The acute effects of intranasal oxytocin on automatic and effortful attentional shifting to emotional faces

Oxytocin is known to promote social affiliation. The mechanism by which this occurs is unknown, but it may involve changes in social information processing. In a placebo‐controlled study, we examined the influence of intranasal oxytocin on effortful and automatic attentional shifting in 57 participants using a spatial cueing task with emotional and neutral faces. For effortful processing, oxytocin decreased the speed of shifting attention to sad faces presented for 750 ms and facilitated disengagement from right hemifield sad and angry faces presented for 200 ms. For automatic processing, symptoms of depression moderated the relationship between drug and disengagement. Oxytocin attenuated an attentional bias to masked angry faces on disengagement trials in persons with high depression scores. Oxytocin's influence on social behavior may occur, in part, by eliciting flexible attentional shifting in the early stages of information processing.     

Selective attention to threatening faces in delusion‐prone individuals

Introduction. Selective attention to threat‐related information has been associated with clinical delusions in schizophrenia and nonclinical delusional ideation in healthy individuals. However, it is unclear whether biased attention for threat reflects early engagement effects on selective attention, or later difficulties in disengaging attention from perceived threat. The present study examined which of these processes operate in nonclinical delusion‐prone individuals.

Methods. A total of 100 psychologically healthy participants completed the Peters et al. () Delusions Inventory (PDI). Twenty‐two scoring in the upper quartile (high‐PDI group) and 22 scoring in the lower quartile (low‐PDI group) completed a modified dot‐probe task. Participants detected dot‐probes appearing 200, 500, or 1250 ms after an angry‐neutral face pair or a happy‐neutral face pair.

Results. High‐PDI individuals responded faster to dot‐probes presented in the same location as angry compared to happy faces at the short 200 ms stimulus onset asynchrony (SOA), but only when the emotional faces were presented to the left visual field. At the two longer SOAs (500 ms, 1250 ms), the high‐PDI group were also faster to respond to dot‐probes presented in the same location as angry compared to happy faces and slower to respond to dot‐probes presented in different spatial locations to angry (vs. happy) faces. The latter effects were seen whether emotional faces were presented to the left or the right visual field.

Conclusions. Results support the operation of emotion‐selective engagement and defective disengagement for threat‐related facial expressions (i.e., anger) in delusion‐prone individuals.     

Differential modulations of reward expectation on implicit facial emotion processing: ERP evidence

Implicit emotional processing refers to the preferential processing of emotional content even if it is task irrelevant. Given that motivation enhances executive control by biasing attentional resources toward target stimuli, here we investigated the effects of reward expectation on implicit facial emotional processing in two experiments using ERPs. A precue signaling additional monetary reward for fast and accurate response for the upcoming trial (incentive condition; relative to a cue indicating no such additional reward, i.e., nonincentive condition) was followed by the presentation of a happy, angry, or neutral face. Participants had to determine the gender of the face in Experiment 1 and decide whether a number superimposed on the face was even or odd in Experiment 2. In both experiments, incentive cues elicited larger P3 and contingent negative variation responses, and the targets following incentive cues elicited more positive‐going ERPs (200–700 ms), compared with the nonincentive condition. Importantly, the N2 responses (200–280 ms) to the target exhibited differential patterns of Reward × Emotion interaction: relative to the nonincentive condition, the N2 amplitude differences between emotional (i.e., happy and/or angry) and neutral faces increased in the incentive condition in Experiment 1, but diminished in Experiment 2. These results indicate that reward expectation can differentially modulate implicit processing of facial expressions, with increased sensitivity to emotions when the processing of whole faces is required, but with reduced sensitivity when the processing of faces is distractive. This study enriches the evidence for interactions between reward‐related executive control and implicit emotional processing.     

