The effect of sleep restriction, with or without high‐intensity interval exercise, on myofibrillar protein synthesis in healthy young men
Open accessAbstract
Key points: Sleep restriction has previously been associated with the loss of muscle mass in both human and animal models. The rate of myofibrillar protein synthesis (MyoPS) is a key variable in regulating skeletal muscle mass and can be increased by performing high‐intensity interval exercise (HIIE), although the effect of sleep restriction on MyoPS is unknown. In the present study, we demonstrate that participants undergoing a sleep restriction protocol (five nights, with 4 h in bed each night) had lower rates of skeletal muscle MyoPS; however, rates of MyoPS were maintained at control levels by performing HIIE during this period. Our data suggest that the lower rates of MyoPS in the sleep restriction group may contribute to the detrimental effects of sleep loss on muscle mass and that HIIE may be used as an intervention to counteract these effects. The present study aimed to investigate the effect of sleep restriction, with or without high‐intensity interval exercise (HIIE), on the potential mechanisms underpinning previously‐reported sleep‐loss‐induced reductions to muscle mass. Twenty‐four healthy, young men underwent a protocol consisting of two nights of controlled baseline sleep and a five‐night intervention period. Participants were allocated into one of three parallel groups, matched for age, , body mass index and habitual sleep duration; a normal sleep (NS) group [8 h time in bed (TIB) each night], a sleep restriction (SR) group (4 h TIB each night), and a sleep restriction and exercise group (SR+EX, 4 h TIB each night, with three sessions of HIIE). Deuterium oxide was ingested prior to commencing the study and muscle biopsies obtained pre‐ and post‐intervention were used to assess myofibrillar protein synthesis (MyoPS) and molecular markers of protein synthesis and degradation signalling pathways. MyoPS was lower in the SR group [fractional synthetic rate (% day –1 ), mean ± SD, 1.24 ± 0.21] compared to both the NS (1.53 ± 0.09) and SR+EX groups (1.61 ± 0.14) ( P < 0.05). However, there were no changes in the purported regulators of protein synthesis (i.e. p‐AKT ser473 and p‐mTOR ser2448 ) and degradation (i.e. Foxo1/3 mRNA and LC3 protein) in any group. These data suggest that MyoPS is acutely reduced by sleep restriction, although MyoPS can be maintained by performing HIIE. These findings may explain the sleep‐loss‐induced reductions in muscle mass previously reported and also highlight the potential therapeutic benefit of HIIE to maintain myofibrillar remodelling in this context.
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Written from the paper’s full text.
TL;DR
Five nights of sleep restriction (4 h time in bed/night) reduced myofibrillar protein synthesis (MyoPS) in healthy young men, but performing three sessions of high-intensity interval exercise (HIIE) during sleep restriction maintained MyoPS at normal-sleep levels. Molecular markers of protein synthesis and degradation signalling did not change in any group.
Key findings
- MyoPS was lower in the sleep restriction (SR) group [fractional synthetic rate (FSR), mean ± SD, 1.24 ± 0.21% day⁻¹] than in both normal sleep (NS; 1.53 ± 0.09% day⁻¹) and sleep restriction plus exercise (SR+EX; 1.61 ± 0.14% day⁻¹) groups (P < 0.05).
- Between-group differences: SR vs NS was −0.29 ± 0.08 FSR % day⁻¹ (95% CI −0.50 to −0.09, P = 0.004); SR vs SR+EX was −0.37 ± 0.09 FSR % day⁻¹ (95% CI −0.58 to −0.17, P < 0.001); NS vs SR+EX did not differ (0.08 ± 0.06 FSR % day⁻¹, 95% CI −0.29 to 0.12, P = 0.95).
- Sleep restriction reduced total sleep time versus baseline in SR (−224 ± 20 min) and SR+EX (−223 ± 9 min), and versus NS during intervention (SR −219 ± 8 min; SR+EX −214 ± 8 min; both P < 0.001).
- There were no changes in purported regulators of protein synthesis (p-AKTser473, p-mTORser2448) or degradation (Foxo1/3 mRNA, LC3 protein) in any group; Murf1 mRNA showed a significant interaction (P = 0.026) but no post hoc between-group differences.
Methods
- Twenty-four healthy, recreationally active young men (18–40 years) were allocated to three parallel groups matched for age, V̇O2peak, BMI and habitual sleep duration: NS (n = 8; 8 h TIB/night), SR (n = 8; 4 h TIB/night for five nights), and SR+EX (n = 8; 4 h TIB/night plus three HIIE sessions on days 4, 5 and 6).
- The protocol included two baseline sleep nights, a five-night intervention, and a final ad libitum recovery night; diet was standardized (carbohydrate 4.5 g kg⁻¹ day⁻¹, protein 1.5 g kg⁻¹ day⁻¹, fat 1 g kg⁻¹ day⁻¹), and HIIE consisted of 10 × 60 s cycling intervals at 90% Wpeak with 75 s active recovery.
- MyoPS was assessed by deuterium oxide tracer and muscle biopsies pre- and post-intervention, with FSR calculated from saliva and myofibrillar ²H enrichment; molecular markers were measured by western blotting and quantitative RT-PCR, with mixed ANOVA and one-way ANOVA used for statistical comparisons.
Limitations
- The paper states that it did not directly measure changes in muscle mass; the intervention was probably too short to detect lean mass changes by dual-energy X-ray absorptiometry, and future studies should include direct measures such as MRI or cross-sectional area.
