Neural markers of a greater female responsiveness to social stimuli

Abstract Background There is fMRI evidence that women are neurally predisposed to process infant laughter and crying. Other findings show that women might be more empathic and sensitive than men to emotional facial expressions. However, no gender difference in the brain responses to persons and unanimated scenes has hitherto been demonstrated. Results Twenty-four men and women viewed 220 images portraying persons or landscapes and ERPs were recorded from 128 sites. In women, but not in men, the N2 component (210–270) was much larger to persons than to scenes. swLORETA showed significant bilateral activation of FG (BA19/37) in both genders when viewing persons as opposed to scenes. Only women showed a source of activity in the STG and in the right MOG (extra-striate body area, EBA), and only men in the left parahippocampal area (PPA). Conclusion A significant gender difference was found in activation of the left and right STG (BA22) and the cingulate cortex for the subtractive condition women minus men, thus indicating that women might have a greater preference or interest for social stimuli (faces and persons).</p

How We Know It Hurts: Item Analysis of Written Narratives Reveals Distinct Neural Responses to Others' Physical Pain and Emotional Suffering

People are often called upon to witness, and to empathize with, the pain and suffering of others. In the current study, we directly compared neural responses to others' physical pain and emotional suffering by presenting participants (n = 41) with 96 verbal stories, each describing a protagonist's physical and/or emotional experience, ranging from neutral to extremely negative. A separate group of participants rated “how much physical pain”, and “how much emotional suffering” the protagonist experienced in each story, as well as how “vivid and movie-like” the story was. Although ratings of Pain, Suffering and Vividness were positively correlated with each other across stories, item-analyses revealed that each scale was correlated with activity in distinct brain regions. Even within regions of the “Shared Pain network” identified using a separate data set, responses to others' physical pain and emotional suffering were distinct. More broadly, item analyses with continuous predictors provided a high-powered method for identifying brain regions associated with specific aspects of complex stimuli – like verbal descriptions of physical and emotional events.United States. Air Force Office of Scientific Research (Office of Naval Research, grant number N000140910845

Reward prediction errors arising from switches between major and minor modes in music: An fMRI study

Evidence has accumulated that prediction error processing plays a role in the enjoyment of music listening. The present study examined listeners' neural responses to the signed reward prediction errors (RPEs) arising from switches between major and minor modes in music. We manipulated the final chord of J. S. Bach's keyboard pieces so that each major-mode passage ended with either the major (Major-Major) or minor (Major-Minor) tonic chord, and each minor-mode passage ended with either the minor (Minor-Minor) or major (Minor-Major) tonic chord. In Western music, the major and minor modes have positive and negative connotations, respectively. Therefore, the outcome of the final chord in Major-Minor stimuli was associated with negative RPE, whereas that in Minor-Major was associated with positive RPE. Twenty-three musically experienced adults underwent functional magnetic resonance imaging while listening to Major-Major, Major-Minor, Minor-Minor, and Minor-Major stimuli. We found that activity in the subgenual anterior cingulate cortex (extending into the ventromedial prefrontal cortex) during the final chord for Major-Major was significantly higher than that for Major-Minor. Conversely, a frontoparietal network for Major-Minor exhibited significantly increased activity compared to Major-Major. The contrasts between Minor-Minor and Minor-Major yielded regions implicated in interoception. We discuss our results in relation to executive functions and the emotional connotations of major versus minor mode.Comment: submitted to Psychophysiolog

スイミン ショウガイ ト パーソナリティ トノ カンレン : fMRI オ モチイタ ケンキュウ

This study is aimed to examine the neural correlates of effect of the total sleep deprivation on the risk-taking of the action observation network (AON) in humans using functional magnetic resonance imaging (fMRI). We also explored the influence of interindividual psychological differences on patterns of activation in the risk-taking of AON, which may mediate the relationship between the lack of sleep and the risk perceptional ability. We first demonstrated that viewing Risk-taking versus Safe actions recruited brain areas involved in the inferior/middle temporal gyrus, inferior/medial/middle frontal gyrus, precentral gyrus, inferior parietal lobule, anterior/posterior cingulate gyrus, precuneus, and insula, and areas thought to be associated with the AON of risk-taking. Next, within these networks, individuals under the well-slept state showed higher signal change in the right middle temporal gyrus, left middle frontal gyrus. In addition, individuals under sleep-deprived conditions showed higher signal change in the insula in the observation of risk-taking than well-slept conditions. The increase in insula activation showed a significant positive correlation with psychological anxiety scores (STAI state). Further, the another anxiety scores (STAI-trait) showed a positive correlation only with neural activity in the insula among the sleep deprivation group. Our findings suggested that the understanding of risk-taking actions that underlies AON is related to neural activation in AON and pain processing related areas, under conditions of both regular sleep and sleep deprivation. Importantly, we found that sleep deprivation was associated with increased neural responses to pain actions in insula. This pattern of activation changes suggests that sleep deprivation may induce hyperactivation for interpreting negative emotional states in AON

