Tuesday, December 24, 2019

The Encoding of Contextual Fear Conditioning - 1296 Words

The formation of new memories requires protein synthesis dependent changes in synaptic structure and plasticity in the hippocampus. Studies in humans and animals suggest that these memories are initially stored in hippocampus but later transferred to cortex for permanent storage. This phenomenon is described as systems consolidation of memories. While the specific role for new protein synthesis in hippocampus in early encoding of memories is established, whether protein synthesis in medial prefrontal cortex play a major role in encoding of memories is unclear. To address this question, we used contextual fear conditioning (CFC) of mouse, a behavior training that induce long lasting memories. A single training session produces robust lifelong memory (8) that can be measured using automated procedures (9). Several studies have used CFC training as a model to study hippocampal-cortical communications and mechanisms underlying systems consolidation of memories. Contextual fear memories a re initially stored in hippocampus and then moved to medial prefrontal cortex (mPFC) for long-term storage. We assume that if encoding of contextual fear memories require protein synthesis at both hippocampus and PFC, we will be able to identify translationally active mRNAs in hippocampus and PFC. Because RNAs associated with polyribosomes indicate translational activation, we first isolated polyribosomes from mPFC and hippocampus at two time points (one hour and six hours, hereafter T1 and T2Show MoreRelatedThe Effect Of New Protein Synthesis At Prl Cortex900 Words   |  4 Pages training. Mice infused with anisomycin (n= 12) immediately after conditioning showed impairment in contextual fear memory compared with vehicle-infused animals (saline, n=18) when tested 24 hours after CFC training (DF=28, F=7.19, t-test: p 0.05) (Figure 2A). 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