de Gelder B.
Nature Review Neuroscience, 7, 242-249
People's faces show fear in many different circumstances. However, when people are terrified, as well as showing emotion, they run for cover. When we see a bodily expression of emotion, we immediately know what specific action is associated with a particular emotion, leaving little need for interpretation of the signal, as is the case for facial expressions. Research on emotional body language is rapidly emerging as a new field in cognitive and affective neuroscience. This article reviews how whole-body signals are automatically perceived and understood, and their role in emotional communication and decision-making.
Friday, February 24, 2006
ARTICLE UPDATE - Attentional modulation of the amygdala varies with personality
Steven B. Most, Marvin M. Chun, Matthew R. Johnson and Kent A. Kiehl
NeuroImage, in press
The amygdala is implicated in emotional processing, and its rich subcortical connections have led to suggestions that processing of emotional stimuli occurs independently of attention. Using a novel attentional manipulation in conjunction with fMRI, we showed that emotion-related amygdala activity was modulated by attention, but that the degree of such modulation correlated with the personality variable harm avoidance, associated with trait anxiety. Participants ignored emotional distractors while searching through a rapid stream of pictures for a target, about which they were provided either specific or nonspecific descriptive information (e.g., “look for a building” versus “look for a landscape or building”). Thus, they employed either a specific or a nonspecific attentional set in order to find the target and ignore distractors. In response to irrelevant emotional distractors, low harm-avoidant participants had relatively little emotion-related amygdala activity regardless of whether they maintained a specific or nonspecific attentional set. High harm-avoidant participants, however, showed strong emotion-related amygdala activity when maintaining a nonspecific attentional set and lower amygdala activity when maintaining a specific attentional set. This decrease was accompanied by increased activation of the rostral anterior cingulate cortex (ACC), which is often linked with the resolution of affective interference. In addition to demonstrating individual differences in attentional modulation of the amygdala, these results may indicate that the rostral ACC is sensitive to the increased effort that high harm-avoidant individuals must recruit in order to modulate amygdala responsivity.
NeuroImage, in press
The amygdala is implicated in emotional processing, and its rich subcortical connections have led to suggestions that processing of emotional stimuli occurs independently of attention. Using a novel attentional manipulation in conjunction with fMRI, we showed that emotion-related amygdala activity was modulated by attention, but that the degree of such modulation correlated with the personality variable harm avoidance, associated with trait anxiety. Participants ignored emotional distractors while searching through a rapid stream of pictures for a target, about which they were provided either specific or nonspecific descriptive information (e.g., “look for a building” versus “look for a landscape or building”). Thus, they employed either a specific or a nonspecific attentional set in order to find the target and ignore distractors. In response to irrelevant emotional distractors, low harm-avoidant participants had relatively little emotion-related amygdala activity regardless of whether they maintained a specific or nonspecific attentional set. High harm-avoidant participants, however, showed strong emotion-related amygdala activity when maintaining a nonspecific attentional set and lower amygdala activity when maintaining a specific attentional set. This decrease was accompanied by increased activation of the rostral anterior cingulate cortex (ACC), which is often linked with the resolution of affective interference. In addition to demonstrating individual differences in attentional modulation of the amygdala, these results may indicate that the rostral ACC is sensitive to the increased effort that high harm-avoidant individuals must recruit in order to modulate amygdala responsivity.
