scholarly journals The relationship between fasting-induced torpor, sleep and waking in laboratory mice

SLEEP ◽  
2021 ◽  
Author(s):  
Yi-Ge Huang ◽  
Sarah J Flaherty ◽  
Carina A Pothecary ◽  
Russell G Foster ◽  
Stuart N Peirson ◽  
...  
Keyword(s):  
Body Temperature ◽  
Rem Sleep ◽  
Brain Activity ◽  
Mammalian Species ◽  
Nrem Sleep ◽  
Laboratory Mice ◽  
State Classification ◽  
Metabolic Suppression ◽  
The Relationship ◽  
Electroencephalogram Eeg

Abstract Study objectives Torpor is a regulated and reversible state of metabolic suppression used by many mammalian species to conserve energy. Whereas the relationship between torpor and sleep has been well-studied in seasonal hibernators, less is known about the effects of fasting-induced torpor on states of vigilance and brain activity in laboratory mice. Methods Continuous monitoring of electroencephalogram (EEG), electromyogram (EMG) and surface body temperature was undertaken in adult, male C57BL/6 mice over consecutive days of scheduled restricted feeding. Results All animals showed bouts of hypothermia that became progressively deeper and longer as fasting progressed. EEG and EMG were markedly affected by hypothermia, although the typical electrophysiological signatures of NREM sleep, REM sleep and wakefulness enabled us to perform vigilance-state classification in all cases. Consistent with previous studies, hypothermic bouts were initiated from a state indistinguishable from NREM sleep, with EEG power decreasing gradually in parallel with decreasing surface body temperature. During deep hypothermia, REM sleep was largely abolished, and we observed shivering-associated intense bursts of muscle activity. Conclusions Our study highlights important similarities between EEG signatures of fasting-induced torpor in mice, daily torpor in Djungarian hamsters and hibernation in seasonally-hibernating species. Future studies are necessary to clarify the effects on fasting-induced torpor on subsequent sleep.

scholarly journals The relationship between fasting-induced torpor, sleep and wakefulness in the laboratory mouse

2020 ◽  
Author(s):  
Yi G. Huang ◽  
Sarah J. Flaherty ◽  
Carina A. Pothecary ◽  
Russell G. Foster ◽  
Stuart N. Peirson ◽  
...  
Keyword(s):  
Body Temperature ◽  
Rem Sleep ◽  
Brain Activity ◽  
Mammalian Species ◽  
Laboratory Mouse ◽  
Nrem Sleep ◽  
Early Ontogeny ◽  
State Classification ◽  
The Relationship ◽  
Electroencephalogram Eeg

AbstractTorpor is a regulated reversible state of metabolic suppression used by many mammalian species to conserve energy. Although torpor has been studied extensively in terms of general physiology, metabolism and neuroendocrinology, the effects of hypometabolism and associated hypothermia on brain activity and states of vigilance have received little attention. Here we performed continuous monitoring of electroencephalogram (EEG), electromyogram (EMG) and peripheral body temperature in adult, male C57BL/6 mice over consecutive days of scheduled restricted feeding. All animals showed prominent bouts of hypothermia that became progressively deeper and longer as fasting progressed. EEG and EMG were markedly affected by hypothermia, although the typical electrophysiological signatures of NREM sleep, REM sleep and wakefulness allowed us to perform vigilance-state classification in all cases. Invariably, hypothermia bouts were initiated from a state indistinguishable from NREM sleep, with EEG power decreasing gradually in parallel with decreasing body temperature. Furthermore, during deep hypothermia REM sleep was largely abolished, but we observed brief and intense bursts of muscle activity, which resembled the regular motor discharges seen during early ontogeny associated with immature sleep patterns. We conclude that torpor and sleep are electrophysiologically on a continuum, and that, in order for torpor to occur, mice need to first transition through euthermic sleep.

