Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/94673
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dc.contributorDepartment of Applied Social Sciencesen_US
dc.creatorZhuo, Sen_US
dc.creatorZhang, Wen_US
dc.creatorFan, Jen_US
dc.creatorWu, Yen_US
dc.creatorWu, Wen_US
dc.creatorPeng, Wen_US
dc.date.accessioned2022-08-26T01:55:11Z-
dc.date.available2022-08-26T01:55:11Z-
dc.identifier.issn0306-4530en_US
dc.identifier.urihttp://hdl.handle.net/10397/94673-
dc.language.isoenen_US
dc.publisherPergamonen_US
dc.rights© 2022 Elsevier Ltd. All rights reserved.en_US
dc.rights© 2022. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/.en_US
dc.rightsThe following publication Zhuo, S., Zhang, W., Fan, J., Wu, Y., Wu, W., & Peng, W. (2022). Single-dose testosterone administration modulates instant empathic responses to others’ pain: An EEG study. Psychoneuroendocrinology, 141, 105768 is available at https://dx.doi.org/10.1016/j.psyneuen.2022.105768.en_US
dc.subjectTestosteroneen_US
dc.subjectPainen_US
dc.subjectEmpathyen_US
dc.subjectAttentionen_US
dc.subjectEvent-related potentialsen_US
dc.subjectPre-stimulus α-oscillationsen_US
dc.titleSingle-dose testosterone administration modulates instant empathic responses to others’ pain : an EEG studyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume141en_US
dc.identifier.doi10.1016/j.psyneuen.2022.105768en_US
dcterms.abstractWhether or not testosterone can impair empathy remains unclear in the literature. Given that empathic responses to others’ emotional experiences depend strongly upon top–down controlled mechanisms of attention, here we investigated whether the effects of testosterone administration on pain empathy could be modulated by manipulating attention. We used a double-blind, placebo-controlled within-participant design, in which either testosterone or placebo was administrated in separate sessions. Images depicting painful or nonpainful scenes were presented to induce instant empathic responses. Experiment 1 adopted the pain-judgment and hands-counting tasks to direct attention toward painful or nonpainful aspect of the images, respectively. Experiment 2 employed the pain-rating task to estimate affective and cognitive aspects of pain empathy. When discriminating nonpainful aspects of the images in the hands-counting task, accuracies were lower and empathic late positive potential responses were greater in testosterone sessions than in placebo sessions. This suggested that testosterone enhanced empathic responses to task-irrelevant pain-related features, which interfered with task performance. When providing empathic ratings to the images in the pain-rating task, empathic event-related potentials in the early stage were only observed in the testosterone session. This suggested that testosterone facilitated automatic affective reactivity to others’ pain when elaborately processing empathic stimuli. Nevertheless, when discriminating painful aspects of the images in the pain-judgment task, we did not observe any significant differences between the two sessions. These results demonstrated that testosterone effects on enhancing brain reactivity to empathic stimuli were dependent upon task demands deploying attention allocation. The enhancement likely arose from the altered brain state (e.g., increased vigilance and arousal levels) after testosterone administration, as evidenced by the reduced amplitude of spontaneous α-oscillation recorded before the onset of the images. It expands our understanding of the neurobiological mechanisms that affect empathy, and highlights the role of testosterone.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationPsychoneuroendocrinology, July 2022, v. 141, 105768en_US
dcterms.isPartOfPsychoneuroendocrinologyen_US
dcterms.issued2022-07-
dc.identifier.isiWOS:000803769800016-
dc.identifier.scopus2-s2.0-85129395253-
dc.identifier.pmid35500352-
dc.identifier.eissn1873-3360en_US
dc.identifier.artn105768en_US
dc.description.validate202208 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera1615-
dc.identifier.SubFormID45622-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
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