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OSU6162 inhibits levodopa-induced dyskinesias in a monkey model of PD

We have studied the effects of two D2 dopamine receptor-selective compounds, (-)-OSU 6162 and raclopride, on levodopa-induced dyskinesias in 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-lesioned common marmosets (Callithrix jacchus).

Three monkeys developed a severe parkinsonian syndrome following administration of MPTP.
In response to daily levodopa treatment the animals developed reproducible and idiosyncratic peak-dose dyskinesias.

Pretreatment with (-)-OSU 6162 and raclopride, in doses increased by multiples of three, both dose-dependently relieved the levodopa-induced dyskinesias.

However, in contrast to when raclopride pretreatment was given, (-)-OSU 6162 pretreatment did not induce akinesia.

Our investigation suggests that (-)-OSU 6162 may be useful an an adjuvant treatment to levodopa in advanced Parkinson's disease to selectively combat levodopa-induced dyskinesias without affecting the antiparkinsonian response.


Neuroreport 1997 Jul 28;8(11):2567-70
Ekesbo A, Andren PE, Gunne LM, Tedroff J
Department of Neurology, University Hospital, Uppsala, Sweden.
PMID: 9261828, UI: 97405158

<http://www.ncbi.nlm.nih.gov/PubMed/>

janet paterson
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