Opioids cause dissociated states of consciousness in C57BL/6J mice

2021 ◽  
Author(s):  
Christopher B O'Brien ◽  
Clarence E Locklear ◽  
Zachary T Glovak ◽  
Diana Zebadúa Unzaga ◽  
Helen A Baghdoyan ◽  
...  
Keyword(s):  
Rem Sleep ◽  
Neuronal Excitability ◽  
Nrem Sleep ◽  
Temporal Organization ◽  
Saline Control ◽  
Organization Of Sleep ◽  
States Of Consciousness ◽  
Surgical Recovery ◽  
Eeg Power ◽  
Electroencephalogram Eeg

The electroencephalogram (EEG) provides an objective, neural correlate of consciousness. Opioid receptors modulate mammalian neuronal excitability, and this fact was used to characterize how opioids administered to mice alter EEG power and states of consciousness. The present study tested the hypothesis that antinociceptive doses of fentanyl, morphine, or buprenorphine differentially alter the EEG and states of sleep and wakefulness in adult, male C57BL/6J mice. Mice were anesthetized and implanted with telemeters that enabled wireless recordings of cortical EEG and electromyogram (EMG). After surgical recovery, EEG and EMG were used to objectively score states of consciousness as wakefulness, rapid eye movement (REM) sleep, or non-REM (NREM) sleep. Measures of EEG power (dB) were quantified as delta (0.5 to 4 Hz), theta (4 to 8 Hz), alpha (8 to 13 Hz), sigma (12 to 15 Hz), beta (13 to 30 Hz), and gamma (30 to 60 Hz). Compared to saline (control), fentanyl and morphine decreased NREM sleep, morphine eliminated REM sleep, and buprenorphine eliminated NREM sleep and REM sleep. Opioids significantly and differentially disrupted the temporal organization of sleep/wake states, altered specific EEG frequency bands, and caused dissociated states of consciousness. The results are discussed relative to the fact that opioids, pain, and sleep modulate interacting states of consciousness.

Enhancement of Eye Motor Response and Electrical Brain Activity during Noise and Vibration in Rabbits

1982 ◽  
Vol 90 (1) ◽  
pp. 130-138 ◽  
Author(s):  
Ilmari Pyykkö ◽  
Izuru Matsuoka ◽  
Shinsuke Ito ◽  
Manabe Hinoki
Keyword(s):  
Motor Response ◽  
Optokinetic Nystagmus ◽  
Dorsal Hippocampus ◽  
Brain Activity ◽  
Noise And Vibration ◽  
Implanted Electrodes ◽  
Theta Waves ◽  
Electrical Brain Activity ◽  
The Relationship ◽  
Electroencephalogram Eeg

The relationship between electroencephalogram (EEG) and eye movements was studied in rabbits during optokinetic, vestibular, and optovestibular tests. EEG was recorded through permanently implanted electrodes. Exposure to noise and vibration increased the frequency and the velocity of optokinetic nystagmus (OKN). The increase was greater during vibration but greatest during combined noise and vibration. EEG activity was closely linked to changes in OKN and was particularly evident with the appearance of theta waves in the dorsal hippocampus. Also, rotation of the rabbit produced considerable activation in the EEG.

Correlations using the NREM-REM sleep cycle frequency support distinct regulation mechanisms for REM and NREM sleep

2002 ◽  
Vol 93 (1) ◽  
pp. 141-146 ◽  
Author(s):  
O. Le Bon ◽  
L. Staner ◽  
S. K. Rivelli ◽  
G. Hoffmann ◽  
I. Pelc ◽  
...  
Keyword(s):  
Rem Sleep ◽  
Healthy Subjects ◽  
Nrem Sleep ◽  
Sleep Cycle ◽  
Cycle Frequency ◽  
Regulation Mechanisms ◽  
The Mean ◽  
Number Of Cycles ◽  
The Relationship ◽  
Sleep Cycles

Polysomnograms of most homeothermic species distinguish two states, rapid eye movement (REM) and non-REM (NREM) sleep. These alternate several times during the night for reasons and following rules that remain poorly understood. It is unknown whether each state has its own function and regulation or whether they represent two facets of the same process. The present study compared the mean REM/NREM sleep ratio and the mean number of NREM-REM sleep cycles across 3 consecutive nights. The rationale was that, if REM and NREM sleep are tightly associated, their ratio should be comparable whatever the cycle frequency in the night. Twenty-six healthy subjects of both sexes were recorded at their home for 4 consecutive nights. The correlation between the REM/NREM sleep ratio and the number of cycles was highly significant. Of the two sleep components, REM sleep was associated to the number of cycles, whereas NREM sleep was not. This suggests that the relationship between REM sleep and NREM sleep is rather weak within cycles, does not support the concept of NREM-REM sleep cycles as miniature units of the sleep process, and favors the concept of distinct mechanisms of regulation for the two components.

