Evidence map›Paper›PMID 26674618›Full record

ArticlePLoS biology2015

Prolonged Intracellular Na+ Dynamics Govern Electrical Activity in Accessory Olfactory Bulb Mitral Cells.

Asaph Zylbertal, Anat Kahan, Yoram Ben-Shaul, Yosef Yarom, Shlomo Wagner

Abstract read
In one paragraph

Article in PLoS biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Spatiotemporal Dynamics of Lateral NaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  2. Spatio-temporal dynamics of lateral NabioRxiv : the preprint server for biology · 2025
    Article
  3. Article
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  7. Interactions among diameter, myelination, and the Na/K pump affect axonal resilience to high-frequency spiking.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  8. Article
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  10. Review
  11. Temporal Response Properties of Accessory Olfactory Bulb Neurons: Limitations and Opportunities for Decoding.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  12. Article
  13. Article
  14. Two-Photon NaFrontiers in cellular neuroscience · 2017
    Article
  15. Interdependent Conductances Drive Infraslow Intrinsic Rhythmogenesis in a Subset of Accessory Olfactory Bulb Projection Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  16. Article
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Asaph ZylbertalDepartment of Neurobiology, Institute of Life Sciences, Hebrew University and the Edmond and Lily Safra Center for Brain Sciences, Jerusalem, Israel.
Anat KahanSchool of Medicine, Department of Medical Neurobiology, Hebrew University, Jerusalem, Israel.
Yoram Ben-ShaulSchool of Medicine, Department of Medical Neurobiology, Hebrew University, Jerusalem, Israel.
Yosef YaromDepartment of Neurobiology, Institute of Life Sciences, Hebrew University and the Edmond and Lily Safra Center for Brain Sciences, Jerusalem, Israel.
Shlomo WagnerSagol Department of Neurobiology, University of Haifa, Haifa, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persistent activity has been reported in many brain areas and is hypothesized to mediate working memory and emotional brain states and to rely upon network or biophysical feedback. Here, we demonstrate a novel mechanism by which persistent neuronal activity can be generated without feedback, relying instead on the slow removal of Na+ from neurons following bursts of activity. We show that mitral cells in the accessory olfactory bulb (AOB), which plays a major role in mammalian social behavior, may respond to a brief sensory stimulation with persistent firing. By combining electrical recordings, Ca2+ and Na+ imaging, and realistic computational modeling, we explored the mechanisms underlying the persistent activity in AOB mitral cells. We found that the exceptionally slow inward current that underlies this activity is governed by prolonged dynamics of intracellular Na+ ([Na+]i), which affects neuronal electrical activity via several pathways. Specifically, elevated dendritic [Na+]i reverses the Na+-Ca2+ exchanger activity, thus modifying the [Ca2+]i set-point. This process, which relies on ubiquitous membrane mechanisms, is likely to play a role in other neuronal types in various brain regions.

Indexed as

Models, NeurologicalNeural ConductionAnimalsComputational BiologyDendritesElectrophysiological PhenomenaFemaleIon Channel GatingKineticsMaleMice, Inbred BALB CMice, Inbred C57BLMicroscopy, FluorescenceMicroscopy, VideoNerve Tissue ProteinsNeuronsNerve Tissue ProteinsSodium-Calcium Exchanger

Identifiers

PMID26674618
PMCPMC4684409

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.