You are not currently logged in.
Access your personal account or get JSTOR access through your library or other institution:
If You Use a Screen ReaderThis content is available through Read Online (Free) program, which relies on page scans. Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Place Cell Firing Correlates with Memory Deficits and Amyloid Plaque Burden in Tg2576 Alzheimer Mouse Model
Francesca Cacucci, Ming Yi, Thomas J. Wills, Paul Chapman and John O'Keefe
Proceedings of the National Academy of Sciences of the United States of America
Vol. 105, No. 22 (Jun. 3, 2008), pp. 7863-7868
Published by: National Academy of Sciences
Stable URL: http://www.jstor.org/stable/25462693
Page Count: 6
Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Preview not available
Alzheimer's disease (AD) is associated with progressive memory decline. Hippocampal place cells are a well understood candidate for the neural basis of one type of memory in rodents; these cells identify the animal's location in an environment and are crucial for spatial memory and navigation. We have recorded place cells in the Tg2576 mouse model of AD, and we report that aged (16 mo) but not young (3 mo) transgenic mice show degraded neuronal representations of the environment. The level of place cell degradation correlates with the animals' (poorer) spatial memory as tested in a forced-choice spatial alternation T-maze task and with hippocampal, but not neocortical, amyloid plaque burden. Place cell recording provides a sensitive assay for measuring the amount and rate of functional deterioration in animal models of dementia as well as providing a quantifiable physiological indication of the beneficial effects of potential therapies.
Proceedings of the National Academy of Sciences of the United States of America © 2008 National Academy of Sciences