Individuals taking tricyclics antidepressants (amitriptyline in particular) had a lower probability of initiating dopaminergic therapy within the first year of their study. This observation suggested to the researchers that treatment with tricyclic antidepressants may delay the need to initiate dopamine therapy for Parkinson’s.
Amitriptyline treatment resulted in an increase in BDNF in the substantia nigra region both before and during ongoing degeneration, suggesting it may contribute to neuroprotection observed in vivo. Amitriptyline treatment also resulted in an increase in GDNF levels but only before the neurotoxin was given
they concluded that the neuroprotective effect seen in their model was most likely due to the increase in BDNF levels.
Tricyclic antidepressant treatment evokes regional changes in neurotrophic factors over time within the intact and degenerating nigrostriatal system
The current study compared three common antidepressant medications, amitriptyline, nortriptyline and venlafaxine, for effects on protecting dopamine nerve cells from degeneration in a toxin model of parkinsonism. No protective effect of any of the drugs or doses tested was found. This is in contrast to our previous work showing that amitriptyline can protect dopamine cells, albeit in a less severe degeneration model. Our tentative conclusion is that while antidepressant medications may have a modest protective effect, this positive influence can be overwhelmed in a model of severe, sudden damage to the dopamine system.
Wouldn't it make more sense to utilise compounds that reduce oxidative stress to prevent degeneration? Things like N-acetylcysteine, melatonin, ivermectin are all very strong antioxidants and anti-inflammatories and when combined work synergistically like panadol and nurofen.
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