安非他明
伏隔核
内源性阿片
壳核
类阿片
医学
麻醉
心理学
内科学
神经科学
中枢神经系统
多巴胺
受体
作者
Inge Mick,Jim Myers,Paul Stokes,David Erritzøe,Alessandro Colasanti,Henrietta Bowden‐Jones,Luke Clark,Roger N. Gunn,Eugenii A. Rabiner,Graham Searle,Adam Waldman,Mark C. Parkin,Alan D. Brailsford,David Nutt,Anne Lingford‐Hughes
标识
DOI:10.1017/s1461145714000704
摘要
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.
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