Monday, February 20, 2006
ARTICLE UPDATE - Facial expressions and complex IAPS pictures: Common and differential networks
Jennifer C. Britton, Stephan F. Taylor, Keith D. Sudheimer and Israel Liberzon
NeuroImage, in press
Neuroimaging studies investigating emotion have commonly used two different visual stimulus formats, facial expressions of emotion or emotionally evocative scenes. However, it remains an important unanswered question whether or not these different stimulus formats entail the same processes. Facial expressions of emotion may elicit more emotion recognition/perception, and evocative pictures may elicit more direct experience of emotion. In spite of these differences, common areas of activation have been reported across different studies, but little work has investigated activations in response to the two stimulus formats in the same subjects. In this fMRI study, we compared BOLD activation patterns to facial expression of emotions and to complex emotional pictures from the International Affective Picture System (IAPS) to determine if these stimuli would activate similar or distinct brain regions. Healthy volunteers passively viewed blocks of expressive faces and IAPS pictures balanced for specific emotion (happy, sad, anger, fear, neutral), interleaved with blocks of fixation. Eye movement, reaction times, and off-line subjective ratings including discrete emotion, valence, and arousal were also recorded. Both faces and IAPS pictures activated similar structures, including the amygdala, posterior hippocampus, ventromedial prefrontal cortex, and visual cortex. In addition, expressive faces uniquely activated the superior temporal gyrus, insula, and anterior cingulate more than IAPS pictures, despite the faces being less arousing. For the most part, these regions were activated in response to all specific emotions; however, some regions responded only to a subset.
NeuroImage, in press
Neuroimaging studies investigating emotion have commonly used two different visual stimulus formats, facial expressions of emotion or emotionally evocative scenes. However, it remains an important unanswered question whether or not these different stimulus formats entail the same processes. Facial expressions of emotion may elicit more emotion recognition/perception, and evocative pictures may elicit more direct experience of emotion. In spite of these differences, common areas of activation have been reported across different studies, but little work has investigated activations in response to the two stimulus formats in the same subjects. In this fMRI study, we compared BOLD activation patterns to facial expression of emotions and to complex emotional pictures from the International Affective Picture System (IAPS) to determine if these stimuli would activate similar or distinct brain regions. Healthy volunteers passively viewed blocks of expressive faces and IAPS pictures balanced for specific emotion (happy, sad, anger, fear, neutral), interleaved with blocks of fixation. Eye movement, reaction times, and off-line subjective ratings including discrete emotion, valence, and arousal were also recorded. Both faces and IAPS pictures activated similar structures, including the amygdala, posterior hippocampus, ventromedial prefrontal cortex, and visual cortex. In addition, expressive faces uniquely activated the superior temporal gyrus, insula, and anterior cingulate more than IAPS pictures, despite the faces being less arousing. For the most part, these regions were activated in response to all specific emotions; however, some regions responded only to a subset.
ARTICLE UPDATE - Neural systems for orienting attention to the location of threat signals: An event-related fMRI study
Gilles Pourtois, Sophie Schwartz, Mohamed L. Seghier, François Lazeyras and Patrik Vuilleumier
NeuroImage, in press
Attention may reflexively shift towards the location of perceived threats, but it is still unclear how these spatial biases recruit the distributed fronto-parietal cortical networks involved in other aspects of selective attention. We used event-related fMRI to determine how brain responses to a neutral visual target are influenced by the emotional expression of faces appearing at the same location during a covert orienting task. On each trial, two faces were briefly presented, one in each upper visual field (one neutral and one emotional, fearful or happy), followed by a unilateral target (a small horizontal or vertical bar) replacing one of the faces. Participants had to discriminate the target orientation, shown on the same (valid) or opposite (invalid) side as the emotional face. Trials with faces but no subsequent target (cue-only trials) were included to disentangle activation due to emotional cues from their effects on target detection. We found increased responses in bilateral temporo-parietal areas and right occipito-parietal cortex for fearful faces relative to happy faces, unrelated to the subsequent target and cueing validity. More critically, we found a selective modulation of intraparietal and orbitofrontal cortex for targets following an invalid fearful face, as well as an increased visual response in right lateral occipital cortex for targets following a valid fearful face. No such effects were observed with happy faces. These results demonstrate that fearful faces can act as exogenous cues by increasing sensory processing in extrastriate cortex for a subsequent target presented at the same location, but also produce a cost in disengaging towards another location by altering the response of IPS to invalidly cued targets. Neural mechanisms responsible for orienting attention towards emotional vs. non-emotional stimuli are thus partly shared in parietal and visual areas, but also partly distinct.
