Introduction: Previous research on the visual processing of threats has largely overlooked the Q8 distinct effects of various types of threats, despite evidence suggesting unique brain activation patterns for specific fears. Our study examines the differential effects of threat types on attentional processes, focusing on snakes and blood-injury-injection (BII) stimuli. We sought to test whether these two types of threat stimuli, as taskirrelevant distractors, would lead to similar effects in a visual search task.
Methods: Participants were exposed to emotionally charged stimuli of varying arousal (medium and high) and neutral pictures of low arousal as task-irrelevant distractors while performing a primary visual search task.
Results: We found that BII-related distractor pictures interfered with attention to the primary task, resulting in slower reaction times compared to snake pictures. In addition, BII-related medium arousal stimuli decreased, but high arousal facilitated both orienting and executive attentional performance. Exploratory analysis of personality traits revealed differential effects of trait anxiety and disgust sensitivity, highlighting the unique mechanisms underlying fear responses. In addition, participants who used adaptive emotion regulation strategies showed better performance in overcoming the interference of threat stimuli on attention.
Discussion: These findings underscore the importance of considering individual differences and emotion regulation strategies in fear research and provide insight into the complex interplay between threat perception and attentional processes.
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http://dx.doi.org/10.3389/fpsyt.2024.1498709 | DOI Listing |
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View Article and Find Full Text PDFBackground: The key advantage of active immunization is the induction of sustained, polyclonal antibody responses that are readily boosted by occasional immunizations. Recent clinical trial outcomes for monoclonal antibodies lecanemab and donanemab, establish the relevance of targeting pathological Abeta for clearing amyloid plaques in Alzheimer's disease. ACI-24.
View Article and Find Full Text PDFBackground: Convergent evidence indicates that deficits in the endosomal recycling pathway underlies pathogenesis of Alzheimer's disease (AD). SORL1 encodes the retromer-associated receptor SORLA that plays an essential role in recycling of AD-associated cargos such as the amyloid precursor protein and the glutamatergic AMPA receptor. Importantly, loss of function pathogenic SORL1 variants are associated with AD.
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View Article and Find Full Text PDFAlzheimers Dement
December 2024
Beckman Research Institute of City of Hope, Duarte, CA, USA.
Background: Brain organoid models were generated from healthy control or Alzheimer's disease patient iPSCs to facilitate our understanding of AD pathogenesis.
Method: ApoE3 and ApoE4 iPSCs were developed into brain organoids using our recently developed brain organoid platform that allows prolonged culture of brain organoids. Human iPSCs were also differentiated into microglia, which were then co-cultured with brain organoids.
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