Large lateralized EDAN‐like brain potentials in a gaze‐shift detection task

Attentional cueing tasks using gaze direction as spatial cues have sometimes yielded an early directing attention negativity (EDAN) component in the ERP, presumably reflecting the initial orienting toward the cued location. However, other studies have failed to identify an EDAN component for gaze cues, yielding an inconsistent picture. In the present study, we re‐examined the EDAN to gaze cueing, using a continuous task where the specific direction of the gaze changes was task irrelevant. Face stimuli changed gaze direction several times during each trial between direct, left‐, and right‐averted positions. Participants counted the number of gaze shifts during the trial. Results showed an unusually large EDAN‐like ERP asymmetry at posterior scalp sites that was of similar amplitude for large and small gaze shifts into the periphery. Shifts from an averted position toward a direct gaze elicited a qualitatively similar but smaller effect than shifts into the periphery. Together, these findings shed new light on gaze‐elicited spatial attention as they indicate a reflexive attention orienting, following the direction of gaze motion, even when the gaze direction itself is irrelevant for the task.     

Target processing is facilitated by motivationally relevant cues

The effect that motivationally relevant stimuli have on processes of attentional engagement and disengagement was investigated during two modified peripheral cueing paradigms. Sexual, mutilation, threatening, and neutral stimuli served as peripheral cues in both experiments. Responses were made to target location in Experiment 1 (N=19 female) and target identity in Experiment 2 (N=18 female). As indexed by enhanced target-evoked P1 and P3b component amplitudes, target processing was facilitated by the presentation of sexual and mutilation stimuli in both experiments. This facilitation in response to targets cued by sexual and mutilation stimuli occurred regardless of whether cueing was valid or invalid as demonstrated by the non-significant cue validity x picture-type interaction. As such, the processes of attentional engagement (as inferred by responses to validly cued targets) and attentional disengagement (as inferred by responses to invalidly cued targets) were not differentially affected by the motivational relevance of the preceding cue. These results indicate that in a non-clinical sample, participants can shift attention rapidly to process information following the onset of motivationally relevant stimuli at attended (valid) and unattended (invalid) locations and that target processing is facilitated by the presence of appetitive and aversive cues.     

Current status of the anger superiority hypothesis: A meta‐analytic review of N2pc studies

Numerous investigators have tested contentions that angry faces capture early attention more completely than happy faces do in the context of other faces. However, syntheses of studies on early event‐related potentials related to the anger superiority hypothesis have yet to be conducted, particularly in relation to the N200 posterior‐contralateral (N2pc) component which provides a reliable electrophysiological index related to orienting of attention suitable for testing this hypothesis. Fifteen samples (N = 534) from 13 studies featuring the assessment of N2pc amplitudes during exposure to angry‐neutral and/or happy‐neutral facial expression arrays were included for meta‐analysis. Moderating effects of study design features and sample characteristics on effect size variability were also assessed. N2pc amplitudes elicited by affectively valenced expressions (angry and happy) were significantly more pronounced than those elicited by neutral expressions. However, the mean effect size difference between angry and happy expressions was ns. N2pc effect sizes were moderated by sample age, number of trials, and nature of facial images used (schematic vs. real) with larger effect sizes observed when samples were comparatively younger, more task trials were presented and schematic face arrays were used. N2pc results did not support anger superiority hypothesis. Instead, attentional resources allocated to angry versus happy facial expressions were similar in early stages of processing. As such, possible adaptive advantages of biases in orienting toward both anger and happy expressions warrant consideration in revisions of related theory.     

Developmental Differences in Cognitive Control of Socio-Affective Processing

We examined developmental differences in cognitive control in the context of distracting communicative cues varying in socio-affective significance. Adults and children (6–13 years) performed a Stroop-type task that required manual responses to a target word (LEFT/RIGHT) in the context of to-be-ignored spatial cues that were symbolic (arrow pointing left or right), social (left/right averted eye gaze in faces), or socio-emotional (happy, angry and fearful faces with left/right averted eye gaze). On the basis of the finding that accuracy was lower in the context of spatially incongruent than congruent cues, it was concluded that spatial direction, cued by both arrows and eye gaze, interfered with response selection. Interference did not differ between adults and children indicating that cognitive control of spatial attention directed by symbolic and social information is mature by 6 years. Interference from averted eye gaze was insensitive to the valence of facial emotion in adults and in children between 6–9 but not 10–13 years. Older children showed more interference from averted eye gaze in angry faces than younger children or adults. Thus, cognitive control of socio-affective processing differs in the preadolescent years relative to earlier in late childhood and adulthood.     