NeuroImage, in press
Attention may reflexively shift towards the location of perceived threats, but it is still unclear how these spatial biases recruit the distributed fronto-parietal cortical networks involved in other aspects of selective attention. We used event-related fMRI to determine how brain responses to a neutral visual target are influenced by the emotional expression of faces appearing at the same location during a covert orienting task. On each trial, two faces were briefly presented, one in each upper visual field (one neutral and one emotional, fearful or happy), followed by a unilateral target (a small horizontal or vertical bar) replacing one of the faces. Participants had to discriminate the target orientation, shown on the same (valid) or opposite (invalid) side as the emotional face. Trials with faces but no subsequent target (cue-only trials) were included to disentangle activation due to emotional cues from their effects on target detection. We found increased responses in bilateral temporo-parietal areas and right occipito-parietal cortex for fearful faces relative to happy faces, unrelated to the subsequent target and cueing validity. More critically, we found a selective modulation of intraparietal and orbitofrontal cortex for targets following an invalid fearful face, as well as an increased visual response in right lateral occipital cortex for targets following a valid fearful face. No such effects were observed with happy faces. These results demonstrate that fearful faces can act as exogenous cues by increasing sensory processing in extrastriate cortex for a subsequent target presented at the same location, but also produce a cost in disengaging towards another location by altering the response of IPS to invalidly cued targets. Neural mechanisms responsible for orienting attention towards emotional vs. non-emotional stimuli are thus partly shared in parietal and visual areas, but also partly distinct.
Friday, February 17, 2006
ARTICLE UPDATE - Task and content modulate amygdala-hippocampal connectivity in emotional retrieval.
Smith AP, Stephan KE, Rugg MD, Dolan RJ.
Neuron, 16, 631-638.
The ability to remember emotional events is crucial for adapting to biologically and socially significant situations. Little is known, however, about the nature of the neural interactions supporting the integration of mnemonic and emotional information. Using fMRI and dynamic models of effective connectivity, we examined regional neural activity and specific interactions between brain regions during a contextual memory retrieval task. We independently manipulated emotional context and relevance of retrieved emotional information to task demands. We show that retrieval of emotionally valenced contextual information is associated with enhanced connectivity from hippocampus to amygdala, structures crucially involved with encoding of emotional events. When retrieval of emotional information is relevant to current behavior, amygdala-hippocampal connectivity increases bidirectionally, under modulatory influences from orbitofrontal cortex, a region implicated in representation of affective value and behavioral guidance. Our findings demonstrate that both memory content and behavioral context impact upon large scale neuronal dynamics underlying emotional retrieval.
Neuron, 16, 631-638.
The ability to remember emotional events is crucial for adapting to biologically and socially significant situations. Little is known, however, about the nature of the neural interactions supporting the integration of mnemonic and emotional information. Using fMRI and dynamic models of effective connectivity, we examined regional neural activity and specific interactions between brain regions during a contextual memory retrieval task. We independently manipulated emotional context and relevance of retrieved emotional information to task demands. We show that retrieval of emotionally valenced contextual information is associated with enhanced connectivity from hippocampus to amygdala, structures crucially involved with encoding of emotional events. When retrieval of emotional information is relevant to current behavior, amygdala-hippocampal connectivity increases bidirectionally, under modulatory influences from orbitofrontal cortex, a region implicated in representation of affective value and behavioral guidance. Our findings demonstrate that both memory content and behavioral context impact upon large scale neuronal dynamics underlying emotional retrieval.
ARTICLE UPDATE - Does emotion help or hinder immediate memory? Arousal versus priority-binding mechanisms.
Hadley CB, Mackay DG.
Journal of Experimental Psychology: Learning, Memory and Cognition, 32, 79-88.
