IP Library Granted Patent US 7,081,444
Granted Patent B2
US 7,081,444 · App. 10/807,553 · Granted Jul 25, 2006

ΨεRACK peptide composition and method for protection against tissue damage due to ischemia

Assignee: The Board of Trustees of the Leland Stanford Junior University
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Quick Facts
Patent No.
US 7,081,444
App. No.
10/807,553
Granted
Jul 25, 2006
Kind
B2
Abstract

A method of reducing damage to cells and tissue caused by an ischemic or hypoxic event is disclosed. The method includes administering to the cell or tissue, either in vivo or ex vivo, ψεRACK peptide. The peptide can be administered before, during or after the ischemic or hypoxic event.

Claims (35)

1. A composition comprising a peptide having a sequence that shares at least 50% identity with SEQ ID NO: 2, said peptide having the ability to selectively activate epsilon protein kinase C (εPKC) function in cardiac myocytes, said peptide attached by an N-terminal cysteine residue to a Tat-derived peptide or to a polyarginine peptide.

2. The composition of claim 1 , wherein said peptide shares a sequence that is at least 70% identity with SEQ ID NO: 2.

3. The composition of claim 1 , wherein said peptide shares a sequence that is at least 80% identity with SEQ ID NO: 2.

4. The composition of claim 1 , wherein said Tat-derived peptide has a sequence identified as SEQ ID NO:5.

5. A method for reducing in vivo damage due to ischemia, hypoxia, or reperfusion injury in a subject, comprising administering to said subject the peptide according to claim 1 .

6. The method of claim 5 , wherein said administering is by a route selected from the group consisting of intravenous, parenteral, subcutaneous, inhalation, intranasal, sublingual, mucosal, and transdermal.

7. The method of claim 5 , wherein said administering is by infusion through coronary arteries to the heart.

8. The method of claim 5 , wherein said administering comprises administering the peptide prior to ischemia, hypoxia, or reperfusion.

9. The method of claim 5 , wherein said administering comprises administering the peptide after ischemia, hypoxia, or reperfusion.

10. The method of claim 5 , wherein said administering comprises administering the peptide during ischemia, hypoxia, or reperfusion.

11. A method for reducing in vivo damage to an organ due to ischemia, hypoxia, or reperfusion injury in a subject, comprising administering to said subject the peptide according to claim 1 .

12. The method of claim 11 , wherein the method is for reducing damage to an organ selected from the group consisting of heart, lung, liver, brain, and kidney.

13. The method of claim 11 , wherein said administering is by a route selected from the group consisting of intravenous, parenteral, subcutaneous, inhalation, intranasal, sublingual, mucosal, and transdermal.

14. The method of claim 11 , wherein said administering is by infusion through coronary arteries to the heart.

15. The method of claim 11 , wherein said administering comprises administering the peptide prior to ischemia, hypoxia, or reperfusion.

16. The method of claim 10 , wherein said administering comprises administering the peptide after ischemia, hypoxia, or reperfusion.

17. The method of claim 10 , wherein said administering comprises administering the peptide during ischemia, hypoxia, or reperfusion.

18. A method for reducing in vivo cellular damage due to ischemia, hypoxia, or reperfusion injury in a subject, comprising administering to said subject the peptide according to claim 1 .

19. The method of claim 18 , wherein the method is for reducing damage to cells selected from the group consisting of heart, lung, liver, brain, and kidney.

20. The method of claim 18 , wherein said administering is by a route selected from the group consisting of intravenous, parenteral, subcutaneous, inhalation, intranasal, sublingual, mucosal, and transdermal.

21. The method of claim 18 , wherein said administering is by infusion through coronary arteries to the heart.

22. The method of claim 18 , wherein said reducing is reducing cellular damage to cardiomyocytes.

23. The method of claim 18 , wherein said administering comprises administering the peptide prior to ischemia, hypoxia, or reperfusion.

24. The method of claim 18 , wherein said administering comprises administering the peptide after ischemia, hypoxia, or reperfusion.

25. The method of claim 18 , wherein said administering comprises administering the peptide during ischemia, hypoxia, or reperfusion.

26. A method for reducing damage to an ex vivo organ due to ischemia, hypoxia, or reperfusion injury, comprising administering to said organ the peptide according to claim 1 .

27. The method of claim 26 , wherein the method is for reducing damage to an organ selected from the group consisting of heart, lung, liver, brain, and kidney.

28. The method of claim 26 , wherein said administering comprises administering the peptide prior to ischemia, hypoxia, or reperfusion.

29. The method of claim 26 , wherein said administering comprises administering the peptide after ischemia, hypoxia, or reperfusion.

30. The method of claim 26 , wherein said administering comprises administering the peptide during ischemia, hypoxia, or reperfusion.

31. A method for reducing damage to a cell due to ischemia, hypoxia, or reperfusion injury, comprising administering to said cell the peptide according to claim 1 .

32. The method of claim 31 , wherein the method is for reducing damage to a cell selected from the group consisting of heart cells, lung cells, liver cells, brain cells, and kidney cells.

33. The method of claim 31 , wherein said administering comprises administering the peptide prior to ischemia, hypoxia, or reperfusion.

34. The method of claim 31 , wherein said administering comprises administering the peptide after ischemia, hypoxia, or reperfusion.

35. The method of claim 31 , wherein said administering comprises administering the peptide during ischemia, hypoxia, or reperfusion.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jun 2, 2011
From: STANFORD UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 026381/0340 →
CONFIRMATORY LICENSE Recorded Nov 23, 2008
From: STANFORD UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021879/0643 →
Continuity (3)
Continuation 1000736300 · Nov 9, 2001
Provisional Application 6024783000 · Nov 10, 2000
Related Publication 20040186055A1 · Sep 23, 2004