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An evolutionary perspective on the behavioral consequences of exogenous oxytocin application

Oxytocin (OT) is released in response to social signals, particularly positive ones like eye contact, social touch, sexual behavior, and affiliative vocalizations. Conversely, exogenous delivery of OT has diverse behavioral effects, sometimes promoting affiliative and prosocial behaviors, but someti...

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Detalles Bibliográficos
Autores principales: Ebitz, R. Becket, Platt, Michael L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894461/
https://www.ncbi.nlm.nih.gov/pubmed/24478646
http://dx.doi.org/10.3389/fnbeh.2013.00225
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author Ebitz, R. Becket
Platt, Michael L.
author_facet Ebitz, R. Becket
Platt, Michael L.
author_sort Ebitz, R. Becket
collection PubMed
description Oxytocin (OT) is released in response to social signals, particularly positive ones like eye contact, social touch, sexual behavior, and affiliative vocalizations. Conversely, exogenous delivery of OT has diverse behavioral effects, sometimes promoting affiliative and prosocial behaviors, but sometimes suppressing them. Here, we argue that one unifying interpretation of these diverse effects is to view OT as an evolutionarily conserved physiological signal indicating affiliative interactions and predicting their behavioral consequences. In this model, OT regulates the way information about the social environment accesses the neural circuitry responsible for social behavior, thereby shaping it in sometimes counter intuitive but adaptive ways. Notably, prosociality is not always the most adaptive response to an affiliative signal from another individual. In many circumstances, an asocial or even antisocial response may confer greater fitness benefits. We argue that the behavioral effects of exogenous OT delivery not only parallel the behavioral effects of affiliative interactions, but are themselves adaptive responses to affiliative interactions. In support of this idea, we review recent evidence that OT does not unilaterally enhance social attention, as previously thought, but rather can reduce the typical prioritization of social information at the expense of other information or goals. Such diminished social vigilance may be an adaptive response to affiliative social interactions because it frees attentional resources for the pursuit of other goals. Finally, we predict that OT may mediate other behavioral consequences of social interactions, such as reduced predator vigilance, and argue that this is a rich avenue for future behavioral and neurobiological study.
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spelling pubmed-38944612014-01-29 An evolutionary perspective on the behavioral consequences of exogenous oxytocin application Ebitz, R. Becket Platt, Michael L. Front Behav Neurosci Neuroscience Oxytocin (OT) is released in response to social signals, particularly positive ones like eye contact, social touch, sexual behavior, and affiliative vocalizations. Conversely, exogenous delivery of OT has diverse behavioral effects, sometimes promoting affiliative and prosocial behaviors, but sometimes suppressing them. Here, we argue that one unifying interpretation of these diverse effects is to view OT as an evolutionarily conserved physiological signal indicating affiliative interactions and predicting their behavioral consequences. In this model, OT regulates the way information about the social environment accesses the neural circuitry responsible for social behavior, thereby shaping it in sometimes counter intuitive but adaptive ways. Notably, prosociality is not always the most adaptive response to an affiliative signal from another individual. In many circumstances, an asocial or even antisocial response may confer greater fitness benefits. We argue that the behavioral effects of exogenous OT delivery not only parallel the behavioral effects of affiliative interactions, but are themselves adaptive responses to affiliative interactions. In support of this idea, we review recent evidence that OT does not unilaterally enhance social attention, as previously thought, but rather can reduce the typical prioritization of social information at the expense of other information or goals. Such diminished social vigilance may be an adaptive response to affiliative social interactions because it frees attentional resources for the pursuit of other goals. Finally, we predict that OT may mediate other behavioral consequences of social interactions, such as reduced predator vigilance, and argue that this is a rich avenue for future behavioral and neurobiological study. Frontiers Media S.A. 2014-01-17 /pmc/articles/PMC3894461/ /pubmed/24478646 http://dx.doi.org/10.3389/fnbeh.2013.00225 Text en Copyright © 2014 Ebitz and Platt. http://creativecommons.org/licenses/by/3.0/ 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
Ebitz, R. Becket
Platt, Michael L.
An evolutionary perspective on the behavioral consequences of exogenous oxytocin application
title An evolutionary perspective on the behavioral consequences of exogenous oxytocin application
title_full An evolutionary perspective on the behavioral consequences of exogenous oxytocin application
title_fullStr An evolutionary perspective on the behavioral consequences of exogenous oxytocin application
title_full_unstemmed An evolutionary perspective on the behavioral consequences of exogenous oxytocin application
title_short An evolutionary perspective on the behavioral consequences of exogenous oxytocin application
title_sort evolutionary perspective on the behavioral consequences of exogenous oxytocin application
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894461/
https://www.ncbi.nlm.nih.gov/pubmed/24478646
http://dx.doi.org/10.3389/fnbeh.2013.00225
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