Synergism of coupled subsarcolemmal Ca2+ clocks and sarcolemmal voltage clocks confers robust and flexible pacemaker function in a novel pacemaker cell model.
暂无分享,去创建一个
[1] D. Noble,et al. A model of sino-atrial node electrical activity based on a modification of the DiFrancesco-Noble (1984) equations , 1984, Proceedings of the Royal Society of London. Series B. Biological Sciences.
[2] Donald M. Bers,et al. Ca2+ Scraps: Local Depletions of Free [Ca2+] in Cardiac Sarcoplasmic Reticulum During Contractions Leave Substantial Ca2+ Reserve , 2003, Circulation research.
[3] K. Sampson,et al. Autonomic Control of Cardiac Action Potentials: Role of Potassium Channel Kinetics in Response to Sympathetic Stimulation , 2005, Circulation research.
[4] D DiFrancesco,et al. Basal responses of the L‐type Ca2+ and hyperpolarization‐activated currents to autonomic agonists in the rabbit sino‐atrial node. , 1996, The Journal of physiology.
[5] Michael D Stern,et al. Diastolic calcium release controls the beating rate of rabbit sinoatrial node cells: numerical modeling of the coupling process. , 2004, Biophysical journal.
[6] E. Lakatta,et al. Rhythmic Ryanodine Receptor Ca2+ Releases During Diastolic Depolarization of Sinoatrial Pacemaker Cells Do Not Require Membrane Depolarization , 2004, Circulation research.
[7] Hiroaki Kitano,et al. Biological robustness , 2008, Nature Reviews Genetics.
[8] E. Lakatta,et al. Dynamic interactions of an intracellular Ca2+ clock and membrane ion channel clock underlie robust initiation and regulation of cardiac pacemaker function. , 2008, Cardiovascular research.
[9] Yasutaka Kurata,et al. Dynamical description of sinoatrial node pacemaking: improved mathematical model for primary pacemaker cell. , 2002, American journal of physiology. Heart and circulatory physiology.
[10] Edward G Lakatta,et al. The emergence of a general theory of the initiation and strength of the heartbeat. , 2006, Journal of pharmacological sciences.
[11] Stefan Herrmann,et al. HCN4 provides a ‘depolarization reserve’ and is not required for heart rate acceleration in mice , 2007, The EMBO journal.
[12] D. Noble,et al. Facilitation of the L-type calcium current in rabbit sino-atrial cells: effect on cardiac automaticity. , 2000, Cardiovascular research.
[13] Itsuo Kodama,et al. Are We Lost in the Labyrinth of the Sinoatrial Node Pacemaker Mechanism? , 2002, Journal of cardiovascular electrophysiology.
[14] Zhilin Qu,et al. Dynamics and Cardiac Arrhythmias , 2006, Journal of cardiovascular electrophysiology.
[15] E. Lakatta,et al. The Integration of Spontaneous Intracellular Ca2+ Cycling and Surface Membrane Ion Channel Activation Entrains Normal Automaticity in Cells of the Heart's Pacemaker , 2006, Annals of the New York Academy of Sciences.
[16] E. Lakatta,et al. Membrane Potential Fluctuations Resulting From Submembrane Ca2+ Releases in Rabbit Sinoatrial Nodal Cells Impart an Exponential Phase to the Late Diastolic Depolarization That Controls Their Chronotropic State , 2006, Circulation research.
[17] D. Bers,et al. Cardiac pacemaking: If vs. Ca2+, is it really that simple? , 2003 .
[18] E. Bozler. TONUS CHANGES IN CARDIAC MUSCLE AND THEIR SIGNIFICANCE FOR THE INITIATION OF IMPULSES , 1943 .
[19] Michael D. Stern,et al. Local Control Models of Cardiac Excitation–Contraction Coupling , 1999, The Journal of general physiology.
[20] D. Noble. Modeling the Heart--from Genes to Cells to the Whole Organ , 2002, Science.
[21] Satoshi Matsuoka,et al. Role of individual ionic current systems in the SA node hypothesized by a model study. , 2003, The Japanese journal of physiology.
[22] H. T. ter Keurs,et al. Calcium and arrhythmogenesis. , 2007, Physiological reviews.
[23] E. Lakatta,et al. Sinoatrial Nodal Cell Ryanodine Receptor and Na + -Ca 2+ Exchanger: Molecular Partners in Pacemaker Regulation , 2001, Circulation research.
