D-Serine and Glycine Differentially Control Neurotransmission during Visual Cortex Critical Period

• Published in: PloS one 2016, Vol.11 (3), p.e0151233-e0151233
• Main Authors: Meunier, Claire N J, Dallérac, Glenn, Le Roux, Nicolas, Sacchi, Silvia, Levasseur, Grégoire, Amar, Muriel, Pollegioni, Loredano, Mothet, Jean-Pierre, Fossier, Philippe
• Format: Article
• Language: English
• Subjects: Activation; Animal cognition; Animals; Binding sites; Biology and Life Sciences; Brain; Critical period; D-Serine; Depolarization; Experiments; Glutamic Acid - metabolism; Glutamic acid receptors (ionotropic); Glycine; Glycine - metabolism; Glycine receptors; Laboratory animals; Life Sciences; Long-term potentiation; Long-Term Potentiation - physiology; Male; Medicine and Health Sciences; N-Methyl-D-aspartic acid receptors; Neurobiology; Neuronal Plasticity - physiology; Neurons and Cognition; Neurosciences; Neurotransmission; Physical Sciences; Plasticity; Pyramidal cells; Pyramidal Cells - metabolism; Pyramidal Cells - physiology; Rats; Rats, Wistar; Receptors; Receptors, Glycine - metabolism; Receptors, N-Methyl-D-Aspartate - metabolism; Rodents; Serine - metabolism; Strychnine; Synapses; Synapses - metabolism; Synaptic plasticity; Synaptic strength; Synaptic Transmission - physiology; Visual cortex; Visual Cortex - metabolism
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0151233

N-methyl-D-aspartate receptors (NMDARs) play a central role in synaptic plasticity. Their activation requires the binding of both glutamate and d-serine or glycine as co-agonist. The prevalence of either co-agonist on NMDA-receptor function differs between brain regions and remains undetermined in the visual cortex (VC) at the critical period of postnatal development. Here, we therefore investigated the regulatory role that d-serine and/or glycine may exert on NMDARs function and on synaptic plasticity in the rat VC layer 5 pyramidal neurons of young rats. Using selective enzymatic depletion of d-serine or glycine, we demonstrate that d-serine and not glycine is the endogenous co-agonist of synaptic NMDARs required for the induction and expression of Long Term Potentiation (LTP) at both excitatory and inhibitory synapses. Glycine on the other hand is not involved in synaptic efficacy per se but regulates excitatory and inhibitory neurotransmission by activating strychnine-sensitive glycine receptors, then producing a shunting inhibition that controls neuronal gain and results in a depression of synaptic inputs at the somatic level after dendritic integration. In conclusion, we describe for the first time that in the VC both D-serine and glycine differentially regulate somatic depolarization through the activation of distinct synaptic and extrasynaptic receptors.