Activation of μ-opioid receptor selectively potentiates NMDA-induced outward currents in rat locus coeruleus neurons

Abstract

We investigated the opioid modulation of N-methyl- d-aspartic acid (NMDA) receptor-mediated response in dissociated LC neurons using nystatin-perforated patch recording. In Mg 2+-free extracellular solution, NMDA induced an inward current ( I NMDA-IN) and a subsequent outward current ( I NMDA-OUT) at a holding potential of −40 mV. A selective μ-opioid receptor agonist, d-Ala 2, N-MePhe 4,Gly 5-ol-enkephalin (DAMGO), potentiated I NMDA-OUT in a concentration-dependent manner with the half-maximal effective concentration of 0.7 μM, while DAMGO (0.1–10 μM) did not affect I NMDA-IN. Under the condition of I NMDA-OUT blockade by the use of Cs-based pipette solution or by buffering intracellular Ca 2+ with a high concentration of EGTA and zero Ca 2+, DAMGO did not change I NMDA-IN. The DAMGO potentiation of I NMDA-OUT was prevented by naloxone, an opioid receptor antagonist. In addition, the DAMGO potentiation of I NMDA-OUT was prevented by treatment with staurosporine, a broad spectrum protein kinase inhibitor. In conclusion, μ-opioid receptor activation selectively potentiated I NMDA-OUT via intracellular signal pathway without affecting I NMDA-IN in LC neurons. We suggest the inhibitory opioid effect through NMDA receptor-mediated response in LC neurons.