Effects of two nights of sleep deprivation on executive function and central and peripheral fatigue during maximal voluntary contraction lasting 60s

Skurvydas, Albertas; Kazlauskaite, Diana; Žlibinaitė, Laura; Čekanauskaitė, Agnė; Valančiene, Dovilė; Karanauskienė, Diana; Zuozienė, Ilona Judita; Majauskienė, Daiva; Mickevičienė, Dalia; Satas, Andrius

doi:10.1016/j.physbeh.2020.113226

Cited by 20 publications

(17 citation statements)

References 44 publications

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“…Sleep is one of the most basic biological activities which is crucial for both high-level cognitive processing and also basic maintenance and restoration of physiological function ( Simpson and Dinges, 2007 ; Fultz et al, 2019 ), and while in sleep the brain, heart rate and breathing will exhibit sleep-related characteristics ( Purves et al, 2011 ). Previous studies suggested that sleep deprivation may affect the function of the central nervous system, ANS, cardiovascular system, and respiratory system ( Zhong et al, 2005 ; Vaara et al, 2009 ; Robillard et al, 2011 ; Chen et al, 2013 ; Glos et al, 2014 ; Sunbul et al, 2014 ; Virtanen et al, 2015 ; Słomko et al, 2018 ; Skurvydas et al, 2021 ; Westphal et al, 2021 ).…”

Section: Discussionmentioning

confidence: 99%

“…In most of the relevant previous studies, sleep deprivation is associated with a decrease in parasympathetic/vagal modulation and baroreflex sensitivity, and an increase in sympathetic modulation and arterial pressure or its variability (Zhong et al, 2005;Chen et al, 2013;Glos et al, 2014;Virtanen et al, 2015;Westphal et al, 2021). In contrast, very few studies have found that sleep deprivation influences cardiovascular autonomic response by increasing parasympathetic modulation (Vaara et al, 2009;Skurvydas et al, 2021). Taken together these observations suggest that previous findings of changed HRV and blood pressure or its variability after 24-hour ATSD might rather reflect the disturbing effect of psychological stress on autonomic function (Pagani et al, 2009).…”

Section: Variablesmentioning

confidence: 99%

“…In previous studies, it has been observed that acute total sleep deprivation (ATSD) may decrease parasympathetic cardiac modulation and/or increase sympathetic activity based on heart rate variability (HRV) analysis (Zhong et al, 2005;Chen et al, 2013;Glos et al, 2014;Virtanen et al, 2015;Westphal et al, 2021). However, other investigations had contradictory results that accumulation of acute sleep loss resulted in decreased heart rate and increased HRV, which reflects the enhancement of vagal outflow (Vaara et al, 2009;Skurvydas et al, 2021). Several studies also found that exposure to continuous ATSD appears to cause hemodynamic dysfunction through raising systolic blood pressure, diastolic blood pressure, arterial stiffness, or lowering baroreflex sensitivity (Robillard et al, 2011;Sunbul et al, 2014;Słomko et al, 2018).…”

Section: Introductionmentioning

confidence: 99%

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Effects of 24-h acute total sleep deprivation on physiological coupling in healthy young adults

Liu

Yu²,

Wang³

et al. 2022

Front. Neurosci.

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Sleep deprivation is associated with dysregulation of the autonomic nervous system, adverse cardiovascular events, cognitive and complex motor performance impairment. Less is known about the effects of acute total sleep deprivation (ATSD) on physiological coupling. We aimed to determine the effects of 24-h ATSD on the physiological coupling between complex subsystems by evaluating the cardiorespiratory, cardiovascular and cortico-cardiac interactions. This study enrolled 38 young healthy participants aged 23.2 ± 2.4 years. Multiple synchronous physiological signals including electrocardiography, photoplethysmography, bio-electrical impedance, electroencephalography, and continuous hemodynamic data, were performed over a baseline night after regular sleep and after a night with 24-h ATSD in the supine position. The magnitude squared coherence, phase synchronization index, and heartbeat evoked potential amplitudes, were obtained from 10-min synchronous physiological recordings to estimate the coupling strength between two time series. Parameters of hemodynamic characteristics and heart rate variability were also calculated to quantify autonomic regulation. Results indicated that the magnitude squared coherence (0.38 ± 0.17 vs. 0.29 ± 0.12, p = 0.015) between respiration and heart rate variability along with the magnitude squared coherence (0.36 ± 0.18 vs. 0.27 ± 0.13, p = 0.012) between respiration and pulse transit time were significantly decreased after 24-h ATSD. There were no significant differences (all p > 0.05) in phase synchronization indices, heartbeat evoked potential amplitudes as well as other analyzed measurements between baseline and 24-h ATSD states. We conclude that exposure to 24-h ATSD appears to weaken the cardiorespiratory and respiratory-cardiovascular coupling strength of young healthy adults. These findings suggest that physiological coupling analysis may serve as a complementary approach for characterizing and understanding the complex effects of sleep deprivation.

