Modulation of direct pathway striatal projection neurons by muscarinic M₄-type receptors

Neuropharmacology. 2015 Feb:89:232-44. doi: 10.1016/j.neuropharm.2014.09.028. Epub 2014 Oct 5.

Abstract

Models of basal ganglia (BG) function posit a dynamic balance between two classes of striatal projection neurons (SPNs): direct pathway neurons (dSPNs) that facilitate movements, and indirect pathway neurons (iSPNs) that repress movement execution. Two main modulatory transmitters regulate the output of these neurons: dopamine (DA) and acetylcholine (ACh). dSPNs express D1-type DA, M1-and M4-type ACh receptors, while iSPNs express D2-type DA and M1-type ACh receptors. Actions of M1-, D1-, and D2-receptors have been extensively reported, but we still ignore most actions of muscarinic M4-type receptors. Here, we used whole-cell recordings in acutely dissociated neurons, pharmacological tools such as mamba-toxins, and BAC D(1 or 2)-eGFP transgenic mice to show that activation of M4-type receptors with bath applied muscarine enhances Ca(2+)-currents through CaV1-channels in dSPNs and not in iSPNs. This action increases excitability of dSPNs after both direct current injection and synaptically driven stimulation. The increases in Ca(2+)-current and excitability were blocked specifically by mamba toxin-3, suggesting mediation via M4-type receptors. M4-receptor activation also increased network activity of dSPNs but not of iSPNs as seen with calcium-imaging techniques. Moreover, actions of D1-type and M4-type receptors may add to produce a larger enhancement of excitability of dSPNs or, paradoxically, oppose each other depending on the order of their activation. Possible implications of these findings are discussed.

Keywords: Acetylcholine; Ca(V)1 Ca(2+)-channels; Excitability; Striatal projection neurons; Striatum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology
  • Animals
  • Calcium Channel Blockers / pharmacology
  • Cells, Cultured
  • Corpus Striatum / cytology*
  • Dopamine / pharmacology
  • In Vitro Techniques
  • Male
  • Membrane Potentials / drug effects
  • Membrane Potentials / genetics
  • Mice
  • Mice, Transgenic
  • Neural Pathways / drug effects
  • Neural Pathways / physiology*
  • Neurons / drug effects
  • Neurons / physiology*
  • Nicardipine / pharmacology
  • Receptor, Muscarinic M4 / metabolism*
  • Receptors, Dopamine D1 / genetics
  • Receptors, Dopamine D2 / genetics
  • Sodium Channel Blockers / pharmacology
  • Tetrodotoxin / pharmacology

Substances

  • Calcium Channel Blockers
  • Receptor, Muscarinic M4
  • Receptors, Dopamine D1
  • Receptors, Dopamine D2
  • Sodium Channel Blockers
  • Tetrodotoxin
  • Nicardipine
  • Acetylcholine
  • Dopamine