Methods of modulation of branched chain acids and uses thereof
View Patent ↗A method of modulating plasma levels of branched chain amino acids and branched chain alpha-keto acids is disclosed, wherein an ammonia scavenger compound or a salt thereof, for example phenylbutyrate or an even numbered congener thereof or a salt thereof, is administered to an individual in need thereof. In various methods, a decrease in plasma levels of branched chain amino acids and branched chain alpha-keto acids is effected to treat individuals suffering from an inborn error in metabolism of amino acids, such as Maple Syrup Urine Disease, for example.
1. A method of decreasing plasma levels of at least one of a branched chain amino acid or branched chain alpha-ketoacid comprising:
administering to an individual having high plasma levels of branched chain amino acids due to an inborn error of metabolism a therapeutically effective amount of at least one compound of the formula:
wherein n is 0, 2, 4, 6 or 8, or
a pharmaceutically acceptable salt thereof, and
wherein said therapeutically effective amount is sufficient to decrease plasma levels of at least one of said branched chain amino acid or branched chain alpha-ketoacid.
2. The method of claim 1 , wherein the amount of said compound administered stimulates the baseline enzymatic activity of the branched chain dehydrogenase enzyme complex protein to levels effective in achieving target plasma levels of branched chain amino acid and/or branched chain alpha-ketoacid for said individual.
3. The method of claim 1 , wherein both branched chain amino acid and branched chain alpha-ketoacid plasma levels are decreased.
4. The method of claim 1 , wherein said compound is phenylbutyrate or a salt or ester or prodrug thereof.
5. The method of claim 4 , wherein said salt is the sodium salt, calcium salt, lithium salt or a potassium salt.
6. The method of claim 4 , wherein said phenylbutyrate or salt or ester or prodrug thereof causes decreased phosphorylation of the S293 and S303 residues of the E1α subunit of the branched chain dehydrogenase enzyme complex protein.
7. The method of claim 1 , wherein said branched chain amino acid is at least one of leucine, isoleucine and valine.
8. The method of claim 1 , wherein said branched chain alpha-ketoacid is at least one of keto-isocaproic acid, keto-methylvaleric acid, and ketoisovaleric acid.
9. The method of claim 1 , wherein said compound is administered orally, intra-peritoneally or intravenously.
10. The method of claim 1 , wherein said inborn error of metabolism is MSUD.
11. The method of claim 10 , wherein said MSUD is selected from a group consisting of the classical form, the intermediate form, the intermittent form and the thiamine-responsive form of the disease.
12. The method of claim 1 , further comprising restricting the dietary branched chain amino acid intake in said individual.
13. The method of claim 4 , wherein said compound is phenylbutyrate or a salt thereof.
14. The method of claim 1 , further comprising assaying for a decrease in plasma levels of at least one of said branched chain amino acid or branched chain alpha-ketoacid.
15. The method of claim 13 , wherein said inborn error of metabolism is MSUD; and
said branched chain amino acid is at least one of leucine, isoleucine and valine or said branched chain alpha-ketoacid is at least one of keto-isocaproic acid, keto-methylvaleric acid, and ketoisovaleric acid.