Double‐pulse calcium channel current facilitation in adult rat sympathetic neurones.
- 1 July 1991
- journal article
- Published by Wiley in The Journal of Physiology
- Vol. 439 (1) , 181-214
- https://doi.org/10.1113/jphysiol.1991.sp018663
Abstract
1. Double-pulse facilitation of Ca2+ channel currents in enzymatically dispersed adult rat superior cervical ganglion neurones was investigated using the whole-cell variant of the patch-clamp technique. Voltage-clamp recordings were performed at room temperature (21-24 degrees C) in solutions designed to isolate Ca2+ channel currents. 2. Ba2+ currents, elicited by a 0 mV test pulse, were increased in amplitude when preceded by a 40 ms pulse to voltages greater than 0 mV. The magnitude of facilitation was dependent on pre-pulse voltage and reached a maximum of 50% (i.e. 1.5 x the current amplitude elicited without a pre-pulse) at a pre-pulse voltage of +80 mV. Half-maximal facilitation occurred at about +25 mV. A small decrease (-6%) in test pulse amplitude was present at pre-pulse voltages between -40 and 0 mV. The magnitude of facilitation was also dependent on test pulse voltage. Facilitation was greatest between test pulse voltages of -10 and 0 mV. 3. Facilitation slowly decreased during prolonged (1 h) dialysis of the neurone even though the Ba2+ current amplitude was well maintained. 4. Increasing the pre-pulse duration over the range 0-120 ms produced an exponential increase in facilitation with a time constant of 17.3 ms. Conversely, lengthening the interpulse duration over the range 5-915 ms, while maintaining a constant pre-pulse amplitude and duration, resulted in an exponential decrease in facilitation with a time constant of 197 ms. 5. At a test potential of 0 mV, the decay of the facilitated Ba2+ current component was fitted to a double exponential function with time constants of about 25 and 150 ms. The time constants had little pre-pulse voltage dependence between +30 to +80 mV. 6. The initial rising phase of both the control and facilitated Ba2+ current were reasonably well described by a single exponential (tau rise) after a delay of 300 microseconds. The tau rise versus test pulse potential relationship was 'bell shaped' over the test pulse voltage of -20 to +30 mV reaching a maximum near -5 mV. tau rise was similar for control and facilitated currents except at potentials greater than +10 mV where the rise of the facilitated current was accelerated. 7. Control and facilitated activation curves, as derived from tail current amplitudes, were described by the sum of two Boltzmann functions. A facilitating pre-pulse produced an increase in the proportion of the current contributed by the component activated at more hyperpolarized test potentials.(ABSTRACT TRUNCATED AT 400 WORDS)Keywords
This publication has 48 references indexed in Scilit:
- The GTPase superfamily: a conserved switch for diverse cell functionsNature, 1990
- Activation of facilitation calcium channels in chromaffin cells by D1 dopamine receptors through a cAMP/protein kinase A-dependent mechanismNature, 1990
- Gene expression of a neuronal growth-associated protein, GAP-43, in the paraganglionic carotid body as well as in the autonomic ganglia of normal adult ratsNeuroscience Letters, 1990
- Mechanism of gating of T-type calcium channels.The Journal of general physiology, 1990
- Modulation of Ca-channel current by an adenosine analog mediated by a GTP-binding protein in chick sensory neuronsPflügers Archiv - European Journal of Physiology, 1989
- Calcium currents in the normal adult rat sympathetic neurone.The Journal of Physiology, 1989
- Two‐suction‐electrode voltage‐clamp analysis of the sustained calcium current in cat sensory neurones.The Journal of Physiology, 1988
- Tetrodotoxin‐resistant sodium current of rat nodose neurones: monovalent cation selectivity and divalent cation block.The Journal of Physiology, 1987
- A quantitative description of the sodium current in the rat sympathetic neurone.The Journal of Physiology, 1986
- BIOSYNTHESIS OF PROSTAGLANDIN E BY RAT SUPERIOR CERVICAL GANGLIA1Journal of Neurochemistry, 1978