Muscarinic receptor activation preferentially inhibits rebound in vulnerable dopaminergic neurons.
Megan L BeaverRebekah C EvansPublished in: bioRxiv : the preprint server for biology (2024)
(SNc) can be divided into functional subpopulations with distinct basal ganglia connectivity and different degeneration patterns in Parkinson's disease. We show that the vulnerable and resilient subpopulations of SNc dopaminergic neurons are differentially modulated by muscarinic receptor activation. Specifically, muscarinic receptor activation inhibits rebound activity more strongly in the vulnerable SNc neurons than in the resilient. We find that this inhibition occurs through a non-canonical rebound-related pathway and is not mediated through the channels best known for modulating rebound in midbrain dopaminergic neurons. These findings are important because they reveal novel acetylcholine-dopamine interactions that occur in the midbrain and affect information processing in distinct basal ganglia circuits.