothesis that there is a decrease in the trigger for SR Ca²⁺ release, or in the availability of the RyR.

View larger version
[in this window]
[in a new window]

Figure 5. Reduced 'fractional' release at higher frequencies
A, the ratio of the amplitude of the [Ca²⁺]_i transients of the conditioning pulses, $Delta$ F/F_c, and the [Ca²⁺]_i transient of caffeine-induced transient $Delta$ F/F_caff, from experiments as shown in the inset, as an estimate of fractional release (mean ± S.E.M., n = 5, P < 0.05). B, for comparison we also calculated the ratio between the amplitude of the [Ca²⁺]_i transients of the conditioning pulses, $Delta$ F/F_c, relative to the [Ca²⁺]_i transient of the test pulse after a 1 s pause, $Delta$ F/F_t, at different frequencies (mean ± S.E.M., n = 5, P < 0.05). Data from the same experiments as shown in Fig. 3.

Changes in I_Ca,L with increasing frequency of stimulation

To measure I_Ca,L we used other solutions than in the previous experiments to exclude contamination by K⁺ and Na⁺ currents (see Methods). The test pulse was set to 0, instead of to +20 mV, to prevent a potential contribution of Cl^- currents. Figure 6A shows the time course of a typical experiment, recording the amplitude of I_Ca,L during different frequencies. During each series of pulses there is decrease in peak current, which is largest for the highest frequencies. The current recovers during rest periods in between trains of stimulation at the various frequencies, excluding that this results from rundown of channels. In Fig. 6B, the average loss of peak current for the three frequencies tested is shown. I_Ca,L is reduced to 88 ± 3 % at 1 Hz, 72 ± 6 % at 2 Hz and 54 ± 8 % at 4 Hz (n = 6, P < 0.05). These data suggest that there is inactivation and incomplete recovery of I_Ca,L at the higher frequencies.

View larger version
[in this window]
[in a new window]

Figure 6. Frequency dependence of L-type Ca²⁺ current
A, time course of a typical experiment measuring I_Ca,L during stimulation at 1, 2 and 4 Hz with a 10 s interval between the different frequencies, showing absolute peak values of I_Ca,L at each frequency. I_Ca,L was measured with 25 ms depolarizing steps from -70 to 0 mV in K⁺-free internal and external solutions. B, peak of steady-state current, expressed as percentage of I₀ (mean ± S.E.M., n = 6). C, recovery from inactivation of I_Ca,L; a 25 ms depolarizing step from -70 to +20 mV was followed by a test step after a 125 ms interval, and this interval was increased by 25 ms steps, interpulse duration was 10 s.

This was tested more directly during an inactivation-recovery protocol as illustrated in Fig. 6C. At the longest interval of 500 ms, recovery is nearly, but not fully complete. On average I_Ca,L recovery was 84 ± 3 % at 250 ms and 95 ± 3 % at 500 ms (n = 7). In the example shown, recovery of the [Ca²⁺]_i transient exceeds the time for recovery of the current, suggesting that release itself may recover more slowly. On average, the recovery of the amplitude of the [Ca²⁺]_i transient, $Delta$ F/F₀, was 38 ± 6 % at 250 ms and 83 ± 6 % at 500 ms.

We also calculated the impact of the reduction of I_Ca,L at higher frequencies on the total Ca²⁺ influx. Using the steady-state data from experiments as shown in Fig. 6, we calculated that the Ca²⁺ influx via I_Ca,L was 3.34 ± 0.65 µm l^-1 s^-1 at 1 Hz, 5.40 ± 1.09 µm l^-1 s^-1 at 2 Hz and 8.06 ± 1.90 µm l^-1 s^-1 at 4 Hz (n = 6, normalized to accessible cell volume).

Frequency dependence of decline of [Ca²⁺]_i

To study the changes in relaxation at different frequencies, we measured the half-time of decay of the [Ca²⁺]_i transient at steady-state stimulation. Because the relaxation is incomplete at the higher frequencies, we measured half-time of decay for the last pulse of a train at each frequency. At 1 Hz the half-time is 126 ± 18 ms, at 2 Hz it is 113 ± 13 ms, and at 4 Hz, 105 ± 9 ms. These data indicate that Ca²⁺ removal is indeed faster at the higher frequencies.

Relation between the frequency dependence of Ca²⁺ release and of contraction

Comparing the frequency dependence of contractions measured in field-stimulated myocytes (Fig. 1), with the frequency dependence of [Ca²⁺]_i transients measured in voltage clamped cells (Fig. 2), it seems that the contraction- frequency relation is more steep than the [Ca²⁺]_i-frequency relation. Since these were independent measurements with possible confounding factors, we loaded cells with the ester form of fluo-3 and recorded simultaneously [Ca²⁺]_i transients and cells shortening in field-stimulated cells. In these cells, as in Fig. 1B, positive, flat and negative relations were observed. In Fig. 7 we have pooled the data of eight cells with a positive contraction-frequency response, together with the [Ca²⁺]_i-frequency relation. These data support the impression from the previous independent measurements, namely that the increase in contraction amplitude is more pronounced than the increase in the [Ca²⁺]_i transient amplitude. Compared to 1 Hz, shortening amplitude, $Delta$ L/L₀, increases approximately 1.2- and 1.8-fold at 2 and 4 Hz respectively, whereas $Delta$ [Ca²⁺]_i increases 1.1- and 1.4-fold.

View larger version
[in this window]
[in a new window]

Figure 7. Simultaneous measurement of cell shortening and [Ca²⁺]_i transients during field stimulation
Pooled data of eight cells loaded with fluo-3AM, and calibrated [Ca²⁺]_i signals. A, amplitude of fractional cell shortening. B, peak ( small square ) and basal ( filled square ) [Ca²⁺]_i of transients. C, relative amplitude of cell shortening ( circle ), calculated as percentage of the amplitude at 1 Hz, compared to the relative increase in the amplitude of the [Ca²⁺]_i transients ( filled circle ).

