Publication | Open Access
Identification of compounds that potentiate CREB signaling as possible enhancers of long-term memory
56
Citations
30
References
2009
Year
Drug TargetMolecular RegulationMolecular BiologyChemical BiologySocial SciencesMemoryCognitive NeuroscienceCell SignalingPossible EnhancersCognitive ScienceCamp ProductionMemory SystemBiochemistryBiochemical InteractionCreb ActivationProtein PhosphorylationSignal TransductionMnemonicNatural SciencesNeuroscienceMolecular NeurobiologyMemory LossLong-term MemoryLead GenerationSmall MoleculesDrug Discovery
The CREB signaling pathway is implicated in long‑term memory. The study aimed to identify small‑molecule enhancers of CREB‑mediated gene expression. The authors screened ~73,000 compounds at 7–15 concentrations in a quantitative high‑throughput format, then systematically profiled mechanisms, revealing modulators of PDE4, PKA, cAMP, and other unknown pathways. The screen identified 1,800 potent CREB enhancers across 96 structural series, showing that qHTS plus pathway interrogation is an efficient lead‑generation strategy.
Many studies have implicated the cAMP Response Element Binding (CREB) protein signaling pathway in long-term memory. To identify small molecule enhancers of CREB activation of gene expression, we screened approximately 73,000 compounds, each at 7-15 concentrations in a quantitative high-throughput screening (qHTS) format, for activity in cells by assaying CREB mediated beta-lactamase reporter gene expression. We identified 1,800 compounds that potentiated CREB mediated gene expression, with potencies as low as 16 nM, comprising 96 structural series. Mechanisms of action were systematically determined, and compounds that affect phosphodiesterase 4, protein kinase A, and cAMP production were identified, as well as compounds that affect CREB signaling via apparently unidentified mechanisms. qHTS followed by interrogation of pathway targets is an efficient paradigm for lead generation for chemical genomics and drug development.
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