Presynaptic Effects of NMDA in Cerebellar Purkinje Cells and Interneurons

• Published in: The Journal of neuroscience Vol. 19; no. 2; pp. 511 - 519
• Main Authors: Glitsch, M, Marty, A
• Format: Journal Article
• Language: English
• Published: United States Soc Neuroscience 15.01.1999; Society for Neuroscience
• Subjects: Animals; Electric Stimulation; Evoked Potentials - drug effects; Evoked Potentials - physiology; Excitatory Amino Acid Agonists - pharmacology; Excitatory Postsynaptic Potentials - drug effects; Excitatory Postsynaptic Potentials - physiology; gamma-Aminobutyric Acid - metabolism; In Vitro Techniques; Interneurons - drug effects; Interneurons - physiology; Magnesium - physiology; N-Methylaspartate - pharmacology; Neural Inhibition - drug effects; Neural Inhibition - physiology; Patch-Clamp Techniques; Purkinje Cells - drug effects; Purkinje Cells - physiology; Rats; Receptors, N-Methyl-D-Aspartate - drug effects; Receptors, N-Methyl-D-Aspartate - physiology; Receptors, Presynaptic - drug effects; Receptors, Presynaptic - physiology
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.19-02-00511.1999

NMDA receptors (NMDARs) are generally believed to mediate exclusively postsynaptic effects at brain synapses. Here we searched for presynaptic effects of NMDA at inhibitory synapses in rat cerebellar slices. In Purkinje cells, application of NMDA enhanced the frequency of miniature IPSCs (mIPSCs) but not that of miniature EPSCs (mEPSCs). This increase in frequency was dependent on the external Mg2+ concentration. In basket and stellate cells, NMDA induced an even larger mIPSC frequency increase than in Purkinje cells, whereas mEPSCs were again not affected. Moreover, NMDA induced an inward current in both types of interneuron, which translated into a small depolarization (approximately 10 mV for 30 microM NMDA) under current-clamp conditions. In paired recordings of connected basket cell-Purkinje cell synapses, depolarizations of 10-30 mV applied to the basket cell soma enhanced the frequency of postsynaptic mIPSCs, suggesting that somatic depolarization was partially transmitted to the terminals in the presence of tetrodotoxin. However, this effect was small and unlikely to account fully for the effects of NMDA on mIPSCs. Consistent with a small number of dendritic NMDARs, evoked EPSCs in interneurons had a remarkably small NMDA component. Evoked IPSCs at interneuron-interneuron synapses were inhibited by NMDA, and the rate of failures was increased, indicating again a presynaptic site of action. We conclude that activation of NMDARs in interneurons exerts complex presynaptic effects, and that the corresponding receptors are most likely located in the axonal domain of the cell.