It is nearly common knowledge that there is a connection between sleep deprivation and obesity, yet there is much to be explored regarding how exactly sleep deprivation affects bodily functions, metabolism, and body mass. Given the rise in obesity and sleep deprivation among the American population and the fact that both are risk factors for different physical and mental illnesses, it is an area of scientific inquiry in need of research. It is generally thought that sleep deprivation causes loss of metabolic function, which means more food is stored as fat; thus, obesity occurs.
In Circadian
Desynchrony and Health, Dr. Turek and Dr. Summa found numerous negative effects
on metabolism due to the inability of healthy sleep function in mice. Using
mice as the model organism, they tested mice with a mutation in the Clock core
circadian gene, a pivotal gene for sleep function. Interestingly, after ten
weeks of diet experimentation, the Clock-mutant mice developed significant
increases in body weight compared to the control mice for both a regular and high-fat
diet. These Clock-mutant mice became sick with glucose metabolic syndromes as
well. The study of islet glucose-stimulated release of insulin demonstrates that
the Clock mutant mice had physiological changes impacting weight. The Clock
mutant mice had a dysfunctional metabolism as they decreased insulin secretion,
which made them prone to issues with glucose homeostasis and an energy
imbalance. Given the metabolic dysregulation somehow indirectly or directly
caused by the Clock gene mutation, it is unsurprising that the Clock mutant mice
were prone to obesity. Through the study of the cellular study of pancreatic
tissue and comparison of body mass in mice, this research demonstrates the dangerous
effects of somatic inhibition of sleep through the central nervous system’s
regulatory function of circadian rhythm.
In Integrated
metabolomics and proteomics analysis reveals energy metabolism disorders in the
livers of sleep-deprived mice, Dr. Hu and his research team impressively
examined the effects of sleep deprivation in mice on body mass, liver health,
and other factors. In this lab, the researchers examined the effects of sleep
deprivation on mice through behavioral intervention. They behaviorally induced
sleep deprivation in mice through an interesting in vivo model of a random
motion platform. The investigation focused on changes to the metabolome, small-molecule
chemicals, and the proteome, a full set of proteins, in the functioning of the
liver. Like Turek’s lab, one of the focuses was on the change in body weight
between the experimental and control mice. This lab recorded the final body
weight at the ten-day mark of their sleep deprivation mouse model. Without a
significant difference, the sleep deprivation group gained more weight than the
control group. Given this experiment lasted a short time in duration, it is
unsurprising that the difference in weight change may not yet have been
significantly different. After ten days of this in-vivo part of the experiment,
the livers were examined, and interesting findings were presented. Three
significant pathways were found including the upregulation of the glutamate and
downregulation of glutamine in the glutathione metabolic pathway. The role of glutathione
metabolism ties in with energy metabolism. Thus, this presents more metabolic evidence
of the negative effects of sleep deprivation on mammalian metabolism and energy
balance.
With different modes of research, both
studies found that lack of sleep causes metabolic dysregulation which induces
obesity in mice. Dr. Turek’s research team focused on somatic inhibition via
the Clock mutation, and Dr. Hu’s team utilized behavioral intervention to sleep
deprive the mice. In conjunction with each other, these findings suggest that
sleep deprivation has a huge impact on the whole-body system at the cellular the
outwardly physical level. It raises further questions about how sleep deprivation
directly affects organ function, and how the functioning or dysfunction of
organs may affect each other.
References:
Vitaterna, M., et al. “Mutagenesis and Mapping of a Mouse Gene,
Clock, Essential for Circadian Behavior.” Science, vol. 264, no.
5159, 29 Apr. 1994, pp. 719–725, https://doi.org/10.1126/science.8171325.
Hu, Shuang, et al. “Integrated Metabolomics and Proteomics
Analysis Reveals Energy Metabolism Disorders in the Livers of Sleep-Deprived
Mice.” Journal of Proteomics, vol. 245, 1 Aug. 2021, pp.
104290–104290, https://doi.org/10.1016/j.jprot.2021.104290. Accessed 17 Feb.
2024.
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