People recall taboo words better than neutral words in many experimental contexts. The present rapid serial visual presentation (RSVP) experiments demonstrated this taboo-superiority effect for immediate recall of mixed lists containing taboo and neutral words matched for familiarity, length, and category coherence. Under binding theory (MacKay et al., 2004), taboo superiority reflects an interference effect: Because the emotional reaction system prioritizes binding mechanisms for linking the source of an emotion to its context, taboo words capture the mechanisms for encoding list context in mixed lists, impairing the encoding of adjacent neutral words when RSVP rates are sufficiently rapid. However, for pure or unmixed lists, binding theory predicted no better recall of taboo-only than of neutral-only lists at fast or slow rates. Present results supported this prediction, suggesting that taboo superiority in immediate recall reflects context-specific binding processes, rather than context-free arousal effects, or emotion-linked differences in rehearsal, processing time, output interference, time-based decay, or guessing biases.
Journal of Experimental Psychology: Learning, Memory and Cognition, 32, 79-88.
People recall taboo words better than neutral words in many experimental contexts. The present rapid serial visual presentation (RSVP) experiments demonstrated this taboo-superiority effect for immediate recall of mixed lists containing taboo and neutral words matched for familiarity, length, and category coherence. Under binding theory (MacKay et al., 2004), taboo superiority reflects an interference effect: Because the emotional reaction system prioritizes binding mechanisms for linking the source of an emotion to its context, taboo words capture the mechanisms for encoding list context in mixed lists, impairing the encoding of adjacent neutral words when RSVP rates are sufficiently rapid. However, for pure or unmixed lists, binding theory predicted no better recall of taboo-only than of neutral-only lists at fast or slow rates. Present results supported this prediction, suggesting that taboo superiority in immediate recall reflects context-specific binding processes, rather than context-free arousal effects, or emotion-linked differences in rehearsal, processing time, output interference, time-based decay, or guessing biases.
ARTICLE UPDATE - Affective context-induced modulation of the error-related negativity.
Larson MJ, Perlstein WM, Stigge-Kaufman D, Kelly KG, Dotson VM.
NeuroReport, 17, 329-333.
The error-related negativity putatively reflects the activity of performance-monitoring processes influenced by motivational factors, and is overactive in certain anxiety states, suggesting that affective factors affect its generation. We examined the effects of emotionally arousing and neutral task-irrelevant backgrounds on the error-related negativity to determine whether an affective context 'mismatch' alters error-related neural processing. Event-related potentials were acquired while healthy participants performed a modified Eriksen flanker task wherein flanker stimuli were superimposed on neutral, pleasant, and unpleasant pictures. The error-related negativity varied as a function of picture valence, peaking both earlier and larger in the context of pleasant backgrounds than neutral or unpleasant backgrounds. Findings support the hypothesis that affective factors influence the error-related negativity, potentially reflecting an affective mismatch associated with performance monitoring.
NeuroReport, 17, 329-333.
The error-related negativity putatively reflects the activity of performance-monitoring processes influenced by motivational factors, and is overactive in certain anxiety states, suggesting that affective factors affect its generation. We examined the effects of emotionally arousing and neutral task-irrelevant backgrounds on the error-related negativity to determine whether an affective context 'mismatch' alters error-related neural processing. Event-related potentials were acquired while healthy participants performed a modified Eriksen flanker task wherein flanker stimuli were superimposed on neutral, pleasant, and unpleasant pictures. The error-related negativity varied as a function of picture valence, peaking both earlier and larger in the context of pleasant backgrounds than neutral or unpleasant backgrounds. Findings support the hypothesis that affective factors influence the error-related negativity, potentially reflecting an affective mismatch associated with performance monitoring.
