Treatment of Ischemic Brain Damage by Perturbing NMDA Receptor- PSD-95 Protein Interactions

Author:

Aarts Michelle1,Liu Yitao234,Liu Lidong234,Besshoh Shintaro5,Arundine Mark1,Gurd James W.5,Wang Yu-Tian234,Salter Michael W.36,Tymianski Michael167

Affiliation:

1. Toronto Western Hospital Research Institute, 11-416 MC-PAV, 399 Bathurst Street, Toronto, Ontario M5T 2S8, Canada.

2. Divisions of Laboratory Medicine and Pathobiology,

3. Programme in Brain and Behaviour, Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada.

4. Brain Research Center and Department of Medicine, Vancouver Hospital and Health Sciences Center, University of British Columbia, Vancouver, British Columbia V6T 1Z3, Canada.

5. Centre for the Neurobiology of Stress, Division of Life Sciences, University of Toronto at Scarborough, Toronto, Ontario M1C 1A3, Canada.

6. Department of Physiology,

7. Department of Surgery, University of Toronto, Toronto, Ontario M5S 1A8, Canada.

Abstract

N -methyl- d -aspartate receptors (NMDARs) mediate ischemic brain damage but also mediate essential neuronal excitation. To treat stroke without blocking NMDARs, we transduced neurons with peptides that disrupted the interaction of NMDARs with the postsynaptic density protein PSD-95. This procedure dissociated NMDARs from downstream neurotoxic signaling without blocking synaptic activity or calcium influx. The peptides, when applied either before or 1 hour after an insult, protected cultured neurons from excitotoxicity, reduced focal ischemic brain damage in rats, and improved their neurological function. This approach circumvents the negative consequences associated with blocking NMDARs and may constitute a practical stroke therapy.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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