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      Habitual physical activity mediates the acute exercise-induced modulation of anxiety-related amygdala functional connectivity

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          Abstract

          Aerobic exercise, in relation to physical activity, has been shown to have beneficial effects on anxiety. However, the underlyig neural mechanism remains elusive. Using a within-subject crossover design, this fMRI study examined how exercise (12-min treadmill running versus walking) mediated amygdala reactivity to explicit and implicit (backward masked) perception of emotional faces in young adults ( N = 40). Results showed that acute exercise-induced differences of state anxiety (STAI-S) varied as a function of individual’s habitual physical activity (IPAQ). Subjects with high IPAQ levels showed significant STAI-S reduction ( P < 0.05). Path analyses indicated that IPAQ explained 14.67% of the variance in acute exercise-induced STAI-S differences. Running elicited stronger amygdala reactivity to implicit happiness than fear, whereas walking did the opposite. The exercise-induced amygdala reactivity to explicit fear was associated with the IPAQ scores and STAI-S differences. Moreover, after running, the amygdala exhibited a positive functional connectivity with the orbitofrontal cortex and insula to implicit happiness, but a negative connectivity with the parahippocampus and subgenual cingulate to implicit fear. The findings suggest that habitual physical activity could mediate acute exercise-induced anxiolytic effects in regards to amygdala reactivity, and help establish exercise training as a form of anxiolytic therapy towards clinical applications.

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          Neural bases of the non-conscious perception of emotional signals.

          Many emotional stimuli are processed without being consciously perceived. Recent evidence indicates that subcortical structures have a substantial role in this processing. These structures are part of a phylogenetically ancient pathway that has specific functional properties and that interacts with cortical processes. There is now increasing evidence that non-consciously perceived emotional stimuli induce distinct neurophysiological changes and influence behaviour towards the consciously perceived world. Understanding the neural bases of the non-conscious perception of emotional signals will clarify the phylogenetic continuity of emotion systems across species and the integration of cortical and subcortical activity in the human brain.
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            Targeting abnormal neural circuits in mood and anxiety disorders: from the laboratory to the clinic.

            Recent decades have witnessed tremendous advances in the neuroscience of emotion, learning and memory, and in animal models for understanding depression and anxiety. This review focuses on new rationally designed psychiatric treatments derived from preclinical human and animal studies. Nonpharmacological treatments that affect disrupted emotion circuits include vagal nerve stimulation, rapid transcranial magnetic stimulation and deep brain stimulation, all borrowed from neurological interventions that attempt to target known pathological foci. Other approaches include drugs that are given in relation to specific learning events to enhance or disrupt endogenous emotional learning processes. Imaging data suggest that common regions of brain activation are targeted with pharmacological and somatic treatments as well as with the emotional learning in psychotherapy. Although many of these approaches are experimental, the rapidly developing understanding of emotional circuit regulation is likely to provide exciting and powerful future treatments for debilitating mood and anxiety disorders.
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              Masked presentations of emotional facial expressions modulate amygdala activity without explicit knowledge.

              Functional magnetic resonance imaging (fMRI) of the human brain was used to study whether the amygdala is activated in response to emotional stimuli, even in the absence of explicit knowledge that such stimuli were presented. Pictures of human faces bearing fearful or happy expressions were presented to 10 normal, healthy subjects by using a backward masking procedure that resulted in 8 of 10 subjects reporting that they had not seen these facial expressions. The backward masking procedure consisted of 33 msec presentations of fearful or happy facial expressions, their offset coincident with the onset of 167 msec presentations of neutral facial expressions. Although subjects reported seeing only neutral faces, blood oxygen level-dependent (BOLD) fMRI signal in the amygdala was significantly higher during viewing of masked fearful faces than during the viewing of masked happy faces. This difference was composed of significant signal increases in the amygdala to masked fearful faces as well as significant signal decreases to masked happy faces, consistent with the notion that the level of amygdala activation is affected differentially by the emotional valence of external stimuli. In addition, these facial expressions activated the sublenticular substantia innominata (SI), where signal increases were observed to both fearful and happy faces--suggesting a spatial dissociation of territories that respond to emotional valence versus salience or arousal value. This study, using fMRI in conjunction with masked stimulus presentations, represents an initial step toward determining the role of the amygdala in nonconscious processing.
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                Author and article information

                Contributors
                ywcheng2@ym.edu.tw
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                24 December 2019
                24 December 2019
                2019
                : 9
                : 19787
                Affiliations
                [1 ]ISNI 0000 0004 1767 1097, GRID grid.470147.1, Department of Physical Medicine and Rehabilitation, , National Yang-Ming University Hospital, ; Yilan, Taiwan
                [2 ]ISNI 0000 0001 0425 5914, GRID grid.260770.4, Institute of Neuroscience and Brain Research Center, , National Yang-Ming University, ; Taipei, Taiwan
                [3 ]ISNI 0000 0000 9337 0481, GRID grid.412896.0, Graduate Institute of Injury Prevention and Control, College of Public Health, , Taipei Medical University, ; Taipei, Taiwan
                [4 ]ISNI 0000 0000 9337 0481, GRID grid.412896.0, Research Center of Brain and Consciousness, Shuang-Ho Hospital, , Taipei Medical University, ; New Taipei City, Taiwan
                [5 ]ISNI 0000 0000 9337 0481, GRID grid.412896.0, Graduate Institute of Mind, Brain and Consciousness, College of Humanities and Social Sciences, , Taipei Medical University, ; Taipei, Taiwan
                [6 ]ISNI 0000 0001 0671 255X, GRID grid.266860.c, Department of Kinesiology, , University of North Carolina at Greensboro, ; Greensboro, NC USA
                [7 ]Department of Research and Education, Taipei City Hospital, Taipei, Taiwan
                [8 ]ISNI 0000 0000 9337 0481, GRID grid.412896.0, Cell Physiology and Molecular Image Research Center, Wan Fang Hospital, , Taipei Medical University, ; Taipei, Taiwan
                Author information
                http://orcid.org/0000-0001-8050-6754
                http://orcid.org/0000-0002-5536-5897
                Article
                56226
                10.1038/s41598-019-56226-z
                6930267
                31875047
                75435cc0-0bdb-41a9-b8b1-fd05c5ad71b4
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 4 June 2019
                : 5 December 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100004700, Taipei Medical University (TMU);
                Award ID: TMU106-AE1-B32
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100004663, Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan);
                Award ID: 106-2410-H-010-002-MY2
                Award Recipient :
                Funded by: Brain research center, National Yang-Ming University from The Featured Areas Research program within the framework of the Higher Education Sprout Project by the Ministry of Education in Taiwan
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                neuroscience,amygdala
                Uncategorized
                neuroscience, amygdala

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