Thursday, February 16, 2006
ARTICLE UPDATE - Brain Systems Mediating Cognitive Interference by Emotional Distraction
Florin Dolcos and Gregory McCarthy
The Journal of Neuroscience, 26, 2072-2079
Flexible behavior depends on our ability to cope with distracting stimuli that can interfere with the attainment of goals. Emotional distracters can be particularly disruptive to goal-oriented behavior, but the neural systems through which these detrimental effects are mediated are not known. We used event-related functional magnetic resonance imaging to investigate the effect of emotional and nonemotional distracters on a delayed-response working memory (WM) task. As expected, this task evoked robust activity during the delay period in typical WM regions (dorsolateral prefrontal cortex and lateral parietal cortex). Presentation of emotional distracters during the delay interval evoked strong activity in typical emotional processing regions (amygdala and ventrolateral prefrontal cortex) while simultaneously evoking relative deactivation of the WM regions and impairing WM performance. These results provide the first direct evidence that the detrimental effect of emotional distracters on ongoing cognitive processes entails the interaction between a dorsal neural system associated with "cold" executive processing and a ventral system associated with "hot" emotional processing.
The Journal of Neuroscience, 26, 2072-2079
Flexible behavior depends on our ability to cope with distracting stimuli that can interfere with the attainment of goals. Emotional distracters can be particularly disruptive to goal-oriented behavior, but the neural systems through which these detrimental effects are mediated are not known. We used event-related functional magnetic resonance imaging to investigate the effect of emotional and nonemotional distracters on a delayed-response working memory (WM) task. As expected, this task evoked robust activity during the delay period in typical WM regions (dorsolateral prefrontal cortex and lateral parietal cortex). Presentation of emotional distracters during the delay interval evoked strong activity in typical emotional processing regions (amygdala and ventrolateral prefrontal cortex) while simultaneously evoking relative deactivation of the WM regions and impairing WM performance. These results provide the first direct evidence that the detrimental effect of emotional distracters on ongoing cognitive processes entails the interaction between a dorsal neural system associated with "cold" executive processing and a ventral system associated with "hot" emotional processing.
Monday, February 13, 2006
ARTICLE UPDATE - The ‘when’ anard ‘where’ of perceiving signals of threat versus non-threat
Leanne M. Williams, Donna Palmer, Belinda J. Liddell, Le Song and Evian Gordon
NeuroImage, in press
We tested the proposal that signals of potential threat are given precedence over positive and neutral signals, reflected in earlier and more pronounced changes in neural activity. The temporal sequence (‘when’) and source localization (‘where’) of event-related potentials (ERPs) elicited by fearful and happy facial expressions, compared to neutral control expressions, were examined for 219 healthy subjects. We scored ERPs over occipito-temporal sites (N80, 50–120 ms; P120, 80–180 ms; N170, 120–220 ms; P230, 180–290 ms; N250, 230–350 ms) and their polarity-reversed counterparts over medial sites (P80, 40–120 ms; N120, 80–150 ms; VPP, 120–220 ms; N200, 150–280 ms; P300, 280–450 ms). In addition to scoring peak amplitude and latency, the anatomical sources of activity were determined using low resolution brain electromagnetic tomography (LORETA). Fearful faces were distinguished by persistent increases in positivity, associated with a dynamical shift from temporo-frontal (first 120 ms) to more distributed cortical sources (120–220 ms) and back (220–450 ms). By contrast, expressions of happiness produced a discrete enhancement of negativity, later in the time course (230–350 ms) and localized to the fusiform region of the temporal cortex. In common, fear and happiness modulated the face-related N170, and produced generally greater right hemisphere activity. These findings support the proposal that fear signals are given precedence in the neural processing systems, such that processing of positive signals may be suppressed until vigilance for potential danger is completed. While fear may be processed via parallel pathways (one initiated prior to structural encoding), neural systems supporting positively valenced input may be more localized and rely on structural encoding.
