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Modulation of dopamine D 1 ‐mediated turning behavior and striatal c‐fos expression by the substantia nigra
Author(s) -
Fenu S.,
Carta A.,
Morelli M.
Publication year - 1995
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/syn.890190402
Subject(s) - nbqx , muscimol , substantia nigra , agonist , chemistry , ampa receptor , dopamine , pharmacology , nmda receptor , glutamate receptor , endocrinology , medicine , neuroscience , receptor , psychology , dopaminergic , biochemistry
In order to study the possible contribution of the substantia nigra (SN) in the positive interaction between dopamine D 1 receptor agonists and glutamate antagonists in unilaterally 6‐hydroxydopamine (6‐OHDA) lesioned rats, the effect of the D 1 agonist, SKF 38393, was studied in combination with intranigral infusions of glutamate antagonists of the NMDA (MK 801, CPP) or AMPA (NBQX) type of receptor. Local infusion into the SN of the 6‐OHDA lesioned side of MK 801, CPP or NBQX at doses inducing no or minimal behavioral effects significantly increased the turning behavior and the expression of c‐fos induced, in the lesioned caudate‐putamen (CPu), by a parenteral administration of SKF 38393. The same result was obtained after intra‐SN infusion of the GABA agonist, muscimol. High doses of MK 801, CPP or muscimol infused into the SN produced intense contralateral turning per se and induced a sparse c‐fos expression in the lesioned CPu which was antagonized by parenteral administration of MK 801. The results indicate that a depression of SN pars reticulata efferent neurons potentiates D 1 ‐mediated responses and suggest that this area may play a role in the positive interaction between glutamate antagonists and D 1 receptor agonists. © 1995 Wiley‐Liss, Inc.