DISCUSSION

Top
Abstract
Introduction
Methods
Results
Discussion
References

In the mouse, the increase in [Ca²⁺]_i transient amplitude with increasing frequencies of stimulation is modest. An unexpected and novel finding was that the frequency-dependent increase in SR content is actually very steep. At the higher frequencies of stimulation a loss of trigger for release offsets this increase in SR Ca²⁺ content, resulting in the rather shallow [Ca²⁺]_i-frequency response. This loss of trigger with increasing frequency has not been reported before. We also observed that the increase in contraction amplitude is disproportionately larger than the increase in the [Ca²⁺]_i transient, suggesting that there may be a regulation downstream of [Ca²⁺]_i.

Increase in SR content with increasing frequency of stimulation

The increase in SR content is consistent with reports in other animal species, including healthy humans. The underlying mechanism must be Ca²⁺ influx exceeding the Ca²⁺ efflux. We calculated that net influx via I_Ca,L is indeed larger at the higher frequencies, despite the reduction in peak current. A reduction of Ca²⁺ efflux via the Na⁺-Ca²⁺ exchanger is due to a shorter time spent at diastolic membrane potentials, and to the increase in [Na⁺]_i at higher frequencies (e.g. Cohen et al. 1982; Frampton et al. 1991; Harrison & Boyett, 1995), which would shift the reversal potential of the exchanger to more negative values. On the other hand, the increase in diastolic [Ca²⁺]_i would counteract this shift. In preliminary experiments on mouse myocytes we observed an increase in cytosolic [Na⁺] in mouse myocytes, but the increase was rather slow compared to the increase in contraction (F. Moccia & K. Mubagwa, unpublished observations). Subsarcolemmal gradients may be more important for shifts in reversal potential of the Na⁺-Ca²⁺ exchange, as suggested by recent studies (Su et al. 2001).

Another potential mechanism for the increase in SR content is increased sarco(endo)plasmic reticulum Ca²⁺-ATPase (SERCA) activity due to Ca²⁺/calmodulin kinase phosphorylation of PLB (Bassani et al. 1995; Hagemann et al. 2000) or through other pathways (Li et al. 1998). Our results are also consistent with a faster SR uptake at higher frequencies.

Lastly, the decrease in I_Ca,L at higher frequency and the decrease in fractional release will reduce the Ca²⁺ efflux via the exchanger and reduce Ca²⁺-dependent inactivation of I_Ca,L, thus increasing SR content (Trafford et al. 2001). This and the above mentioned mechanisms are likely to act in concert to increase SR content.

Loss of I_Ca,L at higher frequencies

In the mouse, the loss of Ca²⁺ current with stimulation at 2 and 4 Hz is apparently related to slow recovery from inactivation. In our experiments [Ca²⁺]_i was not buffered and Ca²⁺-dependent mechanisms are likely to be of major importance, as probably also in vivo. The decay of [Ca²⁺]_i is not complete at 250 ms, as can be seen in Fig. 6, and at steady-state 4 Hz stimulation, diastolic [Ca²⁺]_i is clearly elevated. The time course of beat-to-beat decrease in I_Ca,L does however not occur in parallel with a beat-to-beat increase in diastolic [Ca²⁺]_i. The increase in diastolic [Ca²⁺]_i indeed occurs rather abruptly with the first short stimulation interval (data not shown). [Ca²⁺]_i remains then elevated at the same level, whereas the Ca²⁺ current continues to decline. One explanation is the accumulation of inactivation, as recovery is incomplete. Another factor may be that the subsarcolemmal [Ca²⁺] is more elevated.

The pronounced decrease of I_Ca,L with frequency in normal mouse myocytes has not yet been described. We have however previously observed a loss of I_Ca,L with frequent stimulation in myocytes from failing human hearts, where it will contribute to the negative staircase typical of heart failure (Sipido et al. 1998). The loss of I_Ca,L in the human failing heart occurs at lower frequencies of stimulation (0.5, 1 and 2 Hz), but is also due to slow recovery from inactivation. In the case of the failing heart, the slow removal of Ca²⁺ by the SR has a role in the current inactivation. This loss of I_Ca,L leads to a decrease in the plateau values of the action potential. Li et al. (1999) have also observed a loss of I_Ca,L at higher frequencies of stimulation in human myocytes from the right ventricle (RV) of failing hearts. These authors could show that shortening of the action potential at these higher frequencies is the result of a decrease in I_Ca,L. The decrease in I_Ca,L at higher frequencies in patients is an important mechanism in the negative staircase, and helps to explain the beneficial effects of slowing the heart rate. Our observations in the mouse indicate that this phenomenon may more common than we thought, and may be present in healthy cardiac muscle.

The combination of a reduced I_Ca,L and increasing SR Ca²⁺ content at higher frequencies predicts that the effect of pause as e.g. after an ectopic beat, may have major consequences for both the action potential time course and the amplitude of contraction, because of enhanced recovery of I_Ca,L and increased Ca²⁺ release. This mechanism could be important for arrhythmogenesis.

Our findings of a pronounced loss of I_Ca,L contrasts with several reports on frequency-dependent potentiation of I_Ca,L, which also appears to be Ca²⁺-dependent (see e.g. Zygmunt & Maylie, 1990; Bates & Gurney, 1993; and review in Anderson, 2001). Probably both potentiation and inhibition can occur, and a potential explanation is that both phenomena have a different sensitivity to Ca²⁺. Potentiation is usually observed with small increases in [Ca²⁺]_i when there is moderate [Ca²⁺]_i buffering, e.g. with EGTA (Fedida et al. 1988a; Hryshko & Bers, 1990; Zygmunt & Maylie, 1990). Without [Ca²⁺]_i buffering and with larger increases in [Ca²⁺]_i inhibition occurs (Fedida et al. 1988b). The mechanisms of such a double response remain however elusive. Recent mutational analysis of the $alpha$ 1 subunit identified Ca²⁺/calmodulin binding sites, but the same sites were involved in facilitation as well as inactivation (Zuhlke et al. 2000).

Our data cannot exclude that slow recovery from inactivation of the RyR (reviewed in Bers, 2001) also contributes to the reduced fractional release at higher frequencies. The data of Fig. 6 could be interpreted this way, as Ca²⁺ release recovers more slowly than I_Ca,L. However, as we compare the recovery to a first beat after a 10 s pause, it is possible that the SR Ca²⁺ content is not the same. We therefore cannot establish with certainty the role of RyR recovery.

