IP Library Granted Patent US 7,718,620
Granted Patent B2
US 7,718,620 · App. 11/427,804 · Granted May 18, 2010

Methods for preventing or treating ischemia-reperfusion injury of the kidney

Assignee: Cornell Research Foundation, Inc.
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Quick Facts
Patent No.
US 7,718,620
App. No.
11/427,804
Granted
May 18, 2010
Kind
B2
Abstract

The invention provides a method of treating or preventing ischemia-reperfusion injury of the kidney in a mammal. The method comprises administering an effective amount of an aromatic-cationic peptide having at least one net positive charge; a minimum of four amino acids; a maximum of about twenty amino acids; a relationship between the minimum number of net positive charges (p m ) and the total number of amino acid residues (r) wherein 3p m is the largest number that is less than or equal to r+1; and a relationship between the minimum number of aromatic groups (a) and the total number of net positive charges (p t ) wherein 2 a is the largest number that is less than or equal to p t+1 , except that when a is 1, p t may also be 1.

Claims (69)

1. A method for treating or preventing ischemia-reperfusion injury of the kidney in a mammal, the method comprising administering to the mammal an effective amount of a peptide having the formula selected from the group consisting of:

D-Arg-2′,6′-Dmt-Lys-Phe-NH 2 ,

D-Arg-2′,6′-Dmt-Phe-Lys-NH 2 ,

D-Arg-Phe-Lys-2′,6′-Dmt-NH 2 ,

D-Arg-Phe-2′,6′-Dmt-Lys-NH 2 ,

D-Arg-Lys-2′,6′-Dmt-Phe-NH 2 ,

D-Arg-Lys-Phe-2′,6′-Dmt-NH 2 ,

Phe-Lys-2′,6′-Dmt-D-Arg-NH 2 ,

Phe-Lys-D-Arg-2′,6′-Dmt-NH 2 ,

Phe-D-Arg-2′,6′-Dmt-Lys-NH 2 ,

Phe-D-Arg-Lys-2′,6′-Dmt-NH 2 ,

Phe-D-Arg-Phe-Lys-NH 2 ,

Phe-2′,6′-Dmt-D-Arg-Lys-NH 2 ,

Phe-2′,6′-Dmt-Lys-D-Arg-NH 2 ,

Dmp-D-Arg-Phe-Lys-NH 2 ,

Lys-Phe-2′,6′-Dmt-D-Arg-NH 2 ,

Lys-2′,6′-Dmt-D-Arg-Phe-NH 2 ,

Lys-2′,6′-Dmt-Phe-D-Arg-NH 2 ,

Lys-D-Arg-Phe-2′,6′-Dmt-NH 2 ,

Lys-D-Arg-2′,6′-Dmt-Phe-NH 2 ,

D-Arg-2′,6′-Dmt-D-Arg-Phe-NH 2 ,

D-Arg-2′,6′-Dmt-D-Arg-2′,6′-Dmt-NH 2 ,

D-Arg-2′,6′-Dmt-D-Arg-Tyr-NH 2 ,

D-Arg-2′,6′-Dmt-D-Arg-Trp-NH 2 ,

Trp-D-Arg-Phe-Lys-NH 2 ,

Trp-D-Arg-Tyr-Lys-NH 2 ,

Trp-D-Arg-Trp-Lys-NH 2 ,

Trp-D-Arg-Dmt-Lys-NH 2 ,

D-Arg-Trp-Lys-Phe-NH 2 ,

D-Arg-Trp-Phe-Lys-NH 2 ,

D-Arg-Trp-Lys-Dmt-NH 2 ,

D-Arg-Trp-Dmt-Lys-NH 2 ,

D-Arg-Lys-Trp-Phe-NH 2 ,

D-Arg-Lys-Trp-Dmt-NH 2 ,

Cyclohexyl-D-Arg-Phe-Lys-NH 2 ,

Ala-D-Arg-Phe-Lys-NH 2 ,

Lys-D-Arg-Tyr-NH 2 ,

Trp-D-Lys-Tyr-Arg-NH 2 ,

Phe-Arg-D-His-Asp,

Met-Tyr-D-Lys-Phe-Arg (SEQ. ID. NO: 4),

D-His-Glu-Lys-Tyr-D-Phe-Arg (SEQ. ID. NO: 5),

Lys-D-Gln-Tyr-Arg-D-Phe-Trp-NH 2 (SEQ. ID. NO: 6),

Phe-D-Arg-Lys-Trp-Tyr-D-Arg-His (SEQ. ID. NO: 7),

Gly-D-Phe-Lys-Tyr-His-D-Arg-Tyr-NH 2 (SEQ. ID. NO: 8),

Val-D-Lys-His-Tyr-D-Phe-Ser-Tyr-Arg-NH 2 (SEQ. ID. NO: 9),

Trp-Lys-Phe-D-Asp-Arg-Tyr-D-His-Lys (SEQ. ID. NO: 10),

Lys-Trp-D-Tyr-Arg-Asn-Phe-Tyr-D-His-NH 2 (SEQ. ID. NO: 11),

Thr-Gly-Tyr-Arg-D-His-Phe-Trp-D-His-Lys (SEQ. ID. NO: 12),

