Protocol

Examining Cholinergic Synaptic Signaling in the Thalamic Reticular Nucleus

  1. Michael Beierlein1,2,4
  1. 1Department of Neurobiology and Anatomy, McGovern Medical School at UTHealth, Houston, Texas 77030
  2. 2University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas 77030
  1. 4Correspondence: michael.beierlein{at}uth.tmc.edu
  1. 3 These authors contributed equally to this work.

Abstract

This protocol describes how to obtain monosynaptic cholinergic responses in neurons of the thalamic reticular nucleus (TRN) by making use of extracellular stimulation techniques. These methods are easy to implement and allow for the study of various forms of cholinergic synaptic plasticity and modulation. For many synapses throughout the mammalian brain, short-term plasticity is mediated by endocannabinoids released from postsynaptic neurons that activate presynaptic type I cannabinoid receptors (CB1Rs), resulting in the inhibition of presynaptic Ca2+ channels and a reduction of release probability. Neurons in the TRN are known to liberate endocannabinoids that can control transmitter release at GABAergic terminals. However, expression of CB1Rs on cholinergic terminals contacting the TRN has not been demonstrated. Here we outline strategies aimed to record stable postsynaptic responses and to quantify changes in cholinergic synaptic strength, using presynaptic modulation of acetylcholine (ACh) release by a CB1R agonist as an illustrative example.

Footnotes

  • From the Ion Channels collection, edited by Paul J. Kammermeier, Ian Duguid, and Stephan Brenowitz.

No Related Web Pages
| Table of Contents