Developmental differences in cognitive control of socio-affective processing

We examined developmental differences in cognitive control in the context of distracting communicative cues varying in socio-affective significance. Adults and children (6-13 years) performed a Stroop-type task that required manual responses to a target word (LEFT/RIGHT) in the context of to-be-ignored spatial cues that were symbolic (arrow pointing left or right), social (left/right averted eye gaze in faces), or socio-emotional (happy, angry and fearful faces with left/right averted eye gaze). On the basis of the finding that accuracy was lower in the context of spatially incongruent than congruent cues, it was concluded that spatial direction, cued by both arrows and eye gaze, interfered with response selection. Interference did not differ between adults and children indicating that cognitive control of spatial attention directed by symbolic and social information is mature by 6 years. Interference from averted eye gaze was insensitive to the valence of facial emotion in adults and in children between 6-9 but not 10-13 years. Older children showed more interference from averted eye gaze in angry faces than younger children or adults. Thus, cognitive control of socio-affective processing differs in the preadolescent years relative to earlier in late childhood and adulthood.     

MEG Measures of Covert Orienting and Gaze Processing in Children

We investigated developmental differences in the cortical attention processing network using magnetoencephalography (MEG) and a spatial cueing task in 7–8 and 12–13 year old children. The cueing paradigm consisted of a centrally presented face with left or right averted eye-gaze in the gaze cue condition, and a central face with straight gaze presented with a cue stimulus to the left or right of the face in the peripheral cue condition. Cue congruency was 50 %. MEG was recorded during the two conditions and event-related beamforming was used to determine the timing and location of the brain activity related to target detection with the two types of cueing. The MEG data showed no age differences in the eye-gaze condition, but a developmental difference characterised by slower and more diffuse activations for peripheral cues in the younger versus the older age group. In the 7–8 year olds activation peaked around 300 ms, and was localised to left inferior frontal gyrus as well as posterior areas related to visuo-spatial processing. The 12–13 year olds showed a temporoparietal pattern of activation characteristic of spatial reorientation which resembled that seen for adult participants using the same paradigm (Nagata et al. 2012). The activation peaked around 200 ms and was localised to the left superior frontal gyrus, middle frontal gyrus but bilaterally near the temporoparietal junction. The data indicate maturational changes in brain activity for peripheral cueing.     

Effects of pre-cues on voluntary and reflexive saccade generation I. Anti-cues for pro-saccades

Experiments on visual attention have employed both physical cues and verbal instructions to enable subjects to allocate attention at a location that becomes relevant within a perceptual or motor task some time later (cue lead time, CLT). In this study we have used valid visual peripheral cues (CLT between 100 and 700 ms) to indicate the direction and location of the next saccade. A cue is considered valid or invalid if its meaning with respect to the next saccade is correct or incorrect. A cue is called an anti- or pro-cue if the side of its presentation is opposite to or the same as the direction of the saccade required on a given trial. Correspondingly, a saccade is called an anti- or pro-saccade if it is directed to the side opposite to or the same as the stimulus presentation. A condition in which the cue and the stimulus are presented on opposite sides provides a simple way of dissociating voluntary attention allocation from automatic orienting. This paper considers the anti-cue pro-saccade task: the subjects were instructed to use the cue to direct attention to the opposite side, i.e. the location, where on valid trials the saccade target would occur. In the companion paper we have used the same physical condition, but we have reversed the instructions as to saccade direction and we have reversed the meaning of the cue, i.e. we designed a pro-cue anti-saccade task. In this first paper, the saccadic reaction times (SRTs) of pro-saccades of five adult subjects were measured in the gap paradigm (fixation point offset precedes target onset by 200 ms). With a CLT of 100 ms, valid anti-cues reduced the number of express saccades (i.e. saccades with SRTs in the range 80–120 ms) significantly compared with the control values (no cues). Valid anti-cues with increasingly long CLTs (100–700 ms) resulted in an increasing incidence of anticipatory saccades and saccades with longer SRTs (more than 120 ms), while the frequency of express saccades remained below the control value. When cue and saccade target were dissociated in location or in both location and direction, the effects of the cueing revealed a much lower spatial selectivity as compared to the effects that have been described for voluntary attention allocation by means of central cues. The results suggest that voluntary allocation of attention and cue-induced automatic orienting not only have different time courses but also have opposite effects on the generation of express saccades, and different spatial selectivities. A possible neuronal basis of these results is discussed considering related findings from electrophysiological studies in monkeys. Received: 27 March 1997 / Accepted: 17 December 1997     

