Brain research
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This study aimed to identify the neural correlates of aggression-related attentional selectivity to angry faces in physical aggression. Physical aggression in a non-clinical sample of young men (N = 36) was measured using an aggression questionnaire. Visual attentional bias to angry faces was assessed using a dot-probe task during which angry and neutral faces were presented simultaneously, and EEG was recorded. ⋯ It was concluded that the aggressive males selectively attend to angry faces, and that attentional bias is characterized by undifferentiated P3 amplitude. We propose that this results from an inferior ability to downregulate competing angry face distractors when responding to probes replacing neutral faces (as reflected by the P3 response). These findings indicate that attentional bias to angry faces in individuals with higher physical aggression is characterized by a distinctive ERP signature; this could inform the development of therapeutic interventions seeking to reduce aggression.
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Mas oncogene-related gene receptors (Mrg) are uniquely distributed in small and medium cells of trigeminal and dorsal root ganglia (DRG). The physiological and pharmacological properties of Mrg are unknown. We have shown that intermittent activation of MrgC prevents and reverses morphine tolerance. ⋯ All of these responses were not seen when BAM8-22 or MSH was co-administered with the PKC inhibitor CLT (3 nmol) or GF-109203X (10 nmol). The present study suggested that the chronic activation of MrgC upregulated expressions of pronociceptive mediators via PKC signaling pathway leading to the suppression of antinociceptive property of morphine. These effects are opposite to those occurred when MrgC is activated acutely or moderately.