Methods for modulating the axonal outgrowth of central nervous system neurons
View Patent ↗Methods for modulating the axonal outgrowth of central nervous system neurons are provided. Methods for stimulating the axonal outgrowth of central nervous system neurons following an injury (e.g., stroke, Traumatic Brain Injury, cerebral aneurism, spinal cord injury and the like) and methods for inhibiting the axonal outgrowth of central nervous system neurons are also provided. Finally, a packed formulation comprising a pharmaceutical composition comprising an inosine nucleoside and a pharmaceutically acceptable carrier packed with instructions for use of the pharmaceutical composition for treatment of a central nervous system disorder is provided.
1. A method for stimulating the axonal outgrowth of central nervous system neurons following traumatic brain injury in a mammal, comprising intrathecal administration into the central nervous system of the mammal a pharmaceutical composition consisting essentially of an effective amount of inosine such that axonal outgrowth is stimulated in vivo.
2. A method of treating a mammal having suffered a traumatic brain injury which comprises intrathecal administration of a pharmaceutical composition to said mammal, wherein the active ingredient consists of inosine and a pharmaceutically acceptable carrier, and wherein the pharmaceutical composition is administered in a period from the time of the traumatic brain injury to 100 hours after the traumatic brain injury.
3. The method of claim 1 , or 2 , wherein the inosine is administered to contact CNS neurons in vivo with a concentration of inosine of 5 μM to 1 mM.
4. The method of claim 1 , or 2 , wherein the pharmaceutical composition is introduced into the cerebral spinal fluid of the mammal.
5. The method of claim 4 , wherein the pharmaceutical composition is introduced into a cerebral ventricle.
6. The method of claim 4 , wherein the pharmaceutical composition is introduced into the lumbar area.
7. The method of claim 4 , wherein the pharmaceutical composition is introduced into the cisterna magna.
8. The method of claim 4 , wherein the pharmaceutical composition is administered by the use of an infusion pump.
9. The method of 1 , or 2 , wherein the pharmaceutical composition is administered continually over a period of at least several days.
10. The method of claim 1 , or 2 , wherein the pharmaceutical composition is administered continually over a period of at least four weeks.
11. The method of claim 1 , or 2 , wherein the mammal is human.
12. A method for stimulating the axonal outgrowth of central nervous system neurons following optic nerve injury in a mammal, comprising intrathecal administration into the central nervous system of the mammal a pharmaceutical composition consisting essentially of an effcctive amount of inosine such that axonal outgrowth is stimulated in vivo.
13. A method of treating a mammal having suffered an optic nerve injury which comprises intrathecal administration of a pharmaceutical composition to said mammal, wherein the active ingredient consists of inosine and a pharmaceutically acceptable carrier, and wherein the pharmaceutical composition is administered in a period from the time of the optic nerve injury to 100 hours after the optic nerve injury.
14. The method of claim 12 , or 13 , wherein the inosine is administered to contact CNS neurons in vivo with a concentration of inosine of 5 μM to 1 mM.
15. The method of claims 12 , or 13 , wherein the pharmaceutical composition is administered by the use of an infusion pump.
16. The method of 12 , or 13 , wherein the pharmaceutical composition is administered continually over a period of at least several days.
17. The method of claim 12 , or 13 , wherein the pharmaceutical composition is administered continually over a period of at least four weeks.
18. The method of claim 12 , or 13 , wherein the mammal is human.