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Aβ Accumulation in Vmo Contributes to Masticatory Dysfunction in 5XFAD Mice
1Department of Brain and Cognitive Sciences, College of Natural Sciences, Seoul National University, Seoul, Republic of Korea.
Journal of Dental Research
|March 15, 2021
Summary
Alzheimer's disease (AD) impairs mastication, evidenced by reduced biting force in 5XFAD mice. Amyloid-beta accumulation in the trigeminal motor nucleus (Vmo) likely causes this masticatory dysfunction.
Area of Science:
- Neuroscience
- Pathology
- Animal Models
Background:
- Alzheimer's disease (AD) is characterized by cognitive decline and neural circuit disruption.
- Sensory dysfunctions are recognized early indicators of AD.
- The link between AD and the masticatory system remains unclear, particularly in animal models.
Purpose of the Study:
- To investigate the pathological hallmarks of AD and their impact on masticatory behavior in 5XFAD mice.
- To establish changes in the masticatory system associated with AD progression.
Main Methods:
- Assessment of masticatory efficiency and biting force in 5XFAD mice.
- Evaluation of general motor function.
- Immunohistochemical analysis of the trigeminal motor nucleus (Vmo) and other cranial motor nuclei for amyloid-beta (Aβ) deposition, microglia activation, and cell death.
- Measurement of masseter muscle weight and muscle fiber size.
Main Results:
- 5XFAD mice exhibited decreased masticatory efficiency and maximum biting force.
- No significant changes in general motor function were observed.
- Significant Aβ accumulation, increased microglia, and cell death were found in the Vmo of 5XFAD mice.
- Reduced masseter muscle weight and muscle fiber size were noted in 5XFAD mice.
Conclusions:
- Amyloid-beta accumulation in the Vmo contributes to masticatory dysfunction in 5XFAD mice.
- These findings suggest a strong association between masticatory dysfunction and dementia in Alzheimer's disease.

