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Mild stress facilitates learning and exercise improves retention in aged mice
Paul A Adlard1, Christie Engesser-Cesar, Carl W Cotman
1Institute for Brain Aging and Dementia, University of California Irvine, 1226 Gillespie NRF, Irvine, CA 92697-4540, United States. p.adlard@mhri.edu.au
Experimental Gerontology
|October 19, 2010
Summary
Mild stress aids learning in aged mice, while exercise improves memory retention in both young and aged mice. Voluntary exercise also upregulates key learning/memory genes in older animals.
Area of Science:
- Neuroscience
- Gerontology
- Behavioral Biology
Background:
- Chronic stress negatively impacts the brain, but moderate stress can enhance learning in young animals.
- The effects of mild stress on learning and memory in aged animals remain largely unknown.
- Exercise is known to counteract stress and facilitate cognitive functions.
Purpose of the Study:
- To investigate the impact of mild stress on learning and memory retention in young versus aged mice.
- To determine if voluntary exercise can improve task retention in these age groups.
- To examine the regulation of specific learning/memory genes (BDNF exon VI, synapsin, MAPK, CRFR1) in the hippocampus.
Main Methods:
- Assessment of learning and 1-week retention tasks in young and aged mice.
- Administration of mild stress 24 hours before the initial learning test.
- Implementation of a 1-week voluntary exercise intervention between learning and retention tests.
- Real-time PCR analysis of gene expression (BDNF exon VI, synapsin, MAPK, CRFR1) in the hippocampus.
Main Results:
- Mild stress significantly improved learning performance in aged mice, but not in young mice.
- Voluntary exercise enhanced task retention performance in both young and aged mice.
- In aged mice, exercise led to significant increases in all four examined learning/memory related genes.
Conclusions:
- Mild stress facilitates learning in aged animals.
- Voluntary exercise improves the retention of learned tasks in both young and aged mice.
- Exercise positively influences the expression of key learning and memory genes in the hippocampus of aged mice.