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Section: Discussionmentioning

confidence: 99%

Section: Variablesmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

See 1 more Smart Citation

Effects of 24-h acute total sleep deprivation on physiological coupling in healthy young adults

Liu

Yu²,

Wang³

et al. 2022

Front. Neurosci.

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“…In a study by Kusztor et al [ 21 ], it was noted that cognitive processing in early bottom-up automation appears to be less affected by sleep deprivation compared to more advanced top-down cognitive control. The process of sleep deprivation is accompanied by significant changes in fatigue status [ 64 , 65 , 66 ]. Furthermore, 36 h of sleep deprivation caused participants to experience mental fatigue and reduced central nervous system arousal, leading to impaired sustained attention [ 67 ].…”

Section: Discussionmentioning

confidence: 99%

Acute Sleep Deprivation Impairs Motor Inhibition in Table Tennis Athletes: An ERP Study

Song

Peng

et al. 2022

Brain Sciences

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Excellent response inhibition is the basis for outstanding competitive athletic performance, and sleep may be an important factor affecting athletes’ response inhibition. This study investigates the effect of sleep deprivation on athletes’ response inhibition, and its differentiating effect on non-athlete controls’ performance, with the aim of helping athletes effectively improve their response inhibition ability through sleep pattern manipulation. Behavioral and event-related potential (ERP) data were collected from 36 participants (16 table tennis athletes and 20 general college students) after 36 h of sleep deprivation using ERP techniques and a stop-signal task. Sleep deprivation’s different effects on response inhibition in the two groups were explored through repeated-measures ANOVA. Behavioral data showed that in a baseline state, stop-signal response time was significantly faster in table tennis athletes than in non-athlete controls, and appeared significantly longer after sleep deprivation in both groups. ERP results showed that at baseline state, N2, ERN, and P3 amplitudes were lower in table tennis athletes than in non-athlete controls, and corresponding significant decreases were observed in non-athlete controls after 36 h of sleep deprivation. Table tennis athletes showed a decrease in P3 amplitude and no significant difference in N2 and ERN amplitudes, after 36 h of sleep deprivation compared to the baseline state. Compared to non-athlete controls, table tennis athletes had better response inhibition, and the adverse effects of sleep deprivation on response inhibition occurred mainly in the later top-down motor inhibition process rather than in earlier automated conflict detection and monitoring.

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“…Chase et al demonstrated that a single night of sleep restriction had a significant negative impact on athletic performance the following morning (68), while Rae et al showed that even recovery from exercise was diminished after a single night of sleep deprivation (69). Concomitantly, two -night sleep deprivation affects executive function, as it causes central fatigue, signifying fewer high threshold motor units that can be recruited and, therefore, fewer muscle fibers will be activated to produce work (70).…”

Section: Fatiguementioning

confidence: 99%

Obstructive Sleep Apnea Syndrome: The Effect of Acute and Chronic Responses of Exercise

et al. 2021

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Obstructive Sleep Apnea Syndrome (OSAS) is a sleep disorder with high prevalence in general population, but alarmingly low in clinicians' differential diagnosis. We reviewed the literature on PubMed and Scopus from June 1980–2021 in order to describe the altered systematic pathophysiologic mechanisms in OSAS patients as well as to propose an exercise program for these patients. Exercise prevents a dysregulation of both daytime and nighttime cardiovascular autonomic function, reduces body weight, halts the onset and progress of insulin resistance, while it ameliorates excessive daytime sleepiness, cognitive decline, and mood disturbances, contributing to an overall greater sleep quality and quality of life.

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Effects of two nights of sleep deprivation on executive function and central and peripheral fatigue during maximal voluntary contraction lasting 60s

Cited by 20 publications

References 44 publications

Effects of 24-h acute total sleep deprivation on physiological coupling in healthy young adults

Effects of 24-h acute total sleep deprivation on physiological coupling in healthy young adults

Acute Sleep Deprivation Impairs Motor Inhibition in Table Tennis Athletes: An ERP Study

Obstructive Sleep Apnea Syndrome: The Effect of Acute and Chronic Responses of Exercise

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