RU-2026105456-A - A METHOD FOR TREATMENT OF BRAIN INJURY AFTER A STROKE
RU2026105456ARU 2026105456 ARU2026105456 ARU 2026105456ARU-2026105456-A
Inventors
- ЛЮ, Чжи-жэнь
Assignees
- ПРОДА БАЙОТЕК, ЭлЭлСи
Dates
- Publication Date
- 20260507
- Application Date
- 20240805
- Priority Date
- 20230803
Claims (20)
- 1. A method for treating ischemia-reperfusion injury (IRI) of the brain in a subject, comprising administering a therapeutically effective amount of a PKM2 (pyruvate kinase M2) protein variant, wherein the PKM2 protein variant is delivered systemically and is capable of reducing tissue damage following reperfusion of ischemic brain tissue.
- 2. The method according to claim 1, wherein the variant of the PKM2 protein is the G415R mutant.
- 3. The method according to claim 1, wherein the brain damage is caused by a hemorrhagic stroke.
- 4. The method according to claim 1, wherein the brain damage is caused by ischemic stroke.
- 5. The method according to claim 1, wherein the PKM2 protein variant is administered systemically.
- 6. The method according to claim 1, wherein the PKM2 protein variant is administered at any time and within 2 hours after reperfusion.
- 7. A method for improving tissue recovery and reparation after ischemic stroke and reperfusion, as well as hemorrhagic stroke in a patient in need thereof, comprising administering a therapeutically effective amount of a PKM2 (pyruvate kinase M2) protein variant with the G415R mutation to damaged tissue, wherein the PKM2 protein variant is capable of preventing neuronal death and stimulating regeneration.
- 8. The method of claim 7, wherein the PKM2 protein variant is not a constitutive PKM2.
- 9. The method according to claim 7, wherein the ischemic stroke is an acute ischemic stroke.
- 10. A method for treating brain damage caused by hemorrhagic stroke in a subject, comprising administering a therapeutically effective amount of a PKM2 (pyruvate kinase M2) protein variant, wherein the PKM2 protein variant is delivered systemically and is capable of reducing damage to brain tissue.
- 11. A method for improving tissue recovery and reparation after ischemic stroke and reperfusion, as well as hemorrhagic stroke in a patient in need thereof, comprising administering a therapeutically effective amount of a mutant pyruvate kinase M2 (PKM2) with the G415R mutation to tissue damaged by ischemic stroke, wherein the composition prevents neuronal death and stimulates regeneration.
- 12. The method according to claim 11, wherein the variant RKM2 does not represent a constitutive RKM2.
- 13. The method according to claim 11, which preserves nerve tissue.
- 14. The method of claim 11, wherein the ischemic stroke is an acute ischemic stroke.
- 15. The method of claim 11, wherein the therapeutic agent comprises PKM2 obtained from a human or non-human animal.
- 16. The method of claim 11, wherein the therapeutic agent is placed in a pharmaceutically acceptable carrier.
- 17. The method according to claim 11, wherein the composition is administered systemically.
- 18. The method of claim 11, wherein the composition reduces the death of nerve cells induced by ischemic injury.
- 19. The method according to claim 11, wherein the composition improves the recovery of brain function after a stroke.
- 20. The method according to claim 11, wherein the pyruvate kinase M2 or variant is a dimer.