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Alterations in striatal dopamine overflow during rotational behavior induced by amphetamine, phencyclidine, and MK‐801
Author(s) -
Mele Andrea,
Fontana David,
Pert Agu
Publication year - 1997
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/(sici)1098-2396(199707)26:3<218::aid-syn3>3.0.co;2-a
Subject(s) - phencyclidine , amphetamine , striatum , dopamine , medial forebrain bundle , neuroscience , chemistry , microdialysis , nmda receptor , substantia nigra , dizocilpine , psychology , dopaminergic , biochemistry , receptor
Abstract Rats lesioned unilaterally in the medial forebrain bundle with 6‐OHDA rotated ipsilateral to the lesion following injections of amphetamine, phencyclidine (PCP), and MK‐801. Concurrent measurement of striatal dopamine (DA) in the intact striatum with in vivo microdialysis revealed a dissociation between rotational behavior and alterations in DA overflow induced by the three drugs. Amphetamine produced robust ipsilateral rotational behavior and a substantial elevation in striatal DA (∼130% increase at asymptote). PCP produced comparable increases in rotational behavior, but only ∼30% increase in striatal DA. MK‐801 also had a comparable behavioral effect but failed to alter DA overflow in the intact striatum. Since MK‐801, a noncompetitive NMDA antagonist which does not enhance extracellular dopamine in the striatum, is able to produce ipsilateral rotational behavior in rats with unilateral nigrostriatal lesions, it is likely that the effects of PCP may also be determined predominantly through NMDA blockade in this model. Synapse 26:218–224, 1997. © 1997 Wiley‐Liss Inc.