Neurocognitive effects of HF-rTMS over the dorsolateral prefrontal cortex on the attentional processing of emotional information in healthy women: an event-related fMRI study

Current evidence concerning the neurocircuitry underlying the interplay between attention and emotion is mainly correlational. We used high-frequency repetitive Transcranial Magnetic Stimulation (HF-rTMS) to experimentally manipulate activity within the right or left dorsolateral prefrontal cortex (DLPFC) of healthy women and examined changes in attentional processing of emotional information using an emotional modification of the exogenous cueing task during event-related fMRI. Right prefrontal HF-rTMS resulted in impaired disengagement from angry faces, associated with decreased activation within the right DLPFC, dorsal anterior cingulate cortex (dACC) and left superior parietal gyrus, combined with increased activity within the right amygdala. Left prefrontal HF-rTMS resulted in diminished attentional engagement by angry faces and was associated with increased activity within the right DLPFC, dACC, right superior parietal gyrus and left orbitofrontal cortex. The present observations are in line with reports of a functionally interactive network of cortical-limbic pathways that play a central role in emotion regulation.     

Following the time course of face gender and expression processing: A task-dependent ERP study

The effects of task demands and the interaction between gender and expression in face perception were studied using event-related potentials (ERPs). Participants performed three different tasks with male and female faces that were emotionally inexpressive or that showed happy or angry expressions. In two of the tasks (gender and expression categorization) facial properties were task-relevant while in a third task (symbol discrimination) facial information was irrelevant. Effects of expression were observed on the visual P100 component under all task conditions, suggesting the operation of an automatic process that is not influenced by task demands. The earliest interaction between expression and gender was observed later in the face-sensitive N170 component. This component showed differential modulations by specific combinations of gender and expression (e.g., angry male vs. angry female faces). Main effects of expression and task were observed in a later occipito-temporal component peaking around 230 ms post-stimulus onset (EPN or early posterior negativity). Less positive amplitudes in the presence of angry faces and during performance of the gender and expression tasks were observed. Finally, task demands also modulated a positive component peaking around 400 ms (LPC, or late positive complex) that showed enhanced amplitude for the gender task. The pattern of results obtained here adds new evidence about the sequence of operations involved in face processing and the interaction of facial properties (gender and expression) in response to different task demands.     

Attentional selectivity for emotional faces: Evidence from human electrophysiology

This study investigated the temporal course of attentional biases for threat-related (angry) and positive (happy) facial expressions. Electrophysiological (event-related potential) and behavioral (reaction time [RT]) data were recorded while participants viewed pairs of faces (e.g., angry face paired with neutral face) shown for 500 ms and followed by a probe. Behavioral results indicated that RTs were faster to probes replacing emotional versus neutral faces, consistent with an attentional bias for emotional information. Electrophysiological results revealed that attentional orienting to threatening faces emerged earlier (early N2pc time window; 180–250 ms) than orienting to positive faces (after 250 ms), and that attention was sustained toward emotional faces during the 250–500-ms time window (late N2pc and SPCN components). These findings are consistent with models of attention and emotion that posit rapid attentional prioritization of threat.     

