Abstract:
:Facilitation of social attraction and bonding by the evolutionarily conserved neuropeptide oxytocin is well-established in female mammals. However, accumulating behavioral evidence suggests that oxytocin may have evolved sex-specific functional roles in the domain of human social cognition. A critical question is how oxytocin differentially modulates neural processing of social information in men and women, leading to divergent behavioral responses. Here we show that intranasal oxytocin treatment produces sex- and valence-dependent increases in amygdala activation when women view individuals identified as praising others but in men those who criticize them. Women subsequently show increased liking for the faces of these individuals, whereas in men it is reduced. Thus, oxytocin may act differentially via the amygdala to enhance the salience of positive social attributes in women but negative ones in men. We hypothesize that oxytocin may have evolved different but complementary roles to help ensure successful reproduction by encouraging mothers to promote a prosocial rearing environment for offspring and fathers to protect against antisocial influences.
journal_name
Proc Natl Acad Sci U S Aauthors
Gao S,Becker B,Luo L,Geng Y,Zhao W,Yin Y,Hu J,Gao Z,Gong Q,Hurlemann R,Yao D,Kendrick KMdoi
10.1073/pnas.1602620113subject
Has Abstractpub_date
2016-07-05 00:00:00pages
7650-4issue
27eissn
0027-8424issn
1091-6490pii
1602620113journal_volume
113pub_type
杂志文章abstract::Myasthenia gravis (MG) is a T cell-regulated, antibody-mediated autoimmune disease. Two peptides representing sequences of the human acetylcholine receptor alpha-subunit, p195-212 and p259-271, were previously shown to stimulate peripheral blood lymphocytes of patients with MG and were found to be immunodominant T cel...
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journal_title:Proceedings of the National Academy of Sciences of the United States of America
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