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Updated: Jun 29, 2026

Preparation of Acute Hippocampal Slices from Rats and Transgenic Mice for the Study of Synaptic Alterations during Aging and Amyloid Pathology
Published on: March 23, 2011
Altered dorsal CA1 neuronal population coding in the APP/PS1 mouse model of Alzheimer's disease
Udaysankar Chockanathan1,2,3, Emily J Warner1,2, Loel Turpin1
1Department of Neuroscience, University of Rochester School of Medicine & Dentistry, Rochester, NY, United States.
Abstract:
While the link between amyloid β (Aβ) accumulation and synaptic degradation in Alzheimer's disease (AD) is known, the consequences of this pathology on population coding remain unknown. We found that the entropy, a measure of the diversity of network firing patterns, was lower in the dorsal CA1 region in the APP/PS1 mouse model of Aβ pathology, relative to controls, thereby reducing the population's coding capacity. Our results reveal a network level signature of the deficits Aβ accumulation causes to the computations performed by neural circuits.
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