Methods of using AMPD2 inhibitors for the treatment of fatty liver, obesity and diabetes
The present invention provides compounds and compositions that modulate adenosine monophosphate deaminase (AMPD) and methods for using the same to treat a clinical condition associated with the metabolic syndrome or a disease associated with the metabolic syndrome. In particular, the present invention provides a compound and a composition comprising a selective AMPD2 inhibitor and methods for using the same, for example, to treat a clinical condition associated with metabolic syndrome as well as diseases manifested by the metabolic syndrome.
1. A method for treating a clinical condition associated with metabolic syndrome in a subject comprising administering to the subject in need of such a treatment a therapeutically effective amount of a composition comprising an adenosine monophosphate deaminase 2 (AMPD2) inhibitor, wherein said clinical condition is fatty liver, obesity or diabetes, or a combination thereof.
2. The method of claim 1 , wherein the clinical condition associated with fatty liver comprises nonalcoholic fatty liver disease, nonalcoholic fatty liver disease associated cirrhosis, or a combination thereof.
3. The method of claim 1 , wherein the composition reduces plasma triglycerides.
4. The method of claim 1 , wherein the composition further comprises a xanthine oxidase inhibitor, a uricosuric agent, ketohexokinase (KHK) inhibitor, metformin, thiazolidinediones, an angiotensin-converting enzyme (ACE) inhibitor, an angiotensin receptor blocker, a thiazide diuretic, an antioxidant, catechin, resveratol, a uric acid lowering compound, or a combination thereof.
5. The method of claim 1 , wherein the AMPD2 inhibitor inhibits expression of AMPD2 gene, enzymatic activity of AMPD2 enzyme, or a combination thereof.
6. The method of claim 5 , wherein the AMPD2 inhibitor comprises a siRNA that inhibits expression of AMPD2 gene, an AMPD2 antibody, an AMP analog that inhibits AMPD2, an inhibitor of AMPDX that inhibits AMPD2, carbocyclic coformycin or a derivative thereof, carbocyclic nebularine or a derivative thereof, or deaminoformycin or a derivative thereof.