Caroline Bouter et al., Frontiers in Aging Neuroscience, 2019
The authors have used one of the latest mouse Alzheimer’s Disease (AD) models (Tg4-42 transgenic mutation, which overexpresses the Ab4-42 peptide, which is truncated on the N-terminal region, causing neurotoxicity and Ab aggregation, which are similar to AD). As the AD patients show altered glucose metabolism, the authors chose to follow it with the most common radiopharmaceutical used in PET, namely 18F-FDG, and how it can be used together with the MRI as an early biomarker for AD.
They have found that Tg4-42 mice show a reduction of glucose-metabolism, which correlates with their age, and the decreased 18F-FDG uptake can be shown in early age (3 months).
Results from nanoScan PET/MRI 1T
For the PET/MRI studies, the authors have used a nanoScan PET/MRI 1T, which could provide a fast measurement method together with good statistics. Young (3-4 months) and aged (7-8 months) Tg4-42 (n=7, female) and aged WT C57Bl/6J (7-8 months, n=5, female) control mice were used in this study. The authors have followed the standard 18F-FDG PET/MRI protocol, as the mice were fasted overnight, and 9-21 MBq activity was injected into the tail vein, with a 45 minute long uptake period.
The PET scans were performed for 20 minutes , which was followed by a Tera-Tomo 3D reconstruction method with a 0.3 mm3. For the MRI, the authors have used GRE sequence as a material map for attenuation and scatter correction in the PET reconstruction, and as a brain atlas. The analysis was performed with PMOD software.
Figure 3. shows the main results from the PET/MRI acquisitions: a-c) MRI images were matched with predefined brain regions; axial, coronal and sagittal view. d-f) 18F-FDG-PET images of a WT mouse. g-i) 18F-FDG-PET images of a young Tg4–42 mouse. j-l) 18F-FDG-PET images of an aged Tg4–42 mouse. A, Amygdala; Bs, Brain Stem; C, Cortex; Cb, Cerebellum; H, Hypothalamus; Hc, Hippocampus; Hg, Harderian glands; M, Midbrain; O, Olfactory Bulb; S, Septum/Basal Forebrain; St, Striatum; T, Thalamus.
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