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The Mechanism of Oscillatory Activity at Low Membrane Potentials in Cardiac Purkinje Fibres

Overview
Journal J Physiol
Specialty Physiology
Date 1969 Jan 1
PMID 5761950
Citations 37
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Abstract

1. The mechanism of oscillations at low membrane potentials in Purkinje fibres has been investigated using voltage clamp experiments.2. The oscillations are generated by time-dependent variations in an outward current component, i(x1), that is activated over the voltage range -40 to 10 mV. During normal activity, this current is responsible for initiating full repolarization to the resting potential (Noble & Tsien, 1969b) so that the oscillations represent a failure of the normal repolarization process, probably as a consequence of a small change in background (leakage) current.3. These oscillations are distinct from the normal pacemaker activity of Purkinje fibres which is generated by a separate time-dependent current, i(K2) (Noble & Tsien, 1968). i(K2) shows no time-dependence when the membrane potential variations are entirely positive to -65 mV and cannot, therefore, be involved in the oscillatory activity apart from contributing a background outward current.4. The amplitude and frequency of the oscillations are very sensitive to applied currents less than 1 muA/cm(2). Larger currents abolish the oscillatory activity.5. The mechanism of the oscillations is discussed in relation to the possible mechanisms underlying the natural pacemaker activity of the sino-atrial (SA) node.

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References
1.
Noble D, Tsien R . Outward membrane currents activated in the plateau range of potentials in cardiac Purkinje fibres. J Physiol. 1969; 200(1):205-31. PMC: 1350425. DOI: 10.1113/jphysiol.1969.sp008689. View

2.
Weidmann S . The effect of the cardiac membrane potential on the rapid availability of the sodium-carrying system. J Physiol. 1955; 127(1):213-24. PMC: 1365850. DOI: 10.1113/jphysiol.1955.sp005250. View

3.
TRAUTWEIN W, Kassebaum D . On the mechanism of spontaneous impulse generation in the pacemaker of the heart. J Gen Physiol. 1961; 45:317-30. PMC: 2195170. DOI: 10.1085/jgp.45.2.317. View

4.
Noble D, Tsien R . Reconstruction of the repolarization process in cardiac Purkinje fibres based on voltage clamp measurements of membrane current. J Physiol. 1969; 200(1):233-54. PMC: 1350426. DOI: 10.1113/jphysiol.1969.sp008690. View

5.
Muller P . Ca- and K-free solution and pacemaker activity in mammalian myocardium. Helv Physiol Pharmacol Acta. 1965; 65(1):C38-41. View