Preliminary PET Imaging of Microtubule-Based PET Radioligand [ 11 C]MPC-6827 in a Nonhuman Primate Model of Alzheimer's Disease.
Bhuvanachandra BhoopalKrishna Kumar GollapelliNaresh DamukaMack MillerIvan KrizanAvinash BansodeThomas RegisterBrett M FryeJeongchul KimAkiva MintzMiranda OrrSuzanne CraftChristopher WhitlowSamuel N LockhartCarol ShivelyKiran Kumar Solingapuram SaiPublished in: ACS chemical neuroscience (2023)
The microtubule (MT) instability observed in Alzheimer's disease (AD) is commonly attributed to hyperphosphorylation of the MT-associated protein, tau. In vivo PET imaging offers an opportunity to gain critical information about MT changes with the onset and development of AD and related dementia. We developed the first brain-penetrant MT PET ligand, [ 11 C]MPC-6827, and evaluated its in vivo imaging utility in vervet monkeys. Consistent with our previous in vitro cell uptake and in vivo rodent imaging experiments, [ 11 C]MPC-6827 uptake increased with MT destabilization. Radioactive uptake was inversely related to (cerebrospinal fluid) CSF Aβ 42 levels and directly related to age in a nonhuman primate (NHP) model of AD. Additionally, in vitro autoradiography studies also corroborated PET imaging results. Here, we report the preliminary results of PET imaging with [ 11 C]MPC-6827 in four female vervet monkeys with high or low CSF Aβ 42 levels, which have been shown to correlate with the Aβ plaque burden, similar to humans.
Keyphrases
- pet imaging
- cerebrospinal fluid
- positron emission tomography
- high resolution
- computed tomography
- single cell
- stem cells
- multiple sclerosis
- healthcare
- mild cognitive impairment
- mesenchymal stem cells
- bone marrow
- cognitive impairment
- risk factors
- health information
- photodynamic therapy
- white matter
- brain injury
- blood brain barrier
- resting state