Domain-general Signals in the Cingulo-opercular Network for Visuospatial Attention and Episodic Memory

We investigated the functional properties of a previously described cingulo-opercular network (CON) putatively involved in cognitive control. Analyses of common fMRI task-evoked activity during perceptual and episodic memory search tasks that differently recruited the dorsal attention (DAN) and default mode network (DMN) established the generality of this network. Regions within the CON (anterior insula/frontal operculum and anterior cingulate/presupplementary cortex) displayed sustained signals during extended periods in which participants searched for behaviorally relevant information in a dynamically changing environment or from episodic memory in the absence of sensory stimulation. The CON was activated during all phases of both tasks, which involved trial initiation, target detection, decision, and response, indicating its consistent involvement in a broad range of cognitive processes. Functional connectivity analyses showed that the CON flexibly linked with the DAN or DMN regions during perceptual or memory search, respectively. Aside from the CON, only a limited number of regions, including the lateral pFC, showed evidence of domain-general sustained activity, although in some cases the common activations may have reflected the functional-anatomical variability of domain-specific regions rather than a true domain generality. These additional regions also showed task-dependent functional connectivity with the DMN and DAN, suggesting that this feature is not a specific marker of cognitive control. Finally, multivariate clustering analyses separated the CON from other frontoparietal regions previously associated with cognitive control, indicating a unique fingerprint. We conclude that the CON's functional properties and interactions with other brain regions support a broad role in cognition, consistent with its characterization as a task control network.

[1]  C. Montag,et al.  Susceptibility to everyday cognitive failure is reflected in functional network interactions in the resting brain , 2015, NeuroImage.

[2]  Carol A. Seger,et al.  Neural networks supporting switching, hypothesis testing, and rule application , 2015, Neuropsychologia.

[3]  G. Woodman,et al.  Enhancing long-term memory with stimulation tunes visual attention in one trial , 2014, Proceedings of the National Academy of Sciences.

[4]  J. Mattingley,et al.  Applications of transcranial direct current stimulation for understanding brain function , 2014, Trends in Neurosciences.

[5]  Kathryn R. Cullen,et al.  Developmental Resting State Functional Connectivity for Clinicians , 2014, Current Behavioral Neuroscience Reports.

[6]  Kenneth Y. Kwan,et al.  Nitric oxide signaling in the development and evolution of language and cognitive circuits , 2014, Neuroscience Research.

[7]  Kenneth Y. Kwan,et al.  Dysregulated nitric oxide signaling as a candidate mechanism of fragile X syndrome and other neuropsychiatric disorders , 2014, Front. Genet..

[8]  Mark D'Esposito,et al.  The salience network causally influences default mode network activity during moral reasoning. , 2013, Brain : a journal of neurology.

[9]  A. Zalesky,et al.  Competitive and cooperative dynamics of large-scale brain functional networks supporting recollection , 2012, Proceedings of the National Academy of Sciences.

[10]  M. Corbetta,et al.  Large-scale cortical correlation structure of spontaneous oscillatory activity , 2012, Nature Neuroscience.

[11]  Timothy E. Ham,et al.  Salience network integrity predicts default mode network function after traumatic brain injury , 2012, Proceedings of the National Academy of Sciences.

[12]  Marvin M Chun,et al.  Category-selective background connectivity in ventral visual cortex. , 2012, Cerebral cortex.

[13]  Kimberly L. Ray,et al.  Meta-analytic evidence for a superordinate cognitive control network subserving diverse executive functions , 2012, Cognitive, affective & behavioral neuroscience.

[14]  Kevin S. Brown,et al.  Cooperation between the default mode network and the frontal–parietal network in the production of an internal train of thought , 2012, Brain Research.

[15]  Wei Gao,et al.  Frontal parietal control network regulates the anti‐correlated default and dorsal attention networks , 2012, Human brain mapping.

[16]  Marcia K. Johnson,et al.  Memory: Enduring Traces of Perceptual and Reflective Attention , 2011, Neuron.

[17]  Darren Price,et al.  Investigating the electrophysiological basis of resting state networks using magnetoencephalography , 2011, Proceedings of the National Academy of Sciences.

[18]  Karsten Specht,et al.  Attention and cognitive control networks assessed in a dichotic listening fMRI study , 2011, Brain and Cognition.

[19]  James Z. Chadick,et al.  Differential coupling of visual cortex with default network or frontal-parietal network based on goals , 2011, Nature Neuroscience.

