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      Breathing above the brain stem: volitional control and attentional modulation in humans

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          Abstract

          Whereas the neurophysiology of respiration has traditionally focused on automatic brain stem processes, higher brain mechanisms underlying the cognitive aspects of breathing are gaining increasing interest. Therapeutic techniques have used conscious control and awareness of breathing for millennia with little understanding of the mechanisms underlying their efficacy. Using direct intracranial recordings in humans, we correlated cortical and limbic neuronal activity as measured by the intracranial electroencephalogram (iEEG) with the breathing cycle. We show this to be the direct result of neuronal activity, as demonstrated by both the specificity of the finding to the cortical gray matter and the tracking of breath by the gamma-band (40–150 Hz) envelope in these structures. We extend prior observations by showing the iEEG signal to track the breathing cycle across a widespread network of cortical and limbic structures. We further demonstrate a sensitivity of this tracking to cognitive factors by using tasks adapted from cognitive behavioral therapy and meditative practice. Specifically, volitional control and awareness of breathing engage distinct but overlapping brain circuits. During volitionally paced breathing, iEEG-breath coherence increases in a frontotemporal-insular network, and during attention to breathing, we demonstrate increased coherence in the anterior cingulate, premotor, insular, and hippocampal cortices. Our findings suggest that breathing can act as an organizing hierarchical principle for neuronal oscillations throughout the brain and detail mechanisms of how cognitive factors impact otherwise automatic neuronal processes during interoceptive attention.

          NEW & NOTEWORTHY Whereas the link between breathing and brain activity has a long history of application to therapy, its neurophysiology remains unexplored. Using intracranial recordings in humans, we show neuronal activity to track the breathing cycle throughout widespread cortical/limbic sites. Volitional pacing of the breath engages frontotemporal-insular cortices, whereas attention to automatic breathing modulates the cingulate cortex. Our findings imply a fundamental role of breathing-related oscillations in driving neuronal activity and provide insight into the neuronal mechanisms of interoceptive attention.

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          Most cited references60

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          Interoception: the sense of the physiological condition of the body.

          Converging evidence indicates that primates have a distinct cortical image of homeostatic afferent activity that reflects all aspects of the physiological condition of all tissues of the body. This interoceptive system, associated with autonomic motor control, is distinct from the exteroceptive system (cutaneous mechanoreception and proprioception) that guides somatic motor activity. The primary interoceptive representation in the dorsal posterior insula engenders distinct highly resolved feelings from the body that include pain, temperature, itch, sensual touch, muscular and visceral sensations, vasomotor activity, hunger, thirst, and 'air hunger'. In humans, a meta-representation of the primary interoceptive activity is engendered in the right anterior insula, which seems to provide the basis for the subjective image of the material self as a feeling (sentient) entity, that is, emotional awareness.
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            Automatically Parcellating the Human Cerebral Cortex

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              Dynamic cross-frequency couplings of local field potential oscillations in rat striatum and hippocampus during performance of a T-maze task.

              Oscillatory rhythms in different frequency ranges mark different behavioral states and are thought to provide distinct temporal windows that coherently bind cooperating neuronal assemblies. However, the rhythms in different bands can also interact with each other, suggesting the possibility of higher-order representations of brain states by such rhythmic activity. To explore this possibility, we analyzed local field potential oscillations recorded simultaneously from the striatum and the hippocampus. As rats performed a task requiring active navigation and decision making, the amplitudes of multiple high-frequency oscillations were dynamically modulated in task-dependent patterns by the phase of cooccurring theta-band oscillations both within and across these structures, particularly during decision-making behavioral epochs. Moreover, the modulation patterns uncovered distinctions among both high- and low-frequency subbands. Cross-frequency coupling of multiple neuronal rhythms could be a general mechanism used by the brain to perform network-level dynamical computations underlying voluntary behavior.
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                Author and article information

                Journal
                J Neurophysiol
                J. Neurophysiol
                jn
                J Neurophysiol
                JN
                Journal of Neurophysiology
                American Physiological Society (Bethesda, MD )
                0022-3077
                1522-1598
                1 January 2018
                27 September 2017
                1 January 2019
                : 119
                : 1
                : 145-159
                Affiliations
                [1] 1The Feinstein Institute for Medical Research, Manhasset, New York
                [2] 2Department of Neurosurgery, Hofstra Northwell School of Medicine, Manhasset, New York
                [3] 3Interdepartmental Neuroscience Program and Kellogg School of Management, Northwestern University , Evanston, Illinois
                Author notes
                Address for reprint requests and other correspondence: A. D. Mehta, Northwell Health Physician Partners Neuroscience Institute, 611 Northern Boulevard, Great Neck, NY 11021 (e-mail: amehta@ 123456northwell.edu ).
                Article
                PMC5866472 PMC5866472 5866472 JN-00551-2017 JN-00551-2017
                10.1152/jn.00551.2017
                5866472
                28954895
                cf705b23-28c1-4c27-8dbe-ab4ae1c52fe0
                Copyright © 2018 the American Physiological Society
                History
                : 21 July 2017
                : 25 September 2017
                : 26 September 2017
                Funding
                Funded by: HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 10.13039/100000065
                Award ID: NIH/NINDS U01 NS098976-01
                Funded by: HHS | NIH | National Institute of Mental Health (NIMH) 10.13039/100000025
                Award ID: NIH/NIMH R01 MH111439
                Award ID: NIMH 1R21MH114166-01
                Funded by: Human Frontier Science Program (HFSP) 10.13039/501100000854
                Award ID: LT000151/2012-L/6
                Categories
                Research Article
                Higher Neural Functions and Behavior

                interoceptive attention to breathing,cortical control of breathing,intracranial EEG,oscillations,mind-body

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