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Regulation of Craving: Stress-challenge and re-exposure effects

Regulation of Craving: Stress-challenge and re-exposure effects
渴望的调节:压力挑战和重新暴露的影响
批准号:
417958660
负责人:
Professorin Dr. Tanja Endrass
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Grants
财政年份:
2019
资助国家:
德国
项目状态:
已结题
起止时间:
2018-12-31 至 2023-12-31

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中文摘要
翻译
压力和渴望是物质使用障碍患者复发的重要预测因素。先前的研究表明,当面对物质线索(例如人们吸烟的图像)时,患者可以通过想象使用毒品的长期负面后果来减少自我报告的渴望。从神经上讲,这与前额叶皮层的活动有关,研究表明,与渴望密切相关的腹侧纹状体和杏仁核等区域的活动减少了。第一项研究的目的是检查压力对烟瘾调节能力及其神经基质的影响(使用功能磁共振成像;fMRI)。在fMRI扫描期间,男性重度吸烟者被随机分配到应激诱导(社会评价冷压力任务)或控制条件,并执行涉及吸烟和食物(控制)条件的渴望调节任务。唾液样本将在几个时间点采集,我们假设儿茶酚胺和糖皮质激素的应激诱导效应干扰前额叶介导的控制机制,从而损害调节成功(在行为和神经水平)。此外,我们将评估执行功能水平是否预测在面对压力时保持的监管能力。本研究的第二项目的是利用脑电图(EEG)比较调节渴望的策略及其电生理相关因素的预期效果。在这里,晚期正电位(LPP)将作为物质线索的注意标记及其引发渴望的潜力。在一次脑电图中,重度吸烟者执行一项控制渴望的任务,其中包括想象吸烟的长期负面后果和通过解决算术问题分散注意力。短暂休息后,参与者将再次接触先前呈现的物质线索,而没有指示调节渴望。我们认为,从长远来看,涉及详细阐述物质线索的策略比仅仅通过分散注意力来减少渴望的策略更成功。吸烟者应该能够通过这两种策略迅速减少渴望和与吸烟线索相关的LPP振幅。然而,在再次接触时,吸烟者应该报告更多的渴望和更高的LPP振幅,以回应先前受到分心的吸烟线索,而不是先前受到想象吸烟的长期负面后果的吸烟线索。由于监管策略在实验室中通常是成功的,但在现实生活中实施起来要困难得多,因此该项目将提高我们对促进或损害监管成功的因素以及它们如何相互作用的理解。此外,脑电图研究将有助于理解和表征与某些调节策略相关的“反弹效应”及其对渴望和线索暴露的影响。
英文摘要
Stress and craving are important predictors for relapse in patients with substance use disorders. Prior work has shown that patients can reduce self-reported craving by imagining the long-term negative consequences of using when confronted with substance cues (e.g. images of people smoking). Neurally, this was associated with activity of the prefrontal cortex and it was shown that activity of areas such as the ventral striatum and amygdala, which are closely linked with craving, were reduced.The aim of the first study is to examine the influence of stress on the capacity to regulate craving for cigarettes and its neural substrates (using functional magnetic resonance imaging; fMRI) in heavy smokers. Male heavy smokers are randomly assigned to a stress induction (socially evaluated cold pressor task) or control condition and perform a regulation of craving task involving a smoking and food (control) condition during a fMRI scan. Saliva samples will be taken at several time points and we assume that stress-induced effects of catecholamines and glucocorticoids interfere with prefrontally mediated control mechanisms and thus impair regulatory success (at the behavioral and neural level). Further, we will evaluate whether the level of executive functioning predicts maintained regulatory capacity in the face of stress. The aim of the second study of this proposal is to compare the prospective effects of strategies to regulate craving and its electrophysiological correlates using the electroencephalogram (EEG). Here, the late positive potential (LPP) will serve as a robust marker of attention for substance cues and their potential to elicit craving. During a single EEG session, heavy smokers perform a regulation of craving task, which involves imagination of the long-term negative consequences of smoking and distraction through solving arithmetic problems. After a short break, participants will be re-exposed to the previously presented substance cues, without instructions to regulate craving. We assume that strategies involving elaboration of a substance cue are more successful on the long run than strategies to reduce craving by mere distraction. Smokers should be able to rapidly reduce craving and the LPP amplitude associated with smoking cues through both strategies. However, upon re-exposure, smokers should report more craving and higher LPP amplitudes in response to smoking cues previously subject to distraction relative to smoking cues previously subject to imagining the long-term negative consequences of smoking.Since regulation strategies are frequently successful in the laboratory but much more difficult to implement in real life, this project will improve our understanding of factors facilitating or impairing regulatory success and how they interact. Furthermore, the EEG study will facilitate understanding and characterization of “rebound effects” associated with some regulation strategies and their effects on craving and cue-exposure.
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Emotion regulation in patients with obsessive-compulsive disorder
  • 批准号:
    250782384
  • 项目类别:
    Research Grants
  • 资助金额:
    $0.0万
  • 财政年份:
    2014
  • 负责人:
    Professorin Dr. Tanja Endrass
  • 依托单位:
Neurokognition der Handlungsüberwachung: Funktionelle und räumliche Dissoziation von Komponenten des (gestörten) Monitorings richtiger und falscher Reaktionen
  • 批准号:
    132915092
  • 项目类别:
    Research Units
  • 资助金额:
    $0.0万
  • 财政年份:
    2009
  • 负责人:
    Professorin Dr. Tanja Endrass
  • 依托单位:
Common and Distinct Mechanisms of Social Anxiety and Alcohol Use
海外基金