van de Ven Vincent, Wingen Marleen, Kuypers Kim P C, Ramaekers Johannes G, Formisano Elia
Department of Cognitive Neuroscience, Faculty of Psychology and Neuroscience, Maastricht University, Maastricht, The Netherlands.
PLoS One. 2013 Jun 27;8(6):e68355. doi: 10.1371/journal.pone.0068355. Print 2013.
The default-mode network (DMN), which comprises medial frontal, temporal and parietal regions, is part of the brain's intrinsic organization. The serotonergic (5-HT) neurotransmitter system projects to DMN regions from midbrain efferents, and manipulation of this system could thus reveal insights into the neurobiological mechanisms of DMN functioning. Here, we investigate intrinsic functional connectivity of the DMN as a function of activity of the serotonergic system, through the administration of the selective serotonin reuptake inhibitor (SSRI) escitalopram. We quantified DMN functional connectivity using an approach based on dual-regression. Specifically, we decomposed group data of a subset of the functional time series using spatial independent component analysis, and projected the group spatial modes to the same and an independent resting state time series of individual participants. We found no effects of escitalopram on global functional connectivity of the DMN at the map-level; that is, escitalopram did not alter the global functional architecture of the DMN. However, we found that escitalopram decreased DMN regional pairwise connectivity, which included anterior and posterior cingulate cortex, hippocampal complex and lateral parietal regions. Further, regional DMN connectivity covaried with alertness ratings across participants. Our findings show that escitalopram altered intrinsic regional DMN connectivity, which suggests that the serotonergic system plays an important role in DMN connectivity and its contribution to cognition. Pharmacological challenge designs may be a useful addition to resting-state functional MRI to investigate intrinsic brain functional organization.
默认模式网络(DMN)由内侧额叶、颞叶和顶叶区域组成,是大脑内在组织的一部分。血清素能(5-HT)神经递质系统从中脑传出神经投射到DMN区域,因此对该系统的操纵可能揭示出DMN功能的神经生物学机制。在此,我们通过给予选择性5-羟色胺再摄取抑制剂(SSRI)艾司西酞普兰,研究作为血清素能系统活动函数的DMN内在功能连接性。我们使用基于双回归的方法对DMN功能连接性进行量化。具体而言,我们使用空间独立成分分析对功能时间序列子集的组数据进行分解,并将组空间模式投影到个体参与者的相同和独立静息状态时间序列。我们发现在图谱水平上,艾司西酞普兰对DMN的全局功能连接性没有影响;也就是说,艾司西酞普兰没有改变DMN的全局功能结构。然而,我们发现艾司西酞普兰降低了DMN区域的成对连接性,其中包括前扣带回和后扣带回皮质、海马复合体和外侧顶叶区域。此外,跨参与者的区域DMN连接性与警觉性评分相关。我们的研究结果表明,艾司西酞普兰改变了DMN的内在区域连接性,这表明血清素能系统在DMN连接性及其对认知的贡献中起重要作用。药理学激发设计可能是静息态功能磁共振成像的有益补充,用于研究大脑内在功能组织。