Saturday, March 26, 2005

ARTICLE UPDATE - A common neural basis for receptive and expressive communication of pleasant facial affect

Andreas Hennenlotter, Ulrike Schroeder, Peter Erhard, Florian Castrop, Bernhard Haslinger, Daniela Stoecker, Klaus W. Langed and Andres O. Ceballos-Baumann

NeuroImage, in press

There is accumulating evidence suggesting that the visual representation of facial affect is closely linked to its motor representation. To examine whether perception of pleasant facial affect involves neural circuitries associated with its production, we performed an fMRI experiment with ‘compressed image acquisition' where subjects smiled and observed movies depicting other people smiling within scan-free time intervals between the acquisition of each image volume. Overlaps between the brain activation during observation and execution of smile expressions were located in the right premotor cortex and pars opercularis of the inferior frontal gyrus, right parietal operculum (SII) and left anterior insula. Observation of smile expressions further yielded signal increases within the posterior superior temporal sulcus (STS), fusiform gyrus and ventral amygdala. The results show that perceiving and expressing pleasant facial affect share a common neural basis in areas concerned with motor as well as somato- and limbic-sensory processing. In concert with temporal regions serving the visual analysis of facial expressive features, a mapping of the observed expressions onto neural circuitries associated with the production of these expressions and its somatosensory consequences could provide a description of what the expression would feel like if produced in the observer. Such a mechanism is suggested to be important for empathic understanding of others' feelings.

Tuesday, March 22, 2005

ARTICLE UPDATE - Contributions of amygdala and striatal activity in emotion regulation

Todd A. Hare, Nim Tottenham, Matthew C. Davidson, Gary H. Glover and B.J. Casey

Biological Psychiatry, 57, 624-632

Background
Emotional information can facilitate or interfere with cognitive processes. In this study, we examined the influence of emotional information in biasing performance and the biological basis underlying this influence.

Methods
Ten human subjects (five female) were scanned with functional magnetic resonance imaging while performing an emotional go/nogo task.

Results
Subjects were slower to approach fearful target expressions and had more difficulty avoiding happy nontarget expressions. The amygdala was recruited most for negative emotional context, and activity in this region was positively correlated with response time when detecting negative expressions. Increased signal in the right caudate nucleus was observed when avoiding nontargets and was negatively correlated with the number of false alarms subjects made.

Conclusions
Emotional context can alter behavioral and biological responses when approaching or avoiding a stimulus. We showed that recruitment of the amygdala, a region implicated in evaluating emotional significance, was associated with longer response latencies when approaching negative information, whereas recruitment of the caudate nucleus, a structure previously implicated in reward and impulse control, was most active when avoiding positive information. Our findings have significant implications for exaggerated and inhibited emotional responses that are characteristic of a number of psychiatric disorders.

Monday, March 21, 2005

ARTICLE UPDATE - Neuroimaging of emotion: empirical effects of proportional global signal scaling in fMRI data analysis

Markus Junghöfer, Harald T. Schupp, Rudolf Stark and Dieter Vaitl

NeuroImage, 25, 520-526

Global variations of BOLD-fMRI signal are often considered as nuisance effects. This unwanted source of variance is commonly eliminated using proportional global signal scaling (PGSS). However, application of PGSS relies on the assumption that global variations of BOLD signal and experimental conditions are uncorrelated. It has been shown for cognitive tasks that the unjustified application of PGSS might greatly distort statistical results. The present study examined this issue in the domain of emotion research. Specifically, fMRI data were obtained in a block-design, while 21 subjects passively viewed high and low emotionally arousing pleasant, unpleasant, and neutral pictures. Violations of the orthogonality assumption were found for analyses of emotional pictures high in arousal, causing dramatically different outcomes when compared to analyses performed without PGSS. Application of PGSS was associated with attenuated emotional activation in visual cortical areas, insensitivity to emotional activations in limbic and paralimbic regions, and widely distributed artificial deactivations. In contrast, the orthogonality assumption was not violated for low arousing emotional materials. Thus, the validity of using PGSS varied as a function of the emotional arousal of the stimuli. Taken together, the unwarranted use of PGSS might contribute to conflicting results in affective neuroscience fMRI studies, in particular with respect to limbic and paralimbic structures.

