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Object recognition memory and BDNF expression are reduced in young TgCRND8 mice
Beverly M Francis1, John Kim, Meredith E Barakat
1Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, ON, Canada.
Neurobiology of Aging
|May 8, 2010
Summary
Early Alzheimer
Area of Science:
- Neuroscience
- Alzheimer's Disease Research
- Cognitive Neuroscience
Background:
- Alzheimer's disease (AD) is characterized by amyloid-beta (Aβ) accumulation.
- The TgCRND8 mouse model develops Aβ plaques and cognitive deficits.
- Early functional changes preceding plaque formation are not fully understood.
Purpose of the Study:
- To investigate cognitive function in TgCRND8 mice before macroscopic plaque development.
- To identify early molecular changes associated with cognitive deficits.
Main Methods:
- Object recognition task to assess memory in 8-week-old TgCRND8 mice and controls.
- Morris water maze task to evaluate spatial memory.
- Measurement of brain-derived neurotrophic factor (BDNF) mRNA levels.
Main Results:
- TgCRND8 mice exhibited significant object recognition deficits at 8 weeks of age.
- No impairment was observed in the Morris water maze task at this age.
- Altered BDNF mRNA levels were detected in the frontal cortex and hippocampus of preplaque TgCRND8 mice.
Conclusions:
- Object recognition is a sensitive assay for detecting early cognitive impairment in AD models.
- Functional disruption in frontal cortex and hippocampus occurs before plaque formation.
- Reduced BDNF expression may contribute to early cognitive deficits in TgCRND8 mice.
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