- The paper states that it is unclear how the observed MyoPS rate compares with baseline MyoPS, that a normal sleep plus exercise group would have provided further mechanistic insight, and that findings may not generalize beyond young men without further research including female and older participants.
- Evident from the text: group sizes were small (n = 8 per group), the post-intervention biopsy occurred 48 h after the final exercise session so transient signalling changes may have been missed, p-p70S6Kthr389 could not be assessed because of antibody reliability issues, and RT-PCR data for the NS group included only seven participants because of limited muscle sample collection.
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Claims the paper makes
0 of 59 cited sources checked · 0 supported · 0 flagged
- Findingown data
Following five nights of sleep restriction (4 h TIB each night), the rate of myofibrillar protein synthesis (MyoPS) was significantly lower (by 19%) compared to the normal sleep (NS) and sleep restriction plus exercise (SR+EX) groups.
“We discovered that, following five nights of sleep restriction (4 h TIB, each night), the rate of MyoPS was significantly lower (by 19%) compared to the NS and SR+EX groups.”
Quote in the paperSubstantial claim - Findingown data
There was no difference in rates of MyoPS between the SR+EX and NS groups.
“whereas there was no difference in rates of MyoPS between the SR+HIIE and NS group.”
- Also stated in: § Conclusions · plain
“participants in the SR+EX group had higher rates of MyoPS than the SR group and were similar to those in the NS group.”
Quote in the paperSubstantial claim - Also stated in: § Conclusions · plain
- Findingown data
In healthy young men, myofibrillar protein synthesis (MyoPS) is higher after five nights of sleep restriction with three sessions of high-intensity interval exercise (SR+EX) than after sleep restriction alone (SR).
“Furthermore, MyoPS was significantly lower in the SR group compared to the SR+EX group (−0.37 ± 0.09 FSR % day–1, 95% CI = −0.58 to −0.17 FSR % day–1, P < 0.001).”
- Also stated in: § Abstract · plain
“MyoPS was lower in the SR group [fractional synthetic rate (% day–1), mean ± SD, 1.24 ± 0.21] compared to both the NS (1.53 ± 0.09) and SR+EX groups (1.61 ± 0.14) (P < 0.05).”
- Also stated in: § Key points · plain
“rates of MyoPS were maintained at control levels by performing HIIE during this period.”
Quote in the paperSubstantial claim - Also stated in: § Abstract · plain
- Findingown data
There was a significant interaction effect for Murf1 mRNA gene expression.
“Despite there being a significant interaction effect for Murf1 mRNA gene expression (P = 0.026)”
Quote in the paperNot a substantial claim - Findingown data
In healthy young men, there is no difference in myofibrillar protein synthesis (MyoPS) between normal sleep (NS) and sleep restriction with high-intensity interval exercise (SR+EX).
“There was no difference in MyoPS between the NS and SR+EX groups (0.08 ± 0.06 FSR % day–1, 95% CI = −0.29 to 0.12 FSR % day–1, P = 0.95).”
- Also stated in: § Key points · plain
“rates of MyoPS were maintained at control levels by performing HIIE during this period.”
Quote in the paperSubstantial claim - Also stated in: § Key points · plain
- Findingown data
Post hoc analyses revealed no difference between groups from pre to post-intervention for Murf1 mRNA expression.
“post hoc analyses revealed no difference between groups from pre to post‐intervention (NS: 61 ± 81%, 95% CI = −114 to −9%, P = 0.25), (SR: −26 ± 33%, 95% CI = −23 to 75%, P = 0.27), (SR+EX: −29 ± 35%, 95% CI = −20 to 28%, P = 0.20)”
Quote in the paperNot a substantial claim - Findingown data
There were no changes in the protein degradation markers Foxo1/3 mRNA and LC3 protein in any group.
“However, there were no changes in the purported regulators of protein synthesis (i.e. p‐AKTser473 and p‐mTORser2448) and degradation (i.e. Foxo1/3 mRNA and LC3 protein) in any group.”
Quote in the paperNot a substantial claim - Findingown data
There was no significant interaction effect for mRNA gene expression of Foxo1, Foxo3, Myostatin, Mafbx, Mighty, or p62/SQSTM1 compared to pre-intervention values.
“There was no significant interaction effect for mRNA gene expression of Foxo1 (P = 0.69), Foxo3 (P = 0.74), Myostatin (P = 0.19), Mafbx (P = 0.24), Mighty (P = 0.81) or p62/SQSTM1 (P = 0.09) compared to pre‐intervention values.”
Quote in the paperNot a substantial claim - Findingown data
There were no changes in molecular markers commonly used to indicate activation of the protein synthesis and degradation pathways.
“There were, however, no changes in molecular markers that are commonly used to indicate activation of the protein synthesis and degradation pathways.”
- Also stated in: § Molecular markers of protein turnover · plain
“In the present study, there were no detectable changes in mRNA expression or protein content of markers of either the protein synthesis or degradation signalling pathways (i.e. AKT‐mTOR‐p70S6K, UPS and autophagy pathways).”
Quote in the paperSubstantial claim - Also stated in: § Molecular markers of protein turnover · plain
- Findingown data
In healthy young men, myofibrillar protein synthesis (MyoPS) is lower after five nights of sleep restriction (4 h time in bed per night) than after normal sleep (8 h time in bed per night).
“MyoPS was lower in the SR group [fractional synthetic rate (% day–1), mean ± SD, 1.24 ± 0.21] compared to both the NS (1.53 ± 0.09) and SR+EX groups (1.61 ± 0.14) (P < 0.05).”
