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Oxytocin and vasopressin modulation of prisoner’s dilemma strategies

BACKGROUND: The neuropeptides oxytocin and vasopressin have been repeatedly implicated in social decision making by enhancing social salience and, generally, cooperation. The iterated and sequential version of the prisoner’s dilemma (PD) game is a social dilemma paradigm eliciting strategies of coop...

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Autores principales: Neto, Maria Leonor, Antunes, Marília, Lopes, Manuel, Ferreira, Duarte, Rilling, James, Prata, Diana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583454/
https://www.ncbi.nlm.nih.gov/pubmed/32207359
http://dx.doi.org/10.1177/0269881120913145
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author Neto, Maria Leonor
Antunes, Marília
Lopes, Manuel
Ferreira, Duarte
Rilling, James
Prata, Diana
author_facet Neto, Maria Leonor
Antunes, Marília
Lopes, Manuel
Ferreira, Duarte
Rilling, James
Prata, Diana
author_sort Neto, Maria Leonor
collection PubMed
description BACKGROUND: The neuropeptides oxytocin and vasopressin have been repeatedly implicated in social decision making by enhancing social salience and, generally, cooperation. The iterated and sequential version of the prisoner’s dilemma (PD) game is a social dilemma paradigm eliciting strategies of cooperation versus competition. AIMS: We aimed to characterise the role of PD players’ sex, game partner type (computer vs. human) and oxytocin or vasopressin inhalation on the player’s strategy preference. METHODS: Participants (153 men; 151 women) were randomised to intranasal 24 IU oxytocin, 20 IU vasopressin or placebo, double-blind, and played the PD. We examined main and interactive effects of sex, drug and partner type on strategy preference. RESULTS: We found a pervasive preference for a tit-for-tat strategy (i.e. general sensitivity to the partner’s choices) over unconditional cooperation, particularly when against a human rather than a computer partner. Oxytocin doubled this sensitivity in women (i.e. the preference for tit-for-tat over unconditional cooperation strategies) when playing against computers, which suggests a tendency to anthropomorphise them, and doubled women’s unconditional cooperation preference when playing against humans. Vasopressin doubled sensitivity to the partner’s previous choices (i.e. for tit-for-tat over unconditional cooperation) across sexes and partner types. CONCLUSIONS: These findings suggest that women may be more sensitive to oxytocin’s social effects of anthropomorphism of non-humans and of unconditional cooperation with humans, which may be consistent with evolutionary pressures for maternal care, and that vasopressin, irrespective of sex and partner type, may be generally sensitising humans to others’ behaviour.
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spelling pubmed-75834542020-11-02 Oxytocin and vasopressin modulation of prisoner’s dilemma strategies Neto, Maria Leonor Antunes, Marília Lopes, Manuel Ferreira, Duarte Rilling, James Prata, Diana J Psychopharmacol Original Papers BACKGROUND: The neuropeptides oxytocin and vasopressin have been repeatedly implicated in social decision making by enhancing social salience and, generally, cooperation. The iterated and sequential version of the prisoner’s dilemma (PD) game is a social dilemma paradigm eliciting strategies of cooperation versus competition. AIMS: We aimed to characterise the role of PD players’ sex, game partner type (computer vs. human) and oxytocin or vasopressin inhalation on the player’s strategy preference. METHODS: Participants (153 men; 151 women) were randomised to intranasal 24 IU oxytocin, 20 IU vasopressin or placebo, double-blind, and played the PD. We examined main and interactive effects of sex, drug and partner type on strategy preference. RESULTS: We found a pervasive preference for a tit-for-tat strategy (i.e. general sensitivity to the partner’s choices) over unconditional cooperation, particularly when against a human rather than a computer partner. Oxytocin doubled this sensitivity in women (i.e. the preference for tit-for-tat over unconditional cooperation strategies) when playing against computers, which suggests a tendency to anthropomorphise them, and doubled women’s unconditional cooperation preference when playing against humans. Vasopressin doubled sensitivity to the partner’s previous choices (i.e. for tit-for-tat over unconditional cooperation) across sexes and partner types. CONCLUSIONS: These findings suggest that women may be more sensitive to oxytocin’s social effects of anthropomorphism of non-humans and of unconditional cooperation with humans, which may be consistent with evolutionary pressures for maternal care, and that vasopressin, irrespective of sex and partner type, may be generally sensitising humans to others’ behaviour. SAGE Publications 2020-03-24 2020-08 /pmc/articles/PMC7583454/ /pubmed/32207359 http://dx.doi.org/10.1177/0269881120913145 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Papers
Neto, Maria Leonor
Antunes, Marília
Lopes, Manuel
Ferreira, Duarte
Rilling, James
Prata, Diana
Oxytocin and vasopressin modulation of prisoner’s dilemma strategies
title Oxytocin and vasopressin modulation of prisoner’s dilemma strategies
title_full Oxytocin and vasopressin modulation of prisoner’s dilemma strategies
title_fullStr Oxytocin and vasopressin modulation of prisoner’s dilemma strategies
title_full_unstemmed Oxytocin and vasopressin modulation of prisoner’s dilemma strategies
title_short Oxytocin and vasopressin modulation of prisoner’s dilemma strategies
title_sort oxytocin and vasopressin modulation of prisoner’s dilemma strategies
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583454/
https://www.ncbi.nlm.nih.gov/pubmed/32207359
http://dx.doi.org/10.1177/0269881120913145
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