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      An integrative analysis of 5HTT-mediated mechanism of hyperactivity to non-threatening voices

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          Abstract

          The tonic model delineating the serotonin transporter polymorphism’s ( 5-HTTLPR) modulatory effect on anxiety points towards a universal underlying mechanism involving a hyper-or-elevated baseline level of arousal even to non-threatening stimuli. However, to our knowledge, this mechanism has never been observed in non-clinical cohorts exhibiting high anxiety. Moreover, empirical support regarding said association is mixed, potentially because of publication bias with a relatively small sample size. Hence, how the 5-HTTLPR modulates neural correlates remains controversial. Here we show that 5-HTTLPR short-allele carriers had significantly increased baseline ERPs and reduced fearful MMN, phenomena which can nevertheless be reversed by acute anxiolytic treatment. This provides evidence that the 5-HTT affects the automatic processing of threatening and non-threatening voices, impacts broadly on social cognition, and conclusively asserts the heightened baseline arousal level as the universal underlying neural mechanism for anxiety-related susceptibilities, functioning as a spectrum-like distribution from high trait anxiety non-patients to anxiety patients.

          Abstract

          Chen et al. apply a multi-level approach to show that serotonin signaling modulates neuronal responses to both threatening and non-threatening voices even in the pre-attentive stage. They show that 5-HTTLPR short-allele carriers had higher baseline event-related potentials and lower fearful mismatch negativity, which can be reversed by acute anxiolytic treatment.

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          Most cited references58

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          The mismatch negativity (MMN) in basic research of central auditory processing: a review.

          In the present article, the basic research using the mismatch negativity (MMN) and analogous results obtained by using the magnetoencephalography (MEG) and other brain-imaging technologies is reviewed. This response is elicited by any discriminable change in auditory stimulation but recent studies extended the notion of the MMN even to higher-order cognitive processes such as those involving grammar and semantic meaning. Moreover, MMN data also show the presence of automatic intelligent processes such as stimulus anticipation at the level of auditory cortex. In addition, the MMN enables one to establish the brain processes underlying the initiation of attention switch to, conscious perception of, sound change in an unattended stimulus stream.
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            Serotonin transporter genetic variation and the response of the human amygdala.

            A functional polymorphism in the promoter region of the human serotonin transporter gene (SLC6A4) has been associated with several dimensions of neuroticism and psychopathology, especially anxiety traits, but the predictive value of this genotype against these complex behaviors has been inconsistent. Serotonin [5- hydroxytryptamine, (5-HT)] function influences normal fear as well as pathological anxiety, behaviors critically dependent on the amygdala in animal models and in clinical studies. We now report that individuals with one or two copies of the short allele of the serotonin transporter (5-HTT) promoter polymorphism, which has been associated with reduced 5-HTT expression and function and increased fear and anxiety-related behaviors, exhibit greater amygdala neuronal activity, as assessed by BOLD functional magnetic resonance imaging, in response to fearful stimuli compared with individuals homozygous for the long allele. These results demonstrate genetically driven variation in the response of brain regions underlying human emotional behavior and suggest that differential excitability of the amygdala to emotional stimuli may contribute to the increased fear and anxiety typically associated with the short SLC6A4 allele.
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              Genetic sensitivity to the environment: the case of the serotonin transporter gene and its implications for studying complex diseases and traits.

              Evidence of marked variability in response among people exposed to the same environmental risk implies that individual differences in genetic susceptibility might be at work. The study of such Gene-by-Environment (GxE) interactions has gained momentum. In this article, the authors review research about one of the most extensive areas of inquiry: variation in the promoter region of the serotonin transporter gene (SLC6A4; also known as 5-HTT) and its contribution to stress sensitivity. Research in this area has both advanced basic science and generated broader lessons for studying complex diseases and traits. The authors evaluate four lines of evidence about the 5-HTT stress-sensitivity hypothesis: 1) observational studies about the serotonin transporter linked polymorphic region (5-HTTLPR), stress sensitivity, and depression in humans; 2) experimental neuroscience studies about the 5-HTTLPR and biological phenotypes relevant to the human stress response; 3) studies of 5-HTT variation and stress sensitivity in nonhuman primates; and 4) studies of stress sensitivity and genetically engineered 5-HTT mutations in rodents. The authors then dispel some misconceptions and offer recommendations for GxE research. The authors discuss how GxE interaction hypotheses can be tested with large and small samples, how GxE research can be carried out before as well as after replicated gene discovery, the uses of GxE research as a tool for gene discovery, the importance of construct validation in evaluating GxE research, and the contribution of GxE research to the public understanding of genetic science.
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                Author and article information

                Contributors
                chenyic@tmu.edu.tw
                ywcheng2@ym.edu.tw
                Journal
                Commun Biol
                Commun Biol
                Communications Biology
                Nature Publishing Group UK (London )
                2399-3642
                10 March 2020
                10 March 2020
                2020
                : 3
                : 113
                Affiliations
                [1 ]ISNI 0000 0004 1767 1097, GRID grid.470147.1, Department of Physical Medicine & Rehabilitation, , National Yang-Ming University Hospital, ; Yilan, Taiwan
                [2 ]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
                [3 ]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
                [4 ]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
                [5 ]ISNI 0000 0000 9337 0481, GRID grid.412896.0, Cell Physiology and Molecular Image Research Center, Wan Fang Hospital, , Taipei Medical University, ; Taipei, Taiwan
                [6 ]ISNI 0000 0000 9337 0481, GRID grid.412896.0, Graduate Institute of Medical Sciences, College of Medicine, , Taipei Medical University, ; Taipei, Taiwan
                [7 ]ISNI 0000 0004 1767 1097, GRID grid.470147.1, Department of Surgery, , National Yang-Ming University Hospital, ; Yilan, Taiwan
                [8 ]Department of Education and Research, Taipei City Hospital, Taipei, Taiwan
                [9 ]ISNI 0000 0001 0425 5914, GRID grid.260770.4, Institute of Neuroscience and Brain Research Center, , National Yang-Ming University, ; Taipei, Taiwan
                Author information
                http://orcid.org/0000-0001-8050-6754
                http://orcid.org/0000-0002-5536-5897
                Article
                850
                10.1038/s42003-020-0850-3
                7064530
                32157156
                22e41c9b-51f0-4961-a993-cb908122e297
                © The Author(s) 2020

                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
                : 29 October 2019
                : 21 February 2020
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100004663, Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan);
                Award ID: 108-2410-H-010-005-MY3
                Award ID: 108-2636-H-038-001-
                Award Recipient :
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                © The Author(s) 2020

                amygdala,genetics of the nervous system
                amygdala, genetics of the nervous system

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