A cause of nerve degeneration in patients with Parkinson’s disease may have been discovered by new research, along with a potential treatment that can interrupt the process.
Northwestern University scientists identified a toxic cascade that leads to neuronal degeneration in patients with Parkinson’s disease (PD). They also found that intervening with an antioxidant early in the disease process may break the degenerative cycle and improve neuron function in PD, their study shows.
The scientists further found that mouse models of PD didn’t have the same abnormalities they found in human Parkinson’s disease neurons, revealing the importance of studying human neurons to develop new therapies.
Dopamine Neuron Death
Parkinson’s is the second most common neurodegenerative disorder, primarily caused by the death of dopamine-containing neurons in the substantia nigra, a region of the brain involved in motor control. While people naturally lose dopamine neurons as they age, patients with PD lose a much larger number of these neurons and the remaining cells are no longer able to compensate.
Understanding how and why these neurons die is an important step in identifying treatments, says Dimitri Krainc, a professor and chair of neurology at the Northwestern University Feinberg School of Medicine and the study’s senior author.
Although previous research indicated that the cellular mechanism behind the cell death involved the mitochondria and lysosomes, how these two pathways converge in dopamine neurons to cause cell death remained unknown up until now.
Using human neurons from Parkinson’s patients, Krainc and colleagues identified a toxic cascade of mitochondrial and lysosomal dysfunction initiated by an accumulation of oxidized dopamine and a protein called alpha-synuclein.
Specifically, the current study demonstrated that an accumulation of oxidized dopamine depressed the activity of lysosomal glucocerebrosidase (GCase), an enzyme implicated in PD. That depression in turn weakened overall lysosomal function and contributed to degeneration of neurons.
Critical Disease Pathways
The accretion of oxidized dopamine didn’t just interfere with lysosomes, however. Krainc and his colleagues discovered that the dopamine also damaged the neurons’ mitochondria by increasing mitochondrial oxidant stress. These dysfunctional mitochondria led to increased oxidized dopamine levels, creating a vicious cycle.
“The mitochondrial and lysosomal pathways are two critical pathways in disease development. Combined with the alpha-synuclein accumulation, this study links the major pathological features of PD.”
says Krainc, a professor and chair of neurology at the Northwestern University Feinberg School of Medicine and the study’s senior author.
Once they had catalogued this toxic cascade, Krainc and his colleagues began looking for ways to interrupt it.
“One of the key strategies that worked in our experiments is to treat dopamine neurons early in the toxic cascade with specific antioxidants that improve mitochondrial oxidant stress and lower oxidized dopamine. With this approach, we found that we can attenuate or prevent the downstream toxic effects in human dopaminergic neurons,”
Developing Future Therapies
This approach to interrupting the toxic cascade of oxidized dopamine may provide a target for the development of future therapies. However, identifying patients or subjects with early-stage neurodegeneration can be difficult, because damage has often occurred far before any symptoms are apparent, according to Krainc.
Consequently, genetic testing will be central to future diagnostic efforts. Causative genes are prime candidates for screening, while risk genes such as GBA1 are less conclusive but still important markers, Krainc says.
Early detection will also rely on brain imaging and other clinical signifiers.
Interestingly, when compared to human cellular models, mouse models of PD did not demonstrate the same toxic cascade, according to the study. Krainc and his colleagues showed this is due to differences in metabolism of dopamine between species, and underscored the importance of studying human neurons to discover new targets for drug development.
The work was supported by funding from National Institute of Neurological Disorders and Stroke grants, National Institute on Deafness and Other Communication Disorders, the JPB Foundation, the Michael J. Fox Foundation, the IDP Foundation, the German Academic Exchange Service, the Les Turner ALS Foundation, Target ALS, the German Research Council, and Fond National de Recherche PEARLE Programme.