Nitrated-fatty acids modulation of type II diabetes
View Patent ↗Nitro oleic acid and related metabolites are agonists of PPAR-γ. Surprisingly, nitro oleic acid is a more potent agonist of PPAR-γ, relative to nitro linoleic acid. Thus, nitro oleic acid and its metabolites, as well as their pharmaceutically acceptable salts and prodrug forms, are candidate therapeutics for the treatment of type-2 diabetes, which results from insulin resistance accompanying the improper functioning of PPAR-γ.
1. A method for lowering blood glucose levels, comprising administering a nitro oleic acid, or a metabolite, a pharmaceutically acceptable salt, or prodrug thereof to a subject in need of treatment.
2. The method of claim 1 , wherein administering is carried out by a method selected from the group consisting of topical administration, oral administration, inhalation, intravenous drip, subcutaneous injection, intraperitoneal injection, and intramuscular injection.
3. The method of claim 1 , further comprising administering one or more therapeutic agents in addition to the nitro oleic acid.
4. The method of claim 3 , wherein the one or more therapeutic agents are selected from the group consisting of cytokines, chemokines, and regulators of growth factors.
5. The method of claim 1 , wherein the subject is a human.
6. The method of claim 1 , further comprising administering an anti-microbial agent, an anti-inflammation agent, an anesthetic, or a combination thereof.
7. The method of claim 1 , wherein the nitro oleic acid is a salt of an inorganic base selected from the group consisting of sodium hydroxide, ammonium hydroxide, potassium hydroxide, monoalkyl amine, dialkyl amine, trialkyl amine, aryl amine, substituted ethanolamine, and a combination thereof.
8. The method of claim 1 , wherein the nitro oleic acid is a prodrug selected from the group consisting of a methyl ester of nitro oleic acid or an ethyl ester of nitro oleic acid.
9. The method of claim 1 , wherein the nitro oleic acid, metabolite, salt, or prodrug thereof is in a pharmaceutical composition.
10. The method of claim 9 , wherein the pharmaceutical composition further comprises sodium chloride, Ringer's dextrose, dextrose, lactated Ringer's solution, fluid and nutrient replenishers, or a combination thereof.
11. The method of claim 9 , wherein the pharmaceutical composition is a solution, suspension, solid, or emulsion.
12. The method of claim 9 , wherein the pharmaceutical composition further comprises thickeners, diluents, solvents, buffers, preservatives, surface active agents, excipients, or a combination thereof.