Delta opioids reduce the neurotransmitter release probability by enhancing transient (KV4) K+-currents in corticostriatal synapses as evaluated by the paired pulse protocol

Neurosci Lett. 2007 Mar 6;414(2):150-4. doi: 10.1016/j.neulet.2006.12.010. Epub 2007 Jan 2.

Abstract

Field recordings were used to determine the influence of delta-opioid receptor activation on corticostriatal synaptic transmission. Application of the selective delta-opioid receptor agonist, [Tyr-D-Pen-Gly-Phe-D-Pen]-enkephalin (DPDPE, 1 microM), decreased the amplitude of the field-excitatory synaptic potential and at the same time increased the paired pulse ratio (PPR) suggesting a presynaptic site of action. This response reversed rapidly when DPDPE was washed and blocked by 1 nM of the selective delta-receptor antagonist naltrindole. Neither omega-conotoxin GVIA (1 microM) nor omega-agatoxin TK (400 nM), blockers of N- and P/Q-type Ca2+-channels, respectively, nor TEA (1 mM), blocker of some classes of K+-channels, occluded the effects of DPDPE. Instead, 1 mM 4-AP or 400 microM Ba2+ occluded completely the effects of DPDPE. Therefore, the results suggest that the modulation by delta opioids at corticostriatal terminals is mediated by transient (KV4) K+-conductances.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics, Opioid / pharmacology
  • Animals
  • Calcium Channel Blockers / pharmacology
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / metabolism*
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism*
  • Electric Stimulation
  • Enkephalin, D-Penicillamine (2,5)- / pharmacology*
  • Excitatory Postsynaptic Potentials / drug effects
  • Excitatory Postsynaptic Potentials / physiology
  • Male
  • Narcotic Antagonists / pharmacology
  • Neural Pathways / drug effects
  • Neural Pathways / metabolism*
  • Neurotransmitter Agents / metabolism*
  • Opioid Peptides / metabolism
  • Organ Culture Techniques
  • Potassium Channel Blockers / pharmacology
  • Presynaptic Terminals / drug effects
  • Presynaptic Terminals / metabolism
  • Rats
  • Rats, Wistar
  • Receptors, Opioid, delta / agonists*
  • Receptors, Opioid, delta / antagonists & inhibitors
  • Receptors, Opioid, delta / metabolism
  • Shal Potassium Channels / agonists*
  • Shal Potassium Channels / antagonists & inhibitors
  • Shal Potassium Channels / metabolism
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology

Substances

  • Analgesics, Opioid
  • Calcium Channel Blockers
  • Narcotic Antagonists
  • Neurotransmitter Agents
  • Opioid Peptides
  • Potassium Channel Blockers
  • Receptors, Opioid, delta
  • Shal Potassium Channels
  • Enkephalin, D-Penicillamine (2,5)-