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Three-dimensional scroll waves direct cell movement and gene expression, and induce chaos in the brain and heart. We found an approach to terminate multiple three-dimensional scrolls. A pulse of a properly configured electric field detaches scroll filaments from the surface. They shrink due to filament tension and disappear. Since wave emission from small heterogeneities is not used, this approach requires a much lower electric field. It is not sensitive to the details of the excitable medium. It may affect future studies of low-energy chaos termination in the heart.
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Controlling the complex spatio-temporal dynamics underlying life-threatening cardiac arrhythmias such as fibrillation is extremely difficult, because of the nonlinear interaction of excitation waves in a heterogeneous anatomical substrate. In the absence of a better strategy, strong, globally resetting electrical shocks remain the only reliable treatment for cardiac fibrillation. Here we establish the relationship between the response of the tissue to an electric field and the spatial distribution of heterogeneities in the scale-free coronary vascular structure. We show that in response to a pulsed electric field, E, these heterogeneities serve as nucleation sites for the generation of intramural electrical waves with a source density ρ(E) and a characteristic time, τ, for tissue depolarization that obeys the power law τ â E(α). These intramural wave sources permit targeting of electrical turbulence near the cores of the vortices of electrical activity that drive complex fibrillatory dynamics. We show in vitro that simultaneous and direct access to multiple vortex cores results in rapid synchronization of cardiac tissue and therefore, efficient termination of fibrillation. Using this control strategy, we demonstrate low-energy termination of fibrillation in vivo. Our results give new insights into the mechanisms and dynamics underlying the control of spatio-temporal chaos in heterogeneous excitable media and provide new research perspectives towards alternative, life-saving low-energy defibrillation techniques.
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Fibrilação Atrial/fisiopatologia , Cardioversão Elétrica/métodos , Coração/fisiologia , Coração/fisiopatologia , Fibrilação Ventricular/fisiopatologia , Animais , Meios de Contraste , Vasos Coronários/anatomia & histologia , Cães , Cardioversão Elétrica/instrumentação , Eletrocardiografia , Coração/anatomia & histologia , Microtomografia por Raio-XRESUMO
BACKGROUND: Electrically based therapies for terminating atrial fibrillation (AF) currently fall into 2 categories: antitachycardia pacing and cardioversion. Antitachycardia pacing uses low-intensity pacing stimuli delivered via a single electrode and is effective for terminating slower tachycardias but is less effective for treating AF. In contrast, cardioversion uses a single high-voltage shock to terminate AF reliably, but the voltages required produce undesirable side effects, including tissue damage and pain. We propose a new method to terminate AF called far-field antifibrillation pacing, which delivers a short train of low-intensity electric pulses at the frequency of antitachycardia pacing but from field electrodes. Prior theoretical work has suggested that this approach can create a large number of activation sites ("virtual" electrodes) that emit propagating waves within the tissue without implanting physical electrodes and thereby may be more effective than point-source stimulation. METHODS AND RESULTS: Using optical mapping in isolated perfused canine atrial preparations, we show that a series of pulses at low field strength (0.9 to 1.4 V/cm) is sufficient to entrain and subsequently extinguish AF with a success rate of 93% (69 of 74 trials in 8 preparations). We further demonstrate that the mechanism behind far-field antifibrillation pacing success is the generation of wave emission sites within the tissue by the applied electric field, which entrains the tissue as the field is pulsed. CONCLUSIONS: AF in our model can be terminated by far-field antifibrillation pacing with only 13% of the energy required for cardioversion. Further studies are needed to determine whether this marked reduction in energy can increase the effectiveness and safety of terminating atrial tachyarrhythmias clinically.
