Exaggerated sensitivity to threat and reduced medial prefrontal engagement during threat generalization in reactive aggressive adolescents
Wang, Y., Becker, B., Wang, J., Wang, Y., Zhang, L., Mei, Y., Li, H., & Lei, Y. (2024). Exaggerated sensitivity to threat and reduced medial prefrontal engagement during threat generalization in reactive aggressive adolescents. Neuroimage, 294, Article 120645. https://doi.org/10.1016/j.neuroimage.2024.120645
Julkaistu sarjassa
NeuroimageTekijät
Li, Hong |
Päivämäärä
2024Tekijänoikeudet
© 2024 the Authors
Aggressive adolescents tend to exhibit abnormal fear acquisition and extinction, and reactive aggressive adolescents are often more anxious. However, the relationship between fear generalization and reactive aggression (RA) remains unknown. According to Reactive-Proactive Aggression Questionnaire (RPQ) scores, 61 adolescents were divided into two groups, namely, a high RA group (N = 30) and a low aggression (LA) group (N = 31). All participants underwent three consecutive phases of the Pavlovian conditioning paradigm (i.e., habituation, acquisition, and generalization), and neural activation of the medial prefrontal cortex (mPFC) was assessed by functional near-infrared spectroscopy (fNIRS). The stimuli were ten circles with varying sizes, including two conditioned stimuli (CSs) and eight generalization stimuli (GSs). A scream at 85 dB served as the auditory unconditioned stimulus (US). The US expectancy ratings of both CSs and GSs were higher in the RA group than in the LA group. The fNIRS results showed that CSs and GSs evoked lower mPFC activation in the RA group compared to the LA group during fear generalization. These findings suggest that abnormalities in fear acquisition and generalization are prototypical dysregulations in adolescents with RA. They provide neurocognitive evidence for dysregulated fear learning in the mechanisms underlying adolescents with RA, highlighting the need to develop emotional regulation interventions for these individuals.
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Julkaisija
ElsevierISSN Hae Julkaisufoorumista
1053-8119Asiasanat
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https://converis.jyu.fi/converis/portal/detail/Publication/213665998
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This work was supported by grants from STI 2030—Major Projects 2022ZD0210900, the National Natural Science Foundation of China (NSFC32271142, NSFC82271583 and NSFC 32250610208); Guangdong Key Project in “Development of new tools for diagnosis and treatment of Autism” (2018B030335001); Ministry of Education Key Projects of Philosophy and Social Sciences Research (grant number 21JZD063); Shenzhen Science and Technology Research Funding Program (JCYJ20200109144801736); National Key Research and Development Program of China (2018YFA0701400); China Brain Project (2022ZD0208500). ...Lisenssi
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