Anti-inflammatory compositions for treating brain inflammation
View Patent ↗Compositions with synergistic anti-inflammatory effects in inflammatory diseases resulting from activation and consequent degranulation of mast cells and followed by secretion of inflammatory biochemicals from the activated mast cells, the compositions containing one or more of a flavone or flavonoid glycoside a heavily sulfated, non-bovine proteoglycan, an unrefined olive kernel extract that increases absorption of these compositions in various routes of administration, a hexosamine sulfate such as D-glucosamine sulfate, S-adenosylmethionine, a histamine-1 receptor antagonist, a histamine-3 receptor agonist, an antagonist of the actions of CRR, a long-chain unsaturated fatty acid, a phospholipid, Krill oil, a polyamine, glutiramer acetate and interferon. Certain of the present compositions are useful in protecting against the neuropathological components of multiple sclerosis and similar inflammatory neurological diseases.
1. A method of treating neurodegenerative brain inflammation in a subject, comprising administering to a subject in need thereof an effective amount of a composition comprising a flavonoid or a flavonoid glycoside, olive kernel oil, a proteoglycan and one or more ingredients selected from the group consisting of a polyunsaturated fatty acid and a phospholipid.
2. The method of claim 1 , wherein the composition further comprises an interferon.
3. The method of claim 1 , wherein the composition further comprises glutiramer acetate.
4. The method of claim 1 , wherein the composition further comprises a histamine-1 receptor antagonist.
5. The method of claim 1 , wherein the flavonoid is selected from the group consisting of quercetin, myricetin, genistein, kaempferol, (−)epigallocatechin-3-gallate, luteolin, epigenin, rutin, hesperitin, and hesperidin.
6. The method of claim 1 , wherein the composition comprises a polyunsaturated fatty acid, and wherein the polyunsaturated fatty acid is selected from the group consisting of alphalinoleic acid, eicosapentenoic acid, and docosahexenoic acid.
7. The method of claim 1 , wherein the composition comprises a phospholipid, and wherein the phospholipid is selected from the group consisting of fish oil, Krill oil, and sphingomyelin.
8. The method of claim 1 , wherein the composition comprises chondroitin sulfate, a flavonoid, docosahexenoic acid, Krill oil, and olive kernel oil.
9. The method of claim 8 , wherein the composition further comprises hydroxyzine.
10. The method of claim 8 , wherein the composition is administered orally.
11. The method of claim 1 , wherein each ingredient is in the amount of 100-1,000 mg.
12. The method of claim 1 , wherein the composition comprises chondroitin sulfate, quercetin, rutin, (−)epigallocatechin-3-gallate, docosahexenoic acid, and olive kernel oil.
13. The method of claim 12 , wherein the composition comprises 150 mg of quercetin, 150 mg of rutin, 150 mg of (−)epigallocatechin-3-gallate, 250 mg of docosahexenoic acid, 300 mg of olive kernel oil and chondroitin sulfate.
14. The method of claim 12 , wherein the composition further comprises hydroxyzine.
15. The method of claim 12 , wherein the composition is administered orally.
16. The method of claim 1 , wherein the neurodegenerative brain inflammation includes disruption of the blood-brain barrier.
17. A composition comprising 10-1000 mg of luteolin, 10-1000 mg of quercetin, 10-1000 mg of rutin, 100-1000 mg of (−)epigallocatechin-3-gallate, 100-1000 mg of docosahexenoic acid, 100-1000 mg of krill oil, and 100-1000 mg of olive kernel oil.
18. The composition of claim 17 , wherein the composition further comprises 10-1000 mg of chondroitin sulfate.
19. The composition of claim 18 , wherein the composition comprises 150 mg of luteloin, 150 mg of quercetin, 150 mg of rutin, 150 mg of (−)epigallocatechin-3-gallate, 250 mg of docosahexenoic acid, 300 mg of olive kernel oil and 10-1000 mg of chondroitin sulfate.