Journal
GENES BRAIN AND BEHAVIOR
Volume 20, Issue 4, Pages -Publisher
WILEY
DOI: 10.1111/gbb.12708
Keywords
anxiety; behavior; brain; brown adipose tissue; circadian rhythm; cryptochrome; depression; gene expression; PET; q‐ RT‐ PCR
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Funding
- Varsinais-Suomen Sairaanhoitopiiri [13856]
- Academy of Finland [258814]
- University of Helsinki
- Sigrid Juselius Foundation
- Academy of Finland (AKA) [258814, 258814] Funding Source: Academy of Finland (AKA)
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The study found that Cry2 gene knockout mice exhibited reduced despair-like behavior in the forced swim test and decreased preference for saccharin, indicating increased anhedonia, with no group differences in anxiety-like behavior. These behavioral changes may be associated with alterations in brain metabolism.
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.
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