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Fibrilação Atrial/terapia , Estimulação Cardíaca Artificial/métodos , Simulação por Computador , Modelos Cardiovasculares , Animais , Fibrilação Atrial/fisiopatologia , Cães , Cardioversão Elétrica/métodos , Feminino , Técnicas In Vitro , Masculino , Marca-Passo ArtificialRESUMO
Excitable media show changes in their basic characteristics that reflect temporal changes in the environment. In the photosensitive Belousov-Zhabotinsky (BZ) reaction, excitability is decreased by illumination. We found that a traveling pulse failed to propagate when a certain level of light intensity was switched on abruptly, but the pulse continued propagating when the light intensity reached the same level gradually. We investigated the mechanism of adaptation of pulse propagation to the change in light intensity using two mathematical models, the Oregonator model (a specific model for the photosensitive BZ reaction), and the FitzHugh-Nagumo model (a generic model for excitable media). The appearance of a characteristic such as adaptation is shown to be a general feature for a traveling pulse in excitable media.
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We show that for a class of bistable reaction-diffusion systems, zero-velocity fronts can be robust in the singular limit where one of the diffusion coefficients vanishes. In this case, stationary fronts can persist along variations of the system parameters. This property contrasts with the standard result that the front velocity v(&mgr;), expressed as a function of a control parameter &mgr;, is zero only at some isolated values &mgr;(0), and thus not giving robustness to zero-velocity fronts when &mgr; is varied. (c) 2000 American Institute of Physics.
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We investigate the drift of a spiral wave core in a homogeneous excitable medium under the influence of a periodic stimulation by wave trains close to the core. Two important results were found. First, as opposed to existing theories of spiral wave drift, we observe drift induced by wave trains with periods larger than the period of the freely rotating spiral wave. Second, when investigating the drift of meandering spirals we found that the property of meandering of spirals is not robust against periodic stimulations. Simple phenomenological arguments are provided to explain these observations. (c) 2001 American Institute of Physics.
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Classical theory of potential distribution in cardiac muscle (cable theory) postulates that all effects of electric field (internally or externally applied) should decay exponentially with a space constant of the order of the tissue space constant ( approximately 1 mm). Classical theory does not take into account the cellular structure of the heart. Here, we formulate a mathematical model of excitation propagation taking into account cellular gap junctions. Investigation of the model has shown that the classical description is correct on the macroscopic scale only. At microscopic scale, electric field is modulated with a spatial period equal to the cell size (Plonsey and Barr), with the zero average. A very important new feature found here is that this effect of electric field does not decay at arbitrary big distances from the electrode. It opens the new way to control the excitation propagation in the cardiac muscle. In particular, we show that electric field can modify the velocity of propagation of an impulse in cardiac tissue at arbitrary big distances from electrode. In 2-dimensions, it can make rotating waves drift. To test these predictions, experiments with cardiac preparations are proposed.
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Steady, nonpropagating, fronts in reaction diffusion systems usually exist only for special sets of control parameters. When varying one control parameter, the front velocity may become zero only at isolated values (where the Maxwell condition is satisfied, for potential systems). The experimental observation of fronts with a zero velocity over a finite interval of parameters, e.g., in catalytic experiments [Barelko et al., Chem. Eng. Sci., 33, 805 (1978)], therefore, seems paradoxical. We show that the velocity dependence on the control parameter may be such that velocity is very small over a finite interval, and much larger outside. This happens in a class of reaction diffusion systems with two components, with the extra assumptions that (i) the two diffusion coefficients are very different, and that (ii) the slowly diffusing variables has two stable states over a control parameter range. The ratio of the two velocity scales vanishes when the smallest diffusion coefficient goes to zero. A complete study of the effect is carried out in a model of catalytic reaction. (c) 2000 American Institute of Physics.
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A free vortex in excitable media can be displaced and removed by a wave train. However, simple physical arguments suggest that vortices anchored to large inexcitable obstacles cannot be removed similarly. We show that unpinning of vortices attached to obstacles smaller than the core radius of the free vortex is possible through pacing. The wave-train frequency necessary for unpinning increases with the obstacle size and we present a geometric explanation of this dependence. Our model-independent results suggest that decreasing excitability of the medium can facilitate pacing-induced removal of vortices in cardiac tissue.
