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The Journal of Neurophysiology Vol. 85 No. 1 January 2001, pp. 117-124
Copyright ©2001 by the American Physiological Society
Department of Anatomy and Structural Biology, University of Otago, Dunedin, New Zealand
Kerr, J.N.D. and
J. R. Wickens.
Dopamine D-1/D-5 Receptor Activation Is Required for Long-Term
Potentiation in the Rat Neostriatum In Vitro. J. Neurophysiol. 85: 117-124, 2001. Dopamine and
glutamate are key neurotransmitters involved in learning and memory
mechanisms of the brain. These two neurotransmitter systems converge on
nerve cells in the neostriatum. Dopamine modulation of
activity-dependent plasticity at glutamatergic corticostriatal synapses
has been proposed as a cellular mechanism for learning in the
neostriatum. The present research investigated the role of specific
subtypes of dopamine receptors in long-term potentiation (LTP) in the
corticostriatal pathway, using intracellular recording from striatal
neurons in a corticostriatal slice preparation. In agreement with
previous reports, LTP could be induced reliably under
Mg2+-free conditions. This
Mg2+-free LTP was blocked by dopamine depletion
and by the dopamine D-1/D-5 receptor antagonist SCH 23390 but was not
blocked by the dopamine D-2 receptor antagonist remoxipride or the
GABAA antagonist picrotoxin. In dopamine-depleted
slices, the ability to induce LTP could be restored by bath application
of the dopamine D-1/D-5 receptor agonist, SKF 38393. These results show
that activation of dopamine D-1/D-5 receptors by either endogenous
dopamine or exogenous dopamine agonists is a requirement for the
induction of LTP in the corticostriatal pathway. These findings have
significance for current understanding of learning and memory
mechanisms of the neostriatum and for theoretical understanding of the
mechanism of action of drugs used in the treatment of psychotic
illnesses and Parkinson's disease.
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