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Last Updated: 3 years ago

Possible Interaction: Amphetamine and Raclopride

supplement:

Amphetamine

Research Papers that Mention the Interaction

Amphetamine (1 mg/kg) increased and raclopride (0.3 mg/kg) decreased performance by 63 and 28 %, respectively, with a 20-min injection-test interval.
Psychopharmacology  •  2015  |  View Paper
ResultsSCH 23390, SCH 39166, haloperidol, and raclopride dose-dependently inhibited vocalizations under AMPH and suppressed the proportion of trill calls.
Psychopharmacology  •  2012  |  View Paper
In the first set of experiments, all types of AIMs (axial, limb, orolingual and locomotor) were markedly reduced when amphetamine was co-administered with either the D(2) dopamine receptor antagonist raclopride or the D(1) receptor antagonist SCH23390.
Neurobiology of Disease  •  2009  |  View Paper
Even though the group given SCH23390 or raclopride alone showed profound disruption on DRL behavior by flattening the IRT curve, the co-administration of amphetamine with SCH23390 or raclopride reversed the aforementioned amphetamine-induced behavioral deficiency on DRL task.
The Chinese journal of physiology  •  2007  |  View Paper
The administration of amphetamine (1 mg/kg) induced a clear CPP that was completely blocked by the DA antagonists flupentixol (0.25 mg/kg) or raclopride (0.125 mg/kg).
Behavioral neuroscience  •  2004  |  View Paper
A reduction of 20–30% in raclopride binding was observed 30 min after amphetamine injection (4 mg/kg IP).
Synapse  •  2004  |  View Paper
ResultsAdministration of raclopride or clozapine reversed either an amphetamine or a ketamine-induced PPI deficit, as had the novel mood stabilizer lamotrigine in previous studies.
Psychopharmacology  •  2003  |  View Paper
However, pretreatment with either SCH 23390 or raclopride abolished the stimulatory effect of d‐amphetamine on NT‐LI and NPY‐LI.
Journal of neuroscience research  •  2002  |  View Paper
Pretreatment with either SCH 23390 or raclopride abolished the stimulatory effect of d‐amphetamine on CGRP‐LI levels.
Journal of neuroscience research  •  2001  |  View Paper
In contrast, the D2 receptor‐selective antagonist raclopride induced RGS2 mRNA when administered alone and greatly enhanced stimulation by amphetamine.
Journal of neurochemistry  •  1999  |  View Paper
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