- Also stated in: § MyoPS · plain
“Compared to the NS group, the myofibrillar protein FSR was significantly lower [mean ± SD between‐group difference FSR (% day–1), 95% CI, P value] in the SR group; –0.29 ± 0.08 FSR % day–1, 95% CI [−0.50, −0.09 FSR % day–1], P = 0.004) (Fig. 2).”
- Also stated in: § Key points · plain
“participants undergoing a sleep restriction protocol (five nights, with 4 h in bed each night) had lower rates of skeletal muscle MyoPS”
Quote in the paperSubstantial claim - Also stated in: § MyoPS · plain
- Findingown data
There were no changes in the protein synthesis regulators p-AKTser473 and p-mTORser2448 in any group.
“However, there were no changes in the purported regulators of protein synthesis (i.e. p‐AKTser473 and p‐mTORser2448) and degradation (i.e. Foxo1/3 mRNA and LC3 protein) in any group.”
Quote in the paperSubstantial claim - Findingown data
In the present study, there were no detectable changes in mRNA expression or protein content of markers of either the protein synthesis or degradation signalling pathways (AKT-mTOR-p70S6K, UPS, and autophagy pathways).
“In the present study, there were no detectable changes in mRNA expression or protein content of markers of either the protein synthesis or degradation signalling pathways (i.e. AKT‐mTOR‐p70S6K, UPS and autophagy pathways).”
Quote in the paperSubstantial claim - Findingcitation
The rate of MyoPS was higher in the SR+EX group compared to the SR group.
“The results of the present study demonstrate that the rate of MyoPS was higher in the SR+EX group compared to the SR group.”
Quote in the paperSubstantial claim - Findingown data
The present study showed that, even in the exercise group, there were no changes to MPS and MPB signalling.
“Indeed, the present study showed that, even in the exercise group, there were no changes to MPS and MPB signalling.”
Quote in the paperSubstantial claim - Interpretationown data
Myofibrillar protein synthesis (MyoPS) is acutely reduced by sleep restriction.
“These data suggest that MyoPS is acutely reduced by sleep restriction, although MyoPS can be maintained by performing HIIE.”
Quote in the paperSubstantial claim - Study design and conductown data
There were no statistically significant differences between the three groups for any of the baseline characteristics.
“There were no statistically significant differences between the three groups for any of the baseline characteristics.”
Quote in the paperNot a substantial claim - Interpretationreasoning
The period of five nights of 4 h TIB was probably too short to detect any meaningful reductions in muscle mass or muscle fibre cross-sectional area.
“This period of time was probably too short to detect any meaningful reductions in muscle mass or muscle fibre cross‐sectional area (CSA).”
Quote in the paperSubstantial claim - Premisecitation
Sleep restriction has previously been associated with the loss of muscle mass in both human and animal models.
“Sleep restriction has previously been associated with the loss of muscle mass in both human and animal models.”
- Also stated in: § Introduction · plain
“Sleep has also been causatively implicated in the maintenance of muscle mass (Nedeltcheva et al. 2010; Dattilo et al. 2012), with an increased likelihood of both sarcopenia and lower total skeletal muscle mass in those reporting insufficient (i.e. <7 h per night) or poor sleep quality (Chien et al. 2015; Buchmann et al. 2016; Hu et al. 2017).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Nedeltcheva et al. 2010
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- cites Dattilo et al. 2012
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- Also stated in: § Introduction · plain
- Study design and conductown data
Both sleep-restricted groups had a reduction in total sleep time (TST) during their respective interventions compared to the baseline period.
“Both sleep‐restricted groups had a reduction in TST during their respective interventions compared to the baseline period (SR; –224 ± 20 min, 95% CI = −241 to −203 min, P < 0.001; SR+EX −223 ± 9 min, 95% CI = −242 to −204 min, P < 0.001).”
Quote in the paperSubstantial claim - Study design and conductown data
There were no between-group differences for baseline total sleep time (TST).
“There were no between‐group differences for baseline TST [mean ± SD TST (min) of nights 1 and 2, P value, NS; 448 ± 25 min, SR; 452 ± 17 min, and SR+EX; 459 ± 9 min, P = 0.50].”
Quote in the paperNot a substantial claim - Premisecitation
High-intensity interval exercise (HIIE) is capable of inducing muscle protein synthesis and its associated signalling pathways.
“Although resistance exercise is regarded as the most potent stimulus to induce skeletal muscle protein synthesis, high‐intensity interval exercise (HIIE) is also capable of inducing muscle protein synthesis, and its associated signalling pathways (Miller et al. 2005; Di Donato et al. 2014; Bell et al. 2015).”
Quote in the paperSubstantial claim0 of 3 sources checked- cites Miller et al. 2005
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- cites Di Donato et al. 2014
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- cites Bell et al. 2015
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- Premisecitation
Rates of protein synthesis are the primary driving mechanism for changes in muscle mass (atrophy and hypertrophy).
“Rates of protein synthesis are considered the primary driving mechanism for changes in muscle mass (atrophy and hypertrophy) (Rennie, 1985; Gibson et al. 1987; de Boer et al. 2007).”
Quote in the paperSubstantial claim0 of 3 sources checked- cites Rennie, 1985
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- cites Gibson et al. 1987
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- cites de Boer et al. 2007
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- Study design and conductown data
The normal sleep (NS) group showed no difference in total sleep time (TST) between the baseline and intervention periods.
“The NS group showed no difference in TST between the baseline and intervention periods [mean ± SD difference (min), 95% CI min, P value, 1 ± 28 min, 95% CI = –20 to 17 min, P > 0.99].”