ARTICLE UPDATE - Neural evidence of effects of emotional valence on word recognition

Midori Inaba, Michio Nomura and Hideki Ohira

International Journal of Psychophysiology, in press

There are no clear reports of electrophysiological evidence of the facilitating effect of negative valence on word recognition. However, behavioral psychological studies have suggested that negative words can be recognized more accurately than positive and neutral words. This study aimed to examine whether, and if so how, the valence of words could influence accuracy and event-related potentials (ERPs) in a recognition task. ERPs were recorded from 20 healthy subjects during performance of a word recognition task. We found a behavioral advantage in discriminability between old and new items for negative words. As for ERPs, the positive-going shift was evident for correct responses to targets in late latency at midline and left centro-parietal sites. Additionally, the magnitude of this component was greatest for negative targets, next for positive targets, and least for neutral targets. The findings offer support for the idea that negative content greatly accelerates recognition memory compared to positive and neutral words.

Saturday, March 19, 2005

ARTICLE UPDATE - To what extent are emotional visual stimuli processed without attention and awareness?

Pessoa, L.

Current Opinions in Neurobology, in press


In the past few years, important contributions have been made to the study of emotional visual perception. Researchers have reported responses to emotional stimuli in the human amygdala under some unattended conditions (i.e. conditions in which the focus of attention was diverted away from the stimuli due to task instructions), during visual masking and during binocular suppression. Taken together, these results reveal the relative degree of autonomy of emotional processing. At the same time, however, important limitations to the notion of complete automaticity have been revealed. Effects of task context and attention have been shown, as well as large inter-subject differences in sensitivity to the detection of masked fearful faces (whereby briefly presented, target fearful faces are immediately followed by a neutral face that ‘masks’ the initial face). A better understanding of the neural basis of emotional perception and how it relates to visual attention and awareness is likely to require further refinement of the concepts of automaticity and awareness.

Friday, March 18, 2005

ARTICLE UPDATE - Effects of arousing emotional scenes on the distribution of visuospatial attention: changes with aging and early subcortical vascular

A. Rösler, C. Ulrich, J. Billino, P. Sterzer, S. Weidauer, T. Bernhardt, H. Steinmetz, L. Frölich and A. Kleinschmidt

Journal of the Neurological Sciences, 229-230, 109-116

BACKGROUND: The modulation of attention by emotionally arousing stimuli is highly important for each individual's social function. Disturbances of emotional processing are a supportive feature for the diagnosis of subcortical vascular dementia (SVD). We address here whether these disturbances might be useful as an early disease marker. METHODS: In order to examine the modulation of visual attention by emotionally arousing stimuli of different valence, 12 elderly patients with early SVD, 12 age-comparable healthy adults and 12 young healthy subjects were studied while looking at pairs of pictures from the International Affective Picture Battery that were either neutral-neutral, neutral-positive or neutral-negative in terms of emotional content. Eye movements were recorded with an infrared eye-tracking system. The direction of the first saccade and the dwell time during the 10 s of presentation were measured and compared among groups with parametric tests. RESULTS: All subjects showed a modulation of initial attentional orienting as well as a higher percentage of dwell time towards the pictures containing emotional material. Patients with SVD and old controls did not differ in either experimental measure. Young patients showed a stronger bias towards emotionally negative material than both groups of older individuals. CONCLUSIONS: Modulation of visuospatial attention is preserved in early SVD. This might have implications for therapeutic interventional approaches. A weakened sustained attention towards negative but not positive emotional pictures in the elderly is in accordance with the socioemotional selectivity theory, describing a relative selection of positive stimuli with aging.

ARTICLE UPDATE - Affective consciousness: Core emotional feelings in animals and humans.

Panksepp J.

