Muscarinic inhibition of recurrent glutamatergic excitation in frog tectum column prevents NMDA receptor activation on efferent neuron

Exp Brain Res. 2011 Feb;208(3):323-34. doi: 10.1007/s00221-010-2484-z. Epub 2010 Nov 17.

Abstract

It is widely recognized that neuronal network activity can be modulated via activation of nicotinic and muscarinic acetylcholine receptors located pre- and postsynaptically. It was established in our earlier study that the activation of presynaptic nicotinic receptors greatly facilitates the retinotectal glutamatergic transmission. In the present study, we have determined a transmitter of tectal recurrent excitation and explored the effects of muscarinic acetylcholine receptor activation on the recurrent excitation and the activity of frog tectum column in vivo. Discharge of a single retinal ganglion cell was elicited by a minimal electrical stimulation of the retina. Evoked activity of the tectum column was recorded using the carbon-fiber microelectrode inserted into the tectum layer F. We found the following: 1. The recurrent excitation in the tectum column was not affected by d-tubocurarine (10 μM) and was greatly depressed by the kynurenic acid (500 μM), demonstrating glutamatergic nature of the recurrent excitation. 2. The glutamatergic recurrent excitation was largely reduced by carbamylcholine (100 μM) and oxotremorine-M (10 μM), demonstrating that the activation of muscarinic receptors, located, presumably, on the presynaptic terminals of recurrent pear-shaped neurons, inhibits the recurrent excitation in the tectum column. 3. The muscarinic inhibition of glutamatergic recurrent transmission had critical influence on the activity of the tectum column, preventing the generation of an output signal through suppression of the NMDA receptor activation and establishing necessary conditions for returning of the network to its resting state.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Glutamic Acid / physiology*
  • Nerve Net / drug effects
  • Nerve Net / physiology
  • Neurons, Efferent / drug effects
  • Neurons, Efferent / physiology*
  • Oxotremorine / pharmacology
  • Rana temporaria
  • Receptors, Muscarinic / physiology*
  • Receptors, N-Methyl-D-Aspartate / metabolism*
  • Synaptic Potentials / drug effects
  • Synaptic Potentials / physiology*
  • Tectum Mesencephali / drug effects
  • Tectum Mesencephali / physiology*
  • Tubocurarine / pharmacology

Substances

  • Receptors, Muscarinic
  • Receptors, N-Methyl-D-Aspartate
  • Glutamic Acid
  • Oxotremorine
  • Tubocurarine