MONOTONOUS TASKS AND ALCOHOL CONSUMPTION EFFECTS ON THE BRAIN BY EEG ANALYSIS USING NEURAL NETWORKS

2012 ◽  
Vol 11 (03) ◽  
pp. 1250015 ◽  
Author(s):  
STEPHEN KARUNGARU ◽  
TOSHIHIRO YOSHIDA ◽  
TORU SEO ◽  
MINORU FUKUMI ◽  
KENJI TERADA
Keyword(s):  
Neural Networks ◽  
Mental Stress ◽  
Brain Activity ◽  
Principal Component ◽  
Eeg Signals ◽  
Linear Discriminant ◽  
The Relationship ◽  
Electroencephalogram Eeg ◽  
The Brain ◽  
Eeg Signal Analysis

An analysis of the Electroencephalogram (EEG) signals while performing a monotonous task and drinking alcohol using principal component analysis (PCA), linear discriminant analysis (LDA) for feature extraction and Neural Networks (NNs) for classification is proposed. The EEG is captured while performing a monotonous task that can adversely affect the brain and possibly cause stress. Moreover, we investigate the effects of alcohol on the brain by capturing the data continuously after consumption of equal amounts of alcohol. We hope that our work will shed more light on the relationship between such actions and EEG, and investigate if there is any relation between the tasks and mental stress. EEG signals offers a rare look at brain activity, while, monotonous activities are well known to cause irritation which may contribute to mental stress. We apply PCA and LDA to characterize the change in each component, extract it and discriminate using a NN. After experiments, it was found that PCA and LDA are effective analysis methods in EEG signal analysis.

Hypoxic insomnia: effects of carbon monoxide and acclimatization

1984 ◽  
Vol 57 (6) ◽  
pp. 1696-1703 ◽  
Author(s):  
J. R. Pappenheimer
Keyword(s):  
Rem Sleep ◽  
Slow Wave Sleep ◽  
Nrem Sleep ◽  
Slow Waves ◽  
Partial Recovery ◽  
Peripheral Chemoreceptors ◽  
Loss Of Weight ◽  
Normal Sleep ◽  
Loss Of Appetite ◽  
Electroencephalogram Eeg

Hypoxia causes severe disruption of both rapid-eye-movement (REM) and non-REM (NREM) sleep. Experiments were performed on rats to determine if hypoxic insomnia is mediated by peripheral chemoreceptors and if normal sleep is restored during acclimatization to low O2. Novel methods were devised to measure distribution of amplitudes of cortical slow waves during NREM sleep and to detect REM sleep from the ratio of amplitudes of theta-to delta-frequency bands in the hippocampal electroencephalogram (EEG). Acute exposure of rats to 10.5% O2 (5,030 m altitude equivalent) during daylight hours virtually abolished REM sleep and shifted the distribution of amplitudes of slow-wave sleep EEG toward awake values. Similar disruption of sleep occurred during inhalation of 0.05% CO with steady-state carboxyhemoglobin of approximately 35%. Respiratory rate and alveolar ventilation were greatly increased by 10.5% O2 but were unaffected by CO. Therefore, hypoxic disruption of sleep was not mediated by peripheral chemoreceptors regulating breathing. Partial recovery of sleep occurred after 1-2 wk of hypoxia, but both REM and NREM were still subnormal after 1 mo. Decreased intensity of NREM sleep during hypoxia, measured by amplitude of cortical slow waves, may explain the disparity between subjective complaints of insomnia at altitude and evaluations of sleep by direct observation or by conventional EEG. Loss of appetite, loss of weight, irritability, and other symptoms of altitude sickness may be related to hypoxic insomnia.

