Journal
NEUROCHEMICAL RESEARCH
Volume 33, Issue 6, Pages 1044-1050Publisher
SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11064-007-9548-x
Keywords
glutamate; excitotoxicity; blood glutamate levels; blood glutamate scavenging; oxaloacetate; pyruvate; glutamate-pyruvate transaminase; closed head injury; stroke; neuroprotection; brain to blood glutamate efflux; neurological outcome; antioxidant activity; intravenous injection
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The removal of excess glutamate from brain fluids after acute insults such as closed head injury (CHI) and stroke is expected to prevent excitotoxicity and the ensuing long lasting neurological deficits. Since blood glutamate scavenging accelerates the removal of excess glutamate from brain into blood and causes neuroprotection, we have evaluated here whether the neuroprotective properties of pyruvate could be partly accounted to its blood glutamate scavenging activity. The neurological outcome of rats after CHI improved significantly when treated with intravenous pyruvate (0.9 mmoles/100 g) but not with pyruvate administered together with glutamate. Pyruvate, at 5 mu mole/100 g rat was neither protective not able to decrease blood glutamate but displayed the latter two properties when combined with 60 mu g/100 g of glutamate-pyruvate transaminase. Since the neurological recovery from CHI was correlated with the decrease of blood glutamate levels, we conclude that pyruvate blood glutamate scavenging activity contributes to the spectrum of its neuroprotective mechanisms.
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