Giessing Carsten, Thiel Christiane M
Biological Psychology Lab, Institute of Psychology, University of Oldenburg Oldenburg, Germany.
Front Behav Neurosci. 2012 Aug 28;6:53. doi: 10.3389/fnbeh.2012.00053. eCollection 2012.
Previous studies document that cholinergic and noradrenergic drugs improve attention, memory and cognitive control in healthy subjects and patients with neuropsychiatric disorders. In humans neural mechanisms of cholinergic and noradrenergic modulation have mainly been analyzed by investigating drug-induced changes of task-related neural activity measured with functional magnetic resonance imaging (fMRI). Endogenous neural activity has often been neglected. Further, although drugs affect the coupling between neurons, only a few human studies have explicitly addressed how drugs modulate the functional connectome, i.e., the functional neural interactions within the brain. These studies have mainly focused on synchronization or correlation of brain activations. Recently, there are some drug studies using graph theory and other new mathematical approaches to model the brain as a complex network of interconnected processing nodes. Using such measures it is possible to detect not only focal, but also subtle, widely distributed drug effects on functional network topology. Most important, graph theoretical measures also quantify whether drug-induced changes in topology or network organization facilitate or hinder information processing. Several studies could show that functional brain integration is highly correlated with behavioral performance suggesting that cholinergic and noradrenergic drugs which improve measures of cognitive performance should increase functional network integration. The purpose of this paper is to show that graph theory provides a mathematical tool to develop theory-driven biomarkers of pro-cognitive drug effects, and also to discuss how these approaches can contribute to the understanding of the role of cholinergic and noradrenergic modulation in the human brain. Finally we discuss the "global workspace" theory as a theoretical framework of pro-cognitive drug effects and argue that pro-cognitive effects of cholinergic and noradrenergic drugs might be related to higher network integration.
先前的研究表明,胆碱能和去甲肾上腺素能药物可改善健康受试者以及患有神经精神疾病患者的注意力、记忆力和认知控制能力。在人类中,胆碱能和去甲肾上腺素能调节的神经机制主要通过研究功能磁共振成像(fMRI)测量的与任务相关的神经活动的药物诱导变化来进行分析。内源性神经活动常常被忽视。此外,尽管药物会影响神经元之间的耦合,但只有少数人体研究明确探讨了药物如何调节功能连接组,即大脑内的功能性神经相互作用。这些研究主要集中在大脑激活的同步或相关性上。最近,有一些药物研究使用图论和其他新的数学方法将大脑建模为相互连接的处理节点的复杂网络。使用这些方法不仅可以检测到对功能网络拓扑的局部影响,还能检测到细微的、广泛分布的药物效应。最重要的是,图论方法还可以量化药物诱导的拓扑或网络组织变化是促进还是阻碍信息处理。多项研究表明,功能性脑整合与行为表现高度相关,这表明改善认知表现指标的胆碱能和去甲肾上腺素能药物应能增强功能网络整合。本文的目的是表明图论提供了一种数学工具来开发理论驱动的促认知药物效应生物标志物,并讨论这些方法如何有助于理解胆碱能和去甲肾上腺素能调节在人脑中的作用。最后,我们将“全局工作空间”理论作为促认知药物效应的理论框架进行讨论,并认为胆碱能和去甲肾上腺素能药物的促认知效应可能与更高的网络整合有关。