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Updated: Nov 19, 2025

Morris Water Maze Test: Optimization for Mouse Strain and Testing Environment
Published on: June 22, 2015
Reward motivation and cognitive flexibility in tau null-mutation mice
Sara Oberrauch1, Jeremy A Metha2, Maddison L Brian1
1The Florey Institute of Neuroscience and Mental Health, Parkville Campus, University of Melbourne, Parkville, Australia; Department of Pharmacology & Therapeutics, School of Medicine, Faculty of Medicine, Dentistry and Health Sciences, The University of Melbourne, Parkville, Victoria, Australia.
Mice lacking tau protein showed altered reward processing, eating more and demonstrating higher motivation for rewards. This suggests tau
Area of Science:
- Neuroscience
- Neurology
- Molecular Biology
Background:
- Tauopathies, including Alzheimer's disease (AD) and frontotemporal dementia (FTD), are characterized by cognitive decline and sleep-wake disturbances.
- Alterations in the brain's reward system are observed in AD and FTD patients, but the specific role of tau in these processes remains unclear.
Purpose of the Study:
- To investigate the role of tau in reward processing and reward-motivated cognitive functions.
- To compare reward-related behaviors in tau knockout (tau-/-) mice and wild-type (WT) mice.
Main Methods:
- Utilized progressive ratio and reversal learning tasks in male and female tau-/- and WT mice.
- Assessed operant lever training, home cage food intake, and body weight.
Main Results:
- Tau-/- mice exhibited increased body weight and home cage food consumption compared to WT mice.
- Tau-/- mice demonstrated a higher breakpoint on the progressive ratio task, indicating increased motivation for rewards.
- No significant impairments were observed in reversal learning or reward sensitivity in tau-/- mice.
Conclusions:
- Loss of tau function significantly alters reward processing mechanisms.
- These findings may elucidate aberrant reward-related behaviors observed in tauopathy patients.
- Understanding tau's role in reward pathways offers a potential therapeutic target for anti-tau strategies in neurodegenerative diseases.
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