Synaptic and neuronal loss are major neuropathological characteristics of Parkinson’s disease (PD). Misfolded protein aggregates in the form of Lewy bodies, comprised mainly of α-synuclein (αSyn), are associated with disease progression, and have also been linked to other neurodegenerative diseases, including Lewy body dementia (LBD), Alzheimer’s disease (AD, and Frontotemporal dementia (FTD). However, the effects of αSyn and its mechanism of synaptic damage remain incompletely understood. Here, we show that αSyn oligomers induce Ca2+-dependent release of glutamate from astrocytes obtained from male and female mice, and that mice overexpressing αSyn manifest increased tonic release of glutamate in vivo . In turn, this extracellular glutamate activates glutamate receptors, including extrasynaptic NMDA receptors (eNMDARs), on neurons both in culture and in hippocampal slices of αSyn-overexpressing mice. Additionally, in patch-clamp recording from outside-out patches, we found that oligomerized αSyn can direc...