scholarly journals The hypothalamic link between arousal and sleep homeostasis in mice

2021 ◽  
Vol 118 (51) ◽  
pp. e2101580118
Author(s):  
Tomoko Yamagata ◽  
Martin C. Kahn ◽  
José Prius-Mengual ◽  
Elise Meijer ◽  
Merima Šabanović ◽  
...  
Keyword(s):  
Brain Activity ◽  
Inhibitory Neurons ◽  
State Transitions ◽  
Laboratory Mice ◽  
Sleep Homeostasis ◽  
State Quality ◽  
Electroencephalogram Eeg ◽  
Eeg Pattern ◽  
Female Laboratory

Sleep and wakefulness are not simple, homogenous all-or-none states but represent a spectrum of substates, distinguished by behavior, levels of arousal, and brain activity at the local and global levels. Until now, the role of the hypothalamic circuitry in sleep–wake control was studied primarily with respect to its contribution to rapid state transitions. In contrast, whether the hypothalamus modulates within-state dynamics (state “quality”) and the functional significance thereof remains unexplored. Here, we show that photoactivation of inhibitory neurons in the lateral preoptic area (LPO) of the hypothalamus of adult male and female laboratory mice does not merely trigger awakening from sleep, but the resulting awake state is also characterized by an activated electroencephalogram (EEG) pattern, suggesting increased levels of arousal. This was associated with a faster build-up of sleep pressure, as reflected in higher EEG slow-wave activity (SWA) during subsequent sleep. In contrast, photoinhibition of inhibitory LPO neurons did not result in changes in vigilance states but was associated with persistently increased EEG SWA during spontaneous sleep. These findings suggest a role of the LPO in regulating arousal levels, which we propose as a key variable shaping the daily architecture of sleep–wake states.

scholarly journals Nitric oxide synthase neurons in the preoptic hypothalamus are sleep-active and contribute to regulating NREM and REM sleep and lowering body temperature.

2021 ◽  
Author(s):  
Edward C Harding ◽  
Wei Ba ◽  
Reesha Zahir ◽  
Xiao Yu ◽  
Raquel Yustos ◽  
...  
Keyword(s):  
Nitric Oxide ◽  
Body Temperature ◽  
Nitric Oxide Synthase ◽  
Rem Sleep ◽  
Active Phase ◽  
Nrem Sleep ◽  
Dark Phase ◽  
Dark Light ◽  
Active Population ◽  
Oxide Synthase

When mice are exposed to external warmth, nitric oxide synthase (NOS1) neurons in the median and medial preoptic (MnPO/MPO) hypothalamus induce sleep and concomitant body cooling. However, how these neurons regulate baseline sleep and body temperature is unknown. Using calcium photometry, we show that NOS1 neurons in MnPO/MPO are predominantly NREM active. This is the first instance of a predominantly NREM-active population in the PO area, or to our knowledge, elsewhere in the brain. In addition to releasing nitric oxide, NOS1 neurons in MnPO/MPO can release GABA, glutamate and peptides. We expressed tetanus-toxin light-chain in MnPO/MPO NOS1 cells to reduce vesicular release of transmitters. This induced changes in sleep structure: over 24 hours, mice had less NREM sleep in their dark (active) phase, and more NREM sleep in their light (sleep) phase. REM sleep episodes in the dark phase were longer, and there were fewer REM transitions between other vigilance states. REM sleep had less theta power. Mice with synaptically-blocked MnPO/MPO NOS1 neurons were also warmer. In particular, mice were warmer than control mice at the dark-light transition (ZT0), as well as during the dark phase siesta (ZT16-20), where there is usually a body temperature dip. Also, at this siesta point of cooled body temperature, mice usually have more NREM, but mice with synaptically-blocked MnPO/MPO NOS1 cells showed reduced NREM sleep at this time. Overall, MnPO/MPO NOS1 neurons promote both NREM and REM sleep and contribute to chronically lowering body temperature, particularly at transitions where the mice normally enter NREM sleep.

scholarly journals Nitric Oxide Synthase Neurons in the Preoptic Hypothalamus Are NREM and REM Sleep-Active and Lower Body Temperature

