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Antagonistic odor interactions in olfactory sensory neurons are widespread in freely breathing mice

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  • Joseph D. Zak

    (Harvard University
    Harvard University)

  • Gautam Reddy

    (Harvard University)

  • Massimo Vergassola

    (ENS, Université PSL, CNRS, Sorbonne Université, Université de Paris)

  • Venkatesh N. Murthy

    (Harvard University
    Harvard University)

Abstract

Odor landscapes contain complex blends of molecules that each activate unique, overlapping populations of olfactory sensory neurons (OSNs). Despite the presence of hundreds of OSN subtypes in many animals, the overlapping nature of odor inputs may lead to saturation of neural responses at the early stages of stimulus encoding. Information loss due to saturation could be mitigated by normalizing mechanisms such as antagonism at the level of receptor-ligand interactions, whose existence and prevalence remains uncertain. By imaging OSN axon terminals in olfactory bulb glomeruli as well as OSN cell bodies within the olfactory epithelium in freely breathing mice, we find widespread antagonistic interactions in binary odor mixtures. In complex mixtures of up to 12 odorants, antagonistic interactions are stronger and more prevalent with increasing mixture complexity. Therefore, antagonism is a common feature of odor mixture encoding in OSNs and helps in normalizing activity to reduce saturation and increase information transfer.

Suggested Citation

  • Joseph D. Zak & Gautam Reddy & Massimo Vergassola & Venkatesh N. Murthy, 2020. "Antagonistic odor interactions in olfactory sensory neurons are widespread in freely breathing mice," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17124-5
    DOI: 10.1038/s41467-020-17124-5
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    Cited by:

    1. Joseph D. Zak & Gautam Reddy & Vaibhav Konanur & Venkatesh N. Murthy, 2024. "Distinct information conveyed to the olfactory bulb by feedforward input from the nose and feedback from the cortex," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

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