IP Library Granted Patent US 10,016,486
Granted Patent B1
US 10,016,486 · App. 14/956,042 · Granted Jul 10, 2018

Methods and compositions using AMPK activators for pharmacological prevention of chronic pain

Inventors: Dong-Chul Pyun (Tucson, AZ); Theodore J. Price (Tucson, AZ); Gregory D. Dussor (Tucson, AZ); Dipti Tillu (Tucson, AZ); Bo Lian (Tucson, AZ)
Assignee: ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA
A61K38/2264A61K31/05A61K31/155A61K31/4365A61K31/4375A61K31/4439A61K31/616A61K31/7056A61K38/02A61K38/185A61K38/204
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Quick Facts
Patent No.
US 10,016,486
App. No.
14/956,042
Granted
Jul 10, 2018
Kind
B1
Abstract

Methods and compositions using a combination of adenosine monophosphate protein kinase (AMPK) activators for treating pain such as post-surgical pain or development of chronic pain. The two or more AMPK activators work synergistically and may be administered in individually sub-efficacious doses. The AMPK activators may have different mechanisms of AMPK activation. The AMPK activators may be administered systemically and/or topically in, for example, as a gel, ointment, cream, lotion, suspension, liquid, or transdermal patch.

Claims (7)

1. A method of reducing incision-induced hypersensitivity, incision-induced hyperalgesic priming, or incision-induced development of chronic pain in a subject, said method comprising topically administering to the subject a dosage of a first 5′-adenosine monophosphate-activated protein kinase (AMPK) activator and a dosage of a second AMPK activator, the first AMPK activator is metformin and the second AMPK activator is resveratrol, wherein the dosage of the first AMPK activator is an individually sub-efficacious dose, and the dosage of the second AMPK activator is an individually sub-efficacious dose, wherein the first AMPK activator and the second AMPK activator synergistically reduce incision-induced hypersensitivity, incision-induced hyperalgesic priming, or incision-induced development of chronic pain.

2. The method of claim 1 , wherein the sub-efficacious dose of the first AMPK activator is a dose that is less than the first AMPK activator's threshold dose.

3. The method of claim 1 , wherein the sub-efficacious dose of the second AMPK activator is a dose that is less than the second AMPK activator's threshold dose.

4. The method of claim 1 , wherein the sub-efficacious dose of the first AMPK activator is a dose that is less than the first AMPK activator's EC 50 .

5. The method of claim 1 , wherein the sub-efficacious dose of the second AMPK activator is a dose that is less than the second AMPK activator's EC 50 .

6. The method of claim 1 , wherein the sub-efficacious dose of the first AMPK activator is a dose that is between the first AMPK activator's EC 50 and threshold dose.

7. The method of claim 1 , wherein the sub-efficacious dose of the second AMPK activator is a dose that is between the second AMPK activator's EC 50 and threshold dose.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 4, 2018
From: PYUN, DONG-CHUL; PRICE, THEODORE J.; DUSSOR, GREGORY; TILLU, DIPTI; LIAN, BO
To: ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA
Reel/Frame 045978/0314 →
CONFIRMATORY LICENSE Recorded Jul 6, 2016
From: UNIVERSITY OF ARIZONA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039264/0962 →
Continuity (2)
Continuation In Part 14318245 · Jun 27, 2014
Provisional Application 61840886 · Jun 28, 2013
Cited By (1)
US 12,478,778