Key Points
- This study aims to explore the limitations of the double sucrose gap method for examining slow outward currents in ventricular muscle fibers.
- Described double sucrose gap method for sheep and calf ventricular fibers (0.8-1.2 mm)
- Measured action potentials using micro-electrode recordings to compare slow and rapid currents
- Derived equations for voltage distribution and leakage current in the double sucrose gap
- Good agreement between micro-electrode recordings and externally recorded potentials
- Slow outward current increases do not significantly contribute to repolarization in sheep or calf
- Accumulation of K ions around cells affects potential distribution during clamps
Structured PICO
PPopulationSmall bundles (diameter 0.8-1.2 mm) of sheep or calf ventricular fibres
IInterventionDouble sucrose gap method (voltage clamp)
OOutcomeMeasurement of slow outward current and action potentialssurrogate
The double sucrose gap method is suitable for studying slow currents in mammalian ventricular muscle, revealing that slow outward current contributes little to repolarization in sheep or calf.
Limitations
- The rapid sodium inward current was not controlled on depolarizing clamp steps
- The method is only suitable for a study of slow currents
- Too small a gap causes membrane current to be swamped by leakage current, while too wide a gap gives unequal potential distribution