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Life-threatening cardiac arrhythmias are associated with the existence of stable and unstable spiral waves. Termination of such complex spatio-temporal patterns by local control is substantially limited by anchoring of spiral waves at natural heterogeneities. Far-field pacing (FFP) is a new local control strategy that has been shown to be capable of unpinning waves from obstacles. In this article, we investigate in detail the FFP unpinning mechanism for a single rotating wave pinned to a heterogeneity. We identify qualitatively different phase regimes of the rotating wave showing that the concept of vulnerability is important but not sufficient to explain the failure of unpinning in all cases. Specifically, we find that a reduced excitation threshold can lead to the failure of unpinning, even inside the vulnerable window. The critical value of the excitation threshold (below which no unpinning is possible) decreases for higher electric field strengths and larger obstacles. In contrast, for a high excitation threshold, the success of unpinning is determined solely by vulnerability, allowing for a convenient estimation of the unpinning success rate. In some cases, we also observe phase resetting in discontinuous phase intervals of the spiral wave. This effect is important for the application of multiple stimuli in experiments.
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Estimulação Cardíaca Artificial , Modelos Biológicos , Arritmias Cardíacas/patologia , Arritmias Cardíacas/fisiopatologia , Arritmias Cardíacas/terapia , Estimulação ElétricaRESUMO
For prevention of lethal arrhythmias, patients at risk receive implantable cardioverter-defibrillators, which use high-frequency antitachycardia pacing (ATP) to convert tachycardias to a normal rhythm. One of the suggested ATP mechanisms involves paced-induced drift of rotating waves followed by their collision with the boundary of excitable tissue. This study provides direct experimental evidence of this mechanism. In monolayers of neonatal rat cardiomyocytes in which rotating waves of activity were initiated by premature stimuli, we used the Ca(2+)-sensitive indicator fluo 4 to observe propagating wave patterns. The interaction of the spiral tip with a paced wave was then monitored at a high spatial resolution. In the course of the experiments, we observed spiral wave pinning to local heterogeneities within the myocyte layer. High-frequency pacing led, in a majority of cases, to successful termination of spiral activity. Our data show that 1) stable spiral waves in cardiac monolayers tend to be pinned to local heterogeneities or areas of altered conduction, 2) overdrive pacing can shift a rotating wave from its original site, and 3) the wave break, formed as a result of interaction between the spiral tip and a paced wave front, moves by a paced-induced drift mechanism to an area where it may become unstable or collide with a boundary. The data were complemented by numerical simulations, which was used to further analyze experimentally observed behavior.
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Potenciais de Ação/fisiologia , Mapeamento Potencial de Superfície Corporal/métodos , Estimulação Cardíaca Artificial/métodos , Sistema de Condução Cardíaco/fisiologia , Modelos Cardiovasculares , Miócitos Cardíacos/fisiologia , Animais , Animais Recém-Nascidos , Células Cultivadas , Sistema de Condução Cardíaco/citologia , Miócitos Cardíacos/citologia , RatosRESUMO
High-energy defibrillation shock is the only therapy for ventricular tachyarrhythmias. However, because of adverse side effects, lowering defibrillation energy is desirable. We investigated mechanisms of unpinning, destabilization, and termination of ventricular tachycardia (VT) by low-energy shocks in isolated rabbit right ventricular preparations (n = 22). Stable VT was initiated with burst pacing and was optically mapped. Monophasic "unpinning" shocks (10 ms) of different strengths were applied at various phases throughout the reentry cycle. In 8 of 22 preparations, antitachycardia pacing (ATP: 8-20 pulses, 50-105% of period, 0.8-10 mA) was also applied. Termination of reentry by ATP was achieved in only 5 of 8 preparations. Termination by unpinning occurred in all 22 preparations. Rayleigh's test showed a statistically significant unpinning phase window, during which reentry could be unpinned and subsequently terminated with E80 (magnitude at which 80% of reentries were unpinned) = 1.2 V/cm. All reentries were unpinned with field strengths < or = 2.4 V/cm. Unpinning was achieved by inducing virtual electrode polarization and secondary sources of excitation at the core of reentry. Optical mapping revealed the mechanisms of phase-dependent unpinning of reentry. These results suggest that a 20-fold reduction in energy could be achieved compared with conventional high-energy defibrillation and that the unpinning method may be more effective than ATP for terminating stable, pinned reentry in this experimental model.
