The experience of beauty derived from sorrow

We studied the neural mechanisms that are engaged during the experience of beauty derived from sorrow and from joy, two experiences that share a common denominator (beauty) but are linked to opposite emotional valences. Twenty subjects viewed and rerated, in a functional magnetic resonance imaging s...

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Published in:Human brain mapping Vol. 38; no. 8; pp. 4185 - 4200
Main Authors: Ishizu, Tomohiro, Zeki, Semir
Format: Journal Article
Language:English
Published: United States John Wiley & Sons, Inc 01-08-2017
John Wiley and Sons Inc
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Summary:We studied the neural mechanisms that are engaged during the experience of beauty derived from sorrow and from joy, two experiences that share a common denominator (beauty) but are linked to opposite emotional valences. Twenty subjects viewed and rerated, in a functional magnetic resonance imaging scanner, 120 images which each had classified into the following four categories: beautiful and sad; beautiful and joyful; neutral; ugly. The medial orbito‐frontal cortex (mOFC) was active during the experience of both types of beauty. Otherwise, the two experiences engaged different parts of the brain: joyful beauty engaged areas linked to positive emotions while sorrowful beauty engaged areas linked to negative experiences. Separate regions of the cerebellum were engaged during experience of the two conditions. A functional connectivity analysis indicated that the activity within the mOFC was modulated by the supplementary motor area/middle cingulate cortex, known to be engaged during empathetic experiences provoked by other peoples' sadness. Hum Brain Mapp 38:4185–4200, 2017. © 2017 Wiley Periodicals, Inc.
Bibliography:Tomohiro Ishizu is currently at Department of Basic Psychological Research and Research Methods, University of Vienna
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tomohiro.ishizu@univie.ac.at
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Tomohiro Ishizu is currently at Department of Basic Psychological Research and Research Methods, University of Vienna (tomohiro.ishizu@univie.ac.at).
ISSN:1065-9471
1097-0193
DOI:10.1002/hbm.23657