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Article: Oxytocin Facilitates Pavlovian Fear Learning in Males

TitleOxytocin Facilitates Pavlovian Fear Learning in Males
Authors
Issue Date2016
Citation
Neuropsychopharmacology, 2016, v. 41, n. 4, p. 932-939 How to Cite?
AbstractIn human evolution, social group living and Pavlovian fear conditioning have evolved as adaptive mechanisms promoting survival and reproductive success. The evolutionarily conserved hypothalamic peptide oxytocin is a key modulator of human sociality, but its effects on fear conditioning are still elusive. In the present randomized controlled study involving 97 healthy male subjects, we therefore employed functional magnetic resonance imaging and simultaneous skin conductance response (SCR) measures to characterize the modulatory influence of intranasal oxytocin (24 IU) on Pavlovian fear conditioning. We found that the peptide strengthened conditioning on both the behavioral and neural levels. Specifically, subjects exhibited faster task-related responses and enhanced SCRs to fear-associated stimuli in the late phase of conditioning, which was paralleled by heightened activity in cingulate cortex subregions in the absence of changes in amygdala function. This speaks against amygdalocentric views of oxytocin having pure anxiolytic-like effects. Instead, it suggests that the peptide enables extremely rapid and flexible adaptation to fear signals in social contexts, which may confer clear evolutionary advantages but could also elevate vulnerability for the pathological sequelae of interpersonal trauma.
Persistent Identifierhttp://hdl.handle.net/10722/330520
ISSN
2023 Impact Factor: 6.6
2023 SCImago Journal Rankings: 2.743
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorEckstein, Monika-
dc.contributor.authorScheele, Dirk-
dc.contributor.authorPatin, Alexandra-
dc.contributor.authorPreckel, Katrin-
dc.contributor.authorBecker, Benjamin-
dc.contributor.authorWalter, Annika-
dc.contributor.authorDomschke, Katharina-
dc.contributor.authorGrinevich, Valery-
dc.contributor.authorMaier, Wolfgang-
dc.contributor.authorHurlemann, René-
dc.date.accessioned2023-09-05T12:11:25Z-
dc.date.available2023-09-05T12:11:25Z-
dc.date.issued2016-
dc.identifier.citationNeuropsychopharmacology, 2016, v. 41, n. 4, p. 932-939-
dc.identifier.issn0893-133X-
dc.identifier.urihttp://hdl.handle.net/10722/330520-
dc.description.abstractIn human evolution, social group living and Pavlovian fear conditioning have evolved as adaptive mechanisms promoting survival and reproductive success. The evolutionarily conserved hypothalamic peptide oxytocin is a key modulator of human sociality, but its effects on fear conditioning are still elusive. In the present randomized controlled study involving 97 healthy male subjects, we therefore employed functional magnetic resonance imaging and simultaneous skin conductance response (SCR) measures to characterize the modulatory influence of intranasal oxytocin (24 IU) on Pavlovian fear conditioning. We found that the peptide strengthened conditioning on both the behavioral and neural levels. Specifically, subjects exhibited faster task-related responses and enhanced SCRs to fear-associated stimuli in the late phase of conditioning, which was paralleled by heightened activity in cingulate cortex subregions in the absence of changes in amygdala function. This speaks against amygdalocentric views of oxytocin having pure anxiolytic-like effects. Instead, it suggests that the peptide enables extremely rapid and flexible adaptation to fear signals in social contexts, which may confer clear evolutionary advantages but could also elevate vulnerability for the pathological sequelae of interpersonal trauma.-
dc.languageeng-
dc.relation.ispartofNeuropsychopharmacology-
dc.titleOxytocin Facilitates Pavlovian Fear Learning in Males-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/npp.2015.245-
dc.identifier.pmid26272050-
dc.identifier.scopuseid_2-s2.0-84957847524-
dc.identifier.volume41-
dc.identifier.issue4-
dc.identifier.spage932-
dc.identifier.epage939-
dc.identifier.eissn1740-634X-
dc.identifier.isiWOS:000369786900002-

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