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(18)F-FDG-PET in Mouse Models of Alzheimer's Disease
Suitable animal models and in vivo biomarkers are essential for development and evaluation of new therapeutic strategies in Alzheimer's disease (AD). (18)F-Fluorodeoxyglucose ((18)F-FDG)-positron-emission tomography (PET) is an imaging biomarker that allows the assessment of cerebral glucose me...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482246/ https://www.ncbi.nlm.nih.gov/pubmed/31058151 http://dx.doi.org/10.3389/fmed.2019.00071 |
Sumario: | Suitable animal models and in vivo biomarkers are essential for development and evaluation of new therapeutic strategies in Alzheimer's disease (AD). (18)F-Fluorodeoxyglucose ((18)F-FDG)-positron-emission tomography (PET) is an imaging biomarker that allows the assessment of cerebral glucose metabolism in vivo. While (18)F-FDG-PET/CT is an established tool in the evaluation of AD patients, its role in preclinical studies with AD mouse models remains unclear. Here, we want to review available studies on (18)F-FDG-PET/CT in AD mouse models in order to evaluate the method and its impact in preclinical AD research. Only a limited number of studies using (18)F-FDG-PET in AD mice were carried out so far showing contradictory findings in cerebral FDG uptake. Methodological differences as well as underlying pathological features of used mouse models seem to be accountable for those varying results. However, (18)F-FDG-PET can be a valuable tool in longitudinal in vivo therapy monitoring with a lot of potential for future studies. |
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