NeuroImage, in press
We tested the proposal that signals of potential threat are given precedence over positive and neutral signals, reflected in earlier and more pronounced changes in neural activity. The temporal sequence (‘when’) and source localization (‘where’) of event-related potentials (ERPs) elicited by fearful and happy facial expressions, compared to neutral control expressions, were examined for 219 healthy subjects. We scored ERPs over occipito-temporal sites (N80, 50–120 ms; P120, 80–180 ms; N170, 120–220 ms; P230, 180–290 ms; N250, 230–350 ms) and their polarity-reversed counterparts over medial sites (P80, 40–120 ms; N120, 80–150 ms; VPP, 120–220 ms; N200, 150–280 ms; P300, 280–450 ms). In addition to scoring peak amplitude and latency, the anatomical sources of activity were determined using low resolution brain electromagnetic tomography (LORETA). Fearful faces were distinguished by persistent increases in positivity, associated with a dynamical shift from temporo-frontal (first 120 ms) to more distributed cortical sources (120–220 ms) and back (220–450 ms). By contrast, expressions of happiness produced a discrete enhancement of negativity, later in the time course (230–350 ms) and localized to the fusiform region of the temporal cortex. In common, fear and happiness modulated the face-related N170, and produced generally greater right hemisphere activity. These findings support the proposal that fear signals are given precedence in the neural processing systems, such that processing of positive signals may be suppressed until vigilance for potential danger is completed. While fear may be processed via parallel pathways (one initiated prior to structural encoding), neural systems supporting positively valenced input may be more localized and rely on structural encoding.
ARTICLE UPDATE - The interaction of emotional and cognitive neural systems in emotionally guided response inhibition
Keith M. Shafritz, Susan H. Collins and Hilary P. Blumberg
NeuroImage, in press
The ability to generate appropriate responses in social situations often requires the integration of emotional information conveyed through facial expressions with ongoing cognitive processes. Neuroimaging studies have begun to address how cognitive and emotional neural systems interact, but most of these studies have used emotional oddball stimuli as distractors in order to dissociate emotional from cognitive neural systems. Therefore, the manner in which these systems interact when behavioral responses must be directly guided by the emotional content of stimuli remains elusive. Here, we used functional magnetic resonance imaging (fMRI) to investigate the neural systems involved in response inhibition for faces conveying particular emotions. Participants performed go/no-go tasks involving either letters or happy and sad faces. The fMRI results indicated that inhibiting responses to emotional faces activated inferior frontal/insular cortex, whereas response inhibition during the letter task did not strongly engage this region. In addition, distinct regions of ventral anterior cingulate were preferentially activated for sad faces in the go and no-go conditions. These findings suggest that inhibition within an emotional context recruits a distinct set of brain regions that includes areas beyond those normally activated by response inhibition tasks and that can be modulated by emotional valence.
NeuroImage, in press
The ability to generate appropriate responses in social situations often requires the integration of emotional information conveyed through facial expressions with ongoing cognitive processes. Neuroimaging studies have begun to address how cognitive and emotional neural systems interact, but most of these studies have used emotional oddball stimuli as distractors in order to dissociate emotional from cognitive neural systems. Therefore, the manner in which these systems interact when behavioral responses must be directly guided by the emotional content of stimuli remains elusive. Here, we used functional magnetic resonance imaging (fMRI) to investigate the neural systems involved in response inhibition for faces conveying particular emotions. Participants performed go/no-go tasks involving either letters or happy and sad faces. The fMRI results indicated that inhibiting responses to emotional faces activated inferior frontal/insular cortex, whereas response inhibition during the letter task did not strongly engage this region. In addition, distinct regions of ventral anterior cingulate were preferentially activated for sad faces in the go and no-go conditions. These findings suggest that inhibition within an emotional context recruits a distinct set of brain regions that includes areas beyond those normally activated by response inhibition tasks and that can be modulated by emotional valence.
Friday, February 10, 2006
ARTICLE UPDATE - Anxiety modulates the degree of attentive resources required to process emotional faces
Fox, Elaine; Russo, Riccardo; Georgiou, George A.
Cognitive, Affective, & Behavioral Neuroscience, 5, 396-404
The present study contributes to the ongoing debate over the extent to which attentive resources are required for emotion perception. Although fearful facial expressions are strong competitors for attention, we predict that the magnitude of this effect may be modulated by anxiety. To test this hypothesis, healthy volunteers who varied in their self-reported levels of trait and state anxiety underwent an attentional blink task. Both fearful and happy facial expressions were subject to a strong attentional blink effect for low-anxious individuals. For those reporting high anxiety, a blink occurred for both fearful and happy facial expressions, but the magnitude of the attentional blink was significantly reduced for the fearful expressions. This supports the proposals that emotion perception is not fully automatic and that anxiety is related to a reduced ability to inhibit the processing of threat-related stimuli. Thus, individual differences in self-reported anxiety are an important determinant of the attentional control of emotional processing.
