Neuroimaging Research Branch, National Institute on Drug Abuse, Intramural Research Programs, National Institutes of Health, Baltimore, MD, 21224, USA.
Neuroimaging Research Branch, National Institute on Drug Abuse, Intramural Research Programs, National Institutes of Health, Baltimore, MD, 21224, USA; Harvard Medical School, 25 Shattuck Street, Boston, MA, 02115, USA.
Neuroimage. 2019 Jan 15;185:388-397. doi: 10.1016/j.neuroimage.2018.10.055. Epub 2018 Oct 22.
Deactivation of the default mode network (DMN) is one of the most reliable observations from neuroimaging and has significant implications in development, aging, and various neuropsychiatric disorders. However, the neural mechanism underlying DMN deactivation remains elusive. As the coordination of regional neurochemical substrates and interregional neural interactions are both essential in support of brain functions, a quantitative description of how they impact DMN deactivation may provide new insights into the mechanism. Using an n-back working memory task fMRI and magnetic resonance spectroscopy, we probed the pairwise relationship between task-induced deactivation, interregional functional connectivity and regional excitation-inhibition balance (evaluated by glutamate/GABA ratio) in the posterior cingulate cortex/precuneus (PCC/PCu). Task-induced PCC/PCu deactivation correlated with its excitation-inhibition balance and interregional functional connectivity, where participants with lower glutamate/GABA ratio, stronger intra-DMN connections and stronger antagonistic DMN-SN (salience network)/ECN (executive control network) inter-network connections had greater PCC/PCu deactivation. Mediation analyses revealed that the DMN-SN functional interactions partially mediated the relationship between task-induced deactivation and the excitation-inhibition balance at the PCC/PCu. The triple-relationship discovered in the present study has the potential to bridge DMN-deactivation related findings from various neuroimaging modalities and may provide new insights into the neural mechanism of DMN deactivation. Moreover, this finding may have significant implications for neuropsychiatric disorders related to the DMN dysfunction and suggests an integrated application of pharmacological and neuromodulation-based strategies for rescuing DMN deactivation deficits.
默认模式网络(DMN)的去激活是神经影像学中最可靠的观察结果之一,对发育、衰老和各种神经精神障碍都有重要意义。然而,DMN 去激活的神经机制仍然难以捉摸。由于区域神经化学基质的协调和区域间神经相互作用对于支持大脑功能都是必不可少的,因此对它们如何影响 DMN 去激活的定量描述可能为该机制提供新的见解。我们使用 n-back 工作记忆任务 fMRI 和磁共振波谱,探测了后扣带回皮层/楔前叶(PCC/PCu)中任务诱导去激活、区域间功能连接与区域兴奋-抑制平衡(由谷氨酸/γ-氨基丁酸比评估)之间的两两关系。PCC/PCu 的任务诱导去激活与兴奋-抑制平衡和区域间功能连接相关,其中谷氨酸/γ-氨基丁酸比值较低、内 DMN 连接较强以及拮抗 DMN-SN(突显网络)/ECN(执行控制网络)间网络连接较强的参与者具有更大的 PCC/PCu 去激活。中介分析表明,DMN-SN 功能相互作用部分介导了任务诱导去激活与 PCC/PCu 兴奋-抑制平衡之间的关系。本研究发现的三重关系有可能弥合来自各种神经影像学模态的 DMN 去激活相关发现,并为 DMN 去激活的神经机制提供新的见解。此外,这一发现可能对与 DMN 功能障碍相关的神经精神障碍具有重要意义,并表明了药理学和基于神经调节的策略的综合应用,以挽救 DMN 去激活缺陷。