The scaling behavior of hippocampal activity in sleep/rest predicts spatial memory performance
In the hippocampus, reactivation of spatial memories during sleep enhances consolidation and recall. However, network dynamics may independently influence memory retention. We applied the Phenomenological Renormalization Group to CA1 neuronal activity in rats during sleep/rest epochs surrounding a spatial learning task. The scaling exponent of activity variance (), assessed either before or after learning, predicted subsequent recall performance independently of reactivation. The prediction model was transferable across subjects, suggesting that it is a robust biomarker of learning ability. Single-cell features, such as burst propensity and intrinsic timescales, correlated with and memory, predicted retention even when controlling for these factors. Our results identified a link between scale-free circuit dynamics and memory stabilization, suggesting that the tuning of the underlying dynamical regime near criticality is a key determinant of memory longevity. Targeted modulation of these collective states could offer new avenues for memory enhancement.