Prompted by a new Blaylock paper
and discussion, I browsed the PD glutamate literature and
found Van Laar et al reference describing NAC, parkin, and
excitotoxicity.
Read Van Laar 2015 at: "NAC facilitates Parkin translocation and
mitophagy in neurons following excitotoxic insult – a possible
unexpected role for oxidative stress".
Also read at: "Glutamate exposure causes mitochondrial
depolarization and delayed loss of ATP".
Glutamate excitotoxicity in neurons triggers mitochondrial and
endoplasmic reticulum accumulation of Parkin, and, in the presence
of N-acetyl cysteine, mitophagy.
Van Laar et al 2015,
ncbi.nlm.nih.gov/pmc/articl...
See also:
An update on the potential role of excitotoxicity in the
pathogenesis of Parkinson's disease.
Blandini 2010.
ncbi.nlm.nih.gov/pubmed/209...
Mutant LRRK2 enhances glutamatergic synapse activity and evokes
excitotoxic dendrite degeneration.
ncbi.nlm.nih.gov/pubmed/248...
Neuroprotective and symptomatic effects of targeting group III mGlu
receptors in neurodegenerative disease.
ncbi.nlm.nih.gov/pubmed/242...