Treatment of muscular conditions and muscular dystrophies
The present invention provides methods for improving muscular function or treating a muscular disorder in an individual by administering to the individual a pharmacologically effective amount of a compound that inhibits microtubule-dependent NADPH Oxidase 2 reactive oxygen species signaling production. In addition compounds that block sarcolemmal Ca 2+ channel activation and/or renin-angiotensin signaling may be administered with the inhibitor of microtubule-dependent NADPH Oxidase 2 reactive oxygen species signaling production.
1. A method of improving muscular function in an individual, comprising the steps of:
administering to said individual a pharmacologically effective amount of a compound that inhibits microtubule-dependent NADPH Oxidase 2 reactive oxygen species signaling production;
administering a pharmacologically effective amount of a compound that blocks sarcolemmal Ca 2+ channel activation; and
administering a pharmacologically effective amount of a compound that blocks renin-angiotensin signaling, thereby improving muscular function in said individual.
2. The method of claim 1 , wherein the compound that inhibits microtubule-dependent NADPH Oxidase 2 reactive oxygen species signaling production depolymerizes microtubules.
3. The method of claim 2 , wherein the compound is selected from the group consisting of colchicine, nocodozole, parthenolide, dimethylaminoparthenolide, 2-phenyl-4-quinolone, polygamain, azaindole, vinca alkaloids, colcemid, or their pharmaceutical salts.
4. The method of claim 3 , wherein said compound is colchicine and is administered in an amount from about 5 micrograms/kg to about 20 micrograms/kg of said individual's body weight.
5. The method of claim 1 , wherein the compound that inhibits microtubule-dependent NADPH Oxidase 2 reactive oxygen species signaling production is a NADPH Oxidase 2 inhibitor.
6. The method of claim 5 , wherein the compound that inhibits NADPH Oxidase 2 is selected from the group consisting of fulvene, apocynin, gp91ds comprising a TAT peptide or other peptide enabling cellular uptake thereof, diphenylene iodonium, and pharmaceutical salts thereof.
7. The method of claim 1 , wherein the compound that blocks sarcolemmal Ca 2+ channel activation is selected from the group consisting of GsMTx4, streptomycin, poloxamer P188, ruthenium red, pyrazole-3, 3,5-bis(trifluoromethyl)pyrazole 2, N-(p-amylcinnamoyl)anthranilic acid,4-Methyl-2-(1-piperidinyl)-quinoline, dantrolene sodium, and SKF 96365, or a pharmaceutical salt thereof.
8. The method of claim 1 , wherein the compound that blocks renin-angiotensin signaling is losartan, altace, lisinopril, enalapril, ramparil, zestril, angiotensin converting enzyme inhibitors or a pharmaceutical salt thereof.
9. The method of claim 1 , wherein administration occurs before, during or after onset of muscle damage, activity-induced fatigue or muscle fatigue in said individual.
10. A method of treating an individual having a muscular disorder, comprising the steps of:
administering to said individual a therapeutically effective amount of a compound that inhibits microtubule-dependent NADPH Oxidase 2;
administering a pharmacologically effective amount of a compound that blocks sarcolemmal Ca 2+ channel activation; and
administering a pharmacologically effective amount of a compound that blocks renin-angiotensin signaling, thereby treating said muscular disorder in said individual.
11. The method of claim 10 , wherein the compound that inhibits microtubule-dependent NADPH Oxidase 2 reactive oxygen species signaling production depolymerizes microtubules.
12. The method of claim 11 , wherein said compound is selected from the group consisting of colchicine, nocodozole, parthenolide, dimethylaminoparthenolide 2-phenyl-4-quinolone, polygamain, azaindole, vinca alkaloids, colcemid, or their pharmaceutical salts.
13. The method of claim 10 , wherein the compound that inhibits NADPH Oxidase 2 is selected from the group consisting of fulvene, apocynin, gp91ds comprising a TAT peptide or other peptide enabling cellular uptake thereof, diphenylene iodonium, and pharmaceutical salts thereof.
14. The method of claim 10 , wherein the compound that blocks sarcolemmal Ca 2+ channel activation is selected from the group consisting of GsMTx4, streptomycin, poloxamer P188, ruthenium red, pyrazole-3, 3,5-bis(trifluoromethyl)pyrazole 2, N-(p-amylcinnamoyl)anthranilic acid, 4-Methyl-2-(1-piperidinyl)-quinoline, dantrolene sodium, and an SKF 96365, or a pharmaceutical salt thereof.
15. The method of claim 10 , wherein said renin-angiotensin signaling blocker is losartan, or a pharmaceutical salt thereof.
16. The method of claim 10 , wherein said muscular disorder is Duchenne Muscular Dystrophy, Becker's Muscular Dystrophy, Congenital Muscular Dystrophy, Limb-Girdle Muscular Dystrophy, Limb-Girdle Muscular Dystrophy-2A, Limb-Girdle Muscular Dystrophy-2B, Limb-Girdle Muscular Dystrophy-2D, Limb-Girdle Muscular Dystrophy-2E, Limb-Girdle Muscular Dystrophy-2l, muscle diseases associated with mutations in the delta.-sarcoglycan gene, Ullrich congential muscular dystrophy, congenital merosin-deficient 1A muscular dystrophy, myositis, autophagic vacuolar myopathy, myopathies not associated with a specific protein deficiency, myotonic dystrophy type 1, spinal muscular atrophy, critical care myopathy cases, Pompe disease, or sarcoidosis.