| Literature DB >> 33325370 |
Helen Wong1, Josien Levenga1,2, Lauren LaPlante1, Bailey Keller1, Andrew Cooper-Sansone1, Curtis Borski1, Ryan Milstead3, Marissa Ehringer1,3, Charles Hoeffer1,2,3.
Abstract
AKT is implicated in neurological disorders. AKT has three isoforms, AKT1/AKT2/AKT3, with brain cell type-specific expression that may differentially influence behavior. Therefore, we examined single Akt isoform, conditional brain-specific Akt1, and double Akt1/3 mutant mice in behaviors relevant to neuropsychiatric disorders. Because sex is a determinant of these disorders but poorly understood, sex was an experimental variable in our design. Our studies revealed AKT isoform- and sex-specific effects on anxiety, spatial and contextual memory, and fear extinction. In Akt1 mutant males, viral-mediated AKT1 restoration in the prefrontal cortex rescued extinction phenotypes. We identified a novel role for AKT2 and overlapping roles for AKT1 and AKT3 in long-term memory. Finally, we found that sex-specific behavior effects were not mediated by AKT expression or activation differences between sexes. These results highlight sex as a biological variable and isoform- or cell type-specific AKT signaling as potential targets for improving treatment of neuropsychiatric disorders.Entities:
Keywords: associative memory; extinction; hippocampus; isoform; mouse; neuroscience; prefrontal cortex; spatial learning
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Year: 2020 PMID: 33325370 PMCID: PMC7787664 DOI: 10.7554/eLife.56630
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.713