Omega-conotoxin CVID inhibits a pharmacologically distinct voltage-sensitive calcium channel associated with transmitter release from preganglionic nerve terminals

J Biol Chem. 2003 Feb 7;278(6):4057-62. doi: 10.1074/jbc.M209969200. Epub 2002 Nov 18.

Abstract

Neurotransmitter release from preganglionic parasympathetic neurons is resistant to inhibition by selective antagonists of L-, N-, P/Q-, R-, and T-type calcium channels. In this study, the effects of different omega-conotoxins from genus Conus were investigated on current flow-through cloned voltage-sensitive calcium channels expressed in Xenopus oocytes and nerve-evoked transmitter release from the intact preganglionic cholinergic nerves innervating the rat submandibular ganglia. Our results indicate that omega-conotoxin CVID from Conus catus inhibits a pharmacologically distinct voltage-sensitive calcium channel involved in neurotransmitter release, whereas omega-conotoxin MVIIA had no effect. omega-Conotoxin CVID and MVIIA inhibited depolarization-activated Ba(2+) currents recorded from oocytes expressing N-type but not L- or R-type calcium channels. High affinity inhibition of the CVID-sensitive calcium channel was enhanced when position 10 of the omega-conotoxin was occupied by the smaller residue lysine as found in CVID instead of an arginine as found in MVIIA. Given that relatively small differences in the sequence of the N-type calcium channel alpha(1B) subunit can influence omega-conotoxin access (Feng, Z. P., Hamid, J., Doering, C., Bosey, G. M., Snutch, T. P., and Zamponi, G. W. (2001) J. Biol. Chem. 276, 15728-15735), it is likely that the calcium channel in preganglionic nerve terminals targeted by CVID is a N-type (Ca(v)2.2) calcium channel variant.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Calcium Channel Blockers / chemistry
  • Calcium Channel Blockers / pharmacology*
  • Excitatory Postsynaptic Potentials
  • Ganglia / drug effects*
  • Ganglia / metabolism
  • Ganglia / physiology
  • Ion Channel Gating
  • Molecular Sequence Data
  • Neurotransmitter Agents / metabolism*
  • Presynaptic Terminals / drug effects*
  • Presynaptic Terminals / metabolism
  • Presynaptic Terminals / physiology
  • Protein Conformation
  • Rats
  • Venoms / chemistry
  • Venoms / pharmacology*
  • omega-Conotoxins

Substances

  • AM336
  • Calcium Channel Blockers
  • Neurotransmitter Agents
  • Venoms
  • omega-Conotoxins