Long-term memory consolidation is a dynamic process that requires a heterogeneous ensemble of neurons, each with a highly specialized molecular environment. Considerable effort has been placed into understanding how the molecular mechanisms in specific neuron types are modified in memory, but these studies are often undertaken hours or days after training, when memory is already consolidated. Studies have shown that protein synthesis is elevated during the early stages of consolidation, but there is limited information as to how it impacts neuronal function. We hypothesize that mRNAs being translated during the early stages of consolidation could provide clues as to how diverse neurons involved in memory formation restructure their molecular architecture to support memory formation. Here, we generate a landscape of the translatome of three neuron types in the dorsal hippocampus during the first hour of contextual memory consolidation. Our results show that these neurons share a common