TY - JOUR
T1 - Intranasal oxytocin modulates EEG mu/alpha and beta rhythms during perception of biological motion
AU - Perry, Anat
AU - Bentin, Shlomo
AU - Shalev, Idan
AU - Israel, Salomon
AU - Uzefovsky, Florina
AU - Bar-On, Dori
AU - Ebstein, Richard P.
N1 - Funding Information:
This research was partially funded by the “Hoffman Leadership and Responsibility” fellowship program, at the Hebrew University (AP) and a grant from Autism Speaks (RPE) .
PY - 2010/11
Y1 - 2010/11
N2 - Oxytocin (OT) plays a determining role in social and pair bonding in many vertebrates and increasing evidence suggests it is a social hormone also in humans. Indeed, intranasal administration of OT modulates several social cognitive processes in humans. Electrophysiological studies in humans associated the suppression of EEG in the mu/alpha and beta bands with perception of biological motion and social stimuli. It has been suggested that mu and beta suppression over sensory-motor regions reflects a resonance system in the human brain analogous to mirror neurons in the monkey. We therefore hypothesized that OT, a social hormone, would enhance this suppression, hence, for the first time, link the action of this neuropeptide with a human correlate of mirror neuron activity. Twenty-four students were administered 24. IU of OT or placebo intranasally in a robust, double-blind within-subject design. 45. min later participants were shown a point-light display of continuous biological motion of a human figure's walk. In the 8-10. Hz (low alpha/mu band) and in the 15-25. Hz beta band, a significant main effect of treatment showed that suppression was significantly enhanced in the OT versus the placebo conditions and that this suppression was widespread across the scalp. These results are a first step linking OT to the modulation of EEG rhythms in humans, suggesting that OT may have a role in allocating cortical resources to social tasks partly mediated by mirror neuron activity.
AB - Oxytocin (OT) plays a determining role in social and pair bonding in many vertebrates and increasing evidence suggests it is a social hormone also in humans. Indeed, intranasal administration of OT modulates several social cognitive processes in humans. Electrophysiological studies in humans associated the suppression of EEG in the mu/alpha and beta bands with perception of biological motion and social stimuli. It has been suggested that mu and beta suppression over sensory-motor regions reflects a resonance system in the human brain analogous to mirror neurons in the monkey. We therefore hypothesized that OT, a social hormone, would enhance this suppression, hence, for the first time, link the action of this neuropeptide with a human correlate of mirror neuron activity. Twenty-four students were administered 24. IU of OT or placebo intranasally in a robust, double-blind within-subject design. 45. min later participants were shown a point-light display of continuous biological motion of a human figure's walk. In the 8-10. Hz (low alpha/mu band) and in the 15-25. Hz beta band, a significant main effect of treatment showed that suppression was significantly enhanced in the OT versus the placebo conditions and that this suppression was widespread across the scalp. These results are a first step linking OT to the modulation of EEG rhythms in humans, suggesting that OT may have a role in allocating cortical resources to social tasks partly mediated by mirror neuron activity.
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U2 - 10.1016/j.psyneuen.2010.04.011
DO - 10.1016/j.psyneuen.2010.04.011
M3 - Article
C2 - 20493637
AN - SCOPUS:78650175989
SN - 0306-4530
VL - 35
SP - 1446
EP - 1453
JO - Psychoneuroendocrinology
JF - Psychoneuroendocrinology
IS - 10
ER -