Evidence map›Paper›PMID 24465729›Full record

ArticlePloS one2014

Electrical resonance in the θ frequency range in olfactory amygdala neurons.

Jorge Vera, Maurizio Pezzoli, Ulises Pereira, Juan Bacigalupo, Magdalena Sanhueza

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. αFrontiers in cellular neuroscience · 2022
    Article
  6. IProgress in biophysics and molecular biology · 2021
    Review
  7. Chemical modulation of Kv7 potassium channels.RSC medicinal chemistry · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Competition between Persistent NaFrontiers in cellular neuroscience · 2017
    Article
  13. Article
  14. Review
  15. Article
  16. Article
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

5 authors.

Jorge VeraDepartment of Biology, Faculty of Sciences, University of Chile, Santiago, Chile.
Maurizio PezzoliDepartment of Biology, Faculty of Sciences, University of Chile, Santiago, Chile.
Ulises PereiraDepartment of Biology, Faculty of Sciences, University of Chile, Santiago, Chile.
Juan BacigalupoDepartment of Biology, Faculty of Sciences, University of Chile, Santiago, Chile.
Magdalena SanhuezaDepartment of Biology, Faculty of Sciences, University of Chile, Santiago, Chile.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cortical amygdala receives direct olfactory inputs and is thought to participate in processing and learning of biologically relevant olfactory cues. As for other brain structures implicated in learning, the principal neurons of the anterior cortical nucleus (ACo) exhibit intrinsic subthreshold membrane potential oscillations in the θ-frequency range. Here we show that nearly 50% of ACo layer II neurons also display electrical resonance, consisting of selective responsiveness to stimuli of a preferential frequency (2-6 Hz). Their impedance profile resembles an electrical band-pass filter with a peak at the preferred frequency, in contrast to the low-pass filter properties of other neurons. Most ACo resonant neurons displayed frequency preference along the whole subthreshold voltage range. We used pharmacological tools to identify the voltage-dependent conductances implicated in resonance. A hyperpolarization-activated cationic current depending on HCN channels underlies resonance at resting and hyperpolarized potentials; notably, this current also participates in resonance at depolarized subthreshold voltages. KV7/KCNQ K+ channels also contribute to resonant behavior at depolarized potentials, but not in all resonant cells. Moreover, resonance was strongly attenuated after blockade of voltage-dependent persistent Na+ channels, suggesting an amplifying role. Remarkably, resonant neurons presented a higher firing probability for stimuli of the preferred frequency. To fully understand the mechanisms underlying resonance in these neurons, we developed a comprehensive conductance-based model including the aforementioned and leak conductances, as well as Hodgkin and Huxley-type channels. The model reproduces the resonant impedance profile and our pharmacological results, allowing a quantitative evaluation of the contribution of each conductance to resonance. It also replicates selective spiking at the resonant frequency and allows a prediction of the temperature-dependent shift in resonance frequency. Our results provide a complete characterization of the resonant behavior of olfactory amygdala neurons and shed light on a putative mechanism for network activity coordination in the intact brain.

Indexed as

Electrophysiological PhenomenaAmygdalaAnimalsCerebral CortexComputer SimulationIon Channel GatingIonsKineticsMaleMembrane PotentialsModels, NeurologicalNeuronsOlfactory BulbRatsRats, Sprague-DawleySodium ChannelsIonsSodium Channels

Identifiers

PMID24465729
PMCPMC3897534

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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.