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Mapeamento Potencial de Superfície Corporal , Estimulação Cardíaca Artificial/métodos , Cardioversão Elétrica/métodos , Sistema de Condução Cardíaco/fisiopatologia , Taquicardia Ventricular/fisiopatologia , Taquicardia Ventricular/terapia , Potenciais de Ação , Animais , Técnicas In Vitro , Coelhos , Recuperação de Função Fisiológica/fisiologia , Resultado do TratamentoRESUMO
Many arrhythmias are believed to be triggered by ectopic sources arising from the border of the ischemic tissue. However, the development of ectopic activity from individual sources to a larger mass of cardiac tissue remains poorly understood. To address this critical issue, we used monolayers of neonatal rat cardiomyocytes to create conditions that promoted progression of ectopic activity from single cells to the network that consisted of hundreds of cells. To explain complex spatiotemporal patterns observed in these experiments we introduced a new theoretical framework. The framework's main feature is a parameter space diagram, which uses cell automaticity and coupling as two coordinates. The diagram allows one to depict network behavior, quantitatively address the heterogeneity factor, and evaluate transitions between different regimes. The well-organized wave trains were observed at moderate and high cell coupling values and network heterogeneity was found to be qualitatively unimportant for these regimes. In contrast, at lower values of coupling, spontaneous ectopic activity led to the appearance of fragmented ectopic waves. For these regimes, network heterogeneity played an essential role. The ectopic waves occasionally gave rise to spiral activity in two different regions within the parameter space via two distinct mechanisms. Together, our results suggest that localized ectopic waves represent an essential step in the progression of ectopic activity. These studies add to the understanding of initiation and progression of arrhythmias and can be applied to other phenomena that deal with assemblies of coupled oscillators.
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Potenciais de Ação , Arritmias Cardíacas/fisiopatologia , Relógios Biológicos , Sistema de Condução Cardíaco/fisiopatologia , Modelos Cardiovasculares , Miócitos Cardíacos , Transmissão Sináptica , Animais , Animais Recém-Nascidos , Células Cultivadas , Simulação por Computador , Potenciais da Membrana , Modelos Neurológicos , Ratos , Ratos Sprague-DawleyRESUMO
Recent experiments [R. A. Gray, Phys. Rev. Lett. 87, 168104 (2001)]] have revealed striking standing wave patterns in cardiac muscle. In excitable media, such as cardiac tissue where colliding waves annihilate, standing wave patterns result from a fully nonlinear mechanism. We present a possible physical mechanism explaining these patterns. The phenomenon does not depend on the precise excitable model chosen. Analogies are drawn with weak links in superconductors, and phase-slip solutions in the Ginzburg-Landau equations.
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Coração/fisiologia , Modelos Biológicos , Simulação por Computador , Potenciais da Membrana/fisiologia , Fibras Musculares Esqueléticas/fisiologiaRESUMO
By using both experimental and theoretical means, we have addressed the progression of ectopic activity from individual cardiac cells to a multicellular two-dimensional network. Experimental conditions that favor ectopic activity have been created by local perfusion of a small area of cardiomyocyte network (I-zone) with an isoproterenol-heptanol containing solution. The application of this solution initially slowed down and then fully blocked wave propagation inside the I-zone. After a brief lag period, ectopically active cells appeared in the I-zone, followed by evolution of the ectopic clusters into slowly propagating waves. The changing pattern of colliding and expanding ectopic waves confined to the I-zone persisted for as long as the isoproterenol-heptanol environment was present. On restoration of the control environment, the ectopic waves from the I-zone broke out into the surrounding network causing arrhythmias. The observed sequence of events was also modeled by FitzHugh-Nagumo equations and included a cell's arrangement of two adjacent square regions of 20 x 20 cells. The control zone consisted of well-connected, excitable cells, and the I-zone was made of weakly coupled cells (heptanol effect), which became spontaneously active as time evolved (isoproterenol effect). The dynamic events in the system have been studied numerically with the use of a finite difference method. Together, our experimental and computational data have revealed that the combination of low coupling, increased excitability, and spatial heterogeneity can lead to the development of ectopic waves confined to the injured network. This transient condition appears to serve as an essential step for the ectopic activity to "mature" before escaping into the surrounding control network.