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Neurophysiological contributors to advantageous risk-taking: an experimental psychopharmacological investigation

The ability to learn from experience is critical for determining when to take risks and when to play it safe. However, we know little about how within-person state changes, such as an individual’s degree of neurophysiological arousal, may impact the ability to learn which risks are most likely to fa...

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Autores principales: MacCormack, Jennifer K, Armstrong-Carter, Emma, Humphreys, Kathryn L, Muscatell, Keely A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421704/
https://www.ncbi.nlm.nih.gov/pubmed/33860790
http://dx.doi.org/10.1093/scan/nsab047
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author MacCormack, Jennifer K
Armstrong-Carter, Emma
Humphreys, Kathryn L
Muscatell, Keely A
author_facet MacCormack, Jennifer K
Armstrong-Carter, Emma
Humphreys, Kathryn L
Muscatell, Keely A
author_sort MacCormack, Jennifer K
collection PubMed
description The ability to learn from experience is critical for determining when to take risks and when to play it safe. However, we know little about how within-person state changes, such as an individual’s degree of neurophysiological arousal, may impact the ability to learn which risks are most likely to fail vs succeed. To test this, we used a randomized, double-blind, placebo-controlled design to pharmacologically manipulate neurophysiological arousal and assess its causal impact on risk-related learning and performance. Eighty-seven adults (45% female, M(age) = 20.1 ± 1.46 years) took either propranolol (n = 42), a beta-adrenergic receptor blocker that attenuates sympathetic nervous system–related signaling, or a placebo (n = 45). Participants then completed the Balloon Emotional Learning Task, a risk-taking task wherein experiential learning is necessary for task success. We found that individuals on propranolol, relative to placebo, earned fewer points on the task, suggesting that they were less effective risk-takers. This effect was mediated by the fact that those on propranolol made less optimal decisions in the final phase of the task on trials with the greatest opportunity for advantageous risk-taking. These findings highlight that neurophysiological arousal supports risk-related learning and, in turn, more advantageous decision-making and optimal behavior under conditions of risk.
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spelling pubmed-84217042021-09-09 Neurophysiological contributors to advantageous risk-taking: an experimental psychopharmacological investigation MacCormack, Jennifer K Armstrong-Carter, Emma Humphreys, Kathryn L Muscatell, Keely A Soc Cogn Affect Neurosci Original Manuscript The ability to learn from experience is critical for determining when to take risks and when to play it safe. However, we know little about how within-person state changes, such as an individual’s degree of neurophysiological arousal, may impact the ability to learn which risks are most likely to fail vs succeed. To test this, we used a randomized, double-blind, placebo-controlled design to pharmacologically manipulate neurophysiological arousal and assess its causal impact on risk-related learning and performance. Eighty-seven adults (45% female, M(age) = 20.1 ± 1.46 years) took either propranolol (n = 42), a beta-adrenergic receptor blocker that attenuates sympathetic nervous system–related signaling, or a placebo (n = 45). Participants then completed the Balloon Emotional Learning Task, a risk-taking task wherein experiential learning is necessary for task success. We found that individuals on propranolol, relative to placebo, earned fewer points on the task, suggesting that they were less effective risk-takers. This effect was mediated by the fact that those on propranolol made less optimal decisions in the final phase of the task on trials with the greatest opportunity for advantageous risk-taking. These findings highlight that neurophysiological arousal supports risk-related learning and, in turn, more advantageous decision-making and optimal behavior under conditions of risk. Oxford University Press 2021-04-16 /pmc/articles/PMC8421704/ /pubmed/33860790 http://dx.doi.org/10.1093/scan/nsab047 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Manuscript
MacCormack, Jennifer K
Armstrong-Carter, Emma
Humphreys, Kathryn L
Muscatell, Keely A
Neurophysiological contributors to advantageous risk-taking: an experimental psychopharmacological investigation
title Neurophysiological contributors to advantageous risk-taking: an experimental psychopharmacological investigation
title_full Neurophysiological contributors to advantageous risk-taking: an experimental psychopharmacological investigation
title_fullStr Neurophysiological contributors to advantageous risk-taking: an experimental psychopharmacological investigation
title_full_unstemmed Neurophysiological contributors to advantageous risk-taking: an experimental psychopharmacological investigation
title_short Neurophysiological contributors to advantageous risk-taking: an experimental psychopharmacological investigation
title_sort neurophysiological contributors to advantageous risk-taking: an experimental psychopharmacological investigation
topic Original Manuscript
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421704/
https://www.ncbi.nlm.nih.gov/pubmed/33860790
http://dx.doi.org/10.1093/scan/nsab047
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