Regulation of Craving: Neural Correlates and the Role of Stress and Delay Discounting

IF 2.6 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Solvej Nickel-Grenke, Raoul Wüllhorst, Stefan Scherbaum, Kristina Schwarz, Tanja Endrass
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Abstract

Regulation of craving (ROC) by focusing on long-term negative consequences of drug use has been shown to successfully reduce subjective craving. This process is supported by the dorsolateral prefrontal cortex (dlPFC), which exerts control over reward and value signals in the ventral striatum (VS) and ventromedial prefrontal cortex (vmPFC). As stress impairs cognitive control and addiction is characterized by altered value computations manifesting in delay discounting, we examined how these factors interact with ROC and its neural correlates to better understand the use of ROC in high-risk situations. Sixty-eight male smokers underwent a delay discounting task and either a stress (socially evaluated cold pressor task) or a control condition. They subsequently completed a ROC task during fMRI while focusing on (1) long-term negative consequences (LATER) versus (2) short-term positive consequences (NOW). We found lower subjective craving ratings and attenuated neural responses in the VS (t = 4.33, p = 0.012) and vmPFC (t = 5.79, p < 0.001), as well as higher activation in the dlPFC (t = 4.09, p = 0.038) in the LATER compared to the NOW strategy. Although no neural or behavioural difference in ROC was observed between stress and control groups, both individual stress (cortisol) and delay discounting were positively related to vmPFC activity (NOW > LATER). We replicated previous results on ROC. Importantly, the association of vmPFC signals with stress response and delay discounting suggests that enhancing ROC success may involve reinforcing changes in self-referentiality of future thoughts to subjective value of drug use.

渴望的调节:神经关联及压力和延迟折扣的作用
通过关注药物使用的长期负面后果来调节渴望(ROC)已被证明可以成功地减少主观渴望。这一过程由背外侧前额叶皮层(dlPFC)支持,它控制腹侧纹状体(VS)和腹内侧前额叶皮层(vmPFC)的奖励和价值信号。由于压力损害认知控制和成瘾的特征表现为延迟折扣中价值计算的改变,我们研究了这些因素如何与ROC及其神经相关性相互作用,以更好地理解ROC在高风险情况下的使用。68名男性吸烟者接受延迟折扣任务和压力(社会评估冷压力任务)或控制条件。他们随后在fMRI期间完成ROC任务,同时关注(1)长期负面后果(LATER)和(2)短期积极后果(NOW)。我们发现,与NOW策略相比,LATER策略中VS (t = 4.33, p = 0.012)和vmPFC (t = 5.79, p < 0.001)的主观渴望等级较低,神经反应减弱,dlPFC的激活(t = 4.09, p = 0.038)较高。虽然在应激组和对照组之间没有观察到神经或行为上的差异,但个体应激(皮质醇)和延迟折扣都与vmPFC活动呈正相关(NOW >; LATER)。我们在ROC上重复了之前的结果。重要的是,vmPFC信号与应激反应和延迟折扣的关联表明,提高ROC成功可能涉及加强未来想法对药物使用主观价值的自我参照性变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Addiction Biology
Addiction Biology 生物-生化与分子生物学
CiteScore
8.10
自引率
2.90%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields. Addiction Biology includes peer-reviewed original research reports and reviews. Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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