Abstract
Rationale
Emerging evidence from agonist–antagonist studies suggests a role for the dopamine D3 receptor subtype in the regulation of PPI in animals, but such evidence is lacking for human subjects.
Objectives
This study examines the effect of the preferential D3 agonist ropinirole on PPI in humans.
Methods
PPI was tested in 12 healthy men in three sessions associated with ropinirole 0.25 mg, ropinirole 0.5 mg, or placebo according to a balanced, crossover, double-blind design. Two prepulses (75- and 85-dB white noise bursts) and two lead intervals (50 and 80 ms) were employed.
Results
Ropinirole 0.5 mg significantly reduced prepulse inhibition (PPI) with both prepulses at the 80-ms lead intervals. There was no effect of treatment on startle amplitude and habituation.
Conclusions
These results suggest a role for the dopamine D3 receptor in the mediation of human PPI, although a contribution from ropinirole’s agonistic activity at the D2 receptor cannot be entirely excluded. Firm conclusions on the role of the D3 receptor in the modulation of human PPI can only be drawn with the use of genetic approaches or more selective ligands for this receptor.
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Acknowledgements
The authors have no conflict of interest or any involvement, financial or otherwise, that might have biased the present work. This project was supported by the University of Crete Research Funds Account (E.L.K.E. 1348). The experiments described in the present study comply with the current laws of Greece, where the study was performed.
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Giakoumaki, S.G., Roussos, P., Frangou, S. et al. Disruption of prepulse inhibition of the startle reflex by the preferential D3 agonist ropinirole in healthy males. Psychopharmacology 194, 289–295 (2007). https://doi.org/10.1007/s00213-007-0843-7
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DOI: https://doi.org/10.1007/s00213-007-0843-7