Center for Studies of Addiction, Department of Psychiatry, The University of Pennsylvania Perelman School of Medicine, 3535 Market Street Suite 500, Philadelphia, PA, 19104, USA.
Center for Studies of Addiction, Department of Psychiatry, The University of Pennsylvania Perelman School of Medicine, 3535 Market Street Suite 500, Philadelphia, PA, 19104, USA.
Drug Alcohol Depend. 2021 Apr 1;221:108593. doi: 10.1016/j.drugalcdep.2021.108593. Epub 2021 Feb 13.
Craving is a major contributor to drug-seeking and relapse. Although the ventral striatum (VS) is a primary neural correlate of craving, strategies aimed at manipulating VS function have not resulted in efficacious treatments. This incongruity may be because the VS does not influence craving in isolation. Instead, craving is likely mediated by communication between the VS and other neural substrates. Thus, we examined how striatal functional connectivity (FC) with key nodes of networks involved in addiction affects relief of craving, which is an important step in identifying viable treatment targets.
Twenty-four nicotine-dependent non-abstinent women completed two resting-state (rs) fMRI scans, one before and one following smoking a cigarette in the scanner, and provided craving ratings before and after smoking the cigarette. A seed-based approach was used to examine rsFC between the VS, putamen and germane craving-related brain regions; the dorsolateral prefrontal cortex (dlPFC), the posterior cingulate cortex, and the anterior ventral insula.
Smoking a cigarette was associated with a decrease in craving. Relief of craving correlated with increases in right dlPFC- bilateral VS (r = 0.57, p = 0.003, corrected) as did increased right dlPFC-left putamen coupling (r = 0.62, p = 0.001, corrected).
Smoking-induced relief of craving is associated with enhanced rsFC between the dlPFC, a region that plays a pivotal role in decision making, and the striatum, the neural structure underlying motivated behavior. These findings are highly consistent with a burgeoning literature implicating dlPFC-striatal interactions as a neurobiological substrate of craving.
渴望是导致觅药和复发的主要因素。尽管腹侧纹状体(VS)是渴望的主要神经相关物,但旨在操纵 VS 功能的策略并未产生有效的治疗方法。这种不一致可能是因为 VS 不会孤立地影响渴望。相反,渴望可能是由 VS 与其他神经基质之间的通信介导的。因此,我们研究了纹状体功能连接(FC)与成瘾相关网络的关键节点之间的关系如何影响渴望的缓解,这是确定可行治疗靶点的重要步骤。
24 名尼古丁依赖的非戒断女性完成了两次静息态(rs)fMRI 扫描,一次在扫描前,一次在扫描中吸烟后,并在吸烟前后提供了渴望评分。采用种子方法研究了 VS、壳核和与渴望相关的关键脑区(背外侧前额叶皮层(dlPFC)、后扣带回和前腹侧内脑岛)之间的 rsFC。
吸烟与渴望的减少有关。渴望的缓解与右侧 dlPFC-双侧 VS 的增加相关(r = 0.57,p = 0.003,校正),右侧 dlPFC-左侧壳核的耦合增加也与渴望的缓解相关(r = 0.62,p = 0.001,校正)。
吸烟引起的渴望缓解与 dlPFC 和纹状体之间的 rsFC 增强有关,dlPFC 是决策的关键区域,纹状体是动机行为的神经结构。这些发现与越来越多的文献一致,即 dlPFC-纹状体相互作用是渴望的神经生物学基础。