IP Library Granted Patent US 8,987,332
Granted Patent B2
US 8,987,332 · App. 13/493,241 · Granted Mar 24, 2015

Methods of treating inflammatory conditions

Inventors: Jerrold M. Olefsky (Solana Beach, CA); Da Young Oh (La Jolla, CA)
Assignee: The Regents of the University of California
A61K31/20A61K31/202
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Quick Facts
Patent No.
US 8,987,332
App. No.
13/493,241
Granted
Mar 24, 2015
Kind
B2
Abstract

The present invention provides methods of treating a β-arrestin2 mediated and/or GPR120 mediated response in a subject. The β-arrestin2 mediated and/or GPR120 mediated response can be inflammation, including diabetes, inflammation associated with obesity and obesity. The methods can comprise administering to a subject a therapeutically effective amount of a compound predicted to bind a β-arrestin2 molecule and/or GPR120, wherein the compound selectively activates a β-arrestin2-dependent signaling pathway of GPR120.

Claims (16)

1. A method of treating inflammation in a subject, the method comprising administering a therapeutically effective amount of a compound that binds GPR120, the compound selectively activating a β-arrestin2-dependent signaling pathway of GPR120.

2. The method of claim 1 , wherein the compound that selectively activates a β-arrestin2-dependent signaling pathway is an ω-3 fatty acid.

3. The method of claim 2 , wherein the ω-3 FA is DHA.

4. The method of claim 2 , wherein the ω-3 FA is EPA.

5. The method of claim 1 , wherein the compound selectively activates a β-arrestin2-dependent signaling pathway and does not activate a β-arrestin1-dependent signaling pathway.

6. The method of claim 1 , wherein the inflammation is associated with diabetes.

7. The method of claim 1 , wherein the inflammation is associated with obesity.

8. The method of claim 1 , wherein the subject is a human.

9. A method of treating an inflammatory condition associated with β-arrestin2 function, the method comprising administering a therapeutically effective amount of a β-arrestin2 modulating agent to a subject in need thereof.

10. The method of claim 9 , wherein the inflammatory condition is diabetes.

11. The method of claim 9 , wherein the inflammatory condition is associated with obesity.

12. The method of claim 9 , wherein the β-arrestin2 modulating agent is an ω-3 fatty acid.

13. The method of claim 9 , wherein the ω-3 fatty acid is DHA.

14. The method of claim 9 , wherein the ω-3 fatty acid is EPA.

15. The method of claim 9 , wherein the compound selectively activates a β-arrestin2-dependent signaling pathway and does not activate a β-arrestin2-dependent signaling pathway.

16. The method of claim 9 , wherein the subject is a human.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jul 13, 2012
From: UNIVERSITY OF CALIFORNIA SAN DIEGO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 028553/0832 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2012
From: OLEFSKY, JERROLD M.; OH, DA YOUNG
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 028351/0964 →
Continuity (5)
Continuation PCTUS2010059699 · Dec 9, 2010
Provisional Application 61379626 · Sep 2, 2010
Provisional Application 61377601 · Aug 27, 2010
Provisional Application 61285086 · Dec 9, 2009
Related Publication 20120295975A1 · Nov 22, 2012