We tested twenty healthy adults who underwent 90-min long PET scans collected in 3 randomly ordered sessions (placebo, oral-MP, and IV-MP; double-blind) while simultaneously recording their self-reported ‘high’ ratings (0–10) under resting conditions, using oral- and IV-MP as pharmacological challenges. In each session, each of the 20 participants was given an oral pill (60mg-MP or placebo) 30 min before injection of the PET tracer ([11C]raclopride), followed 30 min after the tracer by an IV administration (0.25 mg/kg-MP or placebo). Note that these IV- and oral-MP doses were selected because they led to roughly equivalent levels of DA transporter occupancy6 (link), and their administration times were chosen to ensure that peak concentrations of MP in the striatum had similar timing for oral-MP and IV-MP, relative to imaging initiation7 (link).
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