Abstract

Unravelling and understanding the molecular and neurochemical changes of the aging brain is key to early intervention strategies. Glutamate (Glu) neurotransmission, the major excitatory neurotransmitter in the brain, is mechanistically involved in memory, learning performance, and other aspects of cognition. Moreover, as the brain ages, the glutamatergic signaling system mediated through brain N‐methyl‐D‐aspartate (NMDA) receptors becomes hypofunctional, and this decline may be associated with cognitive dysfunction in normal aging and in disease states. We have developed an in vitro assay that measures Glu‐stimulated release of neurotransmitters in rat brain slices. Using this assay, we compared changes in Glu‐stimulated release of [3H]‐norepinephrine (NE) from the cerebral cortex and hippocampus in young (2–3 months old) versus old (21–23 months old) Fischer F344 rats. Our findings demonstrate that that there is a pronounced deficit (approximately 30–40%) of Glu‐stimulated [3H]‐NE release in the aged rat brain in comparison to younger controls. In the same tissues, potassium (K+) stimulated‐NE release is similar in brains from young and old rats, suggesting that the age‐related decline in in Glu‐stimulated NE release is related to a change in NMDA receptors. Notably, the deficit in Glu‐stimulated [3H]‐NE release in both brain regions was completely rescued by the addition of 1 uM d‐amphetamine sulfate to the tissue slices. Overall, these findings reveal an important deficit in NE release in the aging brain, which may have important implications for cognitive dysfunction in aging. Moreover, this deficit can be reversed with amphetamine and possibly with similar drugs. These studies have clear clinical implications for the use of CNS stimulants as a therapeutic intervention for early cognitive impairment.This abstract is from the Experimental Biology 2019 Meeting. There is no full text article associated with this abstract published in The FASEB Journal.

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