Cognitive, Affective, & Behavioral Neuroscience, 5, 396-404
The present study contributes to the ongoing debate over the extent to which attentive resources are required for emotion perception. Although fearful facial expressions are strong competitors for attention, we predict that the magnitude of this effect may be modulated by anxiety. To test this hypothesis, healthy volunteers who varied in their self-reported levels of trait and state anxiety underwent an attentional blink task. Both fearful and happy facial expressions were subject to a strong attentional blink effect for low-anxious individuals. For those reporting high anxiety, a blink occurred for both fearful and happy facial expressions, but the magnitude of the attentional blink was significantly reduced for the fearful expressions. This supports the proposals that emotion perception is not fully automatic and that anxiety is related to a reduced ability to inhibit the processing of threat-related stimuli. Thus, individual differences in self-reported anxiety are an important determinant of the attentional control of emotional processing.
ARTICLE UPDATE - The emotional power of music: How music enhances the feeling of affective pictures
Baumgartner T, Lutz K, Schmidt CF, Jancke L.
Brain Research, in press
Music is an intriguing stimulus widely used in movies to increase the emotional experience. However, no brain imaging study has to date examined this enhancement effect using emotional pictures (the modality mostly used in emotion research) and musical excerpts. Therefore, we designed this functional magnetic resonance imaging study to explore how musical stimuli enhance the feeling of affective pictures. In a classical block design carefully controlling for habituation and order effects, we presented fearful and sad pictures (mostly taken from the IAPS) either alone or combined with congruent emotional musical excerpts (classical pieces). Subjective ratings clearly indicated that the emotional experience was markedly increased in the combined relative to the picture condition. Furthermore, using a second-level analysis and regions of interest approach, we observed a clear functional and structural dissociation between the combined and the picture condition. Besides increased activation in brain areas known to be involved in auditory as well as in neutral and emotional visual-auditory integration processes, the combined condition showed increased activation in many structures known to be involved in emotion processing (including for example amygdala, hippocampus, parahippocampus, insula, striatum, medial ventral frontal cortex, cerebellum, fusiform gyrus). In contrast, the picture condition only showed an activation increase in the cognitive part of the prefrontal cortex, mainly in the right dorsolateral prefrontal cortex. Based on these findings, we suggest that emotional pictures evoke a more cognitive mode of emotion perception, whereas congruent presentations of emotional visual and musical stimuli rather automatically evoke strong emotional feelings and experiences.
Brain Research, in press
Music is an intriguing stimulus widely used in movies to increase the emotional experience. However, no brain imaging study has to date examined this enhancement effect using emotional pictures (the modality mostly used in emotion research) and musical excerpts. Therefore, we designed this functional magnetic resonance imaging study to explore how musical stimuli enhance the feeling of affective pictures. In a classical block design carefully controlling for habituation and order effects, we presented fearful and sad pictures (mostly taken from the IAPS) either alone or combined with congruent emotional musical excerpts (classical pieces). Subjective ratings clearly indicated that the emotional experience was markedly increased in the combined relative to the picture condition. Furthermore, using a second-level analysis and regions of interest approach, we observed a clear functional and structural dissociation between the combined and the picture condition. Besides increased activation in brain areas known to be involved in auditory as well as in neutral and emotional visual-auditory integration processes, the combined condition showed increased activation in many structures known to be involved in emotion processing (including for example amygdala, hippocampus, parahippocampus, insula, striatum, medial ventral frontal cortex, cerebellum, fusiform gyrus). In contrast, the picture condition only showed an activation increase in the cognitive part of the prefrontal cortex, mainly in the right dorsolateral prefrontal cortex. Based on these findings, we suggest that emotional pictures evoke a more cognitive mode of emotion perception, whereas congruent presentations of emotional visual and musical stimuli rather automatically evoke strong emotional feelings and experiences.
