Development and Screening of Contrast Agents for In Vivo Imaging of Parkinson’s Disease
Author(s)Neal, Krista L.; Shakerdge, Naomi B.; Hou, Steven S.; Klunk, William E.; Mathis, Chester A.; McLean, Pamela J.; Bacskai, Brian J.; Nesterov, Evgueni; Swager, Timothy M; ... Show more Show less
MetadataShow full item record
Purpose: The goal was to identify molecular imaging probes that would enter the brain, selectively bind to Parkinson’s disease (PD) pathology, and be detectable with one or more imaging modalities. Procedure: A library of organic compounds was screened for the ability to bind hallmark pathology in human Parkinson’s and Alzheimer’s disease tissue, alpha-synuclein oligomers and inclusions in two cell culture models, and alpha-synuclein aggregates in cortical neurons of a transgenic mouse model. Finally, compounds were tested for blood–brain barrier permeability using intravital microscopy. Results: Several lead compounds were identified that bound the human PD pathology, and some showed selectivity over Alzheimer’s pathology. The cell culture models and transgenic mouse models that exhibit alpha-synuclein aggregation did not prove predictive for ligand binding. The compounds had favorable physicochemical properties, and several were brain permeable. Conclusions: Future experiments will focus on more extensive evaluation of the lead compounds as PET ligands for clinical imaging of PD pathology.
DepartmentMassachusetts Institute of Technology. Department of Chemistry
Molecular Imaging and Biology
Neal, Krista L. et al. “Development and Screening of Contrast Agents for In Vivo Imaging of Parkinson’s Disease.” Molecular Imaging and Biology 15.5 (2013): 585–595.
Author's final manuscript