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Volume 17, Number 12,
Issue of June 15, 1997
pp. 4839-4848
Copyright ©1997 Society for Neuroscience
Dual Ultrastructural Localization of µ-Opioid Receptors and
NMDA-Type Glutamate Receptors in the Shell of the Rat Nucleus
Accumbens
Received Jan. 24, 1997; revised March 26, 1997; accepted March 31, 1997.
K. Noelle Gracy,
Adena L. Svingos, and
Virginia M. Pickel
Division of Neurobiology, Department of Neurology and Neuroscience,
Cornell University Medical College, New York, New York 10021
The effectiveness of NMDA antagonists in modulating the motor and
motivational effects of opiates is attributed, in part, to functional
associations involving NMDA receptors and µ-opioid receptors (MORs)
in the shell of the nucleus accumbens (Acb). To determine the
subcellular sites for potential functional interactions between opiate
ligands and NMDA receptors in this region, we examined the
ultrastructural localization of antipeptide antisera against MOR and
the R1 subunit of the NMDA receptor in the Acb shell of the adult rat
brain. MOR-like immunoreactivity (MOR-LI) was seen primarily in
dendrites, whereas NMDAR1-like immunoreactivity (NMDAR1-LI) was
detected more often in axon terminals forming asymmetric synapses. In
these profiles, MOR labeling was localized mainly to extrasynaptic plasma membranes, whereas NMDAR1-LI was associated with both synaptic and extrasynaptic sites. Of 307 MOR-labeled processes, 17.9% of the
dendrites and 9.4% of the axon terminals also contained NMDAR1-LI. In
addition, 24.7% of the dendrites containing only MOR-LI were apposed
to NMDAR1-labeled axons or terminals. We conclude that in the shell of
the Acb, the output of single neurons can be dually modulated by (1)
activation of MOR and NMDA receptors in the same dendrites or (2)
combined activation of presynaptic NMDA receptors in afferents
contacting dendrites containing MOR. In addition, the colocalization of
MOR and NMDAR1 in certain axon terminals in the Acb suggests their dual
involvement in the presynaptic release of neurotransmitters in this
region.
Key words:
opiate;
withdrawal;
locomotion;
addiction;
glutamate;
colocalization;
immunocytochemistry;
morphine;
enkephalin
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