Abstract
To date, the effects of protein synthesis inhibitors (PSI) in learning and memory processes have been attributed to translational arrest and consequent inhibition of de novo protein synthesis. Here we argue that amnesia produced by PSI can be the direct result of their abnormal induction of mRNA-a process termed gene superinduction. This action exerted by PSI involves an abundant and prolonged accumulation of mRNA transcripts of genes that are normally transiently induced. We summarize experimental evidence for the multiple mechanisms and signaling pathways mediating gene superinduction and consider its relevance for PSI-induced amnesia. This mechanistic alternative to protein synthesis inhibition is compared to models of electroconvulsive seizures and fragile × syndrome associated with enhanced mRNA/protein levels and cognitive deficits.
Original language | English (US) |
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Pages (from-to) | 212-218 |
Number of pages | 7 |
Journal | Neurobiology of Learning and Memory |
Volume | 89 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2008 |
Funding
This work was supported by the NIMH Grant MH073669 to J.R.
Keywords
- Anisomycin
- Consolidation
- Cycloheximide
- Extinction
- Gene superinduction
- Memory
- Protein synthesis inhibitor
- Reconsolidation
ASJC Scopus subject areas
- Experimental and Cognitive Psychology
- Cognitive Neuroscience
- Behavioral Neuroscience