Optogenetic analysis of respiratory neuronal networks in the ventral medulla of neonatal rats producing channelrhodopsin in Phox2b-positive cells

Pflugers Arch. 2019 Dec;471(11-12):1419-1439. doi: 10.1007/s00424-019-02317-9. Epub 2019 Oct 20.

Abstract

Paired-like homeobox gene Phox2b is predominantly expressed in pre-inspiratory neurons in the parafacial respiratory group (pFRG) in newborn rat rostral ventrolateral medulla. To analyse detailed local networks of the respiratory centre using optogenetics, the effects of selective activation of Phox2b-positive neurons in the ventral medulla on respiratory rhythm generation were examined in brainstem-spinal cord preparations isolated from transgenic newborn rats with Phox2b-positive cells expressing channelrhodopsin variant ChRFR(C167A). Photostimulation up to 43 s increased the respiratory rate > 200% of control, whereas short photostimulation (1.5 s) of the rostral pFRG reset the respiratory rhythm. At the cellular level, photostimulation depolarised Phox2b-positive pre-inspiratory, inspiratory and respiratory-modulated tonic neurons and Phox2b-negative pre-inspiratory neurons. In contrast, changes in membrane potential of Phox2b-negative inspiratory and expiratory neurons varied depending on characteristics of ongoing synaptic connections in local respiratory networks in the rostral medulla. In the presence of tetrodotoxin, photostimulation depolarised Phox2b-positive cells, but caused no significant changes in membrane potential of Phox2b-negative cells. We concluded that depolarisation of Phox2b-positive neurons was due to cell-autonomous photo-activation and summation of excitatory postsynaptic potentials, whereas membrane potential changes of Phox2b-negative neurons depended on the network configuration. Our findings shed further light on local networks among respiratory-related neurons in the rostral ventrolateral medulla and emphasise the important role of pre-inspiratory neurons in respiratory rhythm generation in the neonatal rat en bloc preparation.

Keywords: Channelrhodopsin; Optogenetics; Parafacial respiratory group; Phox2b; Transgenic rat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Brain Stem / metabolism
  • Channelrhodopsins / metabolism*
  • Female
  • Homeodomain Proteins / metabolism*
  • Male
  • Medulla Oblongata / metabolism*
  • Membrane Potentials / physiology
  • Neurons / metabolism*
  • Optogenetics / methods
  • Rats
  • Respiration
  • Respiratory Center / metabolism*
  • Tetrodotoxin / metabolism
  • Transcription Factors / metabolism*

Substances

  • Channelrhodopsins
  • Homeodomain Proteins
  • NBPhox protein
  • Transcription Factors
  • Tetrodotoxin