Abstract
The d-isomer of aspartate is both a substrate for glutamate transporters and an agonist of N-methyl- d-aspartate (NMDA) receptors. To monitor the behavior of these receptors and transporters in intact tissue we synthesized a new photo-labile analogue of d-aspartate, N-[(6-nitrocoumarin-7-yl)methyl]- d-aspartic acid (Ncm- d-aspartate). This compound was photolyzed rapidly ( t 1/2 = 0.11 μs) by UV light with a quantum efficiency of 0.041 at pH 7.4. In acute hippocampal slices, photolysis of Ncm- d-aspartate by brief (1 ms) exposure to UV light elicited rapidly activating inward currents in astrocytes that were sensitive to inhibition by the glutamate transporter antagonist dl- threo-β-benzyloxyaspartic acid (TBOA). Neither Ncm- d-aspartate nor the photo-released caging group exhibited agonist or antagonist activity at glutamate transporters, and Ncm- d-aspartate did not induce transporter currents prior to photolysis. Glutamate transporter currents were also elicited in cerebellar Purkinje cells in response to photolysis of Ncm- d-aspartate. Photo-release of d-aspartate from Ncm- d-aspartate did not induce α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA)/kainate receptor or metabotropic glutamate receptor (mGluR) currents, but triggered robust NMDA receptor currents in neurons; Ncm- d-aspartate and the photolzyed caging group were similarly inert at NMDA receptors. These results indicate that Ncm- d-aspartate can be used to study NMDA receptors at excitatory synapses and interactions between transporters and receptors in brain tissue.
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