What does the dot‐probe task measure? A reverse correlation analysis of electrocortical activity

The dot‐probe task is considered a gold standard for assessing the intrinsic attentive selection of one of two lateralized visual cues, measured by the response time to a subsequent, lateralized response probe. However, this task has recently been associated with poor reliability and conflicting results. To resolve these discrepancies, we tested the underlying assumption of the dot‐probe task—that fast probe responses index heightened cue selection—using an electrophysiological measure of selective attention. Specifically, we used a reverse correlation approach in combination with frequency‐tagged steady‐state visual potentials (ssVEPs). Twenty‐one participants completed a modified dot‐probe task in which each member of a pair of lateralized face cues, varying in emotional expression (angry‐angry, neutral‐angry, neutral‐neutral), flickered at one of two frequencies (15 or 20 Hz), to evoke ssVEPs. One cue was then replaced by a response probe, and participants indicated the probe orientation (0° or 90°). We analyzed the ssVEP evoked by the cues as a function of response speed to the subsequent probe (i.e., a reverse correlation analysis). Electrophysiological measures of cue processing varied with probe hemifield location: Faster responses to left probes were associated with weak amplification of the preceding left cue, apparent only in a median split analysis. By contrast, faster responses to right probes were systematically and parametrically predicted by diminished visuocortical selection of the preceding right cue. Together, these findings highlight the poor validity of the dot‐probe task, in terms of quantifying intrinsic, nondirected attentive selection irrespective of probe/cue location.     

EEG delta oscillations index inhibitory control of contextual novelty to both irrelevant distracters and relevant task‐switch cues

Delta oscillations contribute to the human P300 event‐related potential evoked by oddball targets, although it is unclear whether they index contextual novelty (event oddballness, novelty P3, nP3), or target‐related processes (event targetness, target P3b). To examine this question, the electroencephalogram (EEG) was recorded during a cued task‐switching version of the Wisconsin card‐sorting test. Each target card was announced by a tone cueing either to switch or repeat the task. Novel sound distracters were interspersed among trials. Time‐frequency EEG analyses revealed bursts of delta (2–4 Hz) power associated with enhanced nP3 amplitudes to both task‐switch cues and novel distracters—but no association with target P3b. These findings indicate that the P300‐delta response indexes contextual novelty regardless of whether novelty emanates from endogenous (new task rules) or exogenous (novel distracters) sources of information.     

The role of top‐down spatial attention in contingent attentional capture

It is well known that attentional capture by an irrelevant salient item is contingent on top‐down feature selection, but whether attentional capture may be modulated by top‐down spatial attention remains unclear. Here, we combined behavioral and ERP measurements to investigate the contribution of top‐down spatial attention to attentional capture under modified spatial cueing paradigms. Each target stimulus was preceded by a peripheral circular cue array containing a spatially uninformative color singleton cue. We varied target sets but kept the cue array unchanged among different experimental conditions. When participants’ task was to search for a colored letter in the target array that shared the same peripheral locations with the cue array, attentional capture by the peripheral color cue was reflected by both a behavioral spatial cueing effect and a cue‐elicited N2pc component. When target arrays were presented more centrally, both the behavioral and N2pc effects were attenuated but still significant. The attenuated cue‐elicited N2pc was found even when participants focused their attention on the fixed central location to identify a colored letter among an RSVP letter stream. By contrast, when participants were asked to identify an outlined or larger target, neither the behavioral spatial cueing effect nor the cue‐elicited N2pc was observed, regardless of whether the target and cue arrays shared same locations or not. These results add to the evidence that attentional capture by salient stimuli is contingent upon feature‐based task sets, and further indicate that top‐down spatial attention is important but may not be necessary for contingent attentional capture.     

Threat‐conditioned contexts modulate the late positive potential to faces—A mobile EEG/virtual reality study

In everyday life, the motivational value of faces is bound to the contexts in which faces are perceived. Electrophysiological studies have demonstrated that inherent negatively valent contexts modulate cortical face processing as assessed with ERP components. However, it is not well understood whether learned (rather than inherent) and three‐dimensional aversive contexts similarly modulate the neural processing of faces. Using full immersive virtual reality (VR) and mobile EEG techniques, 25 participants underwent a differential fear conditioning paradigm, in which one virtual room was paired with an aversive noise burst (threat context) and another with a nonaversive noise burst (safe context). Subsequently, avatars with neutral or angry facial expressions were presented in the threat and safe contexts while EEG was recorded. Analysis of the late positive potential (LPP), which presumably indicates motivational salience, revealed a significant interaction of context (threat vs. safe) and face type (neutral vs. angry). Neutral faces evoked increased LPP amplitudes in threat versus safe contexts, while angry faces evoked increased early LPP amplitudes regardless of context. In addition to indicating that threat‐conditioned contexts alter the processing of ambiguous faces, the present study demonstrates the successful integration of EEG and VR with particular relevance for affective neuroscience research.     

