Murine Non-Transgenic Models of Alzheimer's Disease Pathology: Focus on Risk Factors
Maricarmen Hernández-Rodríguez1, Juan Manuel Vega López2, Martín Martínez-Rosas3
1Laboratorio de Cultivo Celular, Neurofarmacología y Conducta, Escuela Superior de Medicina, Instituto Politécnico Nacional, Plan de San Luis y Díaz Mirón s/n, Mexico City 11340, Mexico.
Brain Sciences
|March 28, 2025
Summary
Alzheimer's disease (AD) research often uses transgenic models. This review explores non-transgenic models, like those induced by streptozotocin or aging, for better Alzheimer's disease therapeutic evaluation.
Area of Science:
- Neuroscience
- Pathology
- Pharmacology
Background:
- Alzheimer's disease (AD) is a major neurodegenerative disorder with unmet therapeutic needs.
- Current AD research heavily relies on amyloid-β (Aβ) transgenic models, with limited therapeutic success.
- Key AD pathologies include Aβ plaques, neurofibrillary tangles, and neuroinflammation.
Purpose of the Study:
- To critically review non-transgenic models for Alzheimer's disease research.
- To assess the utility of models induced by agents like streptozotocin, scopolamine, aging, metals, and diet.
- To enhance the application of these models in evaluating therapeutic interventions for AD.
Main Methods:
- Literature review of existing studies on Alzheimer's disease non-transgenic models.
- Analysis of models induced by specific agents (streptozotocin, scopolamine, metals, etc.) and conditions (aging, mechanical stress, diet).
- Evaluation of how these models mimic AD pathology and risk factors.
Main Results:
- Non-transgenic models offer complementary insights into AD's complex pathology beyond Aβ-centric views.
- Models induced by various factors can recapitulate key AD features like neuroinflammation and cognitive deficits.
- These models are valuable for assessing interventions targeting primary AD risk factors.
Conclusions:
- Non-transgenic models are practical tools for Alzheimer's disease research and therapeutic strategy evaluation.
- Expanding the use of these diverse models can accelerate the development of effective AD treatments.
- Further research into induced non-transgenic models can improve preclinical AD drug discovery.
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