Properties of neurons in the superficial laminae of trigeminal nucleus caudalis

Physiol Rep. 2019 Jul;7(12):e14112. doi: 10.14814/phy2.14112.

Abstract

The trigeminal nucleus caudalis (TNc) receives extensive afferent innervation from peripheral sensory neurons of the trigeminal ganglion (TG), and is the first central relay in the circuitry underpinning orofacial pain. Despite the initial characterization of the neurons in the superficial laminae, many questions remain. Here we report on electrophysiological properties of 535 superficial lamina I/II TNc neurons. Based on their firing pattern, we assigned these cells to five main groups, including (1) tonic, (2) phasic, (3) delayed, (4) H-current, and (5) tonic-phasic neurons, groups that exhibit distinct intrinsic properties and share some similarity with groups identified in the spinal dorsal horn. Driving predominantly nociceptive TG primary afferents using optogenetic stimulation in TRPV1/ChR2 animals, we found that tonic and H-current cells are most likely to receive pure monosynaptic input, whereas delayed neurons are more likely to exhibit inputs that appear polysynaptic. Finally, for the first time in TNc neurons, we used unsupervised clustering analysis methods and found that the kinetics of the action potentials and other intrinsic properties of these groups differ significantly from one another. Unsupervised spectral clustering based solely on a single voltage response to rheobase current was sufficient to group cells with shared properties independent of action potential discharge pattern, indicating that this approach can be effectively applied to identify functional neuronal subclasses. Together, our data illustrate that cells in the TNc with distinct patterns of TRPV1/ChR2 afferent innervation are physiologically diverse, but can be understood as a few major groups of cells having shared functional properties.

Keywords: Craniofacial; electrophysiological properties; neuronal classification; trigeminal; waveform.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology
  • Afferent Pathways / physiology
  • Animals
  • Cluster Analysis
  • Electrophysiological Phenomena
  • Evoked Potentials / physiology
  • Female
  • Male
  • Membrane Potentials / physiology
  • Mice, Knockout
  • Neurons / physiology*
  • Neurons, Afferent / physiology
  • Nuclear Lamina / physiology
  • Optogenetics / methods
  • Patch-Clamp Techniques
  • Photic Stimulation / methods
  • Synapses / physiology
  • TRPV Cation Channels / physiology
  • Trigeminal Nuclei / cytology*
  • Trigeminal Nuclei / physiology

Substances

  • TRPV Cation Channels
  • TRPV1 protein, mouse