Age-dependent effects of oxytocin in brain regions enriched with oxytocin receptors
Although intranasal oxytocin administration to tap into central functions is the most commonly used non-invasive means for exploring oxytocin's role in human cognition and behavior, the way by which intranasal oxytocin acts on the brain is not yet fully understood. Recent research suggests that...
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Published in | Psychoneuroendocrinology Vol. 160; p. 106666 |
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Abstract | Although intranasal oxytocin administration to tap into central functions is the most commonly used non-invasive means for exploring oxytocin's role in human cognition and behavior, the way by which intranasal oxytocin acts on the brain is not yet fully understood. Recent research suggests that brain regions densely populated with oxytocin receptors may play a central role in intranasal oxytocin's action mechanisms in the brain. In particular, intranasal oxytocin may act directly on (subcortical) regions rich in oxytocin receptors via binding to these receptors while only indirectly affecting other (cortical) regions via their neural connections to oxytocin receptor-enriched regions. Aligned with this notion, the current study adopted a novel approach to test 1) whether the connections between oxytocin receptor-enriched regions (i.e., the thalamus, pallidum, caudate nucleus, putamen, and olfactory bulbs) and other regions in the brain were responsive to intranasal oxytocin administration, and 2) whether oxytocin-induced effects varied as a function of age. Forty-six young (24.96 ± 3.06 years) and 44 older (69.89 ± 2.99 years) participants were randomized, in a double-blind procedure, to self-administer either intranasal oxytocin or placebo before resting-state fMRI. Results supported age-dependency in the effects of intranasal oxytocin administration on connectivity between oxytocin receptor-enriched regions and other regions in the brain. Specifically, compared to placebo, oxytocin decreased both connectivity density and connectivity strength of the thalamus for young participants while it increased connectivity density and connectivity strength of the caudate for older participants. These findings inform the mechanisms underlying the effects of exogenous oxytocin on brain function and highlight the importance of age in these processes. |
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AbstractList | Although intranasal oxytocin administration to tap into central functions is the most commonly used non-invasive means for exploring oxytocin's role in human cognition and behavior, the way by which intranasal oxytocin acts on the brain is not yet fully understood. Recent research suggests that brain regions densely populated with oxytocin receptors may play a central role in intranasal oxytocin's action mechanisms in the brain. In particular, intranasal oxytocin may act directly on (subcortical) regions rich in oxytocin receptors via binding to these receptors while only indirectly affecting other (cortical) regions via their neural connections to oxytocin receptor-enriched regions. Aligned with this notion, the current study adopted a novel approach to test 1) whether the connections between oxytocin receptor-enriched regions (i.e., the thalamus, pallidum, caudate nucleus, putamen, and olfactory bulbs) and other regions in the brain were responsive to intranasal oxytocin administration, and 2) whether oxytocin-induced effects varied as a function of age. Forty-six young (24.96 ± 3.06 years) and 44 older (69.89 ± 2.99 years) participants were randomized, in a double-blind procedure, to self-administer either intranasal oxytocin or placebo before resting-state fMRI. Results supported age-dependency in the effects of intranasal oxytocin administration on connectivity between oxytocin receptor-enriched regions and other regions in the brain. Specifically, compared to placebo, oxytocin decreased both connectivity density and connectivity strength of the thalamus for young participants while it increased connectivity density and connectivity strength of the caudate for older participants. These findings inform the mechanisms underlying the effects of exogenous oxytocin on brain function and highlight the importance of age in these processes. Although intranasal oxytocin administration to tap into central functions is the most commonly used non-invasive means for exploring oxytocin's role in human cognition and behavior, the way by which intranasal oxytocin