Keyword search (4,163 papers available)

"slow oscillations" Keyword-tagged Publications:

Title Authors PubMed ID
1 Neurophysiological effects of targeting sleep spindles with closed-loop auditory stimulation Jourde HR; Sobral M; Beltrame G; Coffey EBJ; 40626105
PSYCHOLOGY
2 Phase-Amplitude Coupling of NREM Sleep Oscillations Shows Between-Night Stability and is Related to Overnight Memory Gains Cross N; O' Byrne J; Weiner OM; Giraud J; Perrault AA; Dang-Vu TT; 40214027
PERFORM
3 Sleep spindles and slow oscillations predict cognition and biomarkers of neurodegeneration in mild to moderate Alzheimer's disease Páez A; Gillman SO; Dogaheh SB; Carnes A; Dakterzada F; Barbé F; Dang-Vu TT; Ripoll GP; 39878233
CONCORDIA
4 The neurophysiology of closed-loop auditory stimulation in sleep: A magnetoencephalography study Jourde HR; Merlo R; Brooks M; Rowe M; Coffey EBJ; 37675803
CONCORDIA
5 Sigma oscillations protect or reinstate motor memory depending on their temporal coordination with slow waves Nicolas J; King BR; Levesque D; Lazzouni L; Coffey EBJ; Swinnen S; Doyon J; Carrier J; Albouy G; 35726850
PSYCHOLOGY

 

Title:The neurophysiology of closed-loop auditory stimulation in sleep: A magnetoencephalography study
Authors:Jourde HRMerlo RBrooks MRowe MCoffey EBJ
Link:https://pubmed.ncbi.nlm.nih.gov/37675803/
DOI:10.1111/ejn.16132
Publication:The European journal of neuroscience
Keywords:auditory-evoked responseclosed-loop stimulationelectroencephalography (EEG)magnetoencephalography (MEG)sleepsleep spindlessleep stagesslow oscillations
PMID:37675803 Category: Date Added:2023-09-07
Dept Affiliation: CONCORDIA

Description:

Closed-loop auditory stimulation (CLAS) is a brain modulation technique in which sounds are timed to enhance or disrupt endogenous neurophysiological events. CLAS of slow oscillation up-states in sleep is becoming a popular tool to study and enhance sleep's functions, as it increases slow oscillations, evokes sleep spindles and enhances memory consolidation of certain tasks. However, few studies have examined the specific neurophysiological mechanisms involved in CLAS, in part because of practical limitations to available tools. To evaluate evidence for possible models of how sound stimulation during brain up-states alters brain activity, we simultaneously recorded electro- and magnetoencephalography in human participants who received auditory stimulation across sleep stages. We conducted a series of analyses that test different models of pathways through which CLAS of slow oscillations may affect widespread neural activity that have been suggested in literature, using spatial information, timing and phase relationships in the source-localized magnetoencephalography data. The results suggest that auditory information reaches ventral frontal lobe areas via non-lemniscal pathways. From there, a slow oscillation is created and propagated. We demonstrate that while the state of excitability of tissue in auditory cortex and frontal ventral regions shows some synchrony with the electroencephalography (EEG)-recorded up-states that are commonly used for CLAS, it is the state of ventral frontal regions that is most critical for slow oscillation generation. Our findings advance models of how CLAS leads to enhancement of slow oscillations, sleep spindles and associated cognitive benefits and offer insight into how the effectiveness of brain stimulation techniques can be improved.





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