Relation between the [Ca²⁺]_i and contraction response to frequency

An additional finding was that contraction increased more steeply with frequency, than the amplitude of the [Ca²⁺]_i transient. This is consistent with the previous report by Gao et al. (1998) who measured simultaneously [Ca²⁺]_i and isometric contractions in trabeculae of mouse hearts at room temperature. A phase-plane analysis of force vs. [Ca²⁺]_i showed that the relation between [Ca²⁺]_i and force was dependent on the stimulation frequency, and steeper at higher frequencies. This is an unusual finding not reported in other animal species. The 'sensitization' of myofilaments at higher frequencies could be related to the increase in diastolic [Ca²⁺]_i which may affect phosphorylation of myosin light chains (Morano et al. 1990). The lack of full relaxation of the cell at higher frequencies may be related to such a sensitization phenomenon. Another explanation is that the shift in diastolic [Ca²⁺]_i moves the starting point of the contraction more towards the steep part of the tension-pCa relation. Indeed, the tension-pCa reported by Gao et al. (1998) has a shallow foot, but is then very steep for [Ca²⁺]_i above 500 nM. Although calibration of fluo-3 is not as reliable as for fura-2, our estimate is that basal [Ca²⁺]_i increases from 108 ± 10 nM to 208 ± 30 nM (n = 10) at 4 Hz. This is still below the activation level for contraction, but would reduce the required increase in [Ca²⁺]_i for contraction.

Conclusions

In the mouse the response of contraction to increased frequency of stimulation is a fine balance between positive factors and negative factors, and the frequency response may thus be very sensitive to small changes in any of these factors. This may explain the existence of variability between cells, or between different mouse strains. Indeed, some authors have described a frank negative staircase (Wolska & Solaro, 1996; Ashley et al. 2001). The increase in baseline [Ca²⁺]_i at higher frequencies is likely to be important in the regulation of the frequency response. Higher basal [Ca²⁺]_i may be involved in the loss of I_Ca,L, but also in the increased contractile response, and perhaps in increased SERCA activity by promoting Ca²⁺-dependent phosphorylation.

REFERENCES

Top
Abstract
Introduction
Methods
Results
Discussion
References

ANDERSON, M. E. (2001). Ca²⁺-dependent regulation of cardiac L-type Ca²⁺ channels: is a unifying mechanism at hand? Journal of Molecular and Cellular Cardiology 33, 639-650 [Medline]

BASSANI, R. A., MATTIAZZI, A. & BERS, D. M. (1995). CaMKII is responsible for activity-dependent acceleration of relaxation in rat ventricular myocytes. American Journal of Physiology 268, H703-712 [Medline]

BATES, S. E. & GURNEY, A. M. (1993). Ca²⁺-dependent block and potentiation of L-type calcium current in guinea-pig ventricular myocytes. Journal of Physiology 466, 345-365 [Abstract]

BAUDET, S., DO, E., NOIREAUD, J. & LE-MAREC, H. (1996). Alterations in the force-frequency relationship by tert-butylbenzohydroquinone, a putative SR Ca²⁺ pump inhibitor, in rabbit and rat ventricular muscle. British Journal of Pharmacology 117, 258-267 [Abstract]

BERS, D. M. (2001). Excitation-Contraction Coupling and Cardiac Contractile Force. Kluwer Academic Publishers, The Netherlands

BERS, D. M. & CHRISTENSEN, D. M. (1990). Functional interconversion of rest decay and ryanodine effects in rabbit and rat ventricle depends on Na/Ca exchange. Journal of Molecular and Cellular Cardiology 22, 715-723 [Medline]

CHENG, H., LEDERER, W. J. & CANNELL, M. B. (1993). Calcium sparks: elementary events underlying excitation-contraction coupling in heart muscle. Science 262, 740-744

COHEN, C. J., FOZZARD, H. A. & SHEU, S. S. (1982). Increase in intracellular sodium ion activity during stimulation in mammalian cardiac muscle. Circulation Research 50, 651-662 [Abstract]

FEDIDA, D., NOBLE, D. & SPINDLER, A. J. (1988a). Use-dependent reduction and facilitation of Ca²⁺ current in guinea-pig myocytes. Journal of Physiology 405, 439-460 [Abstract]

FEDIDA, D., NOBLE, D. & SPINDLER, A. J. (1988b). Mechanism of the use dependence of Ca²⁺ current in guinea-pig myocytes. Journal of Physiology 405, 461-475 [Abstract]

FRAMPTON, J. E., HARRISON, S. M., BOYETT, M. R. & ORCHARD, C. H. (1991). Ca²⁺ and Na⁺ in rat myocytes showing different force-frequency relationships. American Journal of Physiology 261, C739-750 [Medline]

GAO, W. D., PEREZ, N. G. & MARBAN, E. (1998). Calcium cycling and contractile activation in intact mouse cardiac muscle. Journal of Physiology 507, 175-184 [Abstract/Full Text]

GEORGAKOPOULOS, D. & KASS, D. A. (2001). Minimal force-frequency modulation of inotropy and relaxation of in situ murine heart. Journal of Physiology 534, 535-545 [Abstract/Full Text]

GWATHMEY, J. K., SLAWSKY, M. T., HAJJAR, R. J., BRIGGS, G. M. & MORGAN, J. P. (1990). Role of intracellular calcium handling in force-interval relationships of human ventricular myocardium. Journal of Clinical Investigation 85, 1599-1613 [Medline]

HAGEMANN, D., KUSCHEL, M., KURAMOCHI, T., ZHU, W., CHENG, H. & XIAO, R. P. (2000). Frequency-encoding Thr17 phospholamban phosphorylation is independent of Ser16 phosphorylation in cardiac myocytes. Journal of Biological Chemistry 275, 22532-22536 [Abstract/Full Text]

HARRISON, S. M. & BOYETT, M. R. (1995). The role of the Na⁺-Ca²⁺ exchanger in the rate-dependent increase in contraction in guinea-pig ventricular myocytes. Journal of Physiology 482, 555-566 [Abstract]