acts on the brain is not yet fully understood. Recent research suggests that brain regions densely populated with oxytocin receptors may play a central role in intranasal oxytocin's action mechanisms in the brain. In particular, intranasal oxytocin may act directly on (subcortical) regions rich in oxytocin receptors via binding to these receptors while only indirectly affecting other (cortical) regions via their neural connections to oxytocin receptor-enriched regions. Aligned with this notion, the current study adopted a novel approach to test 1) whether the connections between oxytocin receptor-enriched regions (i.e., the thalamus, pallidum, caudate nucleus, putamen, and olfactory bulbs) and other regions in the brain were responsive to intranasal oxytocin administration, and 2) whether oxytocin-induced effects varied as a function of age. Forty-six young (24.96 ± 3.06 years) and 44 older (69.89 ± 2.99 years) participants were randomized, in a double-blind procedure, to self-administer either intranasal oxytocin or placebo before resting-state fMRI. Results supported age-dependency in the effects of intranasal oxytocin administration on connectivity between oxytocin receptor-enriched regions and other regions in the brain. Specifically, compared to placebo, oxytocin decreased both connectivity density and connectivity strength of the thalamus for young participants while it increased connectivity density and connectivity strength of the caudate for older participants. These findings inform the mechanisms underlying the effects of exogenous oxytocin on brain function and highlight the importance of age in these processes. |
ArticleNumber | 106666 |
Author | Li, Tie-Qiang Xiao, Shanshan Månsson, Kristoffer N T Ebner, Natalie C Cortes, Diana S Manzouri, Amirhossein Fischer, Håkan |
Author_xml | – sequence: 1 givenname: Shanshan surname: Xiao fullname: Xiao, Shanshan email: shanshan.xiao619@gmail.com organization: Department of Psychology, Stockholm University, Campus Albano hus 4, Albanovägen, SE-114 19 Stockholm, Sweden. Electronic address: shanshan.xiao619@gmail.com – sequence: 2 givenname: Natalie C surname: Ebner fullname: Ebner, Natalie C email: natalie.ebner@ufl.edu organization: Department of Psychology, University of Florida, P.O. Box 112250, Gainesville, FL 32611-2250, USA; Cognitive Aging and Memory Program, Clinical Translational Research Program (CAM-CTRP), University of Florida, 2004 Mowry Road, Gainesville, FL 32611, USA; McKnight Brain Institute, University of Florida, 1149 Newell Drive, Gainesville, FL 32610, USA. Electronic address: natalie.ebner@ufl.edu – sequence: 3 givenname: Amirhossein surname: Manzouri fullname: Manzouri, Amirhossein email: amirhossein.manzouri@ki.se organization: Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet, Norra stationsgatan 69, SE-113 64 Stockholm, Sweden. Electronic address: amirhossein.manzouri@ki.se – sequence: 4 givenname: Tie-Qiang surname: Li fullname: Li, Tie-Qiang email: tie-qiang.li@ki.se organization: Department of Clinical Science, Intervention, and Technology, Karolinska Institutet, Alfred Nobels Allé 8, SE-141 52 Huddinge, Sweden; Department of Medical Radiation Physics and Nuclear Medicine, Karolinska University Hospital, SE-141 86 Stockholm, Sweden. Electronic address: tie-qiang.li@ki.se – sequence: 5 givenname: Diana S surname: Cortes fullname: Cortes, Diana S email: diapi7@gmail.com organization: Department of Psychology, Stockholm University, Campus Albano hus 4, Albanovägen, SE-114 19 Stockholm, Sweden. Electronic address: diapi7@gmail.com – sequence: 6 givenname: Kristoffer N T surname: Månsson fullname: Månsson, Kristoffer N T email: kristoffer.mansson@ki.se organization: Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet, Norra stationsgatan 69, SE-113 64 Stockholm, Sweden. Electronic address: kristoffer.mansson@ki.se – sequence: 7 givenname: Håkan surname: Fischer fullname: Fischer, Håkan email: hakan.fischer@psychology.su.se organization: Department of Psychology, Stockholm University, Campus Albano hus 4, Albanovägen, SE-114 19 Stockholm, Sweden; Stockholm University Brain Imaging Center (SUBIC), SE-106 91 Stockholm, Sweden; Aging Research Center, Karolinska Institutet and Stockholm University, Tomtebodavägen 18 A, SE-171 77 Stockholm, Sweden. Electronic address: hakan.fischer@psychology.su.se |
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Keywords | Resting-state functional connectivity Oxytocin Oxytocin receptor Age Quantitative data-driven analysis framework |
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