{"title":"Neural-behavioral dissociation under acute high-altitude stress: an exploratory ERP study of non-specific neural recruitment and rTMS effects.","authors":"Peng Wu, Lizhi Liu, Huanhuan Li, Jiangheng Guan, Yang Lu, Xianglin Kong, Jian Song, Guozheng Xu","doi":"10.3389/fnbeh.2026.1844235","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Acute high-altitude hypobaric hypoxia impairs executive functions, yet the dynamic relationship between behavioral performance and neuroelectric activity remains unclear. This study aimed to explore the neural compensatory mechanisms underlying cognitive dysfunction induced by high-altitude stress and to conduct an exploratory investigation of the potential modulatory effects of repetitive transcranial magnetic stimulation (rTMS).</p><p><strong>Methods: </strong>Thirty-one healthy adults completed a Flanker task while undergoing EEG recording at three time points in a repeated-measures design: at baseline (G1), immediately after 24 h of simulated high-altitude hypobaric hypoxia (3,600 m; G2), and after three consecutive days of active 1 Hz repetitive transcranial magnetic stimulation (rTMS) applied to the right dorsolateral prefrontal cortex (DLPFC) (G3). We analyzed behavioral (reaction time, accuracy) and event-related potential (N2, P3 amplitude) outcomes. Importantly, we calculated conflict effect difference scores (ΔN2, ΔP3) to isolate neural activity specific to conflict processing.</p><p><strong>Results: </strong>Reaction times were significantly faster at G2 and G3 than at G1 (<i>p</i> < 0.001), with accuracy remaining stable. N2 and P3 amplitudes were significantly enhanced at G2 and G3 relative to G1 (all <i>p</i> < 0.05). ΔN2 did not differ across time points, whereas ΔP3 showed a transient increase from G1 to G2 (<i>p</i> < 0.01) and returned to baseline at G3. As an exploratory study without a sham control, causal interpretations are limited, but the findings reveal clear dissociation between overall neural activity and conflict-specific processing.</p><p><strong>Conclusion: </strong>Acute high-altitude stress increases neural activity related to conflict monitoring and attentional allocation. This enhancement reflects non-specific neural recruitment rather than improved specificity in conflict processing. Exploratory observations indicate that rTMS further elevates P3 amplitude without selectively modulating conflict-specific responses. Conflict effect scores (ΔN2, ΔP3) show promise as sensitive markers for evaluating neurocognitive states under hypoxic stress.</p>","PeriodicalId":12368,"journal":{"name":"Frontiers in Behavioral Neuroscience","volume":"20 ","pages":"1844235"},"PeriodicalIF":3.4000,"publicationDate":"2026-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13328090/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Behavioral Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fnbeh.2026.1844235","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: Acute high-altitude hypobaric hypoxia impairs executive functions, yet the dynamic relationship between behavioral performance and neuroelectric activity remains unclear. This study aimed to explore the neural compensatory mechanisms underlying cognitive dysfunction induced by high-altitude stress and to conduct an exploratory investigation of the potential modulatory effects of repetitive transcranial magnetic stimulation (rTMS).
Methods: Thirty-one healthy adults completed a Flanker task while undergoing EEG recording at three time points in a repeated-measures design: at baseline (G1), immediately after 24 h of simulated high-altitude hypobaric hypoxia (3,600 m; G2), and after three consecutive days of active 1 Hz repetitive transcranial magnetic stimulation (rTMS) applied to the right dorsolateral prefrontal cortex (DLPFC) (G3). We analyzed behavioral (reaction time, accuracy) and event-related potential (N2, P3 amplitude) outcomes. Importantly, we calculated conflict effect difference scores (ΔN2, ΔP3) to isolate neural activity specific to conflict processing.
Results: Reaction times were significantly faster at G2 and G3 than at G1 (p < 0.001), with accuracy remaining stable. N2 and P3 amplitudes were significantly enhanced at G2 and G3 relative to G1 (all p < 0.05). ΔN2 did not differ across time points, whereas ΔP3 showed a transient increase from G1 to G2 (p < 0.01) and returned to baseline at G3. As an exploratory study without a sham control, causal interpretations are limited, but the findings reveal clear dissociation between overall neural activity and conflict-specific processing.
Conclusion: Acute high-altitude stress increases neural activity related to conflict monitoring and attentional allocation. This enhancement reflects non-specific neural recruitment rather than improved specificity in conflict processing. Exploratory observations indicate that rTMS further elevates P3 amplitude without selectively modulating conflict-specific responses. Conflict effect scores (ΔN2, ΔP3) show promise as sensitive markers for evaluating neurocognitive states under hypoxic stress.
期刊介绍:
Frontiers in Behavioral Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the neural mechanisms underlying behavior. Field Chief Editor Nuno Sousa at the Instituto de Pesquisa em Ciências da Vida e da Saúde (ICVS) is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
This journal publishes major insights into the neural mechanisms of animal and human behavior, and welcomes articles studying the interplay between behavior and its neurobiological basis at all levels: from molecular biology and genetics, to morphological, biochemical, neurochemical, electrophysiological, neuroendocrine, pharmacological, and neuroimaging studies.