Consciousness and Cognition, 14, 30-80

The position advanced in this paper is that the bedrock of emotional feelings is contained within the evolved emotional action apparatus of mammalian brains. This dual-aspect monism approach to brain-mind functions, which asserts that emotional feelings may reflect the neurodynamics of brain systems that generate instinctual emotional behaviors, saves us from various conceptual conundrums. In coarse form, primary process affective consciousness seems to be fundamentally an unconditional "gift of nature" rather than an acquired skill, even though those systems facilitate skill acquisition via various felt reinforcements. Affective consciousness, being a comparatively intrinsic function of the brain, shared homologously by all mammalian species, should be the easiest variant of consciousness to study in animals. This is not to deny that some secondary processes (e.g., awareness of feelings in the generation of behavioral choices) cannot be evaluated in animals with sufficiently clever behavioral learning procedures, as with place-preference procedures and the analysis of changes in learned behaviors after one has induced re-valuation of incentives. Rather, the claim is that a direct neuroscientific study of primary process emotional/affective states is best achieved through the study of the intrinsic ("instinctual"), albeit experientially refined, emotional action tendencies of other animals. In this view, core emotional feelings may reflect the neurodynamic attractor landscapes of a variety of extended trans-diencephalic, limbic emotional action systems-including SEEKING, FEAR, RAGE, LUST, CARE, PANIC, and PLAY. Through a study of these brain systems, the neural infrastructure of human and animal affective consciousness may be revealed. Emotional feelings are instantiated in large-scale neurodynamics that can be most effectively monitored via the ethological analysis of emotional action tendencies and the accompanying brain neurochemical/electrical changes. The intrinsic coherence of such emotional responses is demonstrated by the fact that they can be provoked by electrical and chemical stimulation of specific brain zones-effects that are affectively laden. For substantive progress in this emerging research arena, animal brain researchers need to discuss affective brain functions more openly. Secondary awareness processes, because of their more conditional, contextually situated nature, are more difficult to understand in any neuroscientific detail. In other words, the information-processing brain functions, critical for cognitive consciousness, are harder to study in other animals than the more homologous emotional/motivational affective state functions of the brain.

Wednesday, March 16, 2005

new issue of Emotion online now

There are many interesting articles on this issue of "Emotion". The articles are available online now. Duke University has a 4 Telsa scanner... Wow

Tuesday, March 15, 2005

ARTICLE UPDATE - Calling for help is independently modulated by brain systems underlying goal-directed behavior and threat perception

Andrew S. Fox, Terrence R. Oakes, Steven E. Shelton , Alexander K. Converse, Richard J. Davidson, and Ned H. Kalin

PNAS, 102, 4176-4179

In primates, during times of need, calling for help is an universal experience. Calling for help recruits social support and promotes survival. However, calling for help also can attract predators, and it is adaptive to inhibit calls for help when a potential threat is perceived. Based on this, we hypothesized that individual differences in calling for help would be related to the activity of brain systems that mediate goal-directed behavior and the detection of threat. By using high-resolution positron emission tomography in rhesus monkeys undergoing social separation, we demonstrate that increased [18F]-fluoro-2-deoxy-D-glucose uptake in the right dorsolateral prefrontal cortex and decreased uptake in the amygdala independently predict individual differences in calling for help. When taken together, these two regions account for 76% of the variance in calling for help. This result suggests that the drive for affiliation and the perception of threat determine the intensity of an individual's behavior during separation. These findings in monkeys are relevant to humans and provide a conceptual neural framework to understand individual differences in how primates behave when in need of social support.

Monday, March 14, 2005

ARTICLE UPDATE - Pathways for fear perception: modulation of amygdala activity by thalamo-cortical systems

Pritha Das, Andrew H. Kemp, Belinda J. Liddell, Kerri J. Brown, Gloria Olivieri, Anthony Peduto, Evian Gordone and Leanne M. Williams

