Evidence map›Paper›PMID 20826674›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

Kinetic properties and functional dynamics of sodium channels during repetitive spiking in a slow pacemaker neuron.

Lorin S Milescu, Tadashi Yamanishi, Krzysztof Ptak, Jeffrey C Smith

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
0.9field-weighted citation impact, top 30% of its field
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

44 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
  6. Article
  7. Slow negative feedback enhances robustness of square-wave bursting.Journal of computational neuroscience · 2023
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  11. Cell Type-Specific Decrease of the Intrinsic Excitability of Motor Cortical Pyramidal Neurons in Parkinsonism.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  12. Article
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  14. Article
  15. Lateral habenula dysfunctions in Tm4sf2Neurobiology of disease · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Axonal Computations.Frontiers in cellular neuroscience · 2019
    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

4 authors at 2 institutions in 1 country.

Lorin S MilescuDepartment of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, USA. Lorin_Milescu@hms.harvard.edu
Tadashi Yamanishi
Krzysztof Ptak
Jeffrey C Smith
National Institute of Neurological Disorders and Stroke · USHarvard University · US

Funding

Neural Mechanisms Controlling Breathing In MammalsZIANS002899 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI SMITH, JEFFREY C · 2009 to 2023
$21.1M
Intramural NIH HHS Z99 NS999999
6 · The paper itself

Abstract

We examined the kinetic properties of voltage-gated Na(+) channels and their contribution to the repetitive spiking activity of medullary raphé neurons, which exhibit slow pacemaking and strong spiking adaptation. The study is based on a combination of whole-cell patch-clamp, modeling and real-time computation. Na(+) currents were recorded from neurons in brain slices obtained from male and female neonatal rats, using voltage-clamp protocols designed to reduce space-clamp artifacts and to emphasize functionally relevant kinetic features. A detailed kinetic model was formulated to explain the broad range of transient and stationary voltage-dependent properties exhibited by Na(+) currents. The model was tested by injecting via dynamic clamp a model-based current as a substitute for the native TTX-sensitive Na(+) currents, which were pharmacologically blocked. The model-based current reproduced well the native spike shape and spiking frequency. The dynamics of Na(+) channels during repetitive spiking were indirectly examined through this model. By comparing the spiking activities generated with different kinetic models in dynamic-clamp experiments, we determined that state-dependent slow inactivation contributes significantly to spiking adaptation. Through real-time manipulation of the model-based current, we established that suprathreshold Na(+) current mainly controls spike shape, whereas subthreshold Na(+) current modulates spiking frequency and contributes to the pacemaking mechanism. Since the model-based current was injected in the soma, the results also suggest that somatic Na(+) channels are sufficient to establish the essential spiking properties of raphé neurons in vitro.

Indexed as

Nonlinear Dynamics6-Cyano-7-nitroquinoxaline-2,3-dioneAction PotentialsAnimalsAnimals, NewbornBiological ClocksBiophysical PhenomenaCadmium ChlorideExcitatory Amino Acid AntagonistsIn Vitro TechniquesModels, NeurologicalNeuronsPatch-Clamp TechniquesProbabilityRaphe NucleiRats6-Cyano-7-nitroquinoxaline-2,3-dioneCadmium ChlorideExcitatory Amino Acid AntagonistsSodium Channel BlockersSodium ChannelsTetrodotoxin

Identifiers

PMID20826674
PMCPMC2945634
OpenAlexW2003547231

What OpenQuestion holds

Textmetadata
LicenceTDM
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.