Organ cold storage composition and methods of use
View Patent ↗The present invention provides compositions and methods for decreasing oxidative damage to an organ during cold storage.
1. A method of reducing oxidative damage to an organ that occurs during cold storage, the method comprising (i) contacting the organ with a composition comprising mitoquinone and an organ preservation solution, wherein the organ first contacts the composition during cold storage of the organ, and wherein the subject is selected from the group consisting of a rodent, a human, a zoological animal, a companion animal, and a livestock animal; and (ii) cold storing the organ in the composition for at least thirty minutes, such that the composition reduces oxidative damage to an organ that occurs during cold storage.
2. The method of claim 1 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by complex I activity, complex II activity, complex III activity, complex IV activity, or a combination thereof.
3. The method of claim 1 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by MnSOD activity.
4. The method of claim 1 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by measuring creatinine clearance.
5. The method of claim 1 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by measuring nitrotyrosine adduct formation.
6. The method of claim 1 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by measuring superoxide generation.
7. The method of claim 1 , wherein the organ is a kidney.
8. A method of reducing oxidative damage to a kidney that occurs during cold storage, the method comprising (i) contacting the kidney with a composition comprising mitoquinone and an organ preservation solution, wherein the kidney first contacts the composition during cold storage of the kidney, and wherein the subject is selected from the group consisting of a rodent, a human, a zoological animal, a companion animal, and a livestock animal; and (ii) cold storing the kidney in the composition for at least thirty minutes, such that the composition reduces oxidative damage to a kidney that occurs during cold storage.
9. The method of claim 8 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by complex I activity, complex II activity, complex III activity, complex IV activity, or a combination thereof.
10. The method of claim 8 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by MnSOD activity.
11. The method of claim 8 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by measuring creatinine clearance.
12. The method of claim 8 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by measuring nitrotyrosine adduct formation.
13. The method of claim 8 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by measuring superoxide generation.
14. A method of reducing oxidative damage to an organ that occurs during cold storage prior to transplantation of the organ, the method comprising (i) contacting the organ with a composition comprising mitoquinone and an organ preservation solution, wherein the organ first contacts the composition during cold storage of the organ, and wherein the subject is selected from the group consisting of a rodent, a human, a zoological animal, a companion animal, and a livestock animal; and (ii) cold storing the organ in the composition, such that the composition reduces oxidative damage to an organ that occurs during cold storage before transplantation and preserves organ quality for transplantation.
15. The method of claim 14 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by complex I activity, complex II activity, complex III activity, complex IV activity, or a combination thereof.
16. The method of claim 14 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by MnSOD activity, superoxide generation, or nitrotyrosine adduct formation.
17. The method of claim 1 , wherein the method further comprises measuring oxidative damage to the organ and the oxidative damage is measured by measuring creatinine clearance.