4.5 Article

SUBTHALAMIC NUCLEUS EVOKES SIMILAR LONG LASTING GLUTAMATERGIC EXCITATIONS IN PALLIDAL, ENTOPEDUNCULAR AND NIGRAL NEURONS IN THE BASAL GANGLIA SLICE

Journal

NEUROSCIENCE
Volume 166, Issue 3, Pages 808-818

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2010.01.011

Keywords

basal ganglia; glutamate transmission; polysynaptic EPSCs; patch clamp; in vitro

Categories

Funding

  1. Institut National de la Sante et de la Recherche medicate (Inserm)
  2. Centre National de Recherche Scientifique (CNRS)
  3. Association France Parkinson and ERA-Net Neuron (PhysDBS)
  4. Ministere de la recherche (MRT)
  5. Fondation pour la Recherche Medicate (FRM)

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The subthalamic nucleus (STN) modulates the activity of globus pallidus (GP), entopeduncular nucleus (EP) and substantia nigra pars reticulata (SNr) neurons via its direct glutamatergic projections. To investigate the mechanism by which STN affects activity in these structures and whether STN induced activity is comparable among STN target neurons, we performed patch clamp recordings in a tilted, parasagittal, basal ganglia slice (BGS) that preserves these functional connections. We report that single, brief stimulation of the STN generates a brief monosynaptic AMPA-mediated excitatory postsynaptic current (EPSC) in GP, EP and SNr neurons. A higher intensity, supra-threshold activation evokes a compound EPSC consisting of an early monosynaptic component followed by a slow inward NMDA-mediated current with an overlying barrage of AMPA-mediated EPSCs. These late EPSCs were polysynaptic and gave rise to bursts of spikes that lasted several hundreds of milliseconds. They were eliminated by surgical removal of the STN from the BGS slice, indicating that the STN is required for their generation. Reconstruction of biocytin-filled STN neurons revealed that a third of STN neurons project intra-STN axon collaterals that may underlie polysynaptic activity. We propose that activation of the STN yields comparable long lasting excitations in its target neurons by means of a polysynaptic network. (C) 2010 IBRO. Published by Elsevier Ltd. All rights reserved.

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