NeuroImage, in press

Effective perception of fear signals is crucial for human survival and the importance of the amygdala in this process is well documented. Animal, lesion and neuroimaging studies indicate that incoming sensory signals of fear travel from thalamus to amygdala via two neural pathways: a direct subcortical route and an indirect pathway via the sensory cortex. Other lines of research have demonstrated prefrontal modulation of the amygdala. However, no study to date has examined the prefrontal modulation of the thalamo-cortico-amygdala pathways in vivo. We used psychophysiological and physiophysiological interactions to examine the functional connectivity within thalamus, amygdala and sensory (inferior occipital, fusiform) cortices, and the modulation of these networks by the anterior cingulate cortex (ACC). Functional magnetic resonance imaging (fMRI) data were acquired for 28 healthy control subjects during a fear perception task, with neutral as the ‘baseline’ control condition. Main effect analysis, using a region of interest (ROI) approach, confirmed that these regions are part of a distributed neural system for fear perception. Psychophysiological interactions revealed an inverse functional connectivity between occipito-temporal visual regions and the left amygdala, but a positive connectivity between these visual region and the right amygdala, suggesting that there is a hemispheric specialization in the transfer of fear signals from sensory cortices to amygdala. Physiophysiological interactions revealed a dorsal–ventral division in ACC modulation of the thalamus–sensory cortex pathway. While the dorsal ACC showed a positive modulation of this pathway, the ventral ACC exhibited an inverse relationship. In addition, both the dorsal and ventral ACC showed an inverse interaction with the direct thalamus–amygdala pathway. These findings suggest that thalamo-amygdala and cortical regions are involved in a dynamic interplay, with functional differentiation in both lateralized and ventral/dorsal gradients. Breakdowns in these interactions may give rise to affect-related symptoms seen in a range of neuropsychiatric disorders.

Saturday, March 12, 2005

ARTICLE UPDATE - Asymmetrical Activation in the Human Brain during Processing of Fearful Faces

Toemme Noesselt, Jon Driver, Hans-Jochen Heinze and Ray Dolan

Current Biology,15, 424-429

Traditional split-field studies and patient research indicate a privileged role for the right hemisphere in emotional processing [1, 2, 3, 4, 5, 6 and 7], but there has been little direct fMRI evidence for this, despite many studies on emotional-face processing [8, 9 and 10] (see Supplemental Background). With fMRI, we addressed differential hemispheric processing of fearful versus neutral faces by presenting subjects with faces bilaterally [11, 12 and 13] and orthogonally manipulating whether each hemifield showed a fearful or neutral expression prior to presentation of a checkerboard target. Target discrimination in the left visual field was more accurate after a fearful face was presented there. Event-related fMRI showed right-lateralized brain activations for fearful minus neutral left-hemifield faces in right visual areas, as well as more activity in the right than in the left amygdala. These activations occurred regardless of the type of right-hemifield face shown concurrently, concordant with the behavioral effect. No analogous behavioral or fMRI effects were observed for fearful faces in the right visual field (left hemisphere). The amygdala showed enhanced functional coupling with right-middle and anterior-fusiform areas in the context of a left-hemifield fearful face. These data provide behavioral and fMRI evidence for right-lateralized emotional processing during bilateral stimulation involving enhanced coupling of the amygdala and right-hemispheric extrastriate cortex.

Friday, March 11, 2005

ARTICLE UPDATE - Effects of direct and averted gaze on the perception of facially communicated emotion.

Adams RB Jr, Kleck RE.

Emotion, 5, 3-11

Research has largely neglected the effects of gaze direction cues on the perception of facial expressions of emotion. It was hypothesized that when gaze direction matches the underlying behavioral intent (approach-avoidance) communicated by an emotional expression, the perception of that emotion would be enhanced (i.e., shared signal hypothesis). Specifically, the authors expected that (a) direct gaze would enhance the perception of approach-oriented emotions (anger and joy) and (b) averted eye gaze would enhance the perception of avoidance-oriented emotions (fear and sadness). Three studies supported this hypothesis. Study 1 examined emotional trait attributions made to neutral faces. Study 2 examined ratings of ambiguous facial blends of anger and fear. Study 3 examined the influence of gaze on the perception of highly prototypical expressions.

ARTICLE UPDATE - Amygdala activation to sad pictures during high-field (4 tesla) functional magnetic resonance imaging.

