Investigation of nasal CO₂ receptor transduction mechanisms in wild-type and GC-D knockout mice

Chem Senses. 2013 Nov;38(9):769-81. doi: 10.1093/chemse/bjt044. Epub 2013 Oct 11.

Abstract

The main olfactory system of mice contains a small subset of olfactory sensory neurons (OSNs) that are stimulated by CO₂. The objective of this study was to record olfactory receptor responses to a range of CO₂ concentrations to further elucidate steps in the proposed CO₂ transduction pathway in mice. Electro-olfactograms (EOGs) were recorded before and after inhibiting specific steps in the CO₂ transduction pathway with topically applied inhibitors. Inhibition of extracellular carbonic anhydrase (CA) did not significantly affect EOG responses to CO₂ but did decrease EOG responses to several control odorants. Inhibition of intracellular CA or cyclic nucleotide-gated channels attenuated EOG responses to CO₂, confirming the role of these components in CO₂ sensing in mice. We also show that, like canonical OSNs, CO₂-sensitive OSNs depend on Ca²⁺-activated Cl⁻ channels for depolarization of receptor neurons. Lastly, we found that guanylyl cyclase-D knockout mice were still able to respond to CO₂, indicating that other pathways may exist for the detection of low concentrations of nasal CO₂. We discuss these findings as they relate to previous studies on CO₂-sensitive OSNs in mice and other animals.

Keywords: CNG channels; cGMP; carbonic anhydrase; chloride channels; olfaction; olfactory sensory neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbon Dioxide / pharmacology*
  • Chloride Channels / metabolism
  • Cyclic Nucleotide-Gated Cation Channels / metabolism
  • Electrophysiological Phenomena
  • Female
  • Guanylate Cyclase / deficiency
  • Guanylate Cyclase / genetics*
  • Guanylate Cyclase / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nasal Mucosa / drug effects*
  • Nasal Mucosa / physiology
  • Olfactory Receptor Neurons / metabolism
  • Pentanols / pharmacology
  • Receptors, Cell Surface / deficiency
  • Receptors, Cell Surface / genetics*
  • Receptors, Cell Surface / metabolism
  • Signal Transduction / drug effects
  • Smell / physiology

Substances

  • Chloride Channels
  • Cyclic Nucleotide-Gated Cation Channels
  • Pentanols
  • Receptors, Cell Surface
  • Carbon Dioxide
  • amyl acetate
  • Guanylate Cyclase
  • Gucy2d protein, mouse