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The circadian gene Cryptochrome 2 influences stress-induced brain activity and depressive-like behavior in mice
Authors:Ewa Sokolowska  Riikka Viitanen  Zuzanna Misiewicz  Marie Mennesson  Suvi Saarnio  Natalia Kulesskaya  Sanna Kängsep  Heidi Liljenbäck  Päivi Marjamäki  Anu Autio  Saija-Anita Callan  Pirjo Nuutila  Anne Roivainen  Timo Partonen  Iiris Hovatta
Affiliation:1. Molecular and Integrative Biosciences Research Program, University of Helsinki, Helsinki, Finland;2. Turku PET Centre, University of Turku, Turku, Finland;3. Molecular and Integrative Biosciences Research Program, University of Helsinki, Helsinki, Finland

Department of Psychology and Logopedics, University of Helsinki, Helsinki, Finland;4. Molecular and Integrative Biosciences Research Program, University of Helsinki, Helsinki, Finland

Department of Psychology and Logopedics, University of Helsinki, Helsinki, Finland

SleepWell Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland;5. Turku PET Centre, University of Turku, Turku, Finland

Turku Center for Disease Modeling, University of Turku, Turku, Finland;6. Turku PET Centre, University of Turku, Turku, Finland

Department of Endocrinology, Turku University Hospital, Turku, Finland

Turku PET Centre, Turku University Hospital, Turku, Finland;7. Turku PET Centre, University of Turku, Turku, Finland

Turku Center for Disease Modeling, University of Turku, Turku, Finland

Turku PET Centre, Turku University Hospital, Turku, Finland;8. Department of Public Health Solutions, National Institute for Health and Welfare, Helsinki, Finland

Abstract:Cryptochrome 2 (Cry2) is a core clock gene important for circadian regulation. It has also been associated with anxiety and depressive-like behaviors in mice, but the previous findings have been conflicting in terms of the direction of the effect. To begin to elucidate the molecular mechanisms of this association, we carried out behavioral testing, PET imaging, and gene expression analysis of Cry2−/− and Cry2+/+ mice. Compared to Cry2+/+ mice, we found that Cry2−/− mice spent less time immobile in the forced swim test, suggesting reduced despair-like behavior. Moreover, Cry2−/− mice had lower saccharin preference, indicative of increased anhedonia. In contrast, we observed no group differences in anxiety-like behavior. The behavioral changes were accompanied by lower metabolic activity of the ventro-medial hypothalamus, suprachiasmatic nuclei, ventral tegmental area, anterior and medial striatum, substantia nigra, and habenula after cold stress as measured by PET imaging with a glucose analog. Although the expression of many depression-associated and metabolic genes was upregulated or downregulated by cold stress, we observed no differences between Cry2−/− and Cry2+/+ mice. These findings are consistent with other studies showing that Cry2 is required for normal emotional behavior. Our findings confirm previous roles of Cry2 in behavior and extend them by showing that the effects on behavior may be mediated by changes in brain metabolism.
Keywords:anxiety  behavior  brain  brown adipose tissue  circadian rhythm  cryptochrome  depression  gene expression  PET  q-RT-PCR
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