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Does single-dose intranasal oxytocin facilitate neural recruitment in younger and older adults during negative compared to positive dynamic multimodal expressions?
Stockholms universitet, Samhällsvetenskapliga fakulteten, Psykologiska institutionen, Biologisk psykologi.ORCID-id: 0000-0002-4420-2216
Stockholms universitet, Samhällsvetenskapliga fakulteten, Psykologiska institutionen, Biologisk psykologi. Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden; Center for Lifespan Psychology, Max Planck Institute for Human Development, Berlin, Germany; Max Planck UCL Centre for Computational Psychiatry and Ageing Research, Berlin/London.
Stockholms universitet, Samhällsvetenskapliga fakulteten, Psykologiska institutionen, Biologisk psykologi.
Stockholms universitet, Samhällsvetenskapliga fakulteten, Psykologiska institutionen.
Vise andre og tillknytning
(engelsk)Inngår i: Artikkel i tidsskrift (Fagfellevurdert) Submitted
Abstract [en]

Normal adult aging is associated with a decline in socioemotional abilities, and underlying these deficits are age-related neurobiological processes. There is increasing evidence that the neuropeptide oxytocin plays a key role in social cognition, specifically in the ability to recognize emotions. In a randomized, double-blind, placebo controlled within-subjects design, we investigated the extent to which a single dose of 40 IU of intranasal oxytocin facilitates neural recruitment in younger and older adults during negative compared to positive dynamic multimodal expressions. Based on the literature, several regions of interest were selected prior analyses: insula, amygdala, caudate head, fusiform gyrus, superior temporal gyrus, medial prefrontal cortex, medial orbitofrontal cortex, ventral medial prefrontal cortex, and dorsomedial prefrontal cortex. Behavioral data showed that younger adults outperformed older adults. and higher accuracy scores were observed during the PL condition compared to the OT condition. This was further qualified by the brain data, where OT induced brain activity reductions in the fusiform gyrus, dorsomedial prefrontal cortex, and medial orbitofrontal cortex in response to negative compared to positive expressions. Both age groups showed hypoactivity in most regions of interest during auditory stimuli compared to visual and multimodal stimuli. In line with previous research, these findings suggest that the effects of oxytocin may vary due to context, social proficiency, and individual factors (i.e. age). Future studies should target how age, presentation modality, and oxytocin interact.

Emneord [en]
oxytocin, age-related differences, dynamic stimuli, fusiform gyrus, medialorbitofrontal cortex, dorsomedial prefrontal cortex
HSV kategori
Forskningsprogram
psykologi
Identifikatorer
URN: urn:nbn:se:su:diva-184744OAI: oai:DiVA.org:su-184744DiVA, id: diva2:1464533
Forskningsfinansiär
Swedish Research Council, 2013-00854Tilgjengelig fra: 2020-09-07 Laget: 2020-09-07 Sist oppdatert: 2022-02-25
Inngår i avhandling
1. Effects of adult aging on socioemotional perception: Evidence from behavior and brain
Åpne denne publikasjonen i ny fane eller vindu >>Effects of adult aging on socioemotional perception: Evidence from behavior and brain
2020 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Social perception plays a key role in our everyday interactions. It encompasses the ability to identify, understand, and react to the social cues that others express. However, how we process this social and emotional information changes with age and generally speaking, aging brings about a decline in this process, often leading to isolation, loneliness and reduced interpersonal functioning. The overall aim of this thesis was to study the underlying mechanisms of adult age-related changes in socioemotional perception, specifically of social attribute evaluation and emotion recognition. This was done in three studies.

Study I explored age-related differences in the evaluation of seven common social attributes (attractiveness, competence, dominance, extroversion, likeability, threat, and trustworthiness) from computer-generated faces of varying intensity. Older adults rated faces as more attractive across all intensity levels, relative to their younger counterparts. Older adults also rated faces displaying low intensity of likeability as more likeable. Study II examined the effects of age on emotion recognition of positive and negative dynamic visual and auditory emotional expressions presented alone or in combination, and in nonlinguistic vocalizations. Older compared to younger adults showed diminished overall recognition accuracy and age-related differences were mainly observed in the auditory modality. Older adults also showed difficulties in recognizing anger, irritation, and relief expressions. In the case of the nonlinguistic vocalizations, age-related differences were observed for most emotions, regardless of valence. Study III investigated whether a single dose intranasal oxytocin facilitated the recognition of negative emotions from dynamic multimodal expressions and explored the neural correlates of this process with functioning magnetic resonance imaging. Behaviorally, older showed diminished recognition accuracy compared to younger adults but no oxytocin effects were found. Neurally, oxytocin caused brain activity reductions in the fusiform gyrus, dorsomedial prefrontal cortex, and medial orbitofrontal cortex.

The findings of this thesis provide a more nuanced picture of how aging may influence socioemotional perception. Collectively, the findings suggest age comparability for most emotion categories and social attributes. These result patterns may conceivably be due to the computer-generated faces, several positive emotion expressions, and dynamic multimodal stimuli that were included in the studies. The findings also give a neuropsychobiological perspective to socioemotional processing in late adulthood through oxytocin intervention.

sted, utgiver, år, opplag, sider
Stockholm: Department of Psychology, Stockholm University, 2020. s. 102
Emneord
age-related differences; social attributes; emotion recognition; oxytocin; fMRI
HSV kategori
Forskningsprogram
psykologi
Identifikatorer
urn:nbn:se:su:diva-184806 (URN)978-91-7911-294-3 (ISBN)978-91-7911-295-0 (ISBN)
Disputas
2020-10-23, David Magnussonsalen (U31), Frescati Hagväg 8, Stockholm, 10:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2020-09-30 Laget: 2020-09-07 Sist oppdatert: 2022-02-25bibliografisk kontrollert

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