PT - JOURNAL ARTICLE AU - Mark Slifstein AU - Holly Moore AU - Lawrence Kegeles AU - Michelle Duvall AU - Xiaoyan Xu AU - Elizabeth Hackett AU - John Castrillon AU - Olga Kambalov AU - Erica Scher AU - Marc Laruelle AU - Anissa Abi-Dargham TI - Correlation between PET and microdialysis measurements of amphetamine induced DA release in striatal and extrastriatal brain regions in baboons DP - 2007 May 01 TA - Journal of Nuclear Medicine PG - 113P--113P VI - 48 IP - supplement 2 4099 - http://jnm.snmjournals.org/content/48/supplement_2/113P.2.short 4100 - http://jnm.snmjournals.org/content/48/supplement_2/113P.2.full SO - J Nucl Med2007 May 01; 48 AB - 382 Objectives: The amphetamine challenge (AMPH) is a frequently used paradigm for estimating dopamine (DA) release non-invasively in the brain by measuring changes in specific binding of radioligands for D2/D3 receptors. Previous studies have correlated the change in radioligand binding with DA efflux increases following AMPH as measured by microdialysis using radioligands that can only image the striatum. Fallypride (C11 or F18) provides quantifiable images in striatum and extrastrial regions. Here we measured the correlation between changes in [11C] fallypride binding and DA efflux increases following AMPH in baboons. Methods: Three female baboons (A, B and C) were anesthetized and scanned for 2 hr on the HR+ following a bolus injection of [11C] fallypride. After 1 additional hour, amphetamine was administered as a bolus (1 mg/kg ,A and B and 1.5 mg/kg, C). The post AMPH scan began ½ hr following AMPH administration. The parameter V3” was obtained by SRTM with cerebellum as reference region. Change following AMPH was quantified as V3”_post/V3”_ pre – 1 (ΔV3”). Microdialysis was later performed on 2 of the animals (A and C) using the same anesthesia protocol. Probes were placed in striatum, anterior cingulate and thalamus and perfused with aCSF. After probe equilibration, dialysates were collected every 15 min. After 1 hr, animals received the same AMPH dose as during the PET study, and 3 more dialysates were collected. DA concentration was quantified by HPLC-ED. Post-AMPH values were expressed as % increase relative to mean pre-AMPH samples (ΔDA). Average regional ΔDA was correlated with ΔV3" within and across subjects. Results: Regional ΔV3” was highly correlated with ΔDA, both within and across animals: ΔDA = -46.4*ΔV3” – 7.7 for animal A (R2 = 0.97), -12.6*ΔV3” +2.0 for animal C (R2 = 0.80) and -21.7*ΔV3” -0.4 across all 3 animals (R2 = 0.91). Mean ΔV3” was -19 ± 10%, -9 ± 7% and -3 ± 17% in striatum, thalamus and cingulate. Conclusions: The high correlation between ΔV3” and ΔDA supports the validity of PET measurements of DA release following AMPH in extrastriatal regions as well as striatum using fallypride. Research Support (if any): MH0661710-03