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dc.contributor.advisorWood, Shona
dc.contributor.advisorSimonneaux, Valérie
dc.contributor.advisorHazlerigg, David
dc.contributor.authorMarkussen, Fredrik Andreas Fasth
dc.date.accessioned2021-05-25T13:40:35Z
dc.date.available2021-05-25T13:40:35Z
dc.date.issued2020-05-22
dc.description.abstractHibernation is a physiological and behavioural adaptation that permits survival during seasonal periods of energy shortage via a combination of pre-hibernal energy storage and hibernal metabolic depression, i.e. torpor. The central mechanisms in the brain that control torpor expression and arousal from it has been under investigation since the dawn of hibernation research but remains unknown. Recent reports on the role of tanycytes, a specialised glial cell within the brain’s circumventricular organs, in energy homeostasis and metabolic sensing provides a promising avenue for investigation regarding their role in hibernation. One interesting aspect is that tanycytes have been shown to alter brain barrier function depending on organismic energetic state. Therefore, this study aimed to assess brain permeability during torpid and awake states in a true hibernator, the European hamster (<i>Cricetus cricetus</i>), by perfusion of the brain with a small biotinylated tracer molecule. Additionally, a minimally invasive method for hibernation monitoring and detecting arousal events has been validated. We show that small subcutaneous temperature transponders positioned in interscapular brown adipose tissue combined with intraperitoneal temperature loggers allows superior detection of the earliest events of arousal. These data reveal the dynamics of the re-warming (arousal) process, showing brown adipose tissue rewarming precedes core body temperature by up to an hour. We also note that rewarming capacity from torpor is impaired in animals bearing thymus tumours in the thoracic cavity. We found that the blood-brain barrier remains intact both at the level of capillaries and in circumventricular organs during hibernation. This suggests that accessibility of peripheral metabolites to the brain by passive diffusion is not altered during torpor, and may indicate that alterations in intrinsic properties of regulatory neuronal populations regulate torpor arousal cycling. Tanycyte morphology was also unaltered during torpor arousal cycling indicating that further research should focus on the intrinsic properties of these cells rather than the morphology. Taken together, this study provides detailed insight into arousal patterns, brain permeability and tanycyte morphology of the European hamster.en_US
dc.identifier.urihttps://hdl.handle.net/10037/21241
dc.language.isoengen_US
dc.publisherUiT Norges arktiske universiteten_US
dc.publisherUiT The Arctic University of Norwayen_US
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2020 The Author(s)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0en_US
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)en_US
dc.subject.courseIDBIO-3950
dc.subjectVDP::Matematikk og Naturvitenskap: 400::Zoologiske og botaniske fag: 480::Zoofysiologi og komparativ fysiologi: 483en_US
dc.subjectVDP::Mathematics and natural science: 400::Zoology and botany: 480::Zoophysiology and comparative physiology: 483en_US
dc.titleHibernation in European Hamsters (Cricetus crisetus): An assessment of brain permeability during torpor-arousal cyclingen_US
dc.typeMaster thesisen_US
dc.typeMastergradsoppgaveen_US


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Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)