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Toien, O.

Publications and source records attributed to Toien, O..

3 recordsLinked to original sources

Automated sleep scoring in hibernating and non-hibernating American black bears

Hibernating bears show remarkable metabolic suppression. Their decline in core body temperature (Tb) is moderate (from 38{degrees}C to 30-35{degrees}C), but their metabolism declines as much as 75%. To understand the role of sleep in this hypometabolic state, we recorded biotelemetrically EEG, EOG and EMG data over 3500 days from 16 captive American black bears in and out of hibernation under semi-natural conditions. This data set is too large to score manually for Wake, REM- and NREM sleep, so we tested two machine learning classifiers: (1) Somnotate trained on multiple one-day recordings, and (2) Somnivore, trained on a small subset from each recording. As automated scoring methods have not been applied to hibernating species before, a major concern is the effect changing brain temperature has on the EEG and on the machine learning based detection. Therefore, we selected reference data using consensus by 3 manual sleep scorers from each of 6 bears, two one-day recordings at the highest and lowest body temperatures during hibernation when Tb was oscillating in multiday cycles, and a non-hibernating one-day recording in summer. Somnotate results were excellent when trained separately for hibernating and non-hibernating data. Training Somnotate separately for high and low Tb within hibernation did not improve results further. Sleep times in hibernation were about 2x that in summer for both automated scores and manual scores (p<0.0001). There were no significant differences in occupancy of vigilance states between automated and manual scores in hibernation (p>0.05), but a small overestimate of sleep time in summer (p<0.05). Both applications yielded F-measures against manual scores in the 0.90-0.98 range. Outliers in the 0.67-0.88 range were correlated between the two applications, indicating that specific files are more challenging to annotate. We conclude that both applications have accuracies approaching that of manual scorers when trained on high quality data.

neuroscience↗

Transcriptome remodeling and adaptive preservation of muscle protein content in hibernating black bears

Hibernation is an energy-saving adaptation associated with physical inactivity. In contrast to most mammals, hibernating bears demonstrate limited loss of muscle mass and protein content over the prolonged periods of immobility and fasting during winter. This suggests that bears have natural adaptive mechanisms preserving muscle mass and functionality. To identify transcriptional changes that underlie molecular mechanisms attenuating muscle loss, we conducted a large-scale gene expression profiling (14,199 genes) by transcriptome sequencing in quadriceps of adult black bears, comparing hibernating animals (n=5) and summer active animals (n=5). Gene set enrichment analysis showed significant positive correlation between hibernating phenotype and expression changes of genes involved in translation, ribosome and the mTORC1 mediated signaling. In contrast, coordinated transcriptional reduction was detected for genes involved in catabolism of branched chain amino acid (BCAA) suggesting preservation of BCAA. These findings imply maintenance of protein biosynthesis through the mTORC1 signaling positively activated by availability of BCAA in muscle during hibernation. Support for this conclusion comes from overexpression of RRAGD and RRAGB, crucial regulator of the mTORC1 response to leucine availability, and up regulation of EIF4B, downstream target of the mTORC1 signaling. Consistent with the mTORC1 suppression of autophagy-dependent protein degradation, MAP1LC3A and ULK1 were down regulated in hibernating muscle. The maintenance of protein biosynthesis and decrease in protein catabolism through the mTORC1 signaling as response to BCAA availability likely contribute to the preservation of muscle protein through prolonged periods of immobility and fasting during hibernation.

genomics↗

Remodelling of Skeletal Muscle Myosin Metabolic States in Hibernating Mammals

Hibernation is a period of metabolic suppression utilized by many small and large mammal species to survive during winter periods. As the underlying cellular and molecular mechanisms remain incompletely understood, our study aimed to determine whether skeletal muscle myosin and its metabolic efficiency undergo alterations during hibernation to optimize energy utilization. We isolated muscle fibers from small hibernators, Ictidomys tridecemlineatus and Eliomys quercinus and larger hibernators, Ursus arctos and Ursus americanus. We then conducted loaded Mant-ATP chase experiments alongside X-ray diffraction to measure resting myosin dynamics and its ATP demand. In parallel, we performed multiple proteomics analyses. Our results showed a preservation of myosin structure in U. arctos and U. americanus during hibernation, whilst in I. tridecemlineatus and E. quercinus, changes in myosin metabolic states during torpor unexpectedly led to higher levels in energy expenditure of type II, fast-twitch muscle fibers at ambient lab temperatures (20{degrees}C). Upon repeating loaded Mant-ATP chase experiments at 8{degrees}C (near the body temperature of torpid animals), we found that myosin ATP consumption in type II muscle fibers was reduced by 77-107% during torpor compared to active periods. Additionally, we observed Myh2 hyper-phosphorylation during torpor in I. tridecemilineatus, which was predicted to stabilize the myosin molecule. This may act as a potential molecular mechanism mitigating myosin-associated increases in skeletal muscle energy expenditure during periods of torpor in response to cold exposure. Altogether, we demonstrate that resting myosin is altered in hibernating mammals, contributing to significant changes to the ATP consumption of skeletal muscle. Additionally, we observe that it is further altered in response to cold exposure and highlight myosin as a potentially contributor to skeletal muscle non-shivering thermogenesis.

physiology↗