Evidence map›Paper›PMID 20730480›Full record

ArticleJournal of computational neuroscience2011

System identification of Drosophila olfactory sensory neurons.

Anmo J Kim, Aurel A Lazar, Yevgeniy B Slutskiy

Abstract read
In one paragraph

Article in Journal of computational neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

52 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Active sensing in a dynamic olfactory world.Journal of computational neuroscience · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Adaptive temporal processing of odor stimuli.Cell and tissue research · 2021
    Review
  12. Article
  13. Consilience in the Peripheral Sensory Adaptation Response.Frontiers in human neuroscience · 2021
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Competitive binding predicts nonlinear responses of olfactory receptors to complex mixtures.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  19. Odor Stimuli: Not Just Chemical Identity.Frontiers in physiology · 2019
    Review
  20. Independent processing of increments and decrements in odorant concentration by ON and OFF olfactory receptor neurons.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2018
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Anmo J KimDepartment of Electrical Engineering, Columbia University, New York, NY, USA.
Aurel A Lazar
Yevgeniy B Slutskiy

Funding

CRCNS: Input/Output Characterization of the Antennal Lobe of the DrosophilaR01DC008701 · NIDCD · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI LAZAR, AUREL A · 2006 to 2010
$1.3M
NIDCD NIH HHS R01 DC008701NIDCD NIH HHS R01DC008701-01
6 · The paper itself

Abstract

The lack of a deeper understanding of how olfactory sensory neurons (OSNs) encode odors has hindered the progress in understanding the olfactory signal processing in higher brain centers. Here we employ methods of system identification to investigate the encoding of time-varying odor stimuli and their representation for further processing in the spike domain by Drosophila OSNs. In order to apply system identification techniques, we built a novel low-turbulence odor delivery system that allowed us to deliver airborne stimuli in a precise and reproducible fashion. The system provides a 1% tolerance in stimulus reproducibility and an exact control of odor concentration and concentration gradient on a millisecond time scale. Using this novel setup, we recorded and analyzed the in-vivo response of OSNs to a wide range of time-varying odor waveforms. We report for the first time that across trials the response of OR59b OSNs is very precise and reproducible. Further, we empirically show that the response of an OSN depends not only on the concentration, but also on the rate of change of the odor concentration. Moreover, we demonstrate that a two-dimensional (2D) Encoding Manifold in a concentration-concentration gradient space provides a quantitative description of the neuron's response. We then use the white noise system identification methodology to construct one-dimensional (1D) and two-dimensional (2D) Linear-Nonlinear-Poisson (LNP) cascade models of the sensory neuron for a fixed mean odor concentration and fixed contrast. We show that in terms of predicting the intensity rate of the spike train, the 2D LNP model performs on par with the 1D LNP model, with a root mean-square error (RMSE) increase of about 5 to 10%. Surprisingly, we find that for a fixed contrast of the white noise odor waveforms, the nonlinear block of each of the two models changes with the mean input concentration. The shape of the nonlinearities of both the 1D and the 2D LNP model appears to be, for a fixed mean of the odor waveform, independent of the stimulus contrast. This suggests that white noise system identification of Or59b OSNs only depends on the first moment of the odor concentration. Finally, by comparing the 2D Encoding Manifold and the 2D LNP model, we demonstrate that the OSN identification results depend on the particular type of the employed test odor waveforms. This suggests an adaptive neural encoding model for Or59b OSNs that changes its nonlinearity in response to the odor concentration waveforms.

Indexed as

Models, NeurologicalOdorantsAction PotentialsAnimalsDrosophilaLinear ModelsNoiseNonlinear DynamicsOlfactory PathwaysSensory Receptor CellsSmell

Identifiers

PMID20730480
PMCPMC3736744

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.