TY - JOUR
T1 - Amphetamine induced endogenous opioid release in the human brain detected with [11C]carfentanil PET
T2 - replication in an independent cohort
AU - Mick, Inge
AU - Myers, Jim
AU - Stokes, Paul R A
AU - Erritzoe, David
AU - Colasanti, Alessandro
AU - Bowden-Jones, Henrietta
AU - Clark, Luke
AU - Gunn, Roger N
AU - Rabiner, Eugenii A
AU - Searle, Graham E
AU - Waldman, Adam D
AU - Parkin, Mark C
AU - Brailsford, Alan D
AU - Nutt, David J
AU - Lingford-Hughes, Anne R
PY - 2014
Y1 - 2014
N2 - This study aimed to replicate a previous study which showed that endogenous opioid release, following an oral dose of amphetamine, can be detected in the living human brain using [11C]carfentanil positron emission tomography (PET) imaging. Nine healthy volunteers underwent two [11C]carfentanil PET scans, one before and one 3 h following oral amphetamine administration (0.5 mg/kg). Regional changes in [11C]carfentanil BPND from pre- to post-amphetamine were assessed. The amphetamine challenge led to significant reductions in [11C]carfentanil BPND in the putamen, thalamus, frontal lobe, nucleus accumbens, anterior cingulate, cerebellum and insula cortices, replicating our earlier findings. None of the participants experienced significant euphoria/'high', supporting the use of oral amphetamine to characterize in vivo endogenous opioid release following a pharmacological challenge. [11C]carfentanil PET is able to detect changes in binding following an oral amphetamine challenge that reflects endogenous opioid release and is suitable to characterize the opioid system in neuropsychiatric disorders.
AB - This study aimed to replicate a previous study which showed that endogenous opioid release, following an oral dose of amphetamine, can be detected in the living human brain using [11C]carfentanil positron emission tomography (PET) imaging. Nine healthy volunteers underwent two [11C]carfentanil PET scans, one before and one 3 h following oral amphetamine administration (0.5 mg/kg). Regional changes in [11C]carfentanil BPND from pre- to post-amphetamine were assessed. The amphetamine challenge led to significant reductions in [11C]carfentanil BPND in the putamen, thalamus, frontal lobe, nucleus accumbens, anterior cingulate, cerebellum and insula cortices, replicating our earlier findings. None of the participants experienced significant euphoria/'high', supporting the use of oral amphetamine to characterize in vivo endogenous opioid release following a pharmacological challenge. [11C]carfentanil PET is able to detect changes in binding following an oral amphetamine challenge that reflects endogenous opioid release and is suitable to characterize the opioid system in neuropsychiatric disorders.
U2 - 10.1017/S1461145714000704
DO - 10.1017/S1461145714000704
M3 - Article
C2 - 24807268
SN - 1461-1457
VL - N/A
SP - 1
EP - 6
JO - International Journal of Neuropsychopharmacology
JF - International Journal of Neuropsychopharmacology
IS - N/A
M1 - N/A
ER -