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The balanced processing of the internal mental world and the external world is a crucial aspect of everyday well-being. An extensive control of the internal emotional and cognitive world that often results in an internal expression of distress is a common feature of internalizing disorders. However, how depression affects the processing of the external world is still an open question. We, therefore, tested the processing of visual signals in major depressive disorder (MDD). To this end, we recorded the electroencephalogram of 38 MDD patients and 38 controls, while they performed a response-choice task with informative feedback and a passive viewing task. MDD patients differed significantly from controls in the early information processing of visual stimuli. The vertex positive potential (VPP) evoked by feedback in the response-choice task and pictures in the passive viewing task were smaller in MDD patients than in controls. This outcome suggests that depression might subtract attentional resources from external signal processing, with potential consequences in various cognitive domains.

Introduction Responses are optimal when they are accurate and fast. The present experiment investigated whether optimal responses evoke physiological arousal and whether performance affects the processing and evaluation of subsequent emotional material. Methods Participants performed a response‐choice task, where feedback was a colored square reflecting performance quality or a face whose expression (happy or angry) did not indicate any aspect of performance. In the occurrence of an emotional stimulus, participants had to express a judgment about the emotional strength. The experiment focused on differences in the electrodermal and brain electrophysiological activities evoked by optimal (correct‐fast) and suboptimal (correct‐slow) responses, along with modulations on the processing and interpretation of facial emotions. Results The results showed that, compared to correct responses, incorrect responses elicited an augmented phasic skin conductance response (SCR) and enhanced response‐locked event‐related potentials. Importantly, among correct responses, the SCR and the correct‐related negativity (CRN) were larger for correct‐fast than correct‐slow responses. Performance also affected the processing of faces, irrespective of the emotion, but it did not change the subjective interpretation. The EPN evoked by angry and happy faces was less negative after optimal than suboptimal responses. Conclusion These results indicate that the monitoring system is sensitive to detect correct‐fast responses, resulting in a state of physiological arousal that might guide the reinforcement of optimal performances., Optimal performance, like being correct and fast, leads to enhanced response‐related brain activity, increased physiological arousal, and modulations in processing subsequently presented emotional faces. Since these properties are similar to those of error processing, the monitoring system is sensitive to both better‐than‐expected and worse‐than‐expected performance. This sensitivity might lead to learning from the negative reinforcement of errors and the positive reinforcement of optimal responses. ​

We investigated the processing of faces with different smile expressions according to a context of personal performance. Individual judgments of smile happiness were collected to assess the processing of different types of smile when these were presented as a social response in a cognitive conflict task. Two main factors were considered: (a) Expression characteristics of the smile were manipulated: that is, happy (happy-happy), neutral (neutral-happy), or sad (sad-happy) eyes were morphed in faces with smiling mouth; (b) The performance context in which the smiling face appeared as social response (after fast, average, or slow correct response). Participants rated happy-happy faces the happiest followed by neutral-happy faces, then sad-happy faces (happy-happy > neutral-happy > sad-happy). Moreover, faces were rated more happy after fast responses as compared with average or slow responses (fast > average > slow). In addition to subjective ratings, we recorded the electroencephalography (EEG) and calculated event-related brain potentials (ERPs). The ERPs showed modulations of early visual potentials according to the expression characteristics of the face. The P1 was larger for sad-happy than neutral-happy faces. Moreover, the relationship between performance and face had a significant impact on the early posterior negativity (EPN), an ERP component associated with emotion processing. Faces elicited the largest EPN amplitude after average and slow responses as compared with fast responses. These results show that smile processing and interpretation are determined both by the distinctive perceptual features of the smile expression and by the performance context in which the smiling face occurs. (PsycINFO Database Record

According to recent interpretations of repetition priming, response codes are automatically bound to a stimulus and retrieved during successive presentations of the stimulus, hence, affecting its current processing. Despite a solid corpus of behavioural evidence in line with this interpretation, electrophysiological studies have reported contrasting results regarding the nature and the timing of response code retrieval. The present experiment aims to establish at which stage of information processing decision and action codes are retrieved in repetition priming. To this end, the lateralized readiness potential (LRP) was analysed for primed faces to monitor motor cortex activity related to response preparation. Congruent and incongruent responses were obtained by having identical or reversed tasks between study and test. Primed stimuli presented LRP activations with opposite polarities for the two congruency conditions in the time-window 250–300 ms, indicating response-related motor cortex activity resulting from the retrieval of correct and incorrect decision/action codes for congruent and incongruent trials, respectively. This result indicates that decision and action codes bound to a primed stimulus are retrieved at early stages of stimulus processing and that these codes are transmitted to the motor cortex.

Self-absorption describes a pathological tendency towards the internal mental world (internalization) that often conflicts with the accurate monitoring of the external world. In performance monitoring, an augmented electrophysiological response evoked by internal signals in patients with anxiety or depressive disorder seems to reflect this tendency. Specifically, the error-related negativity (Ne/ERN), an index of error processing based on internal signals, is larger in patients compared to controls. In the present experiment, we investigated whether the preferential processing of internal signals in patients is linked to diminished and inflexible external signal processing. To this end, the electrophysiological response evoked by external signals was analysed in patients with panic disorder and healthy controls. Participants performed a choice-response task, where informative or uninformative feedback followed each response, and a passive viewing task. As a replication of previous studies, patients presented an augmented Ne/ERN, indexing enhanced processing of internal signals related to errors. Furthermore, the vertex positive potential (VPP) evoked by visual stimuli was larger in patients than in controls, suggesting enhanced attention to external signals. Moreover, patients and controls showed similar sensitivity to the feedback information content, indicating a normal flexibility in the allocation of monitoring resources to external signals depending on how informative these signals are for performance monitoring. These results suggest that the tendency towards internal signals in patients with panic disorder does not hinder the flexible processing of external signals. On the contrary, external signals seem to attract enhanced processing in patients compared to controls.