T. Hausdorf, A. Ferdinand, P. Koo-Poeggel, M. Mölle, M. Bazhenov, L. Marshall
{"title":"高认知能力受试者睡眠时脑皮层-额皮质阳极电刺激联合闭环声刺激对记忆的影响。","authors":"T. Hausdorf, A. Ferdinand, P. Koo-Poeggel, M. Mölle, M. Bazhenov, L. Marshall","doi":"10.1111/ejn.70266","DOIUrl":null,"url":null,"abstract":"<p>This study investigates the impact of simultaneous anodal transcranial direct-current stimulation (tDCS) and closed-loop acoustic stimulation (CLAS) during slow-wave sleep on memory consolidation and neural oscillations. In this experiment, anodal tDCS was used to modulate cortical excitability, aiming to alter the brain state and investigate the resultant impact of CLAS-induced effects on sleep electroencephalography and overnight memory consolidation. Twenty participants (aged 18–30) completed two experimental nights involving either CLAS alone or tDCS combined with CLAS (AmodCLAS). Offline detected spontaneous SOs were shifted toward negative potential values by AmodCLAS, SO duration was increased, and density decreased. AmodCLAS also decreased sleep efficiency and REM sleep in the second part of the night. Compared with CLAS alone, AmodCLAS failed to influence memory consolidation across all subjects. However, memory retention of participants with higher fluid intelligence (as measured by Raven's Advanced Progressive Matrices) was significantly decreased after AmodCLAS, together with a more pronounced negative shift of SO up-state intervals, yet a weaker reduction in REM sleep. Our findings suggest that individuals with higher cognitive ability exhibit greater susceptibility to sleep-based neuromodulation while possibly possessing greater resilience against sleep perturbance. This highlights the critical role of interindividual cognitive differences in shaping responsiveness to neuromodulation techniques and underscores the need for personalized approaches during such interventions.</p>","PeriodicalId":11993,"journal":{"name":"European Journal of Neuroscience","volume":"62 7","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/ejn.70266","citationCount":"0","resultStr":"{\"title\":\"Stimulating the Stimulated Cortex—Frontocortical Anodal Electric Stimulation Combined With Closed-Loop Acoustic Stimulation During Sleep Impairs Memory in Subjects With High Cognitive Ability\",\"authors\":\"T. Hausdorf, A. Ferdinand, P. Koo-Poeggel, M. Mölle, M. Bazhenov, L. Marshall\",\"doi\":\"10.1111/ejn.70266\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>This study investigates the impact of simultaneous anodal transcranial direct-current stimulation (tDCS) and closed-loop acoustic stimulation (CLAS) during slow-wave sleep on memory consolidation and neural oscillations. In this experiment, anodal tDCS was used to modulate cortical excitability, aiming to alter the brain state and investigate the resultant impact of CLAS-induced effects on sleep electroencephalography and overnight memory consolidation. Twenty participants (aged 18–30) completed two experimental nights involving either CLAS alone or tDCS combined with CLAS (AmodCLAS). Offline detected spontaneous SOs were shifted toward negative potential values by AmodCLAS, SO duration was increased, and density decreased. AmodCLAS also decreased sleep efficiency and REM sleep in the second part of the night. Compared with CLAS alone, AmodCLAS failed to influence memory consolidation across all subjects. However, memory retention of participants with higher fluid intelligence (as measured by Raven's Advanced Progressive Matrices) was significantly decreased after AmodCLAS, together with a more pronounced negative shift of SO up-state intervals, yet a weaker reduction in REM sleep. Our findings suggest that individuals with higher cognitive ability exhibit greater susceptibility to sleep-based neuromodulation while possibly possessing greater resilience against sleep perturbance. 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Stimulating the Stimulated Cortex—Frontocortical Anodal Electric Stimulation Combined With Closed-Loop Acoustic Stimulation During Sleep Impairs Memory in Subjects With High Cognitive Ability
This study investigates the impact of simultaneous anodal transcranial direct-current stimulation (tDCS) and closed-loop acoustic stimulation (CLAS) during slow-wave sleep on memory consolidation and neural oscillations. In this experiment, anodal tDCS was used to modulate cortical excitability, aiming to alter the brain state and investigate the resultant impact of CLAS-induced effects on sleep electroencephalography and overnight memory consolidation. Twenty participants (aged 18–30) completed two experimental nights involving either CLAS alone or tDCS combined with CLAS (AmodCLAS). Offline detected spontaneous SOs were shifted toward negative potential values by AmodCLAS, SO duration was increased, and density decreased. AmodCLAS also decreased sleep efficiency and REM sleep in the second part of the night. Compared with CLAS alone, AmodCLAS failed to influence memory consolidation across all subjects. However, memory retention of participants with higher fluid intelligence (as measured by Raven's Advanced Progressive Matrices) was significantly decreased after AmodCLAS, together with a more pronounced negative shift of SO up-state intervals, yet a weaker reduction in REM sleep. Our findings suggest that individuals with higher cognitive ability exhibit greater susceptibility to sleep-based neuromodulation while possibly possessing greater resilience against sleep perturbance. This highlights the critical role of interindividual cognitive differences in shaping responsiveness to neuromodulation techniques and underscores the need for personalized approaches during such interventions.
期刊介绍:
EJN is the journal of FENS and supports the international neuroscientific community by publishing original high quality research articles and reviews in all fields of neuroscience. In addition, to engage with issues that are of interest to the science community, we also publish Editorials, Meetings Reports and Neuro-Opinions on topics that are of current interest in the fields of neuroscience research and training in science. We have recently established a series of ‘Profiles of Women in Neuroscience’. Our goal is to provide a vehicle for publications that further the understanding of the structure and function of the nervous system in both health and disease and to provide a vehicle to engage the neuroscience community. As the official journal of FENS, profits from the journal are re-invested in the neuroscientific community through the activities of FENS.