Compositions and methods for modulating metabolic pathways
Compositions and methods useful for inducing an increase in fatty acid oxidation or mitochondrial biogenesis, reducing weight gain, inducing weight loss, or increasing Sirt1, Sirt3, or AMPK activity are provided herein. Such compositions can contain synergizing amounts of a sirtuin-pathway activators, including but not limited to resveratrol, in combination with beta-hydroxymethylbutyrate (HMB), keto isocaproic acid (KIC), leucine, or combinations of HMB, KIC and leucine.
1. A method for treating obesity in a subject in need thereof comprising:
a) administering a composition comprising:
i. at least about 500 mg of leucine and/or at least about 200 mg of one or more metabolites thereof, wherein the one or more leucine metabolites are selected from the group consisting of keto-isocaproic acid (KIC), alpha-hydroxy-isocaproic acid, and HMB; and
ii. an amount of at least about 0.5 mg of a sirtuin pathway activator,
wherein the composition is formulated as a tablet, capsule, gel capsule, beverage, snack bar or a food composition,
wherein the composition is substantially free of the individual amino acids alanine, glutamic acid, glycine, isoleucine, valine, and proline,
wherein when (a) is a metabolite of leucine the molar ratio of (a) to (b) is greater than 10; and wherein when (a) is leucine, the molar ratio of (a) to (b) is greater than 500.
2. The method of claim 1 , wherein the sirtuin pathway activator activates one or more of SIRT1, SIRT3, AMPK, and PGC1α.
3. The method of claim 1 , wherein the sirtuin pathway activator is a hydroxycinnamic acid, a stilbene, a polyphenol or a polyphenol precursor.
4. The method of claim 1 , wherein the sirtuin pathway activator is a polyphenol or a polyphenol precursor.
5. The method of claim 4 , wherein the polyphenol or polyphenol precursor is selected from the group consisting of chlorogenic acid, resveratrol, caffeic acid, cinnamic acid, ferulic acid, piceatannol, ellagic acid, epigallocatechin gallate, grape seed extract, and any analog thereof.
6. The method of claim 1 , wherein the sirtuin pathway activator is resveratrol.
7. The method of claim 1 , wherein the sirtuin pathway activator is a phosphodiesterase inhibitor.
8. The method of claim 1 , wherein the sirtuin pathway activator is present in a sub-therapeutic amount.
9. The method of claim 1 , wherein the amount of the sirtuin pathway activator is no more than 5 mg.
10. The method of claim 1 , wherein the amount of the sirtuin pathway activator is no more than 50 mg.
11. The method of claim 1 , wherein the composition further comprises an anti-diabetic agent.
12. The method of claim 11 , wherein the anti-diabetic agent comprises metformin.
13. The method of claim 12 , wherein the composition comprises at least about 25 mg of the metformin.
14. The method of claim 12 , wherein the composition comprises at least about 250 mg of metformin.
15. The method of claim 12 , wherein the composition comprises at least about 400 mg of metformin.
16. The method of claim 1 , wherein the composition is formulated as a unit dose.
17. The method of claim 1 , wherein the composition further comprises at least one pharmaceutically active agent.
18. The method of claim 17 , wherein the pharmaceutically active agent is an anti-obesity agent.
19. The method of claim 18 , wherein the anti-obesity agent is selected from group consisting of: lipase inhibitors, dopaminergic compounds, noradrenergic compounds, serotoninergic compounds, cannabinoid receptor antagonists, exenatide, pramlintide, and CNS agents.
20. The method of claim 1 , wherein treating obesity is characterized by a reduction in body weight, weight gain, visceral adipose tissue mass, fat oxidation and heat production, and respiratory exchange ratio.
21. The method of claim 1 , wherein the subject in need thereof is on a calorie restricted diet.
22. The method of claim 1 , wherein the subject in need thereof is on an unrestricted diet.
23. The method of claim 1 , wherein the subject in need thereof is human.
24. The method of claim 1 , wherein the composition is administered to the subject twice a day.
25. The method of claim 1 , wherein the composition is administered to the subject once a day.