HENDERSON, A. H., BRUTSAERT, D. L., FORMAN, R. & SONNENBLICK, E. H. (1974). Influence of caffeine on force development and force-frequency relations in cat and rat heart muscle. Cardiovascular Research 8, 162-172 [Medline]

HERR, C., SMYTH, N., ULLRICH, S., YUN, F., SASSE, P., HESCHELER, J., FLEISCHMANN, B., LASEK, K., BRIXIUS, K., SCHWINGER, R. H., FASSLER, R., SCHRODER, R. & NOEGEL, A. A. (2001). Loss of annexin A7 leads to alterations in frequency-induced shortening of isolated murine cardiomyocytes. Molecular Cell Biology 21, 4119-4128

HRYSHKO, L. V. & BERS, D. M. (1990). Calcium current facilitation during post-rest recovery depends on Ca entry. American Journal of Physiology 259, H951-961 [Medline]

KADAMBI, V. J., BALL, N., KRANIAS, E. G., WALSH, R. A. & HOIT, B. D. (1999). Modulation of force-frequency relation by phospholamban in genetically engineered mice. American Journal of Physiology 276, H2245-2250 [Medline]

KOCH-WESER, J. & BLINKS, J. R. (1963). The influence of the interval between beats on myocardial contractility. Pharmacological Reviews 15, 601-652

LAYLAND, J. & KENTISH, J. C. (1999). Positive force- and [Ca²⁺]_i frequency relationships in rat ventricular trabeculae at physiological frequencies. American Journal of Physiology 276, H9-18 [Medline]

LI, G. R., YANG, B., FENG, J., BOSCH, R. F., CARRIER, M. & NATTEL, S. (1999). Transmembrane I_Ca contributes to rate-dependent changes of action potentials in human ventricular myocytes. American Journal of Physiology 276, H98-106 [Medline]

LI, L., CHU, G., KRANIAS, E. G. & BERS, D. M. (1998). Cardiac myocyte calcium transport in phospholamban knockout mouse: relaxation and endogenous CaMKII effects. American Journal of Physiology 274, H1335-1347 [Medline]

MORANO, I., ROSCH, J., ARNER, A. & RUEGG, J. C. (1990). Phosphorylation and thiophosphorylation by myosin light chain kinase: different effects on mechanical properties of chemically skinned ventricular fibers from the pig. Journal of Molecular and Cellular Cardiology 22, 805-813 [Medline]

MUBAGWA, K., WEI LIN, SIPIDO, K. R., BOSTEELS, S. & FLAMENG, W. (1997). Monensin-induced reversal of positive force-frequency relationship in cardiac muscle: role of intracellular sodium in rest-dependent potentiation of contraction. Journal of Molecular and Cellular Cardiology 29, 977-989 [Medline]

MULIERI, L. A., HASENFUSS, G., LEAVITT, B., ALLEN, P. D. & ALPERT, N. R. (1992). Altered myocardial force-frequency relation in human heart failure. Circulation 85, 1743-1750 [Abstract]

PIESKE, B., MAIER, L. S., BERS, D. M. & HASENFUSS, G. (1999). Ca²⁺ handling and sarcoplasmic reticulum Ca²⁺ content in isolated failing and nonfailing human myocardium. Circulation Research 85, 38-46 [Abstract/Full Text]

SATOH, H., DELBRIDGE, L. M., BLATTER, L. A. & BERS, D. M. (1996). Surface:volume relationship in cardiac myocytes studied with confocal microscopy and membrane capacitance measurements: species-dependence and developmental effects. Biophysical Journal 70, 1494-1504 [Abstract]

SIPIDO, K. R., MAES, M. M. & VAN DE WERF, F. (1997). Low efficiency of Ca²⁺ entry through the Na/Ca exchanger as trigger for Ca²⁺ release from the sarcoplasmic reticulum. Circulation Research 81, 1034-1044 [Abstract/Full Text]

SIPIDO, K. R., STANKOVICOVA, T., FLAMENG, W., VANHAECKE, J. & VERDONCK, F. (1998). Frequency dependence of Ca²⁺ release from the sarcoplasmic reticulum in human ventricular myocytes from end-stage heart failure. Cardiovascular Research 37, 478-488 [Medline]

SU, Z., SUGISHITA, K., RITTER, M., LI, F., SPITZER, K. W. & BARRY, W. H. (2001). The sodium pump modulates the influence of I_Na on [Ca²⁺]_i transients in mouse ventricular myocytes. Biophysical Journal 80, 1230-1237 [Abstract/Full Text]

TERRACCIANO, C. M., TWEEDIE, D. & MACLEOD, K. T. (1997). The effects of changes to action potential duration on the calcium content of the sarcoplasmic reticulum in isolated guinea- pig ventricular myocytes. Pflügers Archiv 433, 542-544 [Medline]

TRAFFORD, A. W., DIAZ, M. E. & EISNER, D. A. (1999). A novel, rapid and reversible method to measure Ca buffering and time-course of total sarcoplasmic reticulum Ca content in cardiac ventricular myocytes. Pflügers Archiv 437, 501-503 [Medline]

TRAFFORD, A. W., DIAZ, M. E. & EISNER, D. A. (2001). Coordinated control of cell Ca²⁺ loading and triggered release from the sarcoplasmic reticulum underlies the rapid inotropic response to increased L-type Ca²⁺ current. Circulation Research 88, 195-201 [Abstract/Full Text]

VARRO, A., NEGRETTI, N., HESTER, S. B. & EISNER, D. A. (1993). An estimate of the calcium content of the sarcoplasmic reticulum in rat ventricular myocytes. Pflügers Archiv 423, 158-160 [Medline]

WOLSKA, B. M. & SOLARO, R. J. (1996). Method for isolation of adult mouse cardiac myocytes for studies of contraction and microfluorimetry. American Journal of Physiology 271, H1250-1255 [Medline]

ZUHLKE, R. D., PITT, G. S., TSIEN, R. W. & REUTER, H. (2000). Ca²⁺-sensitive inactivation and facilitation of L-type Ca²⁺ channels both depend on specific amino acid residues in a consensus calmodulin-binding motif in the(alpha)1C subunit. Journal of Biological Chemistry 275, 21121-21129 [Abstract/Full Text]

ZYGMUNT, A. C. & MAYLIE, J. (1990). Stimulation-dependent facilitation of the high threshold calcium current in guinea-pig ventricular myocytes. Journal of Physiology 428, 653-671 [Abstract]

Acknowledgements

This study was supported by the FWO, the Flanders Fund for Scientific Research (K.R.S., K.M.).

