Method for treating stroke via administration of NEP1-40 and inosine
Disclosed herein is a method for stimulating axonal outgrowth of central nervous system (CNS) neurons comprising contacting the CNS neurons with an effective amount of NEP1-40 and inosine, to thereby stimulate axonal outgrowth. The method may further comprise contacting the CNS neurons with a cAMP modulator that increases the concentration of intracellular cAMP. Also disclosed is a method for treating a neurological disorder selected from the group consisting of traumatic brain injury, stroke, spinal cord injury, optic neuropathy, retinal nerve damage and optic nerve damage, in a patient in need thereof comprising administering an effective amount of NEP1-40 and inosine to the patient.
1. A method for stimulating axonal outgrowth of mammalian central nervous system (CNS) neurons damaged by stroke comprising contacting the CNS neurons with an effective amount of NEP1-40 and inosine, to thereby stimulate axonal outgrowth.
2. The method of claim 1 , further comprising contacting the CNS neurons with a cAMP modulator that increases the concentration of intracellular cAMP.
3. The method of claim 2 , wherein the cAMP modulator is selected from the group consisting of: cAMP analogues, activators of G protein coupled receptors that activate cAMP, adenylate cyclase activators, calcium ionophores, and phosphodiesterase inhibitors.
4. A method for treating stroke in a patient in need thereof comprising administering an effective amount of NEP1-40 and inosine to the patient, to thereby contact and stimulate axonal outgrowth of central nervous system (CNS) neurons damaged by stroke, to thereby treat the stroke.
5. The method of claim 4 , wherein the NEP1-40 and inosine are administered following an injury to the CNS, to thereby re-establish neural connectivity and/or function of the CNS neurons after the CNS injury.
6. The method of claim 4 , wherein the NEP1-40 and inosine are administered by a route selected from the group consisting of pulmonary, internal topical, interdermal, intravenous, subcutaneous, intranasal, epidermal, ophthalmic, oral, intraventricular, and intrathecal.