Abstract
Glycogen synthase kinase-3β (GSK-3β) is a constitutively active kinase. Since its activation results in neurofibrillary tangle (NFT) deposits in aged and Alzheimer's disease (AD) brains, GSK-3β may be inhibited under normal conditions but activated under pathological conditions. Given its link to NFT formation, we sought to determine whether GSK-3β exists in the brain as a "pathological time bomb" that promotes disease development. To address this hypothesis, we analyzed GSK-3β heterozygote (GSK+/-) mice, which express GSK-3β at 50% wild-type levels. When tested in the Morris water maze test, GSK+/- mice surprisingly exhibited retrograde amnesia. Further analysis indicated that GSK+/- mice had impaired memory reconsolidation but normal memory consolidation. Therefore, we concluded that GSK-3β activation is required for memory reconsolidation in the adult brain. © 2009 The Japanese Pharmacological Society.
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Takashima, A. (2009). Drug development targeting the glycogen synthase kinase-3ß(GSK- 3ß)-mediated signal transduction pathway: Role of GSK-3β in adult brain. Journal of Pharmacological Sciences. Japanese Pharmacological Society. https://doi.org/10.1254/jphs.08R29FM
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