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      Neural and Genetic Correlates of the Social Sharing of Happiness

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          Abstract

          Happiness is regarded as one of the most fundamental human goals. Given recent reports that positive feelings are contagious (e.g., the presence of a happy person enhances others' happiness) because of the human ability to empathize (i.e., sharing emotions), empathic ability may be a key factor in increasing one's own subjective level of happiness. Based on previous studies indicating that a single nucleotide polymorphism in the serotonin 2A receptor gene [ HTR2A rs6311 guanine (G) vs. adenine (A)] is associated with sensitivity to emotional stimuli and several mental disorders such as depression, we predicted that the polymorphism might be associated with the effect of sharing happiness. To elucidate the neural and genetic correlates of the effect of sharing happiness, we first performed functional magnetic resonance imaging (fMRI) during a “happy feelings” evocation task (emotional event imagination task), during which we manipulated the valence of the imagined event (positive, neutral, or negative), as well as the presence of a friend experiencing a positive-valence event (presence or absence). We recruited young adult women for this fMRI study because empathic ability may be higher in women than in men. Participants felt happier ( p < 0.01) and the mentalizing/theory-of-mind network, which spans the medial prefrontal cortex, temporoparietal junction, temporal poles, and precuneus, was significantly more active ( p < 0.05) in the presence condition than in the absence condition regardless of event valence. Moreover, participants with the GG ( p < 0.01) and AG ( p < 0.05) genotypes of HTR2A experienced happier feelings as well as greater activation of a part of the mentalizing/theory-of-mind network ( p < 0.05) during empathy for happiness (neutral/presence condition) than those with the AA genotype. In a follow-up study with a vignette-based questionnaire conducted in a relatively large sample, male and female participants were presented with the same imagined events wherein their valence and the presence of a friend were manipulated. Results showed genetic differences in happiness-related empathy regardless of sex ( p < 0.05). Findings suggest that HTR2A polymorphisms are associated with the effect of sharing happiness by modulating the activity of the mentalizing/theory-of-mind network.

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          Experimental evidence of massive-scale emotional contagion through social networks.

          Emotional states can be transferred to others via emotional contagion, leading people to experience the same emotions without their awareness. Emotional contagion is well established in laboratory experiments, with people transferring positive and negative emotions to others. Data from a large real-world social network, collected over a 20-y period suggests that longer-lasting moods (e.g., depression, happiness) can be transferred through networks [Fowler JH, Christakis NA (2008) BMJ 337:a2338], although the results are controversial. In an experiment with people who use Facebook, we test whether emotional contagion occurs outside of in-person interaction between individuals by reducing the amount of emotional content in the News Feed. When positive expressions were reduced, people produced fewer positive posts and more negative posts; when negative expressions were reduced, the opposite pattern occurred. These results indicate that emotions expressed by others on Facebook influence our own emotions, constituting experimental evidence for massive-scale contagion via social networks. This work also suggests that, in contrast to prevailing assumptions, in-person interaction and nonverbal cues are not strictly necessary for emotional contagion, and that the observation of others' positive experiences constitutes a positive experience for people.
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            Emotional Contagion

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              Ventromedial prefrontal-subcortical systems and the generation of affective meaning.

              The ventromedial prefrontal cortex (vmPFC) comprises a set of interconnected regions that integrate information from affective sensory and social cues, long-term memory, and representations of the 'self'. Alhough the vmPFC is implicated in a variety of seemingly disparate processes, these processes are organized around a common theme. The vmPFC is not necessary for affective responses per se, but is critical when affective responses are shaped by conceptual information about specific outcomes. The vmPFC thus functions as a hub that links concepts with brainstem systems capable of coordinating organism-wide emotional behavior, a process we describe in terms of the generation of affective meaning, and which could explain the common role played by the vmPFC in a range of experimental paradigms. Copyright © 2012 Elsevier Ltd. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Front Neurosci
                Front Neurosci
                Front. Neurosci.
                Frontiers in Neuroscience
                Frontiers Media S.A.
                1662-4548
                1662-453X
                19 December 2017
                2017
                : 11
                : 718
                Affiliations
                [1] 1Department of Health and Psychosocial Medicine, Aichi Medical University School of Medicine , Nagakute, Japan
                [2] 2Division of Cerebral Integration, Department of System Neuroscience, National Institute for Physiological Sciences , Okazaki, Japan
                [3] 3Department of Psychology, Graduate School of Humanities, Kobe University , Kobe, Japan
                [4] 4Department of Psychiatry, Hamamatsu University School of Medicine , Hamamatsu, Japan
                [5] 5Department of Cognitive and Psychological Sciences, Graduate School of Informatics, Nagoya University , Nagoya, Japan
                Author notes

                Edited by: Robert W. Williams, University of Tennessee Health Science Center, United States

                Reviewed by: Khyobeni Mozhui, University of Tennessee Health Science Center, United States; Friederike Klempin, Max Delbrück Center for Molecular Medicine (HZ), Germany

                *Correspondence: Masahiro Matsunaga matsunag@ 123456aichi-med-u.ac.jp

                This article was submitted to Neurogenomics, a section of the journal Frontiers in Neuroscience

                Article
                10.3389/fnins.2017.00718
                5742108
                2ddf37a2-3145-44fb-a1cd-9948b4853ca2
                Copyright © 2017 Matsunaga, Kawamichi, Umemura, Hori, Shibata, Kobayashi, Suzuki, Ishii, Ohtsubo, Noguchi, Ochi, Yamasue and Ohira.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 03 May 2017
                : 08 December 2017
                Page count
                Figures: 7, Tables: 4, Equations: 2, References: 66, Pages: 16, Words: 12218
                Categories
                Neuroscience
                Original Research

                Neurosciences
                happiness,mentalizing/theory-of-mind network,serotonin 2a receptor gene polymorphism,functional magnetic resonance imaging,vignette-based questionnaire

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