Department of Biology, University of Oregon, USA; Department of Human Physiology, University of Oregon, USA; Institute of Neuroscience, University of Oregon, USA.
Department of Psychology, University of Oregon, USA.
Behav Brain Res. 2023 Feb 2;437:114120. doi: 10.1016/j.bbr.2022.114120. Epub 2022 Sep 28.
Models of addiction have identified deficits in inhibitory control, or the ability to inhibit inappropriate or unwanted behaviors, as one factor in the development and maintenance of addictive behaviors. Current literature supports disruption of the prefrontal circuits that mediate reactive inhibitory control processes (i.e., inhibition in response to sudden, unplanned changes in environmental demands) in substance use disorders. However, the relationship between disorders of addiction, such as nicotine dependence, and planned inhibitory processes (i.e., inhibition that occurs after advance warning) is unclear. The goal of the present study was to examine the extent to which reactive and planned inhibitory processes are differentially disrupted in nicotine dependent individuals.
We employed an internet-based novel stop signal task wherein participants were instructed to stop a continuous movement at either a predictable or unpredictable time. This task explicitly separated planned and reactive inhibitory processes and assessed group differences in task performance between smokers (N = 281) and non-smokers (N = 164). The smoker group was defined as any participant that identified as a smoker and reported an average daily nicotine consumption of at least 2 mg. The non-smoker group was defined as any participant that identified as a non-smoker and had not been a former smoker that quit within the last year. The smoker group also completed a questionnaire regarding smoking behaviors which included the Fägerstrom Test of Nicotine Dependence (FTND). We used these data to assess the continuous relation between planned stopping, unplanned stopping, and smoking behaviors.
We found significant differences in stop times for both reactive and planned stopping between groups as well as within the smoker group. Additionally, in the smoker group, dependence as measured by the FTND was associated with longer stop times on planned stop trials. Surprisingly, greater daily average consumption of nicotine was related to faster stopping for both trial types.
These results indicate the relevance of measuring both reactive and planned inhibitory processes for elucidating the relationship between nicotine addiction and mechanisms of inhibitory control.
成瘾模型已经确定,抑制控制缺陷(即抑制不适当或不受欢迎行为的能力)是成瘾行为发展和维持的一个因素。目前的文献支持,在物质使用障碍中,调节反应性抑制控制过程(即对环境需求的突然、无计划变化做出反应的抑制)的前额叶回路受到干扰。然而,尼古丁依赖等成瘾障碍与计划抑制过程(即预先警告后发生的抑制)之间的关系尚不清楚。本研究的目的是考察在尼古丁依赖个体中,反应性和计划性抑制过程的差异受到多大程度的破坏。
我们采用了一种基于互联网的新型停止信号任务,其中要求参与者在可预测或不可预测的时间停止连续运动。该任务明确区分了计划性和反应性抑制过程,并评估了吸烟者(N=281)和非吸烟者(N=164)在任务表现方面的组间差异。吸烟者组定义为任何自我报告吸烟且平均每日尼古丁摄入量至少为 2mg 的参与者。非吸烟者组定义为任何自我报告不吸烟且过去一年未戒烟的参与者。吸烟者组还完成了一份关于吸烟行为的问卷,其中包括 Fagerström 尼古丁依赖测试(FTND)。我们使用这些数据评估计划性停止、非计划性停止和吸烟行为之间的连续关系。
我们发现,在两组之间以及在吸烟者组内,反应性和计划性停止的停止时间都存在显著差异。此外,在吸烟者组中,FTND 测量的依赖程度与计划性停止试验中的停止时间延长有关。令人惊讶的是,每日平均尼古丁摄入量的增加与两种试验类型的更快停止有关。
这些结果表明,测量反应性和计划性抑制过程对于阐明尼古丁成瘾与抑制控制机制之间的关系具有重要意义。