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Mild traumatic brain injury (TBI) is believed to induce glutamate-mediated neurotoxicity, causing alterations in ionotropic glutamate receptors with subsequent brain injury sequelae. In this chapter, the possibility of peptide fragments of ionotropic glutamate receptors detected in the blood of rodents to serve as autoantigens and autoantibodies is explored using experimental models of mild brain injury. Effects of potential endogenous peptide inhibition of ionotropic glutamate receptors for preventive treatment of brain injury are also explored.

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