2019 Volume 34 Issue 3 Pages 228-239
There is much evidence showing that a group of neuropeptides produced in the hypothalamus, oxytocin and orexins, inhibit nociceptive transmission in the rat spinal dorsal horn. In order to reveal cellular mechanisms underlying this antinociception, we examined how oxytocin, orexins A and B affect spontaneous synaptic transmission in rat spinal lamina II (substantia gelatinosa; SG) neurons, which play a pivotal role in regulating nociceptive transmission. The experiments were performed by applying the blind whole–cell patch–clamp technique to SG neurons in adult rat spinal cord slices. Bath–applied oxytocin unaffected glutamatergic spontaneous excitatory transmission while producing an inward current at −70 mV (membrane depolarization) and enhancing both GABAergic and glycinergic spontaneous inhibitory transmissions in >70% of the neurons tested. The depolarization, and increased GABAergic and glycinergic spontaneous inhibitory postsynaptic current (sIPSC) frequencies were concentration–dependent with half–maximal effective concentration (EC50) values of 0.022, 0.024 and 0.038 µM, respectively. On the other hand, orexins A and B produced an inward current at −70 mV and/or increased the frequency of spontaneous excitatory postsynaptic current (sEPSC) without changing its amplitude in some 70% of the neurons examined. EC50 values for orexin A in their effects were 0.0045 and 0.030 µM, respectively; those for orexin B were 0.020 and 0.039 µM, respectively. EC50 value for orexin B in producing inward current was similar to that of oxytocin while being four–fold larger than that of orexin A; EC50 value for orexin B in increasing sEPSC frequency was comparable to orexin A’s one and also to oxytocin’s ones for sIPSC frequency increase. Like oxytocin, orexin A enhanced both GABAergic and glycinergic transmissions in >50% of the neurons tested, whereas orexin B facilitated glycinergic but not GABAergic transmission in the majority (about 70%) of neurons tested. Inhibitory transmission enhancements produced by oxytocin, orexins A and B disappeared in the presence of the voltage–gated Na+–channel blocker tetrodotoxin. Oxytocin activities were mimicked by an oxytocin–receptor agonist TGOT and were inhibited by an oxytocin–receptor antagonist dVOT, indicating an activation of oxytocin receptors. Orexin A activities were inhibited by an orexin–1 receptor antagonist (SB334867) but not an orexin–2 receptor antagonist (JNJ10397049) while orexin B activities were inhibited by JNJ10397049 but not SB334867, indicating that orexins A and B activities are mediated by orexin–1 and –2 receptors, respectively. It is concluded that oxytocin, orexins A and B increase neuronal activity through membrane depolarization and/or increased L–glutamate release from nerve terminals, by activating their specific receptors, which in turn results in GABAergic and/or glycinergic spontaneous inhibitory transmission enhancements, a possible mechanism for antinociception.