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The Journal of Neuroscience, November 15, 1998, 18(22):9453-9470
A Lateralized Deficit in Morphine Antinociception after
Unilateral Inactivation of the Central Amygdala
Barton H.
Manning
Department of Neurology, University of California, San Francisco,
San Francisco, California 94143-0114
The amygdala is a forebrain region that is receiving increasing
attention as a modulator of pain sensation. The amygdala contributes to
antinociception elicited by both psychological factors (e.g., fear) and
exogenous opioid agonists. Unlike the midbrain periaqueductal gray
matter (PAG) or rostral ventromedial medulla, the amygdala is a
pain-modulating region that has clear bilateral representation in the
brain, making it possible to determine whether pain-modulating effects
of this region are lateralized with respect to the
peripheral origin of noxious stimulation. Unilateral inactivation of
the central nucleus of the amygdala (Ce) plus adjacent portions of the
basolateral amygdaloid complex (with either the excitotoxin NMDA
or the GABAA agonist muscimol) reduced the ability of
morphine to suppress prolonged, formalin-induced pain derived from the hindpaw ipsilateral, but not contralateral, to the inactivated region.
This effect was evident regardless of the nociceptive scoring method
used (weighted scores or flinch-frequency method) and was
not accompanied by a concurrent reduction in
morphine-induced hyperlocomotion. Unilateral lesions restricted to the
basolateral amygdaloid complex (i.e., not including the Ce) did not
reduce the ability of morphine to suppress formalin-induced pain
derived from either hindpaw. The results constitute the first report of a lateralized deficit in opioid antinociception after unilateral inactivation of a specific brain area and show the first clear neuroanatomical dissociation between antinociceptive and motor effects
of systemically administered morphine in the rat. The amygdala appears
to modulate nociceptive signals entering the ipsilateral spinal dorsal
horn, probably through monosynaptic connections with ipsilateral
portions of the PAG.
Key words:
pain; antinociception; analgesia; morphine; opioid; formalin test; amygdala; central nucleus; lesion; NMDA; muscimol; inactivation; fear; defense reaction
Copyright © 1998 Society for Neuroscience 0270-6474/98/18229453-18$05.00/0
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