Quote in the paperNot a substantial claim - Interpretationown data
High-intensity interval exercise (HIIE) may be used as an intervention to counteract the detrimental effects of sleep loss on muscle mass.
“Our data suggest that the lower rates of MyoPS in the sleep restriction group may contribute to the detrimental effects of sleep loss on muscle mass and that HIIE may be used as an intervention to counteract these effects.”
- Also stated in: § Abstract · hedged
“These findings may explain the sleep‐loss‐induced reductions in muscle mass previously reported and also highlight the potential therapeutic benefit of HIIE to maintain myofibrillar remodelling in this context.”
Quote in the paperSubstantial claim - Also stated in: § Abstract · hedged
- Premisecitation
Persistent reductions in MyoPS are associated with the loss of muscle mass, as reported with a variety of muscle disuse conditions (step reduction, limb immobilization, and bed rest).
“However, persistent reductions in MyoPS are associated with the loss of muscle mass, as have been reported with a variety of muscle disuse conditions (i.e. step reduction, limb immobilization and bed rest) (de Boer et al. 2007; Breen et al. 2013).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites de Boer et al. 2007
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- cites Breen et al. 2013
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- Study design and conductown data
Compared to the normal sleep (NS) group, total sleep time (TST) during the intervention period was significantly reduced in both the sleep restriction (SR) and sleep restriction plus exercise (SR+EX) groups.
“Compared to the NS group, TST during the intervention period was significantly reduced in both the SR group (−219 ± 8 min, 95% CI = −236 to −202 min, P < 0.001) and SR+EX group (−214 ± 8 min, 95% CI = −231.5 to −197 min, P < 0.001).”
Quote in the paperSubstantial claim - Premisecitation
Changes in muscle mass are, in the short-term (days to weeks), largely determined by the balance between the rates of muscle protein synthesis (MPS) and muscle protein breakdown (MPB).
“Changes in muscle mass are, in the short‐term (i.e. days to weeks), largely determined by the balance between the rates of muscle protein synthesis (MPS) and muscle protein breakdown (MPB) (Rennie, 1985; Gibson et al. 1987).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Rennie, 1985
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- cites Gibson et al. 1987
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- Interpretationown data
The lower rates of myofibrillar protein synthesis (MyoPS) in the sleep restriction group may contribute to the detrimental effects of sleep loss on muscle mass.
“Our data suggest that the lower rates of MyoPS in the sleep restriction group may contribute to the detrimental effects of sleep loss on muscle mass and that HIIE may be used as an intervention to counteract these effects.”
- Also stated in: § Abstract · hedged
“These findings may explain the sleep‐loss‐induced reductions in muscle mass previously reported and also highlight the potential therapeutic benefit of HIIE to maintain myofibrillar remodelling in this context.”
Quote in the paperSubstantial claim - Also stated in: § Abstract · hedged
- Study design and conductown data
There were no significant differences in total sleep time (TST) between the sleep restriction (SR) and sleep restriction plus exercise (SR+EX) groups during the intervention period.
“There were no significant differences in TST between the SR and SR+EX groups during the intervention period (−5 ± 3 min, 95% CI = −23 to 12 min, P = 0.72).”
Quote in the paperNot a substantial claim - Interpretationown data
Myofibrillar protein synthesis (MyoPS) can be maintained by performing high-intensity interval exercise (HIIE) during sleep restriction.
“These data suggest that MyoPS is acutely reduced by sleep restriction, although MyoPS can be maintained by performing HIIE.”
- Also stated in: § Key points · plain
“rates of MyoPS were maintained at control levels by performing HIIE during this period.”
Quote in the paperSubstantial claim - Also stated in: § Key points · plain
- Premisecitation
During periods of energy deficit, a disproportionately greater loss of muscle mass has been reported in humans following sleep restriction (5.5 h time in bed each night for 14 days) compared to normal sleep (8.5 h time in bed each night for 14 days).
“During periods of energy deficit, a disproportionately greater loss of muscle mass has been reported in humans following sleep restriction [5.5 h time in bed (TIB) each night for 14 days] compared to normal sleep (8.5 h TIB each night for 14 days) (Nedeltcheva et al. 2010).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Nedeltcheva et al. 2010
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- Premisecitation
Several studies have reported increases in phosphorylation of AKTser473, mTORser2448 and decreases in eEF2thr56 protein immediately following an endurance exercise session, with levels returning to baseline within 3-4.5 h.
“In the context of exercise, several studies have reported increases in phosphorylation of AKTser473, mTORser2448 and decreases in eEF2thr56 protein, immediately following an endurance exercise session, with levels returning to baseline within 3–4.5 h (Mascher et al. 2007; Di Donato et al. 2014).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Mascher et al. 2007
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- cites Di Donato et al. 2014
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- Premisecitation
Increases in MyoPS have also been observed with endurance exercise (and in particular, HIIE), although the findings appear to be somewhat protocol-dependent.
“However, increases in MyoPS (which may also be associated with skeletal muscle remodelling) have also been observed with endurance exercise (and in particular, HIIE), although the findings appear to be somewhat protocol‐dependent (Di Donato et al. 2014; Konopka & Harber, 2014).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Di Donato et al. 2014
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- cites Konopka & Harber, 2014
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- Premisecitation
Although MPB increases following resistance exercise, it returns to resting values within 48 h.
“Furthermore, although MPB increases following resistance exercise, it returns to resting values within 48 h (Phillips et al. 1997; Kumar et al. 2009).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Phillips et al. 1997
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- cites Kumar et al. 2009
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- Interpretationown data
There was a dissociation between the changes in MyoPS and the molecular signalling pathways that regulate protein synthesis and degradation.
