Abstract
Supraspinal opioid antinociception is mediated by sensitive brain sites capable of supporting this response following microinjection of opioid agonists. These sites include the ventrolateral periaqueductal gray (vlPAG), the rostral ventromedial medulla (RVM), the locus coeruleus and the amygdala. Each of these sites comprise an interconnected anatomical and physiologically relevant system mediating antinociceptive responses through regional interactions. Such interactions have been identified using two pharmacological approaches: (1) the ability of selective antagonists delivered to one site to block antinociception elicited by opioid agonists in a second site, and (2) the presence of synergistic antinociceptive interactions following simultaneous administration of subthreshold doses of opioid agonists into pairs of sites. Thus, the RVM has essential serotonergic, opioid, cholinergic and NMDA synapses that are necessary for the full expression of morphine antinociception elicited from the vlPAG, and the vlPAG has essential opioid synapses that are necessary for the full expression of opioid antinociception elicited from the amygdala. Further, the vlPAG, RVM, locus coeruleus and amygdala interact with each other in synergistically supporting opioid antinociception. Copyright (C) 2000 National Science Council.
Original language | English |
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Pages (from-to) | 181-194 |
Number of pages | 14 |
Journal | Journal of Biomedical Science |
Volume | 7 |
Issue number | 3 |
DOIs | |
State | Published - 2000 |
Externally published | Yes |
Keywords
- Amygdala
- Locus coeruleus
- Medulla, rostral ventromedial
- Opioid antinociception
- Periaqueductal gray, ventrolateral