Asp-D-Trp-Lys-Tyr-D-His-Phe-Arg- D-Gly-Lys-NH 2 (SEQ. ID. NO: 13),

D-His-Lys-Tyr-D-Phe-Glu-D-Asp-D-His-D-Lys-Arg-Trp-NH 2 (SEQ. ID. NO: 14),

Ala-D-Phe-D-Arg-Tyr-Lys-D-Trp-His-D-Tyr-Gly-Phe (SEQ. ID. NO: 15),

Phe-Phe-D-Tyr-Arg-Glu-Asp-D-Lys-Arg-D-Arg-His-Phe-NH 2 (SEQ. ID. NO: 17),

Phe-Tyr-Lys-D-Arg-Trp-His-D-Lys-D-Lys-Glu-Arg-D-Tyr-Thr (SEQ. ID. NO: 18),

Glu-Arg-D-Lys-Tyr-D-Val-Phe-D-His-Trp-Arg-D-Gly-Tyr-Arg-D-Met-NH 2 (SEQ. ID. NO: 20),

Arg-D-Leu-D-Tyr-Phe-Lys-Glu-D-Lys-Arg-D-Trp-Lys-D-Phe-Tyr-D-Arg-Gly (SEQ. ID. NO: 21),

D-Glu-Asp-Lys-D-Arg-D-His-Phe-Phe-D-Val-Tyr-Arg-Tyr-D-Tyr-Arg-His-Phe-NH 2 (SEQ. ID. NO: 22),

Asp-Arg-D-Phe-Cys-Phe-D-Arg-D-Lys-Tyr-Arg-D-Tyr-Trp-D-His-Tyr-D-Phe-Lys-Phe (SEQ. ID. NO: 23),

His-Tyr-D-Arg-Trp-Lys-Phe-D-Asp-Ala-Arg-Cys-D-Tyr-His-Phe-D-Lys-Tyr-His-Ser-NH 2 (SEQ. ID. NO: 24),

Gly-Ala-Lys-Phe-D-Lys-Glu-Arg-Tyr-His-D-Arg-D-Arg-Asp-Tyr-Trp-D-His-Trp-His-D-Lys-Asp (SEQ. ID. NO: 25), and

Thr-Tyr-Arg-D-Lys-Trp-Tyr-Glu-Asp-D-Lys-D-Arg-His-Phe-D-Tyr-Gly-Val-Ile-D-His-Arg-Tyr-Lys-NH 2 (SEQ. ID. NO: 26).

2. The method of claim 1 , wherein the peptide is D-Arg-2′,6′-Dmt-Lys-Phe-NH 2 .

3. The method of claim 1 , wherein the peptide is Phe-D-Arg-Phe-Lys-NH 2 .

4. The method of claim 1 , wherein the peptide is administered after ischemic injury to the kidney in order to treat the ischemia-reperfusion injury.

5. The method of claim 1 , wherein the peptide is administered prior to ischemic injury to the kidney in order to prevent the ischemia-reperfusion injury.

6. The method of claim 1 , wherein the peptide is D-Arg-2′,6′-Dmt-Lys-Phe-NH 2 and is administered after ischemic injury to the kidney.

7. The method of claim 1 ,wherein the peptide is D-Arg-2′,6′-Dmt-Lys-Phe-NH 2 or Phe-D-Arg-Phe-Lys-NH 2 and is administered to the mammal prior to ischemic injury to the kidney.

8. The method of claim 1 , wherein the peptide is administered orally, topically, intranasally, systemically, intravenously, subcutaneously, intramuscularly, or transdermally.

9. The method of claim 1 , wherein the peptide is combined with a pharmaceutically acceptable carrier prior to administration to the mammal.

10. The method of claim 1 , wherein the mammal is a human.

Assignments (4)
CONFIRMATORY LICENSE Recorded Jul 29, 2010
From: CORNELL UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024761/0803 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2009
From: SZETO, HAZEL H.; ZHAO, KESHENG
To: CORNELL RESEARCH FOUNDATION, INC.
Reel/Frame 022325/0970 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2009
From: SCHILLER, PETER W.
To: INSTITUT DE RECHERCHES CLINIQUES DE MONTREAL
Reel/Frame 022326/0007 →
EXECUTIVE ORDER 9424, CONFIRMATORY LICENSE Recorded Feb 17, 2009
From: CORNELL UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022270/0806 →
Continuity (4)
Continuation In Part 1077123200 · Feb 3, 2004
Provisional Application 6044477700 · Feb 4, 2003
Provisional Application 6053569000 · Jan 8, 2004
Related Publication 20070027087A1 · Feb 1, 2007