Group II metabotropic glutamate receptors mediate presynaptic inhibition of excitatory transmission in pyramidal neurons of the human cerebral cortex

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  • Marco Bocchio, Oxford University, Oxford, UK., Aix-Marseille Université
  • ,
  • Istvan P. Lukacs, Oxford University, Oxford, UK.
  • ,
  • Richard Stacey, Oxford University Hospitals NHS Foundation Trust
  • ,
  • Puneet Plaha, Oxford University Hospitals NHS Foundation Trust
  • ,
  • Vasileios Apostolopoulos, Oxford University Hospitals NHS Foundation Trust
  • ,
  • Laurent Livermore, Oxford University Hospitals NHS Foundation Trust
  • ,
  • Arjune Sen, NIHR Biomedical Research Centre, Oxford University, Oxford, UK.
  • ,
  • Olaf Ansorge, Oxford University, Oxford, UK.
  • ,
  • Martin J. Gillies, Oxford University, Oxford, UK.
  • ,
  • Peter Somogyi, Oxford University, Oxford, UK.
  • ,
  • Marco Capogna

Group II metabotropic glutamate receptor (mGluR) ligands are potential novel drugs for neurological and psychiatric disorders, but little is known about the effects of these compounds at synapses of the human cerebral cortex. Investigating the effects of neuropsychiatric drugs in human brain tissue with preserved synaptic circuits might accelerate the development of more potent and selective pharmacological treatments. We have studied the effects of group II mGluR activation on excitatory synaptic transmission recorded from pyramidal neurons of cortical layers 2–3 in acute slices derived from surgically removed cortical tissue of people with epilepsy or tumors. The application of a selective group II mGluR agonist, LY354740 (0.1–1 µM) inhibited the amplitude and frequency of action potential-dependent spontaneous excitatory postsynaptic currents (sEPSCs). This effect was prevented by the application of a group II/III mGluR antagonist, CPPG (0.1 mM). Furthermore, LY354740 inhibited the frequency, but not the amplitude, of action potential-independent miniature EPSCs (mEPSCs) recorded in pyramidal neurons. Finally, LY354740 did slightly reduce cells’ input resistance without altering the holding current of the neurons recorded in voltage clamp at −90 mV. Our results suggest that group II mGluRs are mainly auto-receptors that inhibit the release of glutamate onto pyramidal neurons in layers 2–3 in the human cerebral cortex, thereby regulating network excitability. We have demonstrated the effect of a group II mGluR ligand at human cortical synapses, revealing mechanisms by which these drugs could exert pro-cognitive effects and treat human neuropsychiatric disorders.

OriginalsprogEngelsk
Artikelnummer508
TidsskriftFrontiers in Cellular Neuroscience
Vol/bind12
Antal sider15
ISSN1662-5102
DOI
StatusUdgivet - 4 jan. 2019

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