Friday, February 03, 2006
ARTICLE UPDATE - Temporal course of emotional negativity bias: An ERP study.
Huang YX, Luo YJ.
Neuroscience Letter, in press
There is considerable evidence that people are especially sensitive to emotionally negative materials. However, the temporal course of the negativity bias is still unclear. To address this issue, we observed the changes of P2, late positive components (LPC) and lateralized readiness potential (LRP) under positive, negative and neutral conditions, with International Affective Picture System (IAPS) pictures as emotional stimuli. We found that the amplitude of P2 in the negative block was significantly larger than that in the positive block, indicating that the attentional negativity bias occured very early in emotion perception. The LPC amplitude evoked by negative pictures was larger than that by positive and neutral pictures, suggesting that the negativity bias also occurred in a later evaluation stage of emotion processing. The response-locked LRP interval was shortest in the block of negative pictures, indicating that the negative contents elicited a reaction priming effect. Above all, this research showed that emotional negativity bias could occur in several temporal stages distinguished by attention, evaluation and reaction readiness periods.
Neuroscience Letter, in press
There is considerable evidence that people are especially sensitive to emotionally negative materials. However, the temporal course of the negativity bias is still unclear. To address this issue, we observed the changes of P2, late positive components (LPC) and lateralized readiness potential (LRP) under positive, negative and neutral conditions, with International Affective Picture System (IAPS) pictures as emotional stimuli. We found that the amplitude of P2 in the negative block was significantly larger than that in the positive block, indicating that the attentional negativity bias occured very early in emotion perception. The LPC amplitude evoked by negative pictures was larger than that by positive and neutral pictures, suggesting that the negativity bias also occurred in a later evaluation stage of emotion processing. The response-locked LRP interval was shortest in the block of negative pictures, indicating that the negative contents elicited a reaction priming effect. Above all, this research showed that emotional negativity bias could occur in several temporal stages distinguished by attention, evaluation and reaction readiness periods.
ARTICLE UPDATE - Target Visibility and Visual Awareness Modulate Amygdala Responses to Fearful Faces
Luiz Pessoa, Shruti Japee, David Sturman and Leslie G. Ungerleider
Cerebral Cortex, 16, 366-375
The goals of the present study were twofold. First, we wished to investigate the neural correlates of aware and unaware emotional face perception after characterizing each subject's behavioral performance via signal detection theory methods. Second, we wished to investigate the extent to which amygdala responses to fearful faces depend on the physical characteristics of the stimulus independently of the percept. We show that amygdala responses depend on visual awareness. Under conditions in which subjects were not aware of fearful faces flashed for 33 ms, no differential activation was observed in the amygdala. On the other hand, differential activation was observed for 67 ms fearful targets that the subjects could reliably detect. When trials were divided into hits, misses, correct rejects, and false alarms, we show that target visibility is an important factor in determining amygdala responses to fearful faces. Taken together, our results further challenge the view that amygdala responses occur automatically.
Cerebral Cortex, 16, 366-375
The goals of the present study were twofold. First, we wished to investigate the neural correlates of aware and unaware emotional face perception after characterizing each subject's behavioral performance via signal detection theory methods. Second, we wished to investigate the extent to which amygdala responses to fearful faces depend on the physical characteristics of the stimulus independently of the percept. We show that amygdala responses depend on visual awareness. Under conditions in which subjects were not aware of fearful faces flashed for 33 ms, no differential activation was observed in the amygdala. On the other hand, differential activation was observed for 67 ms fearful targets that the subjects could reliably detect. When trials were divided into hits, misses, correct rejects, and false alarms, we show that target visibility is an important factor in determining amygdala responses to fearful faces. Taken together, our results further challenge the view that amygdala responses occur automatically.
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