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Neurobehavioral deficits in db/db diabetic mice
Ajaykumar N Sharma1, Khalid M Elased, Teresa L Garrett
1Wright State University, Boonshoft School of Medicine, Department of Pharmacology and Toxicology, Dayton, OH 45435, USA.
Physiology & Behavior
|July 20, 2010
Summary
The db/db mouse model exhibits depression and psychosis-like symptoms, suggesting its utility for studying type-2 diabetes neurobehavioral complications. Adult mice show age-dependent progression of these symptoms.
Area of Science:
- Neuroscience
- Endocrinology
- Behavioral Science
Background:
- Clinical studies suggest neurobehavioral disturbances in type-2 diabetes.
- Preclinical research validating these observations is limited.
- The db/db mouse is a recognized model for type-2 diabetes complications.
Purpose of the Study:
- To comprehensively investigate the db/db mouse as a preclinical model for type-2 diabetes-related neurobehavioral complications.
- To assess depression, psychosis-like symptoms, anxiety, locomotor activity, and working memory in db/db mice.
Main Methods:
- Behavioral testing of juvenile and adult db/db mice.
- Forced Swim Test (FST) for depression.
- Pre-Pulse Inhibition (PPI) test for psychosis-like symptoms.
- Elevated Plus Maze (EPM) for anxiety.
- Open Field Test (OFT) for locomotor activity and thigmotaxis.
- Y-maze test for working memory.
Main Results:
- Both juvenile and adult db/db mice showed increased immobility in FST, indicating behavioral despair.
- Adult db/db mice exhibited age-dependent psychosis-like symptoms with disrupted PPI.
- Db/db mice displayed anxiolytic behavior in the EPM test.
- Hypo-locomotion was observed in db/db mice in the OFT.
- No working memory impairment was detected in the Y-maze test.
Conclusions:
- This study provides the first report of depression, psychosis-like symptoms, and anxiolytic behavior in the db/db mouse strain.
- The db/db mouse demonstrates potential as a valuable preclinical model for investigating type-2 diabetes-associated neurobehavioral complications.
- Findings highlight the need for further research into the neurobiological mechanisms underlying these behavioral changes in type-2 diabetes.

