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Serotonergic modulation of receptor occupancy in rats treated with l ‐DOPA after unilateral 6‐OHDA lesioning
Author(s) -
Nahimi Adjmal,
Høltzermann Mette,
Landau Anne M.,
Simonsen Mette,
Jakobsen Steen,
Alstrup Aage Kristian Olsen,
Vang Kim,
Møller Arne,
Wegener Gregers,
Gjedde Albert,
Doudet Doris J.
Publication year - 2012
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2011.07598.x
Subject(s) - raclopride , microdialysis , serotonergic , agonist , pharmacology , dopamine , medicine , striatum , chemistry , endocrinology , neuroscience , serotonin , psychology , receptor
J. Neurochem (2012) 120 , 806–817. Abstract Recent studies suggest that l ‐3,4 dihydroxyphenylalanine (l ‐DOPA)‐induced dyskinesia (LID), a severe complication of conventional l ‐DOPA therapy of Parkinson’s disease, may be caused by dopamine (DA) release originating in serotonergic neurons. To evaluate the in vivo effect of a 5‐HT 1A agonist [(±)‐8‐hydroxy‐2‐(dipropylamino) tetralin hydrobromide, 8‐OHDPAT] on the l ‐DOPA‐induced increase in extracellular DA and decrease in [ 11 C]raclopride binding in an animal model of advanced Parkinson’s disease and LID, we measured extracellular DA in response to l ‐DOPA or a combination of l ‐DOPA and the 5‐HT 1A agonist, 8‐OHDPAT, with microdialysis, and determined [ 11 C]raclopride binding to DA receptors, with micro‐positron emission tomography, as the surrogate marker of DA release. Rats with unilateral 6‐hydroxydopamine lesions had micro‐positron emission tomography scans with [ 11 C]raclopride at baseline and after two pharmacological challenges with l ‐DOPA + benserazide with or without 8‐OHDPAT co‐treatment. Identical challenge regimens were used with the subsequent microdialysis concomitant with ratings of LID severity. The baseline increase of [ 11 C]raclopride‐binding potential (BP ND ) in lesioned striatum was eliminated by the l ‐DOPA challenge, while the concurrent administration of 8‐OHDPAT prevented this l ‐DOPA‐induced displacement of [ 11 C]raclopride significantly in lesioned ventral striatum and near significantly in the dorsal striatum. With microdialysis, the l ‐DOPA challenge raised the extracellular DA in parallel with the emergence of strong LID. Co‐treatment with 8‐OHDPAT significantly attenuated the release of extracellular DA and LID. The 8‐OHDPAT co‐treatment reversed the l ‐DOPA‐induced decrease of [ 11 C]raclopride binding and increase of extracellular DA and reduced the severity of LID. The reversal of the effect of l ‐DOPA on [ 11 C]raclopride binding, extracellular DA and LID by 5‐HT agonist administration is consistent with the notion that part of the DA increase associated with LID originates in serotonergic neurons.