[20]  Daniel L. Schacter,et al.  Solving future problems: Default network and executive activity associated with goal-directed mental simulations , 2011, NeuroImage.

[21]  M. Corbetta,et al.  Episodic Memory Retrieval, Parietal Cortex, and the Default Mode Network: Functional and Topographic Analyses , 2011, The Journal of Neuroscience.

[22]  Theodore P. Zanto,et al.  Causal role of the prefrontal cortex in top-down modulation of visual processing and working memory , 2011, Nature Neuroscience.

[23]  Ethan R. Buch,et al.  Distributed and causal influence of frontal operculum in task control , 2011, Proceedings of the National Academy of Sciences.

[24]  Daryl E. Wilson,et al.  Control of Spatial and Feature-Based Attention in Frontoparietal Cortex , 2010, The Journal of Neuroscience.

[25]  Adrian W. Gilmore,et al.  Default network activity, coupled with the frontoparietal control network, supports goal-directed cognition , 2010, NeuroImage.

[26]  M. Corbetta,et al.  Attention to Memory and the Environment: Functional Specialization and Dynamic Competition in Human Posterior Parietal Cortex , 2010, The Journal of Neuroscience.

[27]  A. Kleinschmidt,et al.  Anterior insula activations in perceptual paradigms: often observed but barely understood , 2010, Brain Structure and Function.

[28]  V. Menon,et al.  Saliency, switching, attention and control: a network model of insula function , 2010, Brain Structure and Function.

[29]  K. Miller Broadband Spectral Change: Evidence for a Macroscale Correlate of Population Firing Rate? , 2010, The Journal of Neuroscience.

[30]  M. Corbetta,et al.  Temporal dynamics of spontaneous MEG activity in brain networks , 2010, Proceedings of the National Academy of Sciences.

[31]  R. Buckner,et al.  Functional-Anatomic Fractionation of the Brain's Default Network , 2010, Neuron.

[32]  E. Maguire,et al.  What does the retrosplenial cortex do? , 2009, Nature Reviews Neuroscience.

[33]  Dirk B. Walther,et al.  Natural Scene Categories Revealed in Distributed Patterns of Activity in the Human Brain , 2009, The Journal of Neuroscience.

[34]  K. Christoff,et al.  Experience sampling during fMRI reveals default network and executive system contributions to mind wandering , 2009, Proceedings of the National Academy of Sciences.

[35]  M. Corbetta,et al.  Interaction of Stimulus-Driven Reorienting and Expectation in Ventral and Dorsal Frontoparietal and Basal Ganglia-Cortical Networks , 2009, The Journal of Neuroscience.

[36]  M. Fox,et al.  The global signal and observed anticorrelated resting state brain networks. , 2009, Journal of neurophysiology.

[37]  S. Yantis,et al.  A Domain-Independent Source of Cognitive Control for Task Sets: Shifting Spatial Attention and Switching Categorization Rules , 2009, The Journal of Neuroscience.

[38]  Kevin Murphy,et al.  The impact of global signal regression on resting state correlations: Are anti-correlated networks introduced? , 2009, NeuroImage.

[39]  M. Rushworth,et al.  Behavioral / Systems / Cognitive Connectivity-Based Parcellation of Human Cingulate Cortex and Its Relation to Functional Specialization , 2008 .

[40]  Justin L. Vincent,et al.  Evidence for a frontoparietal control system revealed by intrinsic functional connectivity. , 2008, Journal of neurophysiology.

[41]  A. Engel,et al.  Neuronal Synchronization along the Dorsal Visual Pathway Reflects the Focus of Spatial Attention , 2008, Neuron.

[42]  Biyu J. He,et al.  Electrophysiological correlates of the brain's intrinsic large-scale functional architecture , 2008, Proceedings of the National Academy of Sciences.

[43]  Russell A. Epstein Parahippocampal and retrosplenial contributions to human spatial navigation , 2008, Trends in Cognitive Sciences.

[44]  V. Menon,et al.  A critical role for the right fronto-insular cortex in switching between central-executive and default-mode networks , 2008, Proceedings of the National Academy of Sciences.

[45]  S. Petersen,et al.  A dual-networks architecture of top-down control , 2008, Trends in Cognitive Sciences.

[46]  D. Schacter,et al.  The Brain's Default Network , 2008, Annals of the New York Academy of Sciences.

[47]  Bharat B. Biswal,et al.  Competition between functional brain networks mediates behavioral variability , 2008, NeuroImage.

