Method Of Reducing Injury To Mammalian Cells

Abstract

A method of inhibiting the binding between N-methyl-D-aspartate receptors and neuronal proteins in a neuron is disclosed. The method comprises administering to the neuron an effective inhibiting amount of a peptide replacement agent for the NMDA receptor or neuronal protein interaction domain that effect said inhibition of the NMDA receptor-neuronal protein interaction. The method is of value in reducing the damaging effect of injury to mammalian cells. Postsynaptic density-95 protein (PSD-95) couples neuronal N-methyl-D-aspartate receptors (NMDARs) to pathways mediating excitotoxicity, ischemic and traumatic brain damage. This coupling was disrupted by transducing neurons with peptides that bind to modular domains on either side of the PSD-95NMDAR interaction complex. This treatment attenuated downstream NMDAR signaling without blocking NMDAR activity, protected cultured cortical neurons from excitotoxic insults, dramatically reduced cerebral infarction volume in rats subjected to transient focal cerebral ischemia, and traumatic brain injury (TBI) in rats.

1 - 2 . (canceled) 
     
     
         3 . A method of reducing the damaging effect of ischemia or traumatic injury to the brain or spinal cord in a mammal, said method comprising treating said mammal with, an effective amount of an agent comprising a tSXV peptide, and a Tat peptide. 
     
     
         4 - 8 . (canceled) 
     
     
         9 . The method as defined in claim  1  wherein said agent is KLSSIESDV [SEQ ID NO:1]. 
     
     
         10 . The method as defined in claim  1  wherein said agent is KLSSIETDV [SEQ ID NO:2] 
     
     
         11 . (canceled) 
     
     
         12 . The method as defined in  claim 3  wherein the Tat peptide has the amino acid sequence YGRKKRRQRRR [SEQ ID NO:3]. 
     
     
         13 - 44 . (canceled)