This article has been cited by other articles:

M. E. Reichelt, L. Willems, B. A. Hack, J. N. Peart, and J. P. Headrick
Cardiac and coronary function in the Langendorff-perfused mouse heart model
Exp Physiol, January 1, 2009; 94(1): 54 - 70.
[Abstract] [Full Text] [PDF]

L. F. Santana
NFAT-Dependent Excitation-Transcription Coupling in Heart
Circ. Res., September 26, 2008; 103(7): 681 - 683.
[Full Text] [PDF]

S. Ozdemir, V. Bito, P. Holemans, L. Vinet, J.-J. Mercadier, A. Varro, and K. R. Sipido
Pharmacological Inhibition of Na/Ca Exchange Results in Increased Cellular Ca2+ Load Attributable to the Predominance of Forward Mode Block
Circ. Res., June 6, 2008; 102(11): 1398 - 1405.
[Abstract] [Full Text] [PDF]

K. M. Dibb, D. A. Eisner, and A. W. Trafford
Regulation of systolic [Ca2+]i and cellular Ca2+ flux balance in rat ventricular myocytes by SR Ca2+, L-type Ca2+ current and diastolic [Ca2+]i
J. Physiol., December 1, 2007; 585(2): 579 - 592.
[Abstract] [Full Text] [PDF]

J.-B. Shen, R. Shutt, A. Pappano, and B. T. Liang
Characterization and mechanism of P2X receptor-mediated increase in cardiac myocyte contractility
Am J Physiol Heart Circ Physiol, November 1, 2007; 293(5): H3056 - H3062.
[Abstract] [Full Text] [PDF]

R. R. Lamberts, N. Hamdani, T. W. Soekhoe, N. M. Boontje, R. Zaremba, L. A. Walker, P. P. de Tombe, J. van der Velden, and G. J. M. Stienen
Frequency-dependent myofilament Ca2+ desensitization in failing rat myocardium
J. Physiol., July 15, 2007; 582(2): 695 - 709.
[Abstract] [Full Text] [PDF]

L. Umans, L. Cox, M. Tjwa, V. Bito, L. Vermeire, K. Laperre, K. Sipido, L. Moons, D. Huylebroeck, and A. Zwijsen
Inactivation of Smad5 in Endothelial Cells and Smooth Muscle Cells Demonstrates that Smad5 Is Required for Cardiac Homeostasis
Am. J. Pathol., May 1, 2007; 170(5): 1460 - 1472.
[Abstract] [Full Text] [PDF]

M. C. de Waard, J. van der Velden, V. Bito, S. Ozdemir, L. Biesmans, N. M. Boontje, D. H.W. Dekkers, K. Schoonderwoerd, H. C.H. Schuurbiers, R. d. Crom, et al.
Early Exercise Training Normalizes Myofilament Function and Attenuates Left Ventricular Pump Dysfunction in Mice With a Large Myocardial Infarction
Circ. Res., April 13, 2007; 100(7): 1079 - 1088.
[Abstract] [Full Text] [PDF]

J.-S. David, C. Ferreti, J. Amour, B. Vivien, O. Eve, P. Petit, B. Riou, and P.-Y. Gueugniaud
Effects of bupivacaine, levobupivacaine and ropivacaine on myocardial relaxation: [Les effets de la bupivacaine, levobupivacaine et ropivacaine sur la relaxation du myocarde]
Can J Anesth, March 1, 2007; 54(3): 208 - 217.
[Abstract] [Full Text] [PDF]

T. Namiki, R. W. Joyner, and M. B. Wagner
Developmental changes in time course of recovery from inactivation in L-type calcium currents of rabbit ventricular myocytes
Am J Physiol Heart Circ Physiol, January 1, 2007; 292(1): H295 - H303.
[Abstract] [Full Text] [PDF]

R. P. Kondo, D. A. Dederko, C. Teutsch, J. Chrast, D. Catalucci, K. R. Chien, and W. R. Giles
Comparison of contraction and calcium handling between right and left ventricular myocytes from adult mouse heart: a role for repolarization waveform
J. Physiol., February 15, 2006; 571(1): 131 - 146.
[Abstract] [Full Text] [PDF]

V. Bito, D. Dauwe, F. Verdonck, K. Mubagwa, and K. R. Sipido
The Amiodarone Derivative KB130015 [2-Methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl)benzofuran] Induces an Na+-Dependent Increase of [Ca2+] in Ventricular Myocytes
J. Pharmacol. Exp. Ther., January 1, 2006; 316(1): 162 - 168.
[Abstract] [Full Text] [PDF]

M. Rota, A. Boni, K. Urbanek, M. E. Padin-Iruegas, T. J. Kajstura, G. Fiore, H. Kubo, E. H. Sonnenblick, E. Musso, S. R. Houser, et al.
Nuclear Targeting of Akt Enhances Ventricular Function and Myocyte Contractility
Circ. Res., December 9, 2005; 97(12): 1332 - 1341.
[Abstract] [Full Text] [PDF]

D. A. Eisner and K. R. Sipido
Sodium Calcium Exchange in the Heart: Necessity or Luxury?
Circ. Res., September 17, 2004; 95(6): 549 - 551.
[Full Text] [PDF]

V. E. Bondarenko, G. P. Szigeti, G. C. L. Bett, S.-J. Kim, and R. L. Rasmusson
Computer model of action potential of mouse ventricular myocytes
Am J Physiol Heart Circ Physiol, September 1, 2004; 287(3): H1378 - H1403.
[Abstract] [Full Text] [PDF]

