Treating neural disease with tyrosine kinase inhibitors
Provided herein are methods of treating or preventing a neurodegenerative disease, a myodegenerative disease or a prion disease in a subject comprising administering a tyrosine kinase inhibitor.
1. A method of treating an α-Synucleinopathy in a subject, comprising:
selecting a subject with an α-Synucleinopathy or at risk for an α-Synucleinopathy; and
systemically administering to the subject an effective amount of nilotinib, wherein the nilotinib is administered to the subject at a dosage of about 5 mg/kg or less.
2. The method of claim 1 , wherein the effective amount of nilotinib promotes Parkin activity.
3. The method of claim 1 , wherein the nilotinib is administered daily.
4. The method of claim 1 , further comprising administering a second therapeutic agent to the subject.
5. A method of inhibiting toxic protein aggregation in a neuron of a subject with an α-Synucleinopathy, comprising contacting the neuron in the subject with an effective amount of nilotinib, wherein the neuron is contacted with nilotinib by systemically administering nilotinib to the subject at a dosage of about 5 mg/kg or less.
6. The method of claim 5 , wherein the protein is selected from the group consisting of alpha-synuclein, and insoluble Parkin.
7. A method of rescuing a neuron from neurodegeneration associated with an α-Synucleinopathy in a subject comprising contacting the neuron in the subject with an effective amount of, nilotinib, wherein the neuron is contacted with the nilotinib by systemically administering a nilotinib to the subject at a dosage of about 5 mg/kg or less.
8. The method of claim 1 , further comprising determining that the subject has a decreased level of parkin activity relative to a control prior to administering to the subject an effective amount of nilotinib.