Konova Anna B, Moeller Scott J, Tomasi Dardo, Goldstein Rita Z
Center for Neural Science, New York University, New York, NY 10003, United States.
Departments of Psychiatry & Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.
Brain Res. 2015 Dec 2;1628(Pt A):147-56. doi: 10.1016/j.brainres.2015.02.002. Epub 2015 Feb 24.
The spatial distribution and strength of information processing 'hubs' are essential features of the brain׳s network topology, and may thus be particularly susceptible to neuropsychiatric disease. Despite growing evidence that drug addiction alters functioning and connectivity of discrete brain regions, little is known about whether chronic drug use is associated with abnormalities in this network-level organization, and if such abnormalities could be targeted for intervention. We used functional connectivity density (FCD) mapping to evaluate how chronic and acute stimulants affect brain hubs (i.e., regions with many short-range or long-range functional connections). Nineteen individuals with cocaine use disorders (CUD) and 15 healthy controls completed resting-state fMRI scans following a randomly assigned dose of methylphenidate (MPH; 20mg) or placebo. Short-range and long-range FCD maps were computed for each participant and medication condition. CUD participants had increased short-range and long-range FCD in the ventromedial prefrontal cortex, posterior cingulate/precuneus, and putamen/amygdala, which in areas of the default mode network correlated with years of use. Across participants, MPH decreased short-range FCD in the thalamus/putamen, and decreased long-range FCD in the supplementary motor area and postcentral gyrus. Increased density of short-range and long-range functional connections to default mode hubs in CUD suggests an overrepresentation of these resource-expensive hubs. While the effects of MPH on FCD were only partly overlapping with those of CUD, MPH-induced reduction in the density of short-range connections to the putamen/thalamus, a network of core relevance to habit formation and addiction, suggests that some FCD abnormalities could be targeted for intervention.
信息处理“枢纽”的空间分布和强度是大脑网络拓扑结构的基本特征,因此可能特别容易受到神经精神疾病的影响。尽管越来越多的证据表明药物成瘾会改变离散脑区的功能和连接性,但对于长期药物使用是否与这种网络层面的组织异常有关,以及这些异常是否可以作为干预靶点,人们知之甚少。我们使用功能连接密度(FCD)映射来评估慢性和急性兴奋剂如何影响脑枢纽(即具有许多短程或长程功能连接的区域)。19名患有可卡因使用障碍(CUD)的个体和15名健康对照在随机分配剂量的哌甲酯(MPH;20mg)或安慰剂后完成静息态功能磁共振成像扫描。为每个参与者和药物条件计算短程和长程FCD图。CUD参与者在腹内侧前额叶皮层、后扣带回/楔前叶以及壳核/杏仁核中的短程和长程FCD增加,在默认模式网络区域中,这些增加与使用年限相关。在所有参与者中,MPH降低了丘脑/壳核中的短程FCD,并降低了辅助运动区和中央后回中的长程FCD。CUD中与默认模式枢纽的短程和长程功能连接密度增加表明这些资源消耗大的枢纽过度代表。虽然MPH对FCD的影响仅部分与CUD的影响重叠,但MPH导致与壳核/丘脑的短程连接密度降低,壳核/丘脑是与习惯形成和成瘾核心相关的网络,这表明一些FCD异常可以作为干预靶点。