V. Bito, F. R. Heinzel, F. Weidemann, C. Dommke, J. van der Velden, E. Verbeken, P. Claus, B. Bijnens, I. De Scheerder, G. J.M. Stienen, et al.
Cellular Mechanisms of Contractile Dysfunction in Hibernating Myocardium
Circ. Res., April 2, 2004; 94(6): 794 - 801.
[Abstract] [Full Text] [PDF]

T. P. Flagg, F. Charpentier, J. Manning-Fox, M. S. Remedi, D. Enkvetchakul, A. Lopatin, J. Koster, and C. Nichols
Remodeling of excitation-contraction coupling in transgenic mice expressing ATP-insensitive sarcolemmal KATP channels
Am J Physiol Heart Circ Physiol, April 1, 2004; 286(4): H1361 - H1369.
[Abstract] [Full Text] [PDF]

K. R. Sipido
Understanding Cardiac Alternans: The Answer Lies in the Ca2+ Store
Circ. Res., March 19, 2004; 94(5): 570 - 572.
[Full Text] [PDF]

P. Tavi, S. Pikkarainen, J. Ronkainen, P. Niemela, M. Ilves, M. Weckstrom, O. Vuolteenaho, J. Bruton, H. Westerblad, and H. Ruskoaho
Pacing-induced calcineurin activation controls cardiac Ca2+ signalling and gene expression
J. Physiol., January 15, 2004; 554(2): 309 - 320.
[Abstract] [Full Text] [PDF]

