Oxytocin and vasopressin modulate risk-taking
Open accessAbstract
The modulation of risk-taking is critical for adaptive and optimal behavior. This study examined how oxytocin (OT) and arginine vasopressin (AVP) influence risk-taking in function of three parameters: sex, risk-valence, and social context. Twenty-nine healthy adults (14 males) completed a risk-taking task, the Stunt task, both in a social-stress (evaluation by unfamiliar peers) and non-social context, in three separate drug treatment sessions. During each session, one of three drugs, OT, AVP, or placebo (PLC), was administered intra-nasally. OT and AVP relative to PLC reduced betting-rate (risk-averse effect). This risk-averse effect was further qualified: AVP reduced risk-taking in the positive risk-valence (high win-probability), and regardless of social context or sex. In contrast, OT reduced risk-taking in the negative risk-valence (low win-probability), and only in the social-stress context and men. The reduction in risk-taking might serve a role in defensive behavior. These findings extend the role of these neuromodulators to behaviors beyond the social realm. How the behavioral modulation of risk-taking maps onto the function of the neural targets of OT and AVP may be the next step in this line of research.
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OT and AVP can have differential effects on neural activity (BOLD fMRI responses) and cognition, at least in some cases, although the effects of OT are more robust.
“These data have, however, found OT and AVP can have differential effects on neural activity (i.e., BOLD fMRI responses) and cognition, at least in some cases although the effects of OT are more robust [84; 86; 87; 88; 89; 90].”
From Cross-talk among oxytocin and arginine-vasopressin receptors: Relevance for basic and clinical studies of the brain and periphery (2018) · cites this paper as [87]
The few studies that have compared the effects of intranasally administered OT and AVP in humans have reported that these peptides do not have opposing roles.
“The few studies that have compared the effects of intranasally administered OT and AVP in humans have reported that these peptides do not have opposing roles.”
From Cross-talk among oxytocin and arginine-vasopressin receptors: Relevance for basic and clinical studies of the brain and periphery (2018) · cites this paper as [87]
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- Authors
- Patel, N., Grillon, C., Pavletic, N., Rosen, D., Pine, D. S., & Ernst, M.
- Affiliations
- National Institutes of Health (US)
- Venue
- Physiology & Behavior
- Publisher
- Elsevier BV
- Published
- 2015-02
- Volume
- 139
- Pages
- 254-260
- ISSN
- 0031-9384 (ISSN-L)
- PMC
- PMC4274653
- OpenAlex
- W2045037937
- Cited by
- 29
- References
- 34
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 1 · 2022: 2 · 2021: 5 · 2020: 2 · 2019: 1 · 2018: 2 · 2017: 3 · 2016: 4 · 2015: 4
- FWCI
- 5.43
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Physiology & Behavior (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (MH002798)
- Topics
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- oxytocin, vasopressin, risk-taking, risk aversion, social stress, sex differences, neuromodulators, defensive behavior
- MeSH terms
- Administration, Intranasal, Adult, Anxiety, Arginine Vasopressin, Double-Blind Method, Female, Humans, Male, Oxytocin, Probability, Psychological Tests, Psychotropic Drugs, Surveys and Questionnaires, Reaction Time, Risk-Taking, Sex Characteristics, Social Behavior, Stress, Psychological, Cross-Over Studies, Young Adult
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