Treatment and prevention of inflammatory disorders
View Patent ↗The invention relates to methods of treating and preventing disorders associated with elevated TNF-α and/or IL-1β by administering therapeutic amounts of stearidonic acid. Further provided are methods for down-regulating TNF-α and/or IL-1β and assays for determining the presence, absence, or quantity of TNF-α and/or IL-1β in a subject in conjunction with a regimen of stearidonic acid administration.
1. A method of increasing eicosapentaenoic acid (20:5, n-3) levels in a human, the method comprising:
(a) identifying a human subject in need of increased eicosapentaenoic acid levels, wherein identifying the human subject comprises screening for an elevated presence of TNF-α and/or IL-1β; and
(b) administering an effective amount of stearidonic acid (18:4, n-3) to the subject over a time period effective to increase eicosapentaenoic acid levels in the subject, wherein the subject metabolizes the stearidonic acid to eicosapentaenoic acid, resulting in increased eicosapentaenoic acid levels.
2. The method of claim 1 , wherein the increased eicosapentaenoic acid (20:5, n-3) levels are present in tissues selected from the group consisting of erythrocyte phospholipids, platelet phospholipids, mononuclear cell phospholipids, plasma phospholipids, triglycerides, and cholesterol esters.
3. The method of claim 1 , wherein the increased eicosapentaenoic acid levels down-regulate TNF-α and/or IL-1β.
4. The method of claim 1 , wherein the effective amount of steeridonic acid administered is from about 0.1 g/day to about 10 g/day.
5. The method of claim 1 , wherein the effective amount of stearidonic acid administered is from about 0.25 g/day to about 8 g/day.
6. The method of claim 1 , wherein the effective amount of stearidonic acid administered is from about 0.5 gfday to about 5 g/day.
7. The method of claim 1 wherein the effective amount of stearidonic acid administered is about 1.5 g/day.
8. The method of claim 1 , wherein identifying the human subject comprises screening for an elevated presence of TNF-α.
9. The method of claim 1 , wherein identifying the human subject comprises screening for an elevated presence of IL-1β.
10. The method of claim 1 , wherein identifying the human subject comprises screening for an elevated presence of TNF-α and IL-1β.