[24] Matteo E Mangoni,et al. Genesis and regulation of the heart automaticity. , 2008, Physiological reviews.
[25] E. Lakatta,et al. Constitutive Phosphodiesterase Activity Restricts Spontaneous Beating Rate of Cardiac Pacemaker Cells by Suppressing Local Ca2+ Releases , 2008, Circulation research.
[26] M. Boyett,et al. Desensitization to acetylcholine in single sinoatrial node cells isolated from rabbit hearts. , 1992, The American journal of physiology.
[27] D. Terrar,et al. Protein kinase C enhances the rapidly activating delayed rectifier potassium current, IKr, through a reduction in C‐type inactivation in guinea‐pig ventricular myocytes , 2000, The Journal of physiology.
[28] Ronald Wilders,et al. Computer modelling of the sinoatrial node , 2007, Medical & Biological Engineering & Computing.
[29] D. Noble. Cardiac Action and Pacemaker Potentials based on the Hodgkin-Huxley Equations , 1960, Nature.
[30] M R Boyett,et al. Correlation between electrical activity and the size of rabbit sino‐atrial node cells. , 1993, The Journal of physiology.
[31] Stanley Nattel,et al. Time-dependent transients in an ionically based mathematical model of the canine atrial action potential. , 2002, American journal of physiology. Heart and circulatory physiology.
[32] R. Tsien,et al. Cellular and subcellular mechanisms of cardiac pacemaker oscillations. , 1979, The Journal of experimental biology.
[33] R L Winslow,et al. Dynamics of abnormal pacemaking activity in cardiac Purkinje fibers. , 1994, Journal of theoretical biology.
[34] J. H. Wang,et al. Dependence of cardiac sarcoplasmic reticulum calcium pump activity on the phosphorylation status of phospholamban. , 1991, The Journal of biological chemistry.
[35] S. Penckofer,et al. Letter by Wallis and Penckofer regarding article, "Calcium/vitamin D supplementation and cardiovascular events". , 2007, Circulation.
[36] D. Terrar,et al. Fundamental importance of Na+–Ca2+ exchange for the pacemaking mechanism in guinea‐pig sino‐atrial node , 2006, The Journal of physiology.
[37] Denis Noble,et al. Role of pacemaking current in cardiac nodes: insights from a comparative study of sinoatrial node and atrioventricular node. , 2008, Progress in biophysics and molecular biology.
[38] John W. Clark,et al. Parasympathetic modulation of sinoatrial node pacemaker activity in rabbit heart: a unifying model. , 1999, American journal of physiology. Heart and circulatory physiology.
[39] D. Rubenstein,et al. Mechanisms of automaticity in subsidiary pacemakers from cat right atrium. , 1989, Circulation research.
[40] J. Lenfant,et al. Mechanism of muscarinic control of the high-threshold calcium current in rabbit sino-atrial node myocytes , 1993, Pflügers Archiv.
[41] D. Noble,et al. Rectifying Properties of Heart Muscle , 1960, Nature.
[42] J. Clark,et al. A mathematical model of a rabbit sinoatrial node cell. , 1994, The American journal of physiology.
[43] Trine Krogh-Madsen,et al. An ionic model for rhythmic activity in small clusters of embryonic chick ventricular cells. , 2005, American journal of physiology. Heart and circulatory physiology.
[44] E. Lakatta,et al. The Missing Link in the Mystery of Normal Automaticity of Cardiac Pacemaker Cells , 2008, Annals of the New York Academy of Sciences.
[45] Donald M Bers,et al. A mathematical treatment of integrated Ca dynamics within the ventricular myocyte. , 2004, Biophysical journal.
[46] E. Lakatta. Beyond Bowditch: the convergence of cardiac chronotropy and inotropy. , 2004, Cell calcium.
[47] D DiFrancesco,et al. Reciprocal role of the inward currents ib, Na and if in controlling and stabilizing pacemaker frequency of rabbit sino-atrial node cells , 1992, Proceedings of the Royal Society of London. Series B: Biological Sciences.
[48] H Honjo,et al. Sarcoplasmic Reticulum Ca2+ Release Is Not a Dominating Factor in Sinoatrial Node Pacemaker Activity , 2003, Circulation research.
[49] E. Lakatta,et al. Calcium Cycling Protein Density and Functional Importance to Automaticity of Isolated Sinoatrial Nodal Cells Are Independent of Cell Size , 2007, Circulation research.