ANDERSON, M. E. (2001). Ca²⁺-dependent regulation of cardiac L-type Ca²⁺ channels: is a unifying mechanism at hand? Journal of Molecular and Cellular Cardiology 33, 639-650	[Medline]
BASSANI, R. A., MATTIAZZI, A. & BERS, D. M. (1995). CaMKII is responsible for activity-dependent acceleration of relaxation in rat ventricular myocytes. American Journal of Physiology 268, H703-712	[Medline]
BATES, S. E. & GURNEY, A. M. (1993). Ca²⁺-dependent block and potentiation of L-type calcium current in guinea-pig ventricular myocytes. Journal of Physiology 466, 345-365	[Abstract]
BAUDET, S., DO, E., NOIREAUD, J. & LE-MAREC, H. (1996). Alterations in the force-frequency relationship by tert-butylbenzohydroquinone, a putative SR Ca²⁺ pump inhibitor, in rabbit and rat ventricular muscle. British Journal of Pharmacology 117, 258-267	[Abstract]
BERS, D. M. (2001). Excitation-Contraction Coupling and Cardiac Contractile Force. Kluwer Academic Publishers, The Netherlands
BERS, D. M. & CHRISTENSEN, D. M. (1990). Functional interconversion of rest decay and ryanodine effects in rabbit and rat ventricle depends on Na/Ca exchange. Journal of Molecular and Cellular Cardiology 22, 715-723	[Medline]
CHENG, H., LEDERER, W. J. & CANNELL, M. B. (1993). Calcium sparks: elementary events underlying excitation-contraction coupling in heart muscle. Science 262, 740-744
COHEN, C. J., FOZZARD, H. A. & SHEU, S. S. (1982). Increase in intracellular sodium ion activity during stimulation in mammalian cardiac muscle. Circulation Research 50, 651-662	[Abstract]
FEDIDA, D., NOBLE, D. & SPINDLER, A. J. (1988a). Use-dependent reduction and facilitation of Ca²⁺ current in guinea-pig myocytes. Journal of Physiology 405, 439-460	[Abstract]
FEDIDA, D., NOBLE, D. & SPINDLER, A. J. (1988b). Mechanism of the use dependence of Ca²⁺ current in guinea-pig myocytes. Journal of Physiology 405, 461-475	[Abstract]
FRAMPTON, J. E., HARRISON, S. M., BOYETT, M. R. & ORCHARD, C. H. (1991). Ca²⁺ and Na⁺ in rat myocytes showing different force-frequency relationships. American Journal of Physiology 261, C739-750	[Medline]
GAO, W. D., PEREZ, N. G. & MARBAN, E. (1998). Calcium cycling and contractile activation in intact mouse cardiac muscle. Journal of Physiology 507, 175-184	[Abstract/Full Text]
GEORGAKOPOULOS, D. & KASS, D. A. (2001). Minimal force-frequency modulation of inotropy and relaxation of in situ murine heart. Journal of Physiology 534, 535-545	[Abstract/Full Text]
GWATHMEY, J. K., SLAWSKY, M. T., HAJJAR, R. J., BRIGGS, G. M. & MORGAN, J. P. (1990). Role of intracellular calcium handling in force-interval relationships of human ventricular myocardium. Journal of Clinical Investigation 85, 1599-1613	[Medline]
HAGEMANN, D., KUSCHEL, M., KURAMOCHI, T., ZHU, W., CHENG, H. & XIAO, R. P. (2000). Frequency-encoding Thr17 phospholamban phosphorylation is independent of Ser16 phosphorylation in cardiac myocytes. Journal of Biological Chemistry 275, 22532-22536	[Abstract/Full Text]
HARRISON, S. M. & BOYETT, M. R. (1995). The role of the Na⁺-Ca²⁺ exchanger in the rate-dependent increase in contraction in guinea-pig ventricular myocytes. Journal of Physiology 482, 555-566	[Abstract]
HENDERSON, A. H., BRUTSAERT, D. L., FORMAN, R. & SONNENBLICK, E. H. (1974). Influence of caffeine on force development and force-frequency relations in cat and rat heart muscle. Cardiovascular Research 8, 162-172	[Medline]
HERR, C., SMYTH, N., ULLRICH, S., YUN, F., SASSE, P., HESCHELER, J., FLEISCHMANN, B., LASEK, K., BRIXIUS, K., SCHWINGER, R. H., FASSLER, R., SCHRODER, R. & NOEGEL, A. A. (2001). Loss of annexin A7 leads to alterations in frequency-induced shortening of isolated murine cardiomyocytes. Molecular Cell Biology 21, 4119-4128
HRYSHKO, L. V. & BERS, D. M. (1990). Calcium current facilitation during post-rest recovery depends on Ca entry. American Journal of Physiology 259, H951-961	[Medline]
KADAMBI, V. J., BALL, N., KRANIAS, E. G., WALSH, R. A. & HOIT, B. D. (1999). Modulation of force-frequency relation by phospholamban in genetically engineered mice. American Journal of Physiology 276, H2245-2250	[Medline]
KOCH-WESER, J. & BLINKS, J. R. (1963). The influence of the interval between beats on myocardial contractility. Pharmacological Reviews 15, 601-652
LAYLAND, J. & KENTISH, J. C. (1999). Positive force- and [Ca²⁺]_i frequency relationships in rat ventricular trabeculae at physiological frequencies. American Journal of Physiology 276, H9-18	[Medline]
LI, G. R., YANG, B., FENG, J., BOSCH, R. F., CARRIER, M. & NATTEL, S. (1999). Transmembrane I_Ca contributes to rate-dependent changes of action potentials in human ventricular myocytes. American Journal of Physiology 276, H98-106	[Medline]
LI, L., CHU, G., KRANIAS, E. G. & BERS, D. M. (1998). Cardiac myocyte calcium transport in phospholamban knockout mouse: relaxation and endogenous CaMKII effects. American Journal of Physiology 274, H1335-1347	[Medline]
MORANO, I., ROSCH, J., ARNER, A. & RUEGG, J. C. (1990). Phosphorylation and thiophosphorylation by myosin light chain kinase: different effects on mechanical properties of chemically skinned ventricular fibers from the pig. Journal of Molecular and Cellular Cardiology 22, 805-813	[Medline]
MUBAGWA, K., WEI LIN, SIPIDO, K. R., BOSTEELS, S. & FLAMENG, W. (1997). Monensin-induced reversal of positive force-frequency relationship in cardiac muscle: role of intracellular sodium in rest-dependent potentiation of contraction. Journal of Molecular and Cellular Cardiology 29, 977-989	[Medline]
MULIERI, L. A., HASENFUSS, G., LEAVITT, B., ALLEN, P. D. & ALPERT, N. R. (1992). Altered myocardial force-frequency relation in human heart failure. Circulation 85, 1743-1750	[Abstract]
PIESKE, B., MAIER, L. S., BERS, D. M. & HASENFUSS, G. (1999). Ca²⁺ handling and sarcoplasmic reticulum Ca²⁺ content in isolated failing and nonfailing human myocardium. Circulation Research 85, 38-46	[Abstract/Full Text]
SATOH, H., DELBRIDGE, L. M., BLATTER, L. A. & BERS, D. M. (1996). Surface:volume relationship in cardiac myocytes studied with confocal microscopy and membrane capacitance measurements: species-dependence and developmental effects. Biophysical Journal 70, 1494-1504	[Abstract]
SIPIDO, K. R., MAES, M. M. & VAN DE WERF, F. (1997). Low efficiency of Ca²⁺ entry through the Na/Ca exchanger as trigger for Ca²⁺ release from the sarcoplasmic reticulum. Circulation Research 81, 1034-1044	[Abstract/Full Text]
SIPIDO, K. R., STANKOVICOVA, T., FLAMENG, W., VANHAECKE, J. & VERDONCK, F. (1998). Frequency dependence of Ca²⁺ release from the sarcoplasmic reticulum in human ventricular myocytes from end-stage heart failure. Cardiovascular Research 37, 478-488	[Medline]
SU, Z., SUGISHITA, K., RITTER, M., LI, F., SPITZER, K. W. & BARRY, W. H. (2001). The sodium pump modulates the influence of I_Na on [Ca²⁺]_i transients in mouse ventricular myocytes. Biophysical Journal 80, 1230-1237	[Abstract/Full Text]
TERRACCIANO, C. M., TWEEDIE, D. & MACLEOD, K. T. (1997). The effects of changes to action potential duration on the calcium content of the sarcoplasmic reticulum in isolated guinea- pig ventricular myocytes. Pflügers Archiv 433, 542-544	[Medline]
TRAFFORD, A. W., DIAZ, M. E. & EISNER, D. A. (1999). A novel, rapid and reversible method to measure Ca buffering and time-course of total sarcoplasmic reticulum Ca content in cardiac ventricular myocytes. Pflügers Archiv 437, 501-503	[Medline]
TRAFFORD, A. W., DIAZ, M. E. & EISNER, D. A. (2001). Coordinated control of cell Ca²⁺ loading and triggered release from the sarcoplasmic reticulum underlies the rapid inotropic response to increased L-type Ca²⁺ current. Circulation Research 88, 195-201	[Abstract/Full Text]
VARRO, A., NEGRETTI, N., HESTER, S. B. & EISNER, D. A. (1993). An estimate of the calcium content of the sarcoplasmic reticulum in rat ventricular myocytes. Pflügers Archiv 423, 158-160	[Medline]
WOLSKA, B. M. & SOLARO, R. J. (1996). Method for isolation of adult mouse cardiac myocytes for studies of contraction and microfluorimetry. American Journal of Physiology 271, H1250-1255	[Medline]
ZUHLKE, R. D., PITT, G. S., TSIEN, R. W. & REUTER, H. (2000). Ca²⁺-sensitive inactivation and facilitation of L-type Ca²⁺ channels both depend on specific amino acid residues in a consensus calmodulin-binding motif in the(alpha)1C subunit. Journal of Biological Chemistry 275, 21121-21129	[Abstract/Full Text]
ZYGMUNT, A. C. & MAYLIE, J. (1990). Stimulation-dependent facilitation of the high threshold calcium current in guinea-pig ventricular myocytes. Journal of Physiology 428, 653-671	[Abstract]

				L. F. Santana NFAT-Dependent Excitation-Transcription Coupling in Heart Circ. Res., September 26, 2008; 103(7): 681 - 683. [Full Text] [PDF]

				S. Ozdemir, V. Bito, P. Holemans, L. Vinet, J.-J. Mercadier, A. Varro, and K. R. Sipido Pharmacological Inhibition of Na/Ca Exchange Results in Increased Cellular Ca2+ Load Attributable to the Predominance of Forward Mode Block Circ. Res., June 6, 2008; 102(11): 1398 - 1405. [Abstract] [Full Text] [PDF]

