Early Detection of Aβ Deposition in the 5xFAD Mouse by Amyloid PET.
Se Jong OhHae-June LeeKyeung Jun KangSang Jin HanYong Jin LeeKyo Chul LeeSang Moo LimDae Yoon ChiKyeong Min KimJi Ae ParkJae Yong ChoiPublished in: Contrast media & molecular imaging (2018)
Purpose.18F-FC119S is a positron emission tomography (PET) tracer for imaging β-amyloid (Aβ) plaques in Alzheimer's disease (AD). The aim of this study is to evaluate the efficacy of 18F-FC119S in quantitating Aβ deposition in a mouse model of early amyloid deposition (5xFAD) by PET. Method. Dynamic 18F-FC119S PET images were obtained in 5xFAD (n = 5) and wild-type (WT) mice (n = 7). The brain PET images were spatially normalized to the M. Mirrione T2-weighted mouse brain MR template, and the volumes of interest were then automatically drawn on the cortex, hippocampus, thalamus, and cerebellum. The specific binding of 18F-FC119S to Aβ was quantified as the distribution volume ratio using Logan graphical analysis with the cerebellum as a reference tissue. The Aβ levels in the brain were also confirmed by immunohistochemical analysis. Result. For the 5xFAD group, radioactivity levels in the cortex, the hippocampus, and the thalamus were higher than those for the WT group. In these regions, specific binding was approximately 1.2-fold higher in 5xFAD mice than in WT. Immunohistochemistry supported these findings; the 5xFAD showed severe Aβ deposition in the cortex and hippocampus in contrast to the WT group. Conclusion. These results demonstrated that 18F-FC119S PET can successfully distinguish Aβ depositions in 5xFAD mice from WT.
Keyphrases
- positron emission tomography
- computed tomography
- pet ct
- pet imaging
- wild type
- functional connectivity
- magnetic resonance
- mouse model
- contrast enhanced
- resting state
- cerebral ischemia
- high fat diet induced
- deep learning
- convolutional neural network
- cognitive impairment
- magnetic resonance imaging
- white matter
- type diabetes
- early onset
- optical coherence tomography
- multiple sclerosis
- machine learning
- metabolic syndrome
- insulin resistance
- dna binding
- blood brain barrier