Neural-behavioral dissociation under acute high-altitude stress: an exploratory ERP study of non-specific neural recruitment and rTMS effects.

IF 3.4 3区 医学 Q2 BEHAVIORAL SCIENCES
Frontiers in Behavioral Neuroscience Pub Date : 2026-06-19 eCollection Date: 2026-01-01 DOI:10.3389/fnbeh.2026.1844235
Peng Wu, Lizhi Liu, Huanhuan Li, Jiangheng Guan, Yang Lu, Xianglin Kong, Jian Song, Guozheng Xu
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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.

急性高海拔应激下的神经行为分离:非特异性神经招募和rTMS效应的探索性ERP研究。
目的:急性高原低气压缺氧损害执行功能,但行为表现与神经电活动之间的动态关系尚不清楚。本研究旨在探讨高原应激导致认知功能障碍的神经代偿机制,并对重复经颅磁刺激(rTMS)的潜在调节作用进行探索性研究。方法:31名健康成人在重复测量设计的三个时间点完成侧卫任务,同时进行脑电图记录:基线(G1), 24小时模拟高空低气压缺氧(3,600 m; G2)后立即,以及连续三天对右背外侧前额叶皮质(DLPFC)施加1 Hz重复经颅磁刺激(rTMS) (G3)后。我们分析了行为(反应时间、准确性)和事件相关电位(N2、P3振幅)结果。重要的是,我们计算了冲突效应差异分数(ΔN2, ΔP3),以隔离特定于冲突处理的神经活动。结果:G2和G3组的反应时间明显快于G1组(p < 0.001),准确度保持稳定。G2、G3时N2、P3波幅较G1显著增强(均p < 0.05)。ΔN2在不同时间点上没有差异,而ΔP3从G1到G2显示短暂的增加(p < 0.01),并在G3时恢复到基线。作为一项没有虚假控制的探索性研究,因果解释是有限的,但研究结果揭示了整体神经活动和冲突特异性处理之间的明确分离。结论:急性高原应激可增加与冲突监测和注意力分配相关的神经活动。这种增强反映了非特异性的神经招募,而不是冲突处理中特异性的提高。探索性观察表明,rTMS进一步提高了P3振幅,但没有选择性地调节冲突特异性反应。冲突效应评分(ΔN2, ΔP3)有望作为评估缺氧应激下神经认知状态的敏感标记。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Behavioral Neuroscience
Frontiers in Behavioral Neuroscience BEHAVIORAL SCIENCES-NEUROSCIENCES
CiteScore
4.70
自引率
3.30%
发文量
506
审稿时长
6-12 weeks
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.
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