Proceedings of the National Academy of Sciences · 2010 · 206 citations · 45 references
Life SciencesNeurobiologyNeuroscienceMolecular NeuroscienceNeuropharmacologySensory PhysiologyAnalgesiaNeurotransmissionPain MechanismsPain NeurobiologyPain NeurosciencePain PhysiologyNeurotransmitter Modulation Of PainNociceptive MechanismsNociceptive TransmissionNociceptor FunctionNociceptor PhysiologyOpioid Modulation Of PainPain Pathway ModulationReceptors
Morphine-induced analgesia and antinociceptive tolerance are known to be modulated by interaction between delta-opioid receptors (DORs) and mu-opioid receptors (MORs) in the pain pathway. However, evidence for expression of DORs in nociceptive small-diameter neurons in dorsal root ganglia (DRG) and for coexistence of DORs with MORs and neuropeptides has recently been challenged. We now report, using in situ hybridization, single-cell PCR, and immunostaining, that DORs are widely expressed not only in large DRG neurons but in small ones and coexist with MORs in peptidergic small DRG neurons, with protachykinin-dependent localization in large dense-core vesicles. Importantly, both DOR and MOR agonists reduce depolarization-induced Ca(2+) currents in single small DRG neurons and inhibit afferent C-fiber synaptic transmission in the dorsal spinal cord. Thus, coexistence of DORs and MORs in small DRG neurons is a basis for direct interaction of opioid receptors in modulation of nociceptive afferent transmission and opioid analgesia.
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