Single Cells Isolated from Human Sinoatrial Node: Action Potentials and Numerical Reconstruction of Pacemaker Current

• Published in: 2007 29th Annual International Conference of the IEEE Engineering in Medicine and Biology Society Vol. 2007; pp. 904 - 907
• Main Authors: Verkerk, A.O., van Borren, M.M.G., Peters, R.J.G., Broekhuis, E., Lam, K.Y., Coronel, R., de Bakker, J.M.T., Tan, H.L., Wilders, R.
• Format: Conference Proceeding Journal Article
• Language: English
• Published: United States IEEE 01-01-2007
• Subjects: Action Potentials - physiology; Animals; Biological Clocks - physiology; Biomembranes; Cells, Cultured; Clamps; Computer Simulation; Humans; IEEE activities; Ion Channel Gating - physiology; Ion Channels - physiology; Kinetic theory; Kirchhoff's Law; Models, Cardiovascular; Myocytes, Cardiac - physiology; Pacemakers; Rabbits; Sinoatrial Node - physiology; Voltage
• ISBN: 9781424407873; 1424407877
• ISSN: 1094-687X; 1557-170X; 1558-4615
• DOI: 10.1109/IEMBS.2007.4352437

Pacemaker activity of the sinoatrial node has extensively been studied in laboratory animals of various species, but is virtually unexplored in man. Most experimental data have been obtained from rabbit, where the hyper- polarization-activated 'funny' current (I f ), also known as the 'pacemaker current', plays an important role in diastolic depolarization and thus in setting pacing rate. Recently, we isolated pacemaker cells from excised human sinoatrial node tissue, and recorded action potentials and I f using the whole- cell patch-clamp technique in current clamp and voltage clamp mode, respectively. Single sinoatrial node pacemaker cells showed a spontaneous beating rate of 73 plusmn 3 beats/min (mean plusmn SEM, n = 3) with a remarkably slow diastolic depolarization. I f was identified in voltage clamp experiments as the 2 mmol/L Cs + -sensitive inward current activating upon 2-s hyper- polarizing voltage clamp steps. The I f reversal potential and (de)activation kinetics were similar to those in rabbit. However, the fully-activated I f conductance was 3-4 times smaller than typically found in rabbit. Furthermore, the half-maximal activation voltage was ~20 mV more negative than in rabbit. These differences would both act to reduce the functional role of I f in human pacemaker cells. To assess this functional role, we carried out a numerical reconstruction of the I f time course during an experimentally recorded human sinoatrial node action potential, based on the obtained data on I f amplitude and kinetics. This reconstruction revealed that If provides a small but significant inward current in the voltage range of diastolic depolarization. We conclude that human sinoatrial node pacemaker cells functionally express I f and that this I f contributes to pacemaking in human sinoatrial node.