| Literature DB >> 33637777 |
Heather Mahoney1,2, Emily Peterson1,2, Hannah Justin1,2, David Gonzalez1,2, Christopher Cardona1,2, Korey Stevanovic3, John Faulkner1,2, Amara Yunus4, Alexandra Portugues1,2, Amy Henriksen1,2, Camden Burns1,2, Cameron McNeill5, Joshua Gamsby1,2, Danielle Gulick6,7.
Abstract
Time-of-day effects have been noted in a wide variety of cognitive behavioral tests, and perturbation of the circadian system, either at the level of the master clock in the SCN or downstream, impairs hippocampus-dependent learning and memory. A number of kinases, including the serine-threonine casein kinase 1 (CK1) isoforms CK1δ/ε, regulate the timing of the circadian period through post-translational modification of clock proteins. Modulation of these circadian kinases presents a novel treatment direction for cognitive deficits through circadian modulation. Here, we tested the potential for PF-670462, a small molecule inhibitor of CK1δ/ε, to improve cognitive performance in C57BL/6J mice in an array of behavioral tests. Compared to vehicle-treated mice tested at the same time of the circadian day, mice treated with PF-670462 displayed better recall of contextual fear conditioning, made fewer working memory errors in the radial arm water maze, and trained more efficiently in the Morris Water Maze. These benefits were accompanied by increased expression of activity-regulated cytoskeleton-associated protein (Arc) in the amygdala in response to an acute learning paradigm. Our results suggest the potential utility of CK1δ/ε inhibition in improving time-of-day cognitive performance.Entities:
Mesh:
Substances:
Year: 2021 PMID: 33637777 PMCID: PMC7910436 DOI: 10.1038/s41598-021-83957-9
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379