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Relative frontal brain asymmetry and cortisol release after social stress: The role of action orientation
•Frontal alpha asymmetries and HPA functioning were assessed before and after standardized public speaking stress test (TSST).•Stronger cortisol response was related to increased left frontal activity.•Moderation analysis showed effect only for low action-oriented participants.•Left frontal activity...
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Published in: | Biological psychology 2016-03, Vol.115, p.86-93 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •Frontal alpha asymmetries and HPA functioning were assessed before and after standardized public speaking stress test (TSST).•Stronger cortisol response was related to increased left frontal activity.•Moderation analysis showed effect only for low action-oriented participants.•Left frontal activity as a prolonged attempt to cope with such situations.
Social evaluation is a potent stressor and consistently leads to an activation of the hypothalamic–pituitary–adrenal system. Here, we investigated whether individual differences in action orientation influence the relationship between the cortisol response to social-evaluative threat and relative left frontal electroencephalographic (EEG) alpha asymmetry as a brain marker of approach motivation. Forty-nine participants were exposed to a camera-based variant of the Trier Social Stress Task while salivary cortisol and resting EEG frontal alpha asymmetry were assessed before and after stress induction. Higher relative left frontal activity was associated with higher changes in cortisol levels as measured by the area under curve with respect to increase, particularly in individuals low in action orientation. We discuss the role of the left frontal cortex in coping, the potential role of oxytocin, and negative health consequences when the left-frontal coping process becomes overstrained. |
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ISSN: | 0301-0511 1873-6246 |
DOI: | 10.1016/j.biopsycho.2016.01.012 |