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1.
J Neurosci ; 43(20): 3675-3686, 2023 05 17.
Article in English | MEDLINE | ID: mdl-37028931

ABSTRACT

Knowledge about one's personality, the self-concept, shapes human experience. Social cognitive neuroscience has made strides addressing the question of where and how the self is represented in the brain. The answer, however, remains elusive. We conducted two functional magnetic resonance imaging experiments (the second preregistered) with human male and female participants employing a self-reference task with a broad range of attributes and carrying out a searchlight representational similarity analysis (RSA). The importance of attributes to self-identity was represented in the medial prefrontal cortex (mPFC), whereas mPFC activation was unrelated both to self-descriptiveness of attributes (experiments 1 and 2) and importance of attributes to a friend's self-identity (experiment 2). Our research provides a comprehensive answer to the abovementioned question: The self-concept is conceptualized in terms of self-importance and represented in the mPFC.SIGNIFICANCE STATEMENT The self-concept comprises beliefs about who one is as an individual (e.g., personality traits, physical characteristics, desires, likes/dislikes, and social roles). Despite researchers' efforts in the last two decades to understand where and how the self-concept is stored in the brain, the question remains elusive. Using a neuroimaging technique, we found that a brain region called medial prefrontal cortex (mPFC) shows differential but systematic activation patterns depending on the importance of presented word stimuli to a participant's self-concept. Our findings suggest that one's sense of the self is supported by neural populations in the mPFC, each of which is differently sensitive to distinct levels of the personal importance of incoming information.


Subject(s)
Brain Mapping , Self Concept , Humans , Male , Female , Brain Mapping/methods , Brain/physiology , Personality , Prefrontal Cortex/diagnostic imaging , Prefrontal Cortex/physiology , Magnetic Resonance Imaging/methods
2.
Hum Brain Mapp ; 42(5): 1328-1342, 2021 04 01.
Article in English | MEDLINE | ID: mdl-33245196

ABSTRACT

Our preferences are influenced by the opinions of others. The past human neuroimaging studies on social conformity have identified a network of brain regions related to social conformity that includes the posterior medial frontal cortex (pMFC), anterior insula, and striatum. Since these brain regions are also known to play important roles in reinforcement learning (i.e., processing prediction error), it was previously hypothesized that social conformity and reinforcement learning have a common neural mechanism. However, although this view is currently widely accepted, these two processes have never been directly compared; therefore, the extent to which they shared a common neural mechanism had remained unclear. This study aimed to formally test the hypothesis. The same group of participants (n = 25) performed social conformity and reinforcement learning tasks inside a functional magnetic resonance imaging (fMRI) scanner. Univariate fMRI data analyses revealed activation overlaps in the pMFC and bilateral insula between social conflict and unsigned prediction error and in the striatum between social conflict and signed prediction error. We further conducted multivoxel pattern analysis (MVPA) for more direct evidence of a shared neural mechanism. MVPA did not reveal any evidence to support the hypothesis in any of these regions but found that activation patterns between social conflict and prediction error in these regions were largely distinct. Taken together, the present study provides no clear evidence of a common neural mechanism between social conformity and reinforcement learning.


Subject(s)
Brain Mapping , Choice Behavior/physiology , Corpus Striatum/physiology , Frontal Lobe/physiology , Gyrus Cinguli/physiology , Insular Cortex/physiology , Reinforcement, Psychology , Social Conformity , Adult , Anticipation, Psychological/physiology , Conflict, Psychological , Corpus Striatum/diagnostic imaging , Female , Frontal Lobe/diagnostic imaging , Gyrus Cinguli/diagnostic imaging , Humans , Insular Cortex/diagnostic imaging , Magnetic Resonance Imaging , Young Adult
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