2021 ◽  
Vol 15 ◽  
Author(s):  
Edward C. Harding ◽  
Wei Ba ◽  
Reesha Zahir ◽  
Xiao Yu ◽  
Raquel Yustos ◽  
...  
Keyword(s):  
Nitric Oxide ◽  
Body Temperature ◽  
Nitric Oxide Synthase ◽  
Rem Sleep ◽  
Active Phase ◽  
Nrem Sleep ◽  
Dark Phase ◽  
Dark Light ◽  
Body Cooling ◽  
Oxide Synthase

When mice are exposed to external warmth, nitric oxide synthase (NOS1) neurons in the median and medial preoptic (MnPO/MPO) hypothalamus induce sleep and concomitant body cooling. However, how these neurons regulate baseline sleep and body temperature is unknown. Using calcium photometry, we show that NOS1 neurons in MnPO/MPO are predominantly NREM and REM active, especially at the boundary of wake to NREM transitions, and in the later parts of REM bouts, with lower activity during wakefulness. In addition to releasing nitric oxide, NOS1 neurons in MnPO/MPO can release GABA, glutamate and peptides. We expressed tetanus-toxin light-chain in MnPO/MPO NOS1 cells to reduce vesicular release of transmitters. This induced changes in sleep structure: over 24 h, mice had less NREM sleep in their dark (active) phase, and more NREM sleep in their light (sleep) phase. REM sleep episodes in the dark phase were longer, and there were fewer REM transitions between other vigilance states. REM sleep had less theta power. Mice with synaptically blocked MnPO/MPO NOS1 neurons were also warmer than control mice at the dark-light transition (ZT0), as well as during the dark phase siesta (ZT16-20), where there is usually a body temperature dip. Also, at this siesta point of cooled body temperature, mice usually have more NREM, but mice with synaptically blocked MnPO/MPO NOS1 cells showed reduced NREM sleep at this time. Overall, MnPO/MPO NOS1 neurons promote both NREM and REM sleep and contribute to chronically lowering body temperature, particularly at transitions where the mice normally enter NREM sleep.

scholarly journals The maturational trajectories of NREM and REM sleep durations differ across adolescence on both school-night and extended sleep

2012 ◽  
Vol 302 (5) ◽  
pp. R533-R540 ◽  
Author(s):  
Irwin Feinberg ◽  
Nicole M. Davis ◽  
Evan de Bie ◽  
Kevin J. Grimm ◽  
Ian G. Campbell
Keyword(s):  
Eye Movement ◽  
Rem Sleep ◽  
Brain Activity ◽  
Physiological Role ◽  
Nrem Sleep ◽  
Sleep Time ◽  
Rapid Eye Movement ◽  
Time In Bed ◽  
Ultimate Explanation ◽  
Brain Changes

We recorded sleep electroencephalogram longitudinally across ages 9–18 yr in subjects sleeping at home. Recordings were made twice yearly on 4 consecutive nights: 2 nights with the subjects maintaining their ongoing school-night schedules, and 2 nights with time in bed extended to 12 h. As expected, school-night total sleep time declined with age. This decline was entirely produced by decreasing non-rapid eye movement (NREM) sleep. Rapid eye movement (REM) sleep durations increased slightly but significantly. NREM and REM sleep durations also exhibited different age trajectories when sleep was extended. Both durations exceeded those on school-night schedules. However, the elevated NREM duration did not change with age, whereas REM durations increased significantly. We interpret the adolescent decline in school-night NREM duration in relation to our hypothesis that NREM sleep reverses changes produced in plastic brain systems during waking. The “substrate” produced during waking declines across adolescence, because synaptic elimination decreases the intensity (metabolic rate) of waking brain activity. Declining substrate reduces both NREM intensity (i.e., delta power) and NREM duration. The absence of a decline in REM sleep duration on school-night sleep and its age-dependent increase in extended sleep pose new challenges to understanding its physiological role. Whatever their ultimate explanation, these robust findings demonstrate that the two physiological states of human sleep respond differently to the maturational brain changes of adolescence. Understanding these differences should shed new light on both brain development and the functions of sleep.

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