“However, there was a dissociation between the changes in MyoPS and the molecular signalling pathways that regulate protein synthesis and degradation.”
Quote in the paperSubstantial claim - Interpretationown data
Sleep restriction can have detrimental effects on the processes that maintain muscle mass, via the potential suppression of MyoPS.
“Although further investigations are needed, these findings suggest that sleep restriction can have detrimental effects on the processes that maintain muscle mass, via the potential suppression of MyoPS.”
Quote in the paperSubstantial claim - Interpretationcitation
The current intervention duration was probably too short to detect changes in lean mass with dual-energy X-ray absorptiometry, given the variability of the measure.
“Nevertheless, the current intervention duration was probably too short to detect changes in lean mass with dual‐energy X‐ray absorptiometry (given the variability of the measure) (Bone et al., 2017)”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Bone et al., 2017
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- Interpretationown data
HIIE could be a viable intervention to mitigate certain detrimental effects associated with sleep loss.
“Our observation that those participants performing HIIE during the SR intervention were able to maintain their rates of MyoPS at levels comparable to the NS group could have important implications for a range of populations experiencing inadequate sleep and lends support to the idea that HIIE could be a viable intervention to mitigate certain detrimental effects associated with sleep loss.”
Quote in the paperSubstantial claim - Interpretationown data
Sleep restriction can inhibit MyoPS.
“Because the SR group had rates of MyoPS that were ∼19% lower than that of the NS or SR+HIIE groups, it may be proposed that sleep restriction can inhibit MyoPS.”
Quote in the paperSubstantial claim - Interpretationcitation
Given the post-intervention biopsy occurred 48 h following the final exercise session, any changes in signalling markers may no longer have been detectable.
“Given our post‐intervention biopsy occurred 48 h following the final exercise session, any changes in signalling markers may no longer have been detectable.”
Quote in the paperSubstantial claim - Interpretationown data
The findings may partly help to explain previous reports of reduced muscle mass in those experiencing insufficient sleep.
“Our findings may partly help to explain previous reports of reduced muscle mass in those experiencing insufficient sleep (Nedeltcheva et al. 2010).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Nedeltcheva et al. 2010
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- Interpretationcitation
The absence of changes to the MPS and MPB signalling pathways may be explained by the transient nature of their regulation and in relation to biopsy timing.
“Furthermore, the absence of changes to the MPS and MPB signalling pathways may be explained by the transient nature of their regulation and in relation to biopsy timing, which has previously been demonstrated in different contexts (de Boer et al. 2007; Atherton et al. 2010).”
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- Interpretationown data
The comparable rates of MyoPS in the SR+EX and NS groups support previous findings that implicate HIIE as a potent stimulus for MyoPS.
“However, the comparable rates of MyoPS in the SR+EX and NS groups support previous findings that implicate HIIE as a potent stimulus for MyoPS.”
Quote in the paperSubstantial claim - Interpretationcitation
The higher MyoPS observed in the SR+EX group compared to the SR group is probably explained by aerobic exercise induced increases in MyoPS.
“The higher MyoPS observed in the SR+EX group compared to the SR group is probably explained by aerobic exercise induced increases in MyoPS (Miller et al. 2005; Di Donato et al. 2014; Bell et al. 2015).”
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- Premisecitation
Similar to the present study, no change in key regulators of the protein synthesis pathway (p-mTORser2448 or p-p70S6Kthr389) were reported following 96 h of sleep deprivation in rats, despite reductions in muscle fibre CSA.
“Similar to the present study, no change in key regulators of the protein synthesis pathway (i.e. p‐mTORser2448 or p‐p70S6Kthr389) were reported following 96 h of sleep deprivation in rats, despite reductions in muscle fibre CSA (Monico‐Neto et al. 2015a ; de Sa Souza et al. 2016).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Monico‐Neto et al. 2015a
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- cites de Sa Souza et al. 2016
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- May combine two claims. 10
- Classified as probably not a substantial claim. 16
May combine two claims.
Findingown dataThere were no changes in protein content of p-AKTser473/AKT (total), p-mTORser2448/mTOR (total), p70S6K, Caspase 3, p-4EBP1thr37/46, p-TSC2thr1462/TSC2 (total), LC3BII:I ratio, or NFκB from pre- to post-intervention.
“There were no changes in p‐AKTser473/AKT (total) (P = 0.15), p‐mTORser2448/mTOR (Total) (P = 0.15), p70S6K (P = 0.28), Caspase 3 (P = 0.19), p‐4EBP1thr37/46 (P = 0.67), p‐TSC2thr1462/TSC2 (Total) (P = 0.29), LC3BII:I ratio (P = 0.88) or NFκB (P = 0.72) protein content from pre‐ to post‐intervention (Fig. 4).”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
PremisecitationReductions in muscle protein synthesis (MPS), and specifically myofibrillar protein synthesis (MyoPS), rather than increases in muscle protein breakdown (MPB), underlie muscle loss induced by interventions such as muscle disuse, limb immobilization and step reduction.
“Interventions known to induce loss of muscle mass (such as muscle disuse, limb immobilization and step reduction) suggest that reductions in MPS, and specifically myofibrillar protein synthesis (MyoPS), rather than increases in MPB, underlie these changes (Symons et al. 2009; Breen et al. 2013; Rudrappa et al. 2016).”
