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Impaired odour discrimination on desynchronization of odour-encoding neural assemblies

Author

Listed:
  • Mark Stopfer

    (California Institute of Technology Biology Division)

  • Seetha Bhagavan

    (Ohio State University
    Georgetown University Medical Center)

  • Brian H. Smith

    (Ohio State University)

  • Gilles Laurent

    (California Institute of Technology Biology Division)

Abstract

Stimulus-evoked oscillatory synchronization of neural assemblies has been described in the olfactory1,2,3,4,5 and visual6,7,8 systems of several vertebrates and invertebrates. In locusts, information about odour identity is contained in the timing of action potentials in an oscillatory population response9,10,11, suggesting that oscillations may reflect a common reference for messages encoded in time. Although the stimulus-evoked oscillatory phenomenon is reliable, its roles in sensation, perception, memory formation and pattern recognition remain to be demonstrated — a task requiring a behavioural paradigm. Using honeybees, we now demonstrate that odour encoding involves, as it does in locusts, the oscillatory synchronization of assemblies of projection neurons and that this synchronization is also selectively abolished by picrotoxin, an antagonist of the GABAA (γ-aminobutyric acid) receptor. By using a behavioural learning paradigm, we show that picrotoxin-induced desynchronization impairs the discrimination of molecularly similar odorants, but not that of dissimilar odorants. It appears, therefore, that oscillatory synchronization of neuronal assemblies is functionally relevant, and essential for fine sensory discrimination. This suggests that oscillatory synchronization and the kind of temporal encoding it affords provide an additional dimension by which the brain could segment spatially overlapping stimulus representations.

Suggested Citation

  • Mark Stopfer & Seetha Bhagavan & Brian H. Smith & Gilles Laurent, 1997. "Impaired odour discrimination on desynchronization of odour-encoding neural assemblies," Nature, Nature, vol. 390(6655), pages 70-74, November.
  • Handle: RePEc:nat:nature:v:390:y:1997:i:6655:d:10.1038_36335
    DOI: 10.1038/36335
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    Cited by:

    1. Rishabh Chandak & Baranidharan Raman, 2023. "Neural manifolds for odor-driven innate and acquired appetitive preferences," Nature Communications, Nature, vol. 14(1), pages 1-21, December.
    2. Montangie, Lisandro & Montani, Fernando, 2015. "Quantifying higher-order correlations in a neuronal pool," Physica A: Statistical Mechanics and its Applications, Elsevier, vol. 421(C), pages 388-400.
    3. Sashi Marella & Bard Ermentrout, 2010. "Amplification of Asynchronous Inhibition-Mediated Synchronization by Feedback in Recurrent Networks," PLOS Computational Biology, Public Library of Science, vol. 6(2), pages 1-11, February.
    4. Seyed-Ali Sadegh-Zadeh & Chandrasekhar Kambhampati & Darryl N. Davis, 2019. "Ionic Imbalances and Coupling in Synchronization of Responses in Neurons," J, MDPI, vol. 2(1), pages 1-24, January.
    5. Einat Granot-Atedgi & Gašper Tkačik & Ronen Segev & Elad Schneidman, 2013. "Stimulus-dependent Maximum Entropy Models of Neural Population Codes," PLOS Computational Biology, Public Library of Science, vol. 9(3), pages 1-14, March.
    6. Wilder Doucette & Diego Restrepo, 2008. "Profound Context-Dependent Plasticity of Mitral Cell Responses in Olfactory Bulb," PLOS Biology, Public Library of Science, vol. 6(10), pages 1-20, October.

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