Wang L, McCarthy G, Song AW, Labar KS

Emotion, 5, 12-22

Fear-related processing in the amygdala has been well documented, but its role in signaling other emotions remains controversial. The authors recovered signal loss in the amygdala at high-field strength using an inward spiral pulse sequence and probed its response to pictures varying in their degree of portrayed sadness. These pictures were presented as intermittent task-irrelevant distractors during a concurrent visual oddball task. Relative to neutral distractors, sad distractors elicited greater activation along ventral brain regions, including the amygdala, fusiform gyrus, and inferior frontal gyrus. In contrast, oddball targets engaged dorsal sectors of frontal, parietal, and cingulate cortices. The amygdala's role in emotional evaluation thus extends to images of grief and despair as well as to those depicting violence and threat.

ARTICLE UPDATE - Attentional interference effects of emotional pictures: threat, negativity, or arousal?

Schimmack U, Derryberry D

Emotion, 5, 55-66

Attentional interference arising from emotional pictures was examined. Participants had to ignore emotional pictures while solving math problems (Study 1, N = 126) or detecting the location of a line (Study 2, N = 60). Data analyses tested predictions of 3 theories. Evolutionary threat theory predicts interference by snake pictures. Categorical negativity theory predicts interference by negative pictures regardless of their intensity. According to arousal theory, arousal level predicts interference effects. The results supported arousal theory, with the most arousing pictures (strong unpleasant pictures, oppositesex models) producing the strongest interference. The findings are interpreted in the context of process models of emotions that postulate an initial relevance check before further processing of valence and other appraisal dimensions.

Wednesday, March 09, 2005

Human evaluate emotion by looking at the eyes

It's a news article from Caltech.
The scientific version could be found on Nature, 433, 68-72. A patient(SM) with amygdala damage has impairment in fear recognition and tends to avoid looking at eyes of the facial expressions presented. They're proposing that amygdala somehow guided visual attention. However, the real casual relationship is still unclear.

ARTICLE UPDATE - Amygdala damage impairs emotional memory for gist but not details of complex stimuli

Ralph Adolphs, Daniel Trane & Tony W Buchanan

Nature Neuroscience, in press

Neurobiological studies demonstrate the amygdala's role in emotional memory, and psychological studies suggest a particular pattern: enhanced memory for the gist but not the details of complex stimuli. We hypothesized that these two findings are related. Whereas normal (n = 52) and brain-damaged (n = 22) controls showed the expected enhancement of gist memory when the encoding context was emotional, persons with unilateral damage to the medial temporal lobe including the amygdala (n = 16) did not show this pattern. Furthermore, amygdala volume showed a significant positive correlation with gist memory but not with overall memory. A further study in four subjects with selective medial temporal damage sparing the amygdala, and one with selective damage confined to the amygdala, confirmed the specificity of this effect to the amygdala. The data support a model whereby the amygdala focuses processing resources on gist, possibly accounting for features of traumatic memories and eyewitness testimony in real life.

Monday, March 07, 2005

ARTICLE UPDATE - Brain mechanisms for mood congruent memory facilitation

P.A. Lewiw, H.D. Critchley, A.P. Smith and R.J. Dolan

NeuorImage, in press

Emotional information is better remembered when mood at the time of retrieval matches it in valence (positive mood, positive material). An associative memory model predicts that this ‘mood congruent’ facilitation is due to the mood-related reactivation at retrieval of emotional responses which were linked to valenced information at encoding. To test this model, we presented subjects with positive and negative words at study and manipulated their mood at test while using functional imaging to monitor brain activity. Subjective mood ratings and heart rate variability both indicated that the manipulation was effective, and memory performance showed a strong trend towards facilitation in congruent conditions. In the functional imaging data, valence-specific conjunctions between encoding activity predicting subsequent memory in a congruent mood and retrieval activity relating to mood congruent recollection revealed shared responses in subgenual cingulate for positive valence and posteriolateral orbitofrontal cortex for negative valence, thus supporting the associative model. To elucidate the mnemonic basis of facilitation, independent of valence, we examined the shared correlates of positive and negative congruence and found that parts of the episodic memory system were activated by congruence in correct rejection trials, but no part of this system was activated by congruence in correctly remembered trials. This pattern suggests that mood congruent facilitation occurs at the level of attempted recall rather than that of successful recollection.

