Amyloid pathology reduces dynamic range and disrupts neural coding in a mouse model of Alzheimer’s Disease

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Abstract

Alzheimer’s Disease (AD) disrupts neural circuits vital for memory and cognition. We used two-photon microscopy to investigate these disruptions in behaving mice, focusing on the link between amyloid plaques - a hallmark of AD - and aberrant neural activity. Using the 5xFAD mouse model, we observed significant changes in hippocampal neurons, including elevated baseline activity and reduced locomotion-driven firing, leading to a diminished neuronal dynamic range. These abnormalities were more pronounced near amyloid plaques. We also found degraded spatial coding, reduced synchrony, and increased variability in neuronal responses. Furthermore, place fields emerged more slowly in both familiar and novel environments, indicative of recall and learning impairments respectively. By showing a specific link between plaque vicinity and neural coding deficits including reduced dynamic range in mice performing spatial tasks, our study offers new insights into the circuit basis of progressive cognitive degradation in AD.

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