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Computational Model of a Positive BDNF Feedback Loop in Hippocampal Neurons Following Inhibitory Avoidance Training

Inhibitory avoidance (IA) training in rodents initiates a molecular cascade within hippocampal neurons. This cascade contributes to the transition of short- to long-term memory (i.e., consolidation). Here, a differential equation-based model was developed to describe a positive feedback loop within...

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Bibliographic Details
Published in:Learning & memory (Cold Spring Harbor, N.Y.) N.Y.), 2016-12, Vol.23 (12), p.714-722
Main Authors: Zhang, Yili, Smolen, Paul, Alberini, Cristina M, Baxter, Douglas A, Byrne, John H
Format: Article
Language:English
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Summary:Inhibitory avoidance (IA) training in rodents initiates a molecular cascade within hippocampal neurons. This cascade contributes to the transition of short- to long-term memory (i.e., consolidation). Here, a differential equation-based model was developed to describe a positive feedback loop within this molecular cascade. The feedback loop begins with an IA-induced release of brain-derived neurotrophic factor (BDNF), which in turn leads to rapid phosphorylation of the cAMP response element-binding protein (pCREB), and a subsequent increase in the level of the ß isoform of the CCAAT/enhancer binding protein (C/EBPß). Increased levels of C/EBPß lead to increased "bdnf" expression. Simulations predicted that an empirically observed delay in the BDNF-pCREB-C/EBPß feedback loop has a profound effect on the dynamics of consolidation. The model also predicted that at least two independent self-sustaining signaling pathways downstream from the BDNF-pCREB-C/EBPß feedback loop contribute to consolidation. Currently, the nature of these downstream pathways is unknown.
ISSN:1072-0502
1549-5485
1549-5485
DOI:10.1101/lm.042044.116