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Article: Oxytocin facilitates protective responses to aversive social stimuli in males

TitleOxytocin facilitates protective responses to aversive social stimuli in males
Authors
KeywordsCognition
Emotion
Functional imaging
Psychophysiology
Issue Date2012
Citation
Proceedings of the National Academy of Sciences of the United States of America, 2012, v. 109, n. 44, p. 18144-18149 How to Cite?
AbstractThe neuropeptide oxytocin (OXT) can enhance the impact of positive social cues but may reduce that of negative ones by inhibiting amygdala activation, although it is unclearwhether the latter causes blunted emotional and mnemonic responses. In two independent double-blind placebo-controlled experiments, each involving over 70 healthy male subjects, we investigated whether OXT affects modulation of startle reactivity by aversive social stimuli as well as subsequent memory for them. Intranasal OXT potentiated acoustic startle responses to negative stimuli, without affecting behavioral valence or arousal judgments, and biased subsequent memory toward negative rather than neutral items. A functional MRI analysis of this mnemonic effect revealed that, whereas OXT inhibited amygdala responses to negative stimuli, it facilitated left insula responses for subsequently remembered items and increased functional coupling between the left amygdala, left anterior insula, and left inferior frontal gyrus. Our results therefore show that OXT can potentiate the protective and mnemonic impact of aversive social information despite reducing amygdala activity, and suggest that the insula may play a role in emotional modulation of memory.
Persistent Identifierhttp://hdl.handle.net/10722/330507
ISSN
2022 Impact Factor: 11.1
2020 SCImago Journal Rankings: 5.011
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorStriepens, Nadine-
dc.contributor.authorScheele, Dirk-
dc.contributor.authorKendrick, Keith M.-
dc.contributor.authorBecker, Benjamin-
dc.contributor.authorSchäfer, Lea-
dc.contributor.authorSchwalba, Knut-
dc.contributor.authorReul, Jürgen-
dc.contributor.authorMaier, Wolfgang-
dc.contributor.authorHurlemann, René-
dc.date.accessioned2023-09-05T12:11:18Z-
dc.date.available2023-09-05T12:11:18Z-
dc.date.issued2012-
dc.identifier.citationProceedings of the National Academy of Sciences of the United States of America, 2012, v. 109, n. 44, p. 18144-18149-
dc.identifier.issn0027-8424-
dc.identifier.urihttp://hdl.handle.net/10722/330507-
dc.description.abstractThe neuropeptide oxytocin (OXT) can enhance the impact of positive social cues but may reduce that of negative ones by inhibiting amygdala activation, although it is unclearwhether the latter causes blunted emotional and mnemonic responses. In two independent double-blind placebo-controlled experiments, each involving over 70 healthy male subjects, we investigated whether OXT affects modulation of startle reactivity by aversive social stimuli as well as subsequent memory for them. Intranasal OXT potentiated acoustic startle responses to negative stimuli, without affecting behavioral valence or arousal judgments, and biased subsequent memory toward negative rather than neutral items. A functional MRI analysis of this mnemonic effect revealed that, whereas OXT inhibited amygdala responses to negative stimuli, it facilitated left insula responses for subsequently remembered items and increased functional coupling between the left amygdala, left anterior insula, and left inferior frontal gyrus. Our results therefore show that OXT can potentiate the protective and mnemonic impact of aversive social information despite reducing amygdala activity, and suggest that the insula may play a role in emotional modulation of memory.-
dc.languageeng-
dc.relation.ispartofProceedings of the National Academy of Sciences of the United States of America-
dc.subjectCognition-
dc.subjectEmotion-
dc.subjectFunctional imaging-
dc.subjectPsychophysiology-
dc.titleOxytocin facilitates protective responses to aversive social stimuli in males-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1073/pnas.1208852109-
dc.identifier.pmid23074247-
dc.identifier.scopuseid_2-s2.0-84868089510-
dc.identifier.volume109-
dc.identifier.issue44-
dc.identifier.spage18144-
dc.identifier.epage18149-
dc.identifier.eissn1091-6490-
dc.identifier.isiWOS:000311149900091-

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