Sylvain Giroud
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Assistant Professor
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About
Sylvain Giroud is an Assistant Professor at Northern Michigan University, USA. His research primarily focuses on hibernation physiology, including the role of microRNA in hepatic metabolism, telomere length dynamics, and the evolutionary trade-offs associated with dormancy. He has published articles exploring the physiological and behavioral adaptations of hibernating species, contributing significantly to the understanding of their survival strategies in changing environments.
Recent Grants
Grant: Close
HYPOxia and HYPOthermia in foraging elephant seals: diving into physiological conundrums (‘Hypo2’)
Open Date: 2021-01-01
Close Date: 2023-12-01
Grant: Close
Comparison of life-history traits between fat and foodstoring hibernators
Open Date: 2019-01-01
Close Date: 2021-12-01
Grant: Close
Plasticity of ontogeny of energy saving mechanisms in heterothermic mammals
Open Date: 2018-08-01
Close Date: 2022-04-01
Grant: Close
Evolution of mammalian life history in continental Iberian ecosystems from the Miocene to Pleistocene: correlation with climatic changes
Open Date: 2016-01-01
Close Date: 2019-01-01
Grant: Close
Polyunsaturated fatty acids and hibernation: underlying mechanisms and consequences for ageing
Open Date: 2014-09-01
Close Date: 2017-08-01
Articles (17)
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2025
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2025
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2024
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2024
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2024
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2023
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2023
Torpor or heterothermy is an energy‐saving mechanism used by endotherms to overcome harsh environmental conditions. During winter, the garden dormouse ( Eliomys quercinus ) hibernates with multiday torpor bouts and body temperatures of a few degrees Celsius, interrupted by brief euthermic phases. This study investigates gene expression within the hypothalamus, the key brain area controlling energy balance, adding information on differential gene expression potentially relevant to orchestrate torpor. A de novo assembled transcriptome of the hypothalamus was generated from garden dormice hibernating under constant darkness without food and water at 5 °C. Samples were collected during early torpor, late torpor, and interbout arousal. During early torpor, 765 genes were differentially expressed as compared with interbout arousal. Twenty‐seven pathways were over‐represented, including pathways related to hemostasis, extracellular matrix organization, and signaling of small molecules. Only 82 genes were found to be differentially expressed between early and late torpor, and no pathways were over‐represented. During late torpor, 924 genes were differentially expressed relative to interbout arousal. Despite the high number of differentially expressed genes, only 10 pathways were over‐represented. Of these, eight were also observed to be over‐represented when comparing early torpor and interbout arousal. Our results are largely consistent with previous findings in other heterotherms. The addition of a transcriptome of a novel species may help to identify species‐specific and overarching torpor mechanisms through future species comparisons.
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2023
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2023
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2022
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2021
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2021
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2021
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2021
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2020
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2020
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2020
Collaborators (7)
Jonas Kindberg
Head of Research
Norwegian Institute for Nature Research
Thomas Ruf
University of Veterinary Medicine
Alina Lynn Evans
Associate Professor
Inland Norway University of Applied Sciences
Annika Herwig
-
Birgitta Strandvik
Karolinska Institutet
Jon M Arnemo
Professor
Inland Norway University of Applied Sciences
Claudia Bieber
Head Research Institute of Wildlife Ecology, Uni.-Prof.
University of Veterinary Medicine Vienna
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