Quote in the paperSubstantial claim0 of 3 sources checked- cites Symons et al. 2009
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- cites Breen et al. 2013
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- cites Rudrappa et al. 2016
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Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationSleep was assessed using wrist-watch activity devices with a validated automated scoring algorithm.
“Sleep was assessed using wrist‐watch activity devices worn on the non‐dominant wrist (Actiwatch 2; Philips Respironics, Murrysville, PA, USA) with device activity sensitivity set to medium (40 activity counts per 30 s epoch) (Kosmadopoulos et al. 2014; Sargent et al. 2016), collected at 32 Hz and scored using a validated automated scoring algorithm (Oakley, 1997).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Oakley, 1997
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Classified as probably not a substantial claim.
PremisecitationPrevious reports have shown reductions in muscle mass when obtaining insufficient sleep.
“Previous reports have shown reductions in muscle mass when obtaining insufficient sleep (Nedeltcheva et al. 2010; Dattilo et al. 2012; de Sa Souza et al. 2016)”
Quote in the paperSubstantial claim0 of 3 sources checked- cites Nedeltcheva et al. 2010
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- cites Dattilo et al. 2012
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- cites de Sa Souza et al. 2016
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Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationProtein synthesis is regulated via activation of the AKT-mTOR-p70S6K signalling pathway, which subsequently leads to increases in strength and muscle mass over time.
“At the molecular level, protein synthesis is regulated via the activation of the AKT‐mTOR‐p70S6K signalling pathway, which subsequently leads to increases in strength and muscle mass over time (Bodine et al. 2001).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Bodine et al. 2001
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenParticipants were monitored at all times throughout the study by a member of the research team to ensure adherence to the protocol.
“Participants were monitored at all times throughout the study by a member of the research team to ensure adherence to the protocol.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataThere were no significant differences between daily step counts, habitually and within the study protocol, in any of the groups.
“There were no significant differences between daily step counts, habitually and within the study protocol, in any of the groups.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductcitationThe fractional synthetic rate (FSR) of myofibrillar protein synthesis (MyoPS) was assessed via the D2O tracer technique as previously reported.
“The fractional synthetic rate (FSR) of MyoPS was assessed via the D2O tracer technique as previously reported (Wilkinson et al. 2014).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Wilkinson et al. 2014
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPrevious interventions where MyoPS is reduced in response to step reduction have suggested the development of an 'anabolic resistance', such that the amino acid-induced stimulation of MyoPS is blunted.
“Previous interventions where MyoPS is reduced in response to step reduction have suggested the development of an ‘anabolic resistance’, such that the amino acid‐induced stimulation of MyoPS is blunted (Breen et al. 2013).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Breen et al. 2013
Not checked in the free run.
May combine two claims.
Interpretationown dataThe capacity for HIIE to promote MyoPS and the findings of the present study suggest that HIIE may be capable of maintaining regular rates of MyoPS during periods of sleep restriction.
“Given the capacity for HIIE to promote MyoPS (Di Donato et al. 2014; Bell et al. 2015) and the findings of the present study suggesting that HIIE may be capable of maintaining regular rates of MyoPS during periods of sleep restriction”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Di Donato et al. 2014
Not checked in the free run.
- cites Bell et al. 2015
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May combine two claims.
InterpretationreasoningWhen taken together with previous literature, changes in the molecular signalling pathways for MPS and MPB probably occur during the earlier stages of the sleep intervention or accumulated throughout the day as the homeostatic drive for sleep increased (rather than the hours immediately following sleep) and/or in the hours immediately following HIIE.
“When taken together with previous literature, this probably means that changes in the molecular signalling pathways for MPS and MPB occur during the earlier stages of the sleep intervention or accumulated throughout the day as the homeostatic drive for sleep increased (rather than the hours immediately following sleep) and/or in the hours immediately following HIIE (de Boer et al. 2007; Greenhaff”
Quote in the paperSubstantial claim0 of 3 sources checked- cites de Boer et al. 2007
Not checked in the free run.
- cites Greenhaff et al. 2008
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- cites Atherton et al. 2010
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationResistance exercise is well known to increase rates of MyoPS in skeletal muscle with subsequent increases in muscle mass.
“Resistance exercise is well known to increase rates of MyoPS in skeletal muscle with subsequent increases in muscle mass suggesting this exercise modality warrants further investigation in the context of sleep loss (Konopka & Harber, 2014; Brook et al. 2015; Brook et al. 2016; Robinson et al. 2017).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites Konopka & Harber, 2014
Not checked in the free run.
- cites Brook et al. 2015
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- cites Brook et al. 2016
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Probably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).
Study design and conductnone givenThe addition of a normal sleep and exercise group may have provided further mechanistic insight into the effect of sleep restriction and HIIE on MyoPS.
“Furthermore, as eluded to previously, the addition of a normal sleep and exercise group may have provided further mechanistic insight into the effect of sleep restriction and HIIE on MyoPS.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationThe lower rate of MyoPS reported in the present study aligns with previous observations of decreases in muscle fibre CSA in rodents following 96 h of sleep deprivation and increased loss of muscle mass with sleep restriction in humans.
“As such, the lower rate of MyoPS reported here aligns with observations of decreases in muscle fibre CSA, reported previously in rodents (following 96 h of sleep deprivation) (Dattilo et al. 2012; Monico‐Neto et al. 2015a ; de Sa Souza et al. 2016) and increased loss of muscle mass with sleep restriction in humans (Nedeltcheva et al. 2010).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites Dattilo et al. 2012
Not checked in the free run.
- cites Monico‐Neto et al. 2015a
Not checked in the free run.