[50] D. Kass,et al. Wall Tension Is a Potent Negative Regulator of In Vivo Thrombomodulin Expression , 2003, Circulation Research.
[51] Dario DiFrancesco,et al. Direct activation of cardiac pacemaker channels by intracellular cyclic AMP , 1991, Nature.
[52] Jürgen Kurths,et al. Synchronization - A Universal Concept in Nonlinear Sciences , 2001, Cambridge Nonlinear Science Series.
[53] S. Matsuoka,et al. Ionic mechanisms underlying the positive chronotropy induced by beta1-adrenergic stimulation in guinea pig sinoatrial node cells: a simulation study. , 2008, The journal of physiological sciences : JPS.
[54] H. Cheng,et al. Sinoatrial node pacemaker activity requires Ca(2+)/calmodulin-dependent protein kinase II activation. , 2000, Circulation research.
[55] J Jalife,et al. Mutual entrainment and electrical coupling as mechanisms for synchronous firing of rabbit sino‐atrial pace‐maker cells. , 1984, The Journal of physiology.
[56] C. Luo,et al. A dynamic model of the cardiac ventricular action potential. I. Simulations of ionic currents and concentration changes. , 1994, Circulation research.
[57] E. Lakatta,et al. High Basal Protein Kinase A–Dependent Phosphorylation Drives Rhythmic Internal Ca2+ Store Oscillations and Spontaneous Beating of Cardiac Pacemaker Cells , 2006, Circulation research.
[58] Jürgen Kurths,et al. Synchronization: Phase locking and frequency entrainment , 2001 .
[59] E. Lakatta,et al. Cardiac pacemaker cell failure with preserved I(f), I(CaL), and I(Kr): a lesson about pacemaker function learned from ischemia-induced bradycardia. , 2007, Journal of molecular and cellular cardiology.
[60] D DiFrancesco,et al. The contribution of the ‘pacemaker’ current (if) to generation of spontaneous activity in rabbit sino‐atrial node myocytes. , 1991, The Journal of physiology.
[61] C Antzelevitch,et al. Electrotonic Modulation of Pacemaker Activity Further Biological and Mathematical Observations on the Behavior of Modulated Parasystole , 1982, Circulation.
[62] W. Trautwein,et al. Relaxation of the ACh-induced potassium current in the rabbit sinoatrial node cell , 1978, Pflügers Archiv.
[63] A E Becker,et al. Functional and Morphological Organization of the Rabbit Sinus Node , 1980, Circulation research.
[64] D. Bers. The beat goes on: diastolic noise that just won't quit. , 2006, Circulation research.
[65] H Zhang,et al. Mathematical models of action potentials in the periphery and center of the rabbit sinoatrial node. , 2000, American journal of physiology. Heart and circulatory physiology.
[66] E. Lakatta,et al. Cyclic Variation of Intracellular Calcium: A Critical Factor for Cardiac Pacemaker Cell Dominance , 2003, Circulation research.
[67] Christopher J. Davidson,et al. A novel mechanism of pacemaker control that depends on high levels of cAMP and PKA-dependent phosphorylation: a precisely controlled biological clock. , 2006, Circulation research.
[68] S Guan,et al. A discussion about the DiFrancesco-Noble model. , 1997, Journal of theoretical biology.
[69] Zhengfeng Zhou,et al. Na(+)‐Ca2+ exchange current in latent pacemaker cells isolated from cat right atrium. , 1993, The Journal of physiology.
[70] Yasutaka Kurata,et al. Roles of L-type Ca2+ and delayed-rectifier K+ currents in sinoatrial node pacemaking: insights from stability and bifurcation analyses of a mathematical model. , 2003, American journal of physiology. Heart and circulatory physiology.
[71] Jörg Hüser,et al. Intracellular Ca2+ release contributes to automaticity in cat atrial pacemaker cells , 2000, The Journal of physiology.
[72] Edward G Lakatta,et al. &bgr;-Adrenergic Stimulation Modulates Ryanodine Receptor Ca2+ Release During Diastolic Depolarization to Accelerate Pacemaker Activity in Rabbit Sinoatrial Nodal Cells , 2002, Circulation research.
[73] Y Rudy,et al. Ionic charge conservation and long-term steady state in the Luo-Rudy dynamic cell model. , 2001, Biophysical journal.