阿片能调节货币激励延迟fMRI反应。

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Samuel Turton, Peter C T Hawkins, Christopher Muller-Pollard, Evangelos Zois, Patricia Conrod, Fernando Zelaya, Mitul A Mehta
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引用次数: 0

摘要

理由:据推测,纹状体多巴胺能信号的调节在阿片类药物的奖赏效应中起着关键作用。金钱奖励延迟(MID)任务是一种功能磁共振成像(fMRI)范例,用于研究纹状体在预期金钱奖励时的反应,这可能反映了纹状体多巴胺的释放:我们假设芬太尼会调节纹状体 MID 任务的血液氧合水平依赖性(BOLD)反应,从而反映出阿片类药物对纹状体多巴胺能信号的调节。方法:24 名右撇子男性接受了四次核磁共振成像扫描,在扫描期间,他们在静脉注射两种剂量的芬太尼(50 µg/70kg)、纳洛酮(400 µg)或安慰剂(0.9% 生理盐水)中的一种后 15 分钟完成了一项 MID 任务。收集潮气末二氧化碳数据以控制呼吸抑制:结果:在感兴趣区(ROI)和全脑分析中,与安慰剂和纳洛酮相比,我们发现芬太尼诱导的 MID 任务奖励和预期 BOLD 损失增加。这些结果出现在皮质区域,包括舌回、楔前区、扣带回后部和额极,而不是纹状体:我们的研究结果表明,芬太尼对 MID 预期 BOLD 的主要影响位于与准备对突出视觉线索做出运动反应相关的区域,而不是通常与奖赏处理相关的区域,如纹状体。这表明阿片类激动剂不会影响纹状体在 MID 任务中的激活。使用自然奖赏的任务,例如喂食、性或社会接触等会诱发内源性阿片类物质信号的任务,可能更适合用来探究芬太尼对奖赏处理的影响。这些结果来自男性参与者的数据,因此可能无法推广到女性参与者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Opioidergic modulation of monetary incentive delay fMRI responses.

Rationale: It is hypothesised that modulation of striatal dopaminergic signalling plays a key role in the rewarding effects of opioids. The monetary incentive delay (MID) task is a functional magnetic resonance imaging (fMRI) paradigm used to investigate striatal responses, which may reflect striatal dopamine release, during the anticipation of a financial reward.

Objectives: We hypothesised that fentanyl would modulate striatal MID task Blood Oxygenation Level Dependent (BOLD) responses, reflecting opioidergic modulation of striatal dopaminergic signalling.

Methods: 24 right-handed males who undertook four MRI scanning sessions, during which they completed an MID task 15 min after receiving an intravenous infusion of either one of two doses of fentanyl (50 µg/70kg), naloxone (400 µg) or placebo (saline 0.9%), were included in the analyses. End tidal CO2 data were collected to control for respiratory depression.

Results: We demonstrated fentanyl induced increases in MID task reward and loss anticipation BOLD compared with placebo and naloxone in both region of interest (ROI) and whole brain analyses. These results were in cortical regions including the lingual gyrus, precuneus, posterior cingulate and frontal pole rather than the striatum.

Conclusions: Our results show the primary effects of fentanyl on MID anticipation BOLD in regions associated with the preparation of a motor response to a salient visual cue, rather than in regions typically associated with reward processing such as the striatum. This suggests that opioid agonists do not affect striatal activation during the MID task. Tasks using naturalistic rewards, for example feeding, sex or social contact which induce endogenous opioid signalling, may be more appropriate to probe the effects of fentanyl on reward processing. These results are from male participants' data and therefore may not be generalisable to female participants.

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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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