Characterization of calcium currents in aortic baroreceptor neurons

J Neurophysiol. 1992 Aug;68(2):509-17. doi: 10.1152/jn.1992.68.2.509.

Abstract

1. Calcium currents in identified rat aortic baroreceptors were characterized with the perforated patch whole-cell voltage-clamp technique. Aortic baroreceptors were distinguished from other neurons by the presence of a fluorescent tracer that was previously applied to the aortic depressor nerve. The diversity of calcium currents in unidentified neurons dissociated from neonatal rat nodose ganglia were also examined. 2. A population of aortic baroreceptors (63%, 7 of 11) possessed a low-threshold, also referred to as a T-type, calcium current. This current was typically less than 100 pA in 2 mM Ca [72.7 +/- 20.9 (SE) pA, n = 7], had a rapid activation and inactivation, and inactivated completely at conditioning voltages positive to -50 mV. 3. All aortic baroreceptors possessed high-threshold calcium currents that were activated at voltages positive to -30 mV, with typical maximum amplitudes of 600-1,000 pA (826 +/- 79 pA, n = 11). 4. The high-threshold current inactivated with three exponential rates of decay of tau = 10.7 +/- 2.2 ms, 138 +/- 14.6 ms, and a third tau greater than 3 s. It was not possible to separate the kinetic components of inactivation with conditioning voltages (voltage-dependent inactivation), activation thresholds, deactivation kinetics, or calcium-channel antagonists. 5. The voltage-dependent inactivation of high-threshold calcium currents began at voltages positive to -70 mV and became steeply voltage dependent between -60 and -10 mV. Unexpectedly, the three decay constants were present after all conditioning voltages. There were no conditioning voltages that excluded any component.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Animals, Newborn
  • Aorta, Thoracic / innervation
  • Calcium Channel Blockers / pharmacology
  • Calcium Channels / drug effects*
  • Electrophysiology
  • In Vitro Techniques
  • Kinetics
  • Membrane Potentials / drug effects
  • Neurons / drug effects
  • Neurons / metabolism*
  • Nimodipine / pharmacology
  • Nodose Ganglion / cytology
  • Nodose Ganglion / drug effects
  • Peptides, Cyclic / pharmacology
  • Pressoreceptors / drug effects*
  • Rats
  • Rats, Inbred Strains
  • omega-Conotoxins*

Substances

  • Calcium Channel Blockers
  • Calcium Channels
  • Peptides, Cyclic
  • omega-Conotoxins
  • Conus magus toxin
  • Nimodipine