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The Journal of Neuroscience, July 1, 2002, 22(13):5619-5629
Mice Lacking Dopamine D2 and D3 Receptors
Have Spatial Working Memory Deficits
Sara B.
Glickstein1, 2,
Patrick R.
Hof3, and
Claudia
Schmauss1, 2
Departments of 1 Psychiatry and
2 Neuroscience, Columbia University and New York State
Psychiatric Institute, New York, New York 10032, and
3 Kastor Neurobiology of Aging Laboratories and Fishberg
Center for Neurobiology, Mount Sinai School of Medicine, New York, New
York 10029
Mice deficient for dopamine D2 and D3
receptors exhibit blunted c-fos responses to
D1 agonist stimulation. Stereologic cell counting revealed
decreased numbers of medial prefrontal cortex neurons that express Fos
immunoreactivity in all layers, particularly in the prelimbic and
anterior cingulate subregions. Pretreatment of these mutants with a
single, low dose of methamphetamine (METH) led to a sustained increase
in the number of neurons that express Fos immunoreactivity in response
to a D1 agonist challenge, which was most significant in
prelimbic and anterior cingulate subregions. The increased
c-fos responses reached wild-type-like levels in METH-pretreated D2 mutants but remained submaximal in
METH-pretreated D3 mutants. Additional studies tested the
performance of wild type and mutants in a delayed alternation test, a
cognitive task critically dependent on optimal activation of prefrontal
cortical D1 receptors by synaptically released dopamine.
Both D2 and D3 mutants exhibited deficits in
their spatial working memory, with increasing impairments at increasing
delays. Whereas METH pretreatment rescued the spatial working memory of
D2 mutants, it had no effect on D3 mutants.
These data suggest that the sustained improvement of spatial working
memory in METH-pretreated D2 mutants is attributable to D1 receptor-mediated mechanisms.
Key words:
dopamine D1 receptors; D2-receptor knock-out; D3-receptor
knock-out; prefrontal cortex; stereology; c-fos; working
memory
Copyright © 2002 Society for Neuroscience 0270-6474/02/22135619-11$05.00/0
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