- cites de Sa Souza et al. 2016
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Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationThese same studies reported an increase in markers of the UPS and autophagy signalling pathways (p-FOXO3, LC3, and p62/SQSTM protein content), indicating that sleep deprivation increases MPB in rats.
“By contrast to our findings, however, these same studies reported an increase in markers of the UPS and autophagy signalling pathways (i.e. p‐FOXO3, LC3 and p62/SQSTM protein content) (Monico‐Neto et al. 2015a ; de Sa Souza et al. 2016) indicating that sleep deprivation increases MPB in rats.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Monico‐Neto et al. 2015a
Not checked in the free run.
- cites de Sa Souza et al. 2016
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Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe prevalence of sarcopenia in older adults (>65 years of age) is increased in those who report sleeping <6 h per night.
“Furthermore, the prevalence of sarcopenia in older adults (>65 years of age) is increased in those who report sleeping <6 h per night (Chien et al. 2015; Buchmann et al. 2016; Hu et al. 2017).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites Chien et al. 2015
Not checked in the free run.
- cites Buchmann et al. 2016
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- cites Hu et al. 2017
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May combine two claims.
PremisecitationMiller et al. (2005) reported increases in MyoPS following 1 h of single-leg kicking (67% W max), which remained elevated at 48 and 72 h post-exercise.
“Indeed, Miller et al. (2005) reported increases in MyoPS following 1 h of single‐leg kicking (67% W max), which remained elevated at 48 and 72 h post‐exercise.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Miller et al. (2005)
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningWith the present study design, it is unclear how the observed lower rate of MyoPS with sleep restriction compares to baseline rates of MyoPS.
“Although our data report a significantly lower rate of MyoPS (∼19%) with sleep restriction, with the present study design, it is unclear how this compares to baseline rates of MyoPS.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationPrevious research has observed dual-energy X-ray absorptiometry-derived losses in fat-free soft tissue mass across a 14-day sleep restriction period, although the magnitude of this effect was probably enhanced by the calorie-restricted diet employed.
“Previous research has observed dual‐energy X‐ray absorptiometry‐derived losses in fat‐free soft tissue mass across a 14‐day sleep restriction period, although the magnitude of this effect was probably enhanced by the calorie‐restricted diet employed (Nedeltcheva et al. 2010).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Nedeltcheva et al. 2010
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationAlthough some evidence supports corresponding changes in MyoPS and its associated signalling responses, dissociations similar to those reported in the present study are not uncommon.
“Although some evidence supports corresponding changes in MyoPS and its associated signalling responses (Brook et al. 2015), dissociations similar to those reported in the present study are not uncommon (de Boer et al. 2007; Greenhaff et al. 2008; Atherton et al. 2010).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites Brook et al. 2015
Not checked in the free run.
- cites de Boer et al. 2007
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- cites Greenhaff et al. 2008
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Classified as probably not a substantial claim.
Study design and conductnone givenThe present study did not employ direct measurements of changes in muscle mass.
“Although previous research suggests that alterations to MyoPS underlie changes in muscle mass (Rennie, 1985; Gibson et al. 1987; de Boer et al. 2007), the present study did not employ direct measurements of changes in muscle mass.”
Quote in the paperSubstantial claim
The paper relies on this without support.
No study to date has investigated the effects of sleep restriction on muscle protein synthesis (MPS), in whole or fractionated human skeletal muscle, or the potential catabolic influence of sleep restriction on markers of muscle protein breakdown (MPB).
“Nonetheless, no study to date has investigated the effects of sleep restriction on MPS, in whole or fractionated human skeletal muscle, or the potential catabolic influence of sleep restriction on markers of MPB.”
The paper relies on this without support.
The effects of sleep restriction and high-intensity interval exercise (HIIE) on myofibrillar protein synthesis (MyoPS) and its associated signalling pathways have not previously been investigated in humans.
“The effects of sleep restriction and HIIE on MyoPS and its associated signalling pathways have not previously been investigated in humans.”
The paper relies on this without support.
The effect of sleep restriction on myofibrillar protein synthesis (MyoPS) is unknown.
“although the effect of sleep restriction on MyoPS is unknown.”
The authors state this as an assumption.
The present study is the first to demonstrate a lower rate of MyoPS in a sleep restriction group following 4 h TIB for five consecutive nights, and the first observation of a sleep-restriction-induced change in MyoPS in humans.
“however, the present study is the first to demonstrate a lower rate of MyoPS in a SR group following 4 h TIB for five consecutive nights.”
“To our knowledge, this is the first observation of a sleep‐restriction‐induced change in MyoPS in humans.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Five consecutive nights of sleep restriction (4 hr per night) reduced myofibrillar protein synthesis in healthy young males compared with normal sleep patterns.
“To expand on this acute model, investigators recently demonstrated that five consecutive nights of sleep restriction (4 hr per night) reduced myofibrillar protein synthesis in healthy young males when compared to normal sleep patterns (Saner et al., 2020).”
From The effect of acute sleep deprivation on skeletal muscle protein synthesis and the hormonal environment (2021) · cites this paper as Saner et al., 2020
The findings support those by Saner et al. that sleep restriction reduces muscle protein synthesis.
“Despite employing a different stable isotope (phenylalanine vs. deuterated water), study design (acute cross‐over design vs. chronic parallel design), and population (males and females vs. males only), our findings support those by Saner et al.”
From The effect of acute sleep deprivation on skeletal muscle protein synthesis and the hormonal environment (2021) · cites this paper as Saner et al., 2020
Habitual daily step counts were monitored using validated step-counting applications and replicated throughout the study.
