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Exposure to Hedione Increases Reciprocity in Humans

Cooperation among unrelated humans is frequently regarded as a defining feature in the evolutionary success of our species. Whereas, much research has addressed the strategic and cognitive mechanisms that underlie cooperation, investigations into chemosensory processes have received very limited res...

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Autores principales: Berger, Sebastian, Hatt, Hanns, Ockenfels, Axel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411439/
https://www.ncbi.nlm.nih.gov/pubmed/28512400
http://dx.doi.org/10.3389/fnbeh.2017.00079
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author Berger, Sebastian
Hatt, Hanns
Ockenfels, Axel
author_facet Berger, Sebastian
Hatt, Hanns
Ockenfels, Axel
author_sort Berger, Sebastian
collection PubMed
description Cooperation among unrelated humans is frequently regarded as a defining feature in the evolutionary success of our species. Whereas, much research has addressed the strategic and cognitive mechanisms that underlie cooperation, investigations into chemosensory processes have received very limited research attention. To bridge that gap, we build on recent research that has identified the chemically synthesized odorant Hedione (HED) as a ligand for the putative human pheromone receptor (VN1R1) expressed in the olfactory mucosa, and hypothesize that exposure to HED may increase reciprocity. Applying behavioral economics paradigms, the present research shows that exposure to the ligand causes differentiated behavioral effects in reciprocal punishments (Study 1) as well as rewards (Study 2), two types of behaviors that are frequently regarded as essential for the development and maintenance of cooperation.
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spelling pubmed-54114392017-05-16 Exposure to Hedione Increases Reciprocity in Humans Berger, Sebastian Hatt, Hanns Ockenfels, Axel Front Behav Neurosci Neuroscience Cooperation among unrelated humans is frequently regarded as a defining feature in the evolutionary success of our species. Whereas, much research has addressed the strategic and cognitive mechanisms that underlie cooperation, investigations into chemosensory processes have received very limited research attention. To bridge that gap, we build on recent research that has identified the chemically synthesized odorant Hedione (HED) as a ligand for the putative human pheromone receptor (VN1R1) expressed in the olfactory mucosa, and hypothesize that exposure to HED may increase reciprocity. Applying behavioral economics paradigms, the present research shows that exposure to the ligand causes differentiated behavioral effects in reciprocal punishments (Study 1) as well as rewards (Study 2), two types of behaviors that are frequently regarded as essential for the development and maintenance of cooperation. Frontiers Media S.A. 2017-05-02 /pmc/articles/PMC5411439/ /pubmed/28512400 http://dx.doi.org/10.3389/fnbeh.2017.00079 Text en Copyright © 2017 Berger, Hatt and Ockenfels. http://creativecommons.org/licenses/by/4.0/ 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.
spellingShingle Neuroscience
Berger, Sebastian
Hatt, Hanns
Ockenfels, Axel
Exposure to Hedione Increases Reciprocity in Humans
title Exposure to Hedione Increases Reciprocity in Humans
title_full Exposure to Hedione Increases Reciprocity in Humans
title_fullStr Exposure to Hedione Increases Reciprocity in Humans
title_full_unstemmed Exposure to Hedione Increases Reciprocity in Humans
title_short Exposure to Hedione Increases Reciprocity in Humans
title_sort exposure to hedione increases reciprocity in humans
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411439/
https://www.ncbi.nlm.nih.gov/pubmed/28512400
http://dx.doi.org/10.3389/fnbeh.2017.00079
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