Brain energy metabolism and neuroinflammation in ageing APP/PS1-21 mice using longitudinal 18F-FDG and 18F-DPA-714 PET imaging

A1 Originalartikel i en vetenskaplig tidskrift (referentgranskad)

Interna författare/redaktörer

Publikationens författare: Takkinen JS, Lopez-Picon FR, Al Majidi R, Eskola O, Krzyczmonik A, Keller T, Loyttyniemi E, Solin O, Rinne JO, Haaparanta-Solin M
Publiceringsår: 2017
Tidskrift: Journal of Cerebral Blood Flow and Metabolism
Tidskriftsakronym: J CEREBR BLOOD F MET
Volym: 37
Artikelns första sida, sidnummer: 2870
Artikelns sista sida, sidnummer: 2882
Antal sidor: 13
ISSN: 0271-678X


Preclinical animal model studies of brain energy metabolism and neuroinflammation in Alzheimer's disease have produced conflicting results, hampering both the elucidation of the underlying disease mechanism and the development of effective Alzheimer's disease therapies. Here, we aimed to quantify the relationship between brain energy metabolism and neuroinflammation in the APP/PS1-21 transgenic mouse model of Alzheimer's disease using longitudinal in vivo F-18-FDG and F-18-DPA-714) PET imaging and ex vivo brain autoradiography. APP/PS1-21 (TG, n = 9) and wild type control mice (WT, n = 9) were studied longitudinally every third month from age 6 to 15 months with F-18 -FDG and F-18-DPA-714 with a one-week interval between the scans. Additional TG (n = 52) and WT (n = 29) mice were used for ex vivo studies. In vivo, the F-18-FDG SUVs were lower and the F-18-DPA-714 binding ratios relative to the cerebellum were higher in the TG mouse cortex and hippocampus than in WT mice at age 12 to 15 months (p<0.05). The ex vivo cerebellum binding ratios supported the results of the in vivo F-18-DPA-714 studies but not the F-18-FDG studies. This longitudinal PET study demonstrated decreased energy metabolism and increased inflammation in the brains of APP/PS1-21 mice compared to WT mice.


Alzheimer's disease, F-18-DPA-714, F-18-FDG, longitudinal imaging, PET

Senast uppdaterad 2020-10-04 vid 08:17