Automatic emotion regulation in response inhibition: The temporal dynamics of emotion counter‐regulation during a go/no‐go task

Recent behavioral studies indicate that emotion counter‐regulation automatically allocates attention to events that are opposite in the valence to the experienced emotional state. The present study explored the effect of emotion counter‐regulation on response inhibition by using ERPs in a go/no‐go paradigm. We recruited 58 subjects and randomly assigned them to either the angry priming group (watching Nanjing Massacre movie clips) or the neutral priming group (watching “mending a computer” movie clips). The behavioral results revealed that participants in the angry priming group responded significantly more accurately to go happy and no‐go angry faces than go angry and no‐go happy faces. The analyses of ERPs revealed that the amplitudes of the no‐go N2 and no‐go P3 were significantly larger for the happy faces than for the angry faces in the angry priming group. However, no such effects were found in the neutral priming group. These results suggest that highly aroused angry emotion could prompt a priority response to happy emotion stimuli and restrict the responses to angry emotion stimuli through emotion counter‐regulation.     

Attentional biases for angry faces in unipolar depression

BACKGROUND: Past research has demonstrated that depression is associated with dysfunctional processing of emotional information. Recent studies demonstrate that a bias in the attentional processing of negative information may be an important cognitive vulnerability factor underlying the onset and maintenance of depression. However, to date, the nature of this attentional bias is still poorly understood and further exploration of this topic to advance current knowledge of attentional biases in depression seems imperative. METHOD: This study examined attentional biases for angry facial expressions presented for 1000 ms in 20 patients with major depressive disorder (MDD) and 20 non-depressed control participants (NC) matched for age and gender using an emotional modification of the Exogenous Cueing task. RESULTS: Patients with MDD showed maintained attention for angry faces compared with neutral faces. In comparison with non-depressed participants they showed a stronger attentional engagement for angry faces. In contrast, the NC group directed attention away from angry faces, more rapidly disengaging their attention compared with neutral faces. CONCLUSIONS: This pattern of results supports the assumption that MDD is characterized by deficits in the attentional processing of negative, interpersonal information and suggests a 'protective' bias in non-depressed individuals. Implications in relation to previous research exploring cognitive and interpersonal functioning in depression are discussed.     

重度抑郁症对负性情绪面孔的注意偏向

目的:探讨重度抑郁症患者对负性情绪面孔的注意偏向.方法:从35名符合中国精神疾病诊断与分类手册第三版(CCMD-3)抑郁症诊断标准的被试中,筛选出符合汉密尔顿抑郁量表( Hamilton Depression Scale,HAMD)及Beck抑郁自评问卷(Beck Depression Inventory,BDI)重度抑郁症诊断标准的重度抑郁症患者(抑郁组)20名.选取在年龄、性别及受教育程度方面与抑郁组相匹配的正常对照20名.采用NimStim情绪面孔图片库中的负性情绪面孔和中性情绪面孔作为刺激材料,应用注意偏向研究中常用的线索-靶子任务进行研究,比较两组被试线索效应、注意施加、注意解除得分.结果:抑郁组对负性情绪面孔线索效应得分大于对中性情绪面孔线索效应得分(21.73 ms vs.3.91 ms,P<0.01);抑郁组注意施加得分大于对照组(17.25 ms vs.1.64 ms,P<0.001);对照组与抑郁组注意解除得分差别无统计学意义(-1.50 ms vs.0.57 ms, P>0.05).结论:抑郁症患者对负性情绪信息加工存在注意偏向,对负性情绪信息缺乏保护性偏向.