Glycine Release Is Upregulated by Metabotropic Glutamate Receptor 1 in Mouse Hippocampus

<b>Background/Objectives</b>: The neurotransmitter glycine is involved in several physiological and pathological conditions in the Central Nervous System. Different biological structures, including glycine receptors and transporters, are under study as targets for potential drugs acting against serious neurological and psychiatric disorders. The regulation of glycine release from nerve terminals is only partially understood. We report here preliminary evidence of the modulation of glycine release through presynaptic metabotropic glutamate receptors 1 (mGlu1) from glycinergic nerve terminals in mouse hippocampi. <b>Methods</b>: Purified mouse hippocampal synaptosomes labeled with [³H]glycine were used to study glycine release under superfusion conditions. <b>Results</b>: The group I metabotropic glutamate receptor agonist 3,5-DHPG potentiated depolarization-evoked [³H]glycine release from hippocampal synaptosomes, an effect strongly counteracted by the selective mGlu1 antagonist LY 367385. 3,5-DHPG failed to increase [³H]glycine release in <i>Grm1^crv4/crv4</i> mice, a mouse model lacking mGlu1. Although further research is needed to clarify these mechanisms, data suggest that glycine-releasing hippocampal nerve terminals are endowed with presynaptic mGlu1 receptors whose activation potentiates glycine release. <b>Conclusions</b>: Considering that in the hippocampus, glycine is relevant as a co-agonist of glutamate at NMDA receptors and that mGlu1 receptor ligands are under study as potential drugs, we propose that the possible effects of these agents on the release of glycine should be considered when studying these compounds.