[48]  David Badre,et al.  Functional Magnetic Resonance Imaging Evidence for a Hierarchical Organization of the Prefrontal Cortex , 2007, Journal of Cognitive Neuroscience.

[49]  Elisabeth J. Ploran,et al.  Evidence Accumulation and the Moment of Recognition: Dissociating Perceptual Recognition Processes Using fMRI , 2007, The Journal of Neuroscience.

[50]  Walter Schneider,et al.  The cognitive control network: Integrated cortical regions with dissociable functions , 2007, NeuroImage.

[51]  Justin L. Vincent,et al.  Distinct brain networks for adaptive and stable task control in humans , 2007, Proceedings of the National Academy of Sciences.

[52]  Timothy Edward John Behrens,et al.  Triangulating a Cognitive Control Network Using Diffusion-Weighted Magnetic Resonance Imaging (MRI) and Functional MRI , 2007, The Journal of Neuroscience.

[53]  Biyu J. He,et al.  Breakdown of Functional Connectivity in Frontoparietal Networks Underlies Behavioral Deficits in Spatial Neglect , 2007, Neuron.

[54]  G. Glover,et al.  Dissociable Intrinsic Connectivity Networks for Salience Processing and Executive Control , 2007, The Journal of Neuroscience.

[55]  Benjamin J. Shannon,et al.  Coherent spontaneous activity identifies a hippocampal-parietal memory network. , 2006, Journal of neurophysiology.

[56]  Kristina M. Visscher,et al.  A Core System for the Implementation of Task Sets , 2006, Neuron.

[57]  D. C. V. Essen A Population-Average, Landmark- and Surface-based (PALS) atlas of human cerebral cortex , 2005, NeuroImage.

[58]  P. Fries A mechanism for cognitive dynamics: neuronal communication through neuronal coherence , 2005, Trends in Cognitive Sciences.

[59]  Maurizio Corbetta,et al.  The human brain is intrinsically organized into dynamic, anticorrelated functional networks. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[60]  M. Corbetta,et al.  Quantitative analysis of attention and detection signals during visual search. , 2003, Journal of neurophysiology.

[61]  S. Yantis,et al.  Transient neural activity in human parietal cortex during spatial attention shifts , 2002, Nature Neuroscience.

[62]  M. Corbetta,et al.  Control of goal-directed and stimulus-driven attention in the brain , 2002, Nature Reviews Neuroscience.

[63]  M. Corbetta,et al.  Separating Processes within a Trial in Event-Related Functional MRI I. The Method , 2001, NeuroImage.

[64]  M. Corbetta,et al.  Separating Processes within a Trial in Event-Related Functional MRI II. Analysis , 2001, NeuroImage.

[65]  G. Shulman,et al.  INAUGURAL ARTICLE by a Recently Elected Academy Member:A default mode of brain function , 2001 .

[66]  J. Duncan,et al.  Common regions of the human frontal lobe recruited by diverse cognitive demands , 2000, Trends in Neurosciences.

[67]  Leslie G. Ungerleider,et al.  Mechanisms of visual attention in the human cortex. , 2000, Annual review of neuroscience.

[68]  M. Corbetta,et al.  Areas Involved in Encoding and Applying Directional Expectations to Moving Objects , 1999, The Journal of Neuroscience.

[69]  M. Corbetta,et al.  Common Blood Flow Changes across Visual Tasks: II. Decreases in Cerebral Cortex , 1997, Journal of Cognitive Neuroscience.

[70]  D. Heeger,et al.  Linear Systems Analysis of Functional Magnetic Resonance Imaging in Human V1 , 1996, The Journal of Neuroscience.

[71]  S. Monsell,et al.  Costs of a predictible switch between simple cognitive tasks. , 1995 .

[72]  Ricardo Nitrini,et al.  Effects of Aerobic Training on Cognition and Brain Glucose Metabolism in Subjects with Mild Cognitive Impairment. , 2015, Journal of Alzheimer's disease : JAD.

[73]  Daniel L. Schacter,et al.  Intrinsic Architecture Underlying the Relations among the Default, Dorsal Attention, and Frontoparietal Control Networks of the Human Brain , 2013, Journal of Cognitive Neuroscience.

[74]  R. Passingham,et al.  Prefrontal interactions reflect future task operations , 2003, Nature Neuroscience.

[75]  E. Miller,et al.  An integrative theory of prefrontal cortex function. , 2001, Annual review of neuroscience.

[76]  D. M. Green,et al.  Signal detection theory and psychophysics , 1966 .

[77]  Behavioral Neuroscience , 2022 .