Blockade of D-1 dopamine receptors by SCH 23390 prevents EEG and behavioral activation induced by l-DOPA

Administration of l-DOPA, a precursor of dopamine, induced EEG activation, arousal and signs of behavioral excitation in the rabbit. The effects were fully prevented by pretreatment with minute doses (0.01 mg/kg i.v.) of the selective D-1 antagonist SCH 23390. Conversely, its S-enantiomer SCH 23388,...

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Veröffentlicht in:Neuroscience letters 1987-11, Vol.82 (2), p.206-210
Hauptverfasser: Ongini, E., Caporali, M.G., Longo, V.G.
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Sprache:eng
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Zusammenfassung:Administration of l-DOPA, a precursor of dopamine, induced EEG activation, arousal and signs of behavioral excitation in the rabbit. The effects were fully prevented by pretreatment with minute doses (0.01 mg/kg i.v.) of the selective D-1 antagonist SCH 23390. Conversely, its S-enantiomer SCH 23388, which has weak actions on D-1 receptors, displayed relatively low inhibition of l-DOPA effects. (−)-Sulpiride (12.5 mg/kg), a selective D-2 antagonist, and haloperidol (0.1–0.3 mg/kg), a neuroleptic that interacts preferentially with D-2 receptors, both inhibited behavioral effects but failed to block EEG activation. The data indicate that D-1 receptors play an essential role in mediating EEG activation induced by l-DOPA.
ISSN:0304-3940
1872-7972
DOI:10.1016/0304-3940(87)90131-5