Suppression of glial fibrillary acidic protein

1. A method of treating Alexander disease in a subject in need thereof comprising:

administering to a subject at risk of or diagnosed with Alexander disease a therapeutically effective amount of a glial fibrillary acidic protein (GFAP) lowering compound, wherein the GFAP lowering compound comprises a polyphenol compound selected from the group consisting of epigallocatechin 3,5-digallate EGCDG embelin, irigenol, pyrogallin, chrysophanol, ritodrine, methylnorlichexanthone and combinations thereof; and the effective amount is sufficient to reduce GFAP levels in the subject.

2. The method of claim 1 , wherein the polyphenol compound is EGCDG.

3. The method of claim 1 , wherein the polyphenol compound comprises EGCDG.

4. The method of claim 1 , wherein the polyphenol compound comprises irigenol.

5. The method of claim 1 , wherein the polyphenol compound comprises chrysophanol.

6. The method of claim 1 , wherein the GFAP lowering compound further comprises a compound selected from the group consisting of chlorprothixene, mundoserone, tamoxifen citrate, amlodipine, thioridazine, ritanserin, fluccinonide, hexetidine, estradiol benzoate, ketotifen, clobetasol propionate, colecalciferol, fluphenazine, kanmycin, azinphos methyl, 4-acetamidophenyl salicylate, oxotremorine, 5-nitro-2-phenylpropyl-aminobenzoic acid (NPPB), chloramphenicol, terfenadine, phosphocreatine, betulinic acid, betulinic acid derivatives, coumophos, swietenolide-3-acetate, decarbazine, veratic acid, pantothenic acid, neamine, amylodipine besylate, 7-desacetoxy-6,7-dehydrogedunin and combinations thereof.

7. The method of claim 1 , wherein the GFAP lowering compound further comprises a compound selected from the group consisting of mundoserone, amlodipine besylate, 7-desacetoxy-6,7-dehydrogedunin and combinations thereof.

8. A method of treating Alexander disease in a subject in need thereof comprising:

administering to a subject at risk of or diagnosed with Alexander disease a therapeutically effective amount of a glial fibrillary acidic protein (GFAP) lowering compound, wherein the GFAP lowering compound comprises betulinic acid and/or a betulinic acid derivative; and the effective amount is sufficient to reduce GFAP levels in the subject;

wherein the betulinic acid derivative is selected from the group consisting of 3-O—(N-xylosyl-N-methoxyglycyl)betulinic acid, 3-O—(N-altrosyl-N-methoxyglycyl)betulinic acid, 3-O—(N-xvlosyl-N-methoxyglycyl)-3-aminobetulinic acid, 3-O—(N-altrosyl-N-methoxyglycgl)-3-aminobetulinic acid, and 3-aminobetulinic acid.

9. The method of claim 8 , wherein the GFAP lowering compound further comprises a compound selected from the group consisting of chrysophanol, chlorprothixene, EGCDG, mundoserone, tamoxifen citrate, amlodipine, embelin, thioridazine, ritanserin, irigenol, fluccinonide, hexetidine, estradiol benzoate, ketotifen, clobetasol propionate, colecalciferol, fluphenazine, pyrogallin, kanmycin, azinphos methyl, 4-acetamidophenyl salicylate, oxotremorine, ritodrine, 5-nitro-2-phenylpropyl-aminobenzoic acid (NPPB), chloramphenicol, terfenadine, phosphocreatine, methylnorlichexanthone, coumophos, swietenolide-3-acetate, decarbazine, veratic acid, pantothenic acid, neamine, amylodipine besylate, 7-desacetoxy-6,7-dehydrogedunin and combinations thereof.

10. The method of claim 8 , wherein the GFAP lowering compound further comprises a compound selected from the group consisting of EGCDG, mundoserone, irigenol, amlodipine besylate, 7-desacetoxy-6, 7-dehydrogedunin and combinations thereof.

11. The method of claim 8 , wherein the GFAP lowering compound further comprises a polyphenol compound selected from the group consisting of EGCDG, embelin, irigenol, pyrogallin, chrysophanol, ritodrine, methylnorlichexanthone and combinations thereof.

12. The method of claim 8 , wherein the GFAP lowering compound further comprises a quinone compound selected from the group consisting of chrysophanol, embelin and combinations thereof.

13. A method of treating Alexander disease in a subject in need thereof comprising:

administering to a subject at risk of or diagnosed with Alexander disease a therapeutically effective amount of a glial fibrillary acidic protein (GFAP) lowering compound, wherein the GFAP lowering compound comprises mundoserone; and the effective amount is sufficient to reduce GFAP levels in the subject.

14. The method of claim 13 , wherein the GFAP lowering compound further comprises a compound selected from the group consisting of chrysophanol, chlorprothixene, EGCDG, tamoxifen citrate, amlodipine, embelin, thioridazine, ritanserin, irigenol, fluccinonide, hexetidine, estradiol benzoate, ketotifen, clobetasol propionate, colecalciferol, fluphenazine, pyrogallin, kanmycin, azinphos methyl, 4-acetamidophenyl salicylate, oxotremorine, ritodrine, 5-nitro-2-phenylpropyl-aminobenzoic acid (NPPB), chloramphenicol, terfenadine, phosphocreatine, betulinic acid, betulinic acid derivatives, methylnorlichexanthone, coumophos, swietenolide-3-acetate, decarbazine, veratic acid, pantothenic acid, neamine, amylodipine besylate, 7-desacetoxy-6,7-dehydrogedunin and combinations thereof.

15. The method of claim 13 , wherein the GFAP lowering compound further comprises a compound selected from the group consisting of EGCDG, irigenol, amlodipine besylate, 7-desacetoxy-6,7-dehydrogedunin and combinations thereof.

16. The method of claim 13 , wherein the GFAP lowering compound further comprises a c-pendant amino tricyclic compound selected from the group consisting of chlorprothixene, fluphenazine, ketotifen, thioridazine and combinations thereof.

17. The method of claim 13 , wherein the GFAP lowering compound further comprises a polyphenol compound selected from the group consisting of EGCDG, embelin, irigenol, pyrogallin, chrysophanol, ritodrine, methylnorlichexanthone and combinations thereof.