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However, reactivation after aversive trials more closely mirrors the original neural patterns. Here, we show that dh and vh awake swrs occur asynchronously and activate distinct and opposing patterns of nac spiking Here, we review the literature in rodents highlighting the anatomical and functional properties of the hippocampus along its dorsoventral axis that underlie its role in contextual and emotional memory encoding, consolidation, and retrieval.
We recorded neuronal ensembles in the hippocampus and bla while rats learned the location of an aversive air puff on a linear track, as well as during sleep before and after training. How this increase in firing rates and synchrony after learning is counterbalanced to preserve network stability is not understood. We simulated memory (re)consolidation using a connectionist model of the hippocampus that explicitly accounted for its dorsoventral organization and for ca1 proximodistal processing
Replicating human and rodent (re)consolidation studies yielded the following results.
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