Effects of Oxytocin and Prosocial Behavior on Brain Responses to Direct and Vicariously Experienced Pain

In this study, we tested the validity of 2 popular assumptions about empathy: (a) empathy can be enhanced by oxytocin, a neuropeptide known to be crucial in affiliative behavior, and (b) individual differences in prosocial behavior are positively associated with empathic brain responses. To do so, we measured brain activity in a double-blind placebo-controlled study of 20 male participants either receiving painful stimulation to their own hand (self condition) or observing their female partner receiving painful stimulation to her hand (other condition). Prosocial behavior was measured using a monetary economic interaction game with which participants classified as prosocial (N = 12) or selfish (N = 6), depending on whether they cooperated with another player. Empathy-relevant brain activation (anterior insula) was neither enhanced by oxytocin nor positively associated with prosocial behavior. However, oxytocin reduced amygdala activation when participants received painful stimulation themselves (in the nonsocial condition). Surprisingly, this effect was driven by “selfish” participants. The results suggest that selfish individuals may not be as rational and unemotional as usually suggested, their actions being determined by their feeling anxious rather than by reason

Localizing Pain Matrix and Theory of Mind networks with both verbal and non-verbal stimuli

Functional localizer tasks allow researchers to identify brain regions in each individual's brain, using a combination of anatomical and functional constraints. In this study, we compare three social cognitive localizer tasks, designed to efficiently identify regions in the "Pain Matrix," recruited in response to a person's physical pain, and the "Theory of Mind network," recruited in response to a person's mental states (i.e. beliefs and emotions). Participants performed three tasks: first, the verbal false-belief stories task; second, a verbal task including stories describing physical pain versus emotional suffering; and third, passively viewing a non-verbal animated movie, which included segments depicting physical pain and beliefs and emotions. All three localizers were efficient in identifying replicable, stable networks in individual subjects. The consistency across tasks makes all three tasks viable localizers. Nevertheless, there were small reliable differences in the location of the regions and the pattern of activity within regions, hinting at more specific representations. The new localizers go beyond those currently available: first, they simultaneously identify two functional networks with no additional scan time, and second, the non-verbal task extends the populations in whom functional localizers can be applied. These localizers will be made publicly available.National Institutes of Health (U.S.) (Grant 1R01 MH096914-01A1

The Empathic Brain of Psychopaths: From Social Science to Neuroscience in Empathy

Empathy is a crucial human ability, because of its importance to prosocial behavior, and for moral development. A deficit in empathic abilities, especially affective empathy, is thought to play an important role in psychopathic personality. Empathic abilities have traditionally been studied within the social and behavioral sciences using behavioral methods, but recent work in neuroscience has begun to elucidate the neural underpinnings of empathic processing in relation to psychopathy. In this review, current knowledge in the social neuroscience of empathy is discussed and a comprehensive view of the neuronal mechanisms that underlie empathy in psychopathic personality is provided. Furthermore, it will be argued that using classification based on overt behavior, we risk failin

Evidencing a place for the hippocampus within the core scene processing network

Functional neuroimaging studies have identified several “core” brain regions that are preferentially activated by scene stimuli, namely posterior parahippocampal gyrus (PHG), retrosplenial cortex (RSC), and transverse occipital sulcus (TOS). The hippocampus (HC), too, is thought to play a key role in scene processing, although no study has yet investigated scene-sensitivity in the HC relative to these other “core” regions. Here, we characterised the frequency and consistency of individual scene-preferential responses within these regions by analysing a large dataset (n = 51) in which participants performed a one-back working memory task for scenes, objects, and scrambled objects. An unbiased approach was adopted by applying independently-defined anatomical ROIs to individual-level functional data across different voxel-wise thresholds and spatial filters. It was found that the majority of subjects had preferential scene clusters in PHG (max = 100% of participants), RSC (max = 76%), and TOS (max = 94%). A comparable number of individuals also possessed significant scene-related clusters within their individually defined HC ROIs (max = 88%), evidencing a HC contribution to scene processing. While probabilistic overlap maps of individual clusters showed that overlap “peaks” were close to those identified in group-level analyses (particularly for TOS and HC), inter-individual consistency varied across regions and statistical thresholds. The inter-regional and inter-individual variability revealed by these analyses has implications for how scene-sensitive cortex is localised and interrogated in functional neuroimaging studies, particularly in medial temporal lobe regions, such as the H