“Many of the current therapeutic compounds focus on boosting the dopamine output of surviving cells, but this is effective only as long as there are still enough cells to do the job,” said Jeremy Lee, a biochemist from Saskatchewan. “Our approach aims to protect dopamine-producing cells by preventing a-synuclein from mis-folding in the first place,” said Lee. Although the chemistry was challenging, Lee explained the team synthesised 30 different “bifunctional dimer” drugs, that is, molecules that link two different substances known to have an effect on dopamine-producing cells. They started with a caffeine “scaffold,” guided by literature that shows the stimulant has a protective effect against Parkinson’s. From this base, they added other compounds with known effects: nicotine, the diabetes drug metformin, and aminoindan, a research chemical similar to the Parkinson’s drug rasagiline.
Using a yeast model of Parkinson’s disease, researchers discovered two of the compounds prevented the AS protein from clumping, effectively allowing the cells to grow normally. “Our results suggest these novel bifunctional dimers show promise in preventing the progression of Parkinson’s disease,” Lee said. The findings were published in the journal ACS Chemical Neuroscience.