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   <subfield code="a">Modulation of an AMPA-like glutamate receptor (SqGluR) gating by L- and D-aspartic acids</subfield>
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   <subfield code="c">[E. R. Brown, S. Piscopo, J.-T. Chun, M. Francone, I. Mirabile, A. D'Aniello]</subfield>
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   <subfield code="a">Summary.: L- and D-aspartic acids (L-Asp and D-Asp) are present in the majority of nervous systems. In phylogeny, significant levels have been reported in mollusc brains, particularly cephalopods. To examine the role of L- and D-Asp on a cephalopod receptor, we studied ligand gating of a squid glutamate receptor (SqGluR) expressed in HEK 239 (human embryonic kidney) cells. Under voltage clamp, application of L-glutamate (L-Glu; 1-30 mM), but not D-glutamate (D-Glu), or L- or D-Asp, evoked an inward current of 0.1 nA. L- or D-Asp (200 µM) applied with 20 mM L-Glu, slowed the time course of activation and inactivation of the L-Glu gated current (time constant increased from 1 s (L-Glu alone) to 3 s (D-Asp and L-Glu) and to 19 s (L-Asp and L-Glu)). Our results suggest that in molluscan systems, aspartic acid could act as a neuromodulator during glutamatergic transmission and could significantly alter synaptic integration by slowing glutamate receptor gating.</subfield>
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   <subfield code="a">Keywords: Glutamate receptor - SqGluR - Heterologous expression - L- and D-aspartic acid - Neuromodulation</subfield>
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