Saturday, March 05, 2005

ARTICLE UPDATE - Two electrophysiological stages of spatial orienting towards fearful faces: early temporo-parietal activation preceding gain control

Gilles Pourtois, Gregor Thut, Rolando Grave de Peralt, Christoph Michel and Patrik Vuilleumier

NeuroImage, in press

Visuo-spatial attention tends to be prioritized towards emotionally negative stimuli such as fearful faces, as opposed to neutral or positive stimuli. Using a covert orienting task, we previously showed that a lateral occipital P1 component, with extrastriate neural sources, was selectively enhanced to lateralized visual targets replacing a fearful face (fear-valid trial) than the same targets replacing a neutral face (fear-invalid trial), providing evidence for exogenous spatial orienting of attention towards threat cues. Here, we describe a new analysis of these data, using topographic evoked potentials mapping methods combined with a distributed source localization technique. We show that an early field topography (40–80 ms post-target onset) with a centro-parietal negativity and a left posterior parietal source distinguished fear-valid from fear-invalid trials, whereas a distinct activity with anterior cingulate sources was selectively evoked during fear-invalid trials. At the same latency, or later, no difference in field topography was found for valid compared to invalid trials with happy faces. The early parietal map preceded a modulation in amplitude of the field strength (130ms), corresponding to the enhanced lateral occipital P1 during valid trials in the fear condition. Furthermore, this early topography at 40–80 ms was positively correlated with the subsequent amplitude modulation of P1 at 130–160 ms in the fear condition, suggesting a possible functional coupling between these two successive events. These data have important implications for models of spatial attention and interactions with emotion. They suggest two successive stages of neural activity during exogenous orienting of attention towards visual targets following fearful faces, including an early posterior parietal negativity, followed by gain control mechanisms enhancing visual responses in extrastriate occipital cortex.

Friday, March 04, 2005

ARTICLE UPDATE - An examination of the right-hemisphere hypothesis of the lateralization of emotion.

Stephen D. Smith, and M. Barbara Bulman-Fleming

Brain and Cognition, 57, 210-213

The Right-Hemisphere Hypothesis posits that emotional stimuli are perceived more efficiently by the right hemisphere than by the left hemisphere. The current research examines this hypothesis by examining hemispheric asymmetries for the conscious and unconscious perception of emotional stimuli. Negative, positive, and neutral words were presented for 17 ms to one visual field or the other. Conscious perception was measured by using a subjective report-of-awareness measure reported by participants on each trial. Unconscious perception was measured using an “exclusion task,” a form of word-stem-completion task. Consistent with previous research, there was a right-hemisphere advantage for the conscious perception of negative information. As in previous studies, this advantage for conscious perception occurred at the expense of unconscious perception. Specifically, there was a right-hemisphere inferiority for the unconscious perception of negative information. Contrary to the predictions of the Right-Hemisphere Hypothesis, there were no hemispheric asymmetries for the perception of positive emotional information, thus suggesting that the Right-Hemisphere Hypothesis may not be applicable to all behavioral studies.

ARTICLE UPDATE - Viewing facial expressions of pain engages cortical areas involved in the direct experience of pain.

Botvinick M, Jha AP, Bylsma LM, Fabian SA, Solomon PE, Prkachin KM.

Neuroimage, 25, 312-319

Recent neuroimaging and neuropsychological work has begun to shed light on how the brain responds to the viewing of facial expressions of emotion. However, one important category of facial expression that has not been studied on this level is the facial expression of pain. We investigated the neural response to pain expressions by performing functional magnetic resonance imaging (fMRI) as subjects viewed short video sequences showing faces expressing either moderate pain or, for comparison, no pain. In alternate blocks, the same subjects received both painful and non-painful thermal stimulation. Facial expressions of pain were found to engage cortical areas also engaged by the first-hand experience of pain, including anterior cingulate cortex and insula. The reported findings corroborate other work in which the neural response to witnessed pain has been examined from other perspectives. In addition, they lend support to the idea that common neural substrates are involved in representing one's own and others' affective states.