Methods and compounds for inhibiting amyloid deposits
Methods and compositions which are useful in the treatment of amyloidosis. In particular, methods and compositions are provided for inhibiting, preventing and treating amyloid deposition, e.g., in pancreatic islets, wherein the amyloidotic deposits are islet amyloid polypeptide (IAPP)-associated amyloid deposition or deposits. The methods of the invention involve administering to a subject a therapeutic compound which inhibits IAPP-associated amyloid deposits. Accordingly, the compositions and methods of the invention are useful for inhibiting IAPP-associated amyloidosis in disorders in which such amyloid deposition occurs, such as diabetes.
1. A method for inhibiting IAPP-associated amyloid deposits in a subject, comprising administering to said subject an effective amount of an IAPP-inhibiting compound, selected from 3-(3-hydroxy-1-propyl)amino-1-propanesulfonic acid, 2-amino-5-phosphonovaleric acid, 4-phenyl-1-(3′-sulfopropyl) 1,2,3,6-tetrahydropyridine, O-phosphono-L-serine and 3-amino-2-hydroxy-1-propanesulfonic acid and pharmaceutically acceptable esters, acids or salts thereof, such that said IAPP-associated amyloid deposits are inhibited.
2. The method of claim 1 , wherein said subject has IAPP-associated amyloid deposits in pancreatic islets.
3. A method for inhibiting IAPP fibrillogenesis in a subject, comprising administering to said subject an effective amount of an IAPP inhibiting compound, selected from 3-(3-hydroxy-1-propyl)amino-1-propanesulfonic acid, 2-amino-5-phosphonovaleric acid, 4-phenyl-1-(3′-sulfopropyl) 1,2,3,6-tetrahydropyridine, O-phosphono-L-serine and 3-amino-2-hydroxy-1-propanesulfonic acid and pharmaceutically acceptable esters, acids or salts thereof, such that IAPP fibrillogenesis is inhibited.
4. A method for reducing IAPP-associated amyloid deposits in a subject having IAPP-associated amyloid deposits, the method comprising administering to said subject an effective amount of an IAPP inhibiting compound, selected from 3-(3-hydroxy-1-propyl)amino-1-propanesulfonic acid, 2-amino-5-phosphonovaleric acid, 4-phenyl-1-(3′-sulfopropyl) 1,2,3,6-tetrahydropyridine, O-phosphono-L-serine and 3-amino-2-hydroxy-1-propanesulfonic acid and pharmaceutically acceptable esters, acids or salts thereof, such that said IAPP-associated amyloid deposits are inhibited.
5. The method of claim 4 , wherein said subject has IAPP-associated amyloid deposits in pancreatic islets.
6. A method for inhibiting amyloid deposits in a subject, comprising administering to said subject an effective amount of a compound selected from 3-(3-hydroxy-1-propyl)amino-1-propanesulfonic acid, 2-amino-5-phosphonovaleric acid, 4-phenyl-1-(3′-sulfopropyl) 1,2,3,6-tetrahydropyridine, O-phosphono-L-serine and 3-amino-2-hydroxy-1-propanesulfonic acid and pharmaceutically acceptable esters, acids, or salts thereof such that said amyloid deposits are inhibited.
7. The method of claim 1 , wherein said compound is 3-(3-hydroxy-1-propyl)amino-1-propanesulfonic acid, or a pharmaceutically acceptable salt thereof.
8. The method of claim 4 , wherein said compound is 3-(3-hydroxy-1-propyl)amino-1-propanesulfonic acid, or a pharmaceutically acceptable salt thereof.
9. The method of claim 6 , wherein said compound is 3-(3-hydroxy-1-propyl)amino-1-propanesulfonic acid, or a pharmaceutically acceptable salt thereof.