Compositions and methods for the treatment of tauopathies
Disclosed herein are compositions and methods for treating tauopathies such as Alzheimer's disease (AD). Also provided herein are methods of reducing or disrupting tau aggregation in a subject, and methods of reducing tau protein in a subject. The methods may include administering to the subject a therapeutic amount of hexachlorophene, or a pharmaceutically acceptable salt thereof. Further provided herein are pharmaceutical compositions comprising hexachlorophene, or a pharmaceutically acceptable salt thereof, for the treatment of a tauopathy in a subject.
1. A method of treating a tauopathy in a subject, the method comprising administering to the subject a therapeutic amount of hexachlorophene, or a pharmaceutically acceptable salt thereof.
2. The method of claim 1 , wherein the level of phosphorylated tau protein is reduced.
3. The method of claim 2 , wherein the level is reduced a least 10%.
4. The method of claim 3 , wherein the level is reduced at least 50%.
5. The method of claim 4 , wherein the level is reduced at least 80%.
6. The method of claim 1 , wherein the level of total tau protein is reduced.
7. The method of claim 1 , wherein tau aggregation is reduced.
8. The method of claim 7 , wherein tau aggregation is reduced a least 10%.
9. The method of claim 8 , wherein tau aggregation is reduced at least 50%.
10. The method of claim 9 , wherein tau aggregation is reduced at least 80%.
11. The method of claim 1 , wherein the tauopathy is selected from neurodegenerative disease, Alzheimer's disease (AD), Parkinson's disease, Huntington's disease, neuronal loss, cognitive defect, primary age-related tauopathy (PART)/Neurofibrillary tangle-predominant senile dementia, chronic traumatic encephalopathy including dementia pugilistica, progressive supranuclear palsy, Pick's Disease, corticobasal degeneration, some forms of frontotemporal lobar degeneration, frontotemporal dementia and parkinsonism linked to chromosome 17, Lytico-Bodig disease (Parkinson-dementia complex of Guam), ganglioglioma, gangliocytoma, meningioangiomatosis, postencephalitic parkinsonism, subacute sclerosing panencephalitis, lead encephalopathy, tuberous sclerosis, Hallervorden-Spatz disease, and lipofuscinosis.
12. The method of claim 11 , wherein the tauopathy comprises Alzheimer's disease (AD).
13. The method of claim 1 , wherein the hexachlorophene or salt is present in a therapeutically effective amount in a pharmaceutical composition.
14. The method of claim 1 , wherein the hexachlorophene or salt is administered to the subject intravenously, intraarterially, or intraperitoneally.
15. The method of claim 14 , wherein the hexachlorophene or salt is delivered to the brain of the subject.
16. The method of claim 1 , wherein the hexachlorophene or salt is administered by gavage.
17. A method of reducing or disrupting tau aggregation in a subject, the method comprising administering to the subject a therapeutic amount of hexachlorophene, or a pharmaceutically acceptable salt thereof.
18. A method of reducing tau protein in a subject, the method comprising administering to the subject a therapeutic amount of hexachlorophene, or a pharmaceutically acceptable salt thereof.
19. A pharmaceutical composition comprising hexachlorophene, or a pharmaceutically acceptable salt thereof, for the treatment of a tauopathy in a subject.
20. The pharmaceutical composition of claim 19 , wherein the tauopathy comprises Alzheimer's disease (AD).