“Habitual daily step counts were monitored using validated step-counting applications on the participants’ personal mobile phone devices (i-Health app, Apple Inc., Cupertino, CA, USA; and Samsung Health, Samsung Electronics Co., Ltd., Suwon, South Korea) and these step counts were replicated throughout the study (Supplementary Table 1) (data modified from [36]).”
From Exercise mitigates sleep-loss-induced changes in glucose tolerance, mitochondrial function, sarcoplasmic protein synthesis, and diurnal rhythms (2021) · cites this paper as [36]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Discussion contradicts introduction on the cited rat study's mTOR result
MinorThe introduction says de Sa Souza et al. reported increased p‐mTORser2448 after 96 hours of sleep deprivation. The discussion instead includes that study among reports of no change in p‐mTORser2448.
“or an increase in p‐mTORser2448 and p‐4EBP1ser65 (de Sa Souza et al. 2016) were observed in rodent skeletal muscle.”
“no change in key regulators of the protein synthesis pathway (i.e. p‐mTORser2448 or p‐p70S6Kthr389) were reported following 96 h of sleep deprivation in rats, despite reductions in muscle fibre CSA (Monico‐Neto et al. 2015a ; de Sa Souza et al. 2016).”
TSC2 phosphorylation site differs between results and figure
MinorThe results identify the measured TSC2 phosphorylation site as thr1462, but the caption for the corresponding panel labels it thr462.
“p‐TSC2thr1462/TSC2 (Total) (P = 0.29)”
“p‐TSC2thr462/TSC2 (total) (C)”
NS Murf1 estimate falls outside its reported confidence interval
MinorThe NS change is reported as positive 61%, whereas its stated 95% confidence interval runs from −114% to −9% and does not contain that estimate.
“NS: 61 ± 81%”
“95% CI = −114 to −9%”
NS-SR+EX confidence interval is centred on the opposite-signed difference
MinorThe reported difference is +0.08, but the midpoint of its stated confidence interval is −0.085. The interval appears to use the opposite direction of subtraction from the reported difference.
Reported 0.08 · recomputed -0.085
“There was no difference in MyoPS between the NS and SR+EX groups (0.08 ± 0.06 FSR % day–1, 95% CI = −0.29 to 0.12 FSR % day–1, P = 0.95).”
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Acute Sleep Restriction Affects Sport-Specific But Not Athletic Performance in Junior Tennis Players
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The Sleep, Recovery, and Nutrition Characteristics of Elite Adolescent Athletes
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The Development and Evaluation of a Training Monitoring System for Amateur Rugby Union
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Rest, Repair, Repeat: The Complex Relationship of Autophagy and Sleep
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Links Between Autophagy and Healthy Aging
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No time to sleep on it – start exercising!
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Social jetlag alters markers of exercise-induced mitochondrial adaptations in the heart
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Sarcopenia Seems to Be Common in Older Patients With Restless Legs Syndrome
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Linking Biomarkers with Causes, Lifestyle Factors, and Management of Sarcopenia
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Intentional Weight Gain Strategies in Young Adult Athletic Individuals
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Sleep, exercise, and insulin sensitivity
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Can you out‐exercise a bad sleep? A muscle‐centric view
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Perfil del patrón de sueño en deportistas universitarios
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An examination of injury risk and subjective measures of training in amateur Rugby Union
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Some Australian Open matches run extremely late. How would that impact player sleep and recovery?
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Sleep Quality and Falls Risk in the ELSA Study: A Cross‐Sectional and Prospective Cohort Study
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- Authors
- Saner, N. J., Lee, M. J. ‐., Pitchford, N. W., Kuang, J., Roach, G. D., Garnham, A., Stokes, T., Phillips, S. M., Bishop, D. J., & Bartlett, J. D.
- Affiliations
- Victoria University (AU)
- University of Tasmania (AU)
- Central Queensland University (AU)
- McMaster University (CA)
- Edith Cowan University (AU)
- Corresponding author
- Bartlett, Jonathan D.
- ORCID
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 2020-03-11
- Volume
- 598
- Issue
- 8
- Pages
- 1523-1536
- ISSN
- 0022-3751 (ISSN-L)
- 1469-7793
- PMC
- PMC7217042
- OpenAlex
- W3008175177
- Semantic Scholar
- 8f2bfe762f7e6ba15ceff15eac4ce7f4c2d51bd1
- Cited by
- 68
- References
- 56
- Citations by year
- 2026: 11 · 2025: 9 · 2024: 11 · 2023: 9 · 2022: 6 · 2021: 15 · 2020: 7
- FWCI
- 4.61
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- The Journal of Physiology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- UTAS Research Repository (acceptedVersion)
- Victoria University Research Repository (Victoria University) (submittedVersion, cc-by)
- Australasian Journal of Paramedicine (submittedVersion, cc-by)
- Deakin Research Online (Deakin University) (submittedVersion)
- Figshare (submittedVersion, cc-by)
- Figshare (submittedVersion)
- Funders
- Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada (No number)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
- Keywords
- sleep restriction, high-intensity interval exercise, myofibrillar protein synthesis, skeletal muscle mass, muscle protein synthesis, protein degradation, mTOR signaling, Akt signaling, LC3, sleep deprivation, exercise countermeasures, healthy young men, muscle biopsy, time in bed
- MeSH terms
- Humans, Male, Myofibrils, Sleep, Protein Biosynthesis, Exercise, Muscle, Skeletal
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