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Norepinephrine Transporter Imaging in Alchohol Dependence and Obesity (Project 8

Norepinephrine Transporter Imaging in Alchohol Dependence and Obesity (Project 8
酒精依赖和肥胖中的去甲肾上腺素转运蛋白成像(项目 8
批准号:
7815609
负责人:
ALEXANDER NEUMEISTER
金额:
$11.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-25 至 2010-02-28

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Evidence from different disciplines suggests that acute and chronic stress-related mechanisms play an important role in the development of and the chronic, relapsing nature of addiction. These brain stress systems, including the central and peripheral catecholaminergic systems or endocannabinoid (eCB) systems, are linked to each other and both are implicated in the development of addictive behaviors. To better understand the relative contributions of NE and eCB systems in alcohol dependence, we propose to study both, the role of NET and CB1 receptor in the brain of alcohol dependent patients under resting conditions using (S,S)-[11C]MRB and [11C]OMAR, respectively and positron emission tomography (PET) on a high resolution research tomograph (HRRT). To understand the role of eCB in modulating alcohol cue induced craving and regulation of stress responses, we propose to study the CB1 receptor in vivo in patients with alcohol dependence during neutral conditions and during stress exposure using the selective CBi receptor radioligand [11C]OMAR and PET. We propose to study alcohol dependent patients who are recruited for the already ongoing project. The supplement Will be completed in 2 phases: phase 1] CB1 PET study in alcohol dependent patients (N=8) and controls (N=8) under resting conditions; followed by phase 2] to scan alcohol dependent patients (N=6) and individually matched controls (N=6) during neutral-relaxing experiences and during an alcohol cue exposure manipulation which are given in randomized order using [11C] OMAR and PET. Plasma eCB concentrations and behavioral ratings will be collected repeatedly during the PET imaging sessions and correlated with brain GB, expression.
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