				K. M. Dibb, D. A. Eisner, and A. W. Trafford Regulation of systolic [Ca2+]i and cellular Ca2+ flux balance in rat ventricular myocytes by SR Ca2+, L-type Ca2+ current and diastolic [Ca2+]i J. Physiol., December 1, 2007; 585(2): 579 - 592. [Abstract] [Full Text] [PDF]

				J.-B. Shen, R. Shutt, A. Pappano, and B. T. Liang Characterization and mechanism of P2X receptor-mediated increase in cardiac myocyte contractility Am J Physiol Heart Circ Physiol, November 1, 2007; 293(5): H3056 - H3062. [Abstract] [Full Text] [PDF]

				R. R. Lamberts, N. Hamdani, T. W. Soekhoe, N. M. Boontje, R. Zaremba, L. A. Walker, P. P. de Tombe, J. van der Velden, and G. J. M. Stienen Frequency-dependent myofilament Ca2+ desensitization in failing rat myocardium J. Physiol., July 15, 2007; 582(2): 695 - 709. [Abstract] [Full Text] [PDF]

				L. Umans, L. Cox, M. Tjwa, V. Bito, L. Vermeire, K. Laperre, K. Sipido, L. Moons, D. Huylebroeck, and A. Zwijsen Inactivation of Smad5 in Endothelial Cells and Smooth Muscle Cells Demonstrates that Smad5 Is Required for Cardiac Homeostasis Am. J. Pathol., May 1, 2007; 170(5): 1460 - 1472. [Abstract] [Full Text] [PDF]

				M. C. de Waard, J. van der Velden, V. Bito, S. Ozdemir, L. Biesmans, N. M. Boontje, D. H.W. Dekkers, K. Schoonderwoerd, H. C.H. Schuurbiers, R. d. Crom, et al. Early Exercise Training Normalizes Myofilament Function and Attenuates Left Ventricular Pump Dysfunction in Mice With a Large Myocardial Infarction Circ. Res., April 13, 2007; 100(7): 1079 - 1088. [Abstract] [Full Text] [PDF]

				J.-S. David, C. Ferreti, J. Amour, B. Vivien, O. Eve, P. Petit, B. Riou, and P.-Y. Gueugniaud Effects of bupivacaine, levobupivacaine and ropivacaine on myocardial relaxation: [Les effets de la bupivacaine, levobupivacaine et ropivacaine sur la relaxation du myocarde] Can J Anesth, March 1, 2007; 54(3): 208 - 217. [Abstract] [Full Text] [PDF]

				T. Namiki, R. W. Joyner, and M. B. Wagner Developmental changes in time course of recovery from inactivation in L-type calcium currents of rabbit ventricular myocytes Am J Physiol Heart Circ Physiol, January 1, 2007; 292(1): H295 - H303. [Abstract] [Full Text] [PDF]

				R. P. Kondo, D. A. Dederko, C. Teutsch, J. Chrast, D. Catalucci, K. R. Chien, and W. R. Giles Comparison of contraction and calcium handling between right and left ventricular myocytes from adult mouse heart: a role for repolarization waveform J. Physiol., February 15, 2006; 571(1): 131 - 146. [Abstract] [Full Text] [PDF]

				V. Bito, D. Dauwe, F. Verdonck, K. Mubagwa, and K. R. Sipido The Amiodarone Derivative KB130015 [2-Methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl)benzofuran] Induces an Na+-Dependent Increase of [Ca2+] in Ventricular Myocytes J. Pharmacol. Exp. Ther., January 1, 2006; 316(1): 162 - 168. [Abstract] [Full Text] [PDF]

				M. Rota, A. Boni, K. Urbanek, M. E. Padin-Iruegas, T. J. Kajstura, G. Fiore, H. Kubo, E. H. Sonnenblick, E. Musso, S. R. Houser, et al. Nuclear Targeting of Akt Enhances Ventricular Function and Myocyte Contractility Circ. Res., December 9, 2005; 97(12): 1332 - 1341. [Abstract] [Full Text] [PDF]

				D. A. Eisner and K. R. Sipido Sodium Calcium Exchange in the Heart: Necessity or Luxury? Circ. Res., September 17, 2004; 95(6): 549 - 551. [Full Text] [PDF]

				V. E. Bondarenko, G. P. Szigeti, G. C. L. Bett, S.-J. Kim, and R. L. Rasmusson Computer model of action potential of mouse ventricular myocytes Am J Physiol Heart Circ Physiol, September 1, 2004; 287(3): H1378 - H1403. [Abstract] [Full Text] [PDF]

				V. Bito, F. R. Heinzel, F. Weidemann, C. Dommke, J. van der Velden, E. Verbeken, P. Claus, B. Bijnens, I. De Scheerder, G. J.M. Stienen, et al. Cellular Mechanisms of Contractile Dysfunction in Hibernating Myocardium Circ. Res., April 2, 2004; 94(6): 794 - 801. [Abstract] [Full Text] [PDF]

				T. P. Flagg, F. Charpentier, J. Manning-Fox, M. S. Remedi, D. Enkvetchakul, A. Lopatin, J. Koster, and C. Nichols Remodeling of excitation-contraction coupling in transgenic mice expressing ATP-insensitive sarcolemmal KATP channels Am J Physiol Heart Circ Physiol, April 1, 2004; 286(4): H1361 - H1369. [Abstract] [Full Text] [PDF]

				K. R. Sipido Understanding Cardiac Alternans: The Answer Lies in the Ca2+ Store Circ. Res., March 19, 2004; 94(5): 570 - 572. [Full Text] [PDF]

				P. Tavi, S. Pikkarainen, J. Ronkainen, P. Niemela, M. Ilves, M. Weckstrom, O. Vuolteenaho, J. Bruton, H. Westerblad, and H. Ruskoaho Pacing-induced calcineurin activation controls cardiac Ca2+ signalling and gene expression J. Physiol., January 15, 2004; 554(2): 309 - 320. [Abstract] [Full Text] [PDF]