Evidence map›Paper›PMID 23990770›Full record

ArticlePLoS computational biology2013

Causes and consequences of hyperexcitation in central clock neurons.

Casey O Diekman, Mino D C Belle, Robert P Irwin, Charles N Allen, Hugh D Piggins, Daniel B Forger

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 41 citations in OpenAlex.

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  5. The E3 ubiquitin ligase adaptorProceedings of the National Academy of Sciences of the United States of America · 2021
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  6. Bright daytime light enhances circadian amplitude in a diurnal mammal.Proceedings of the National Academy of Sciences of the United States of America · 2021
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  7. Article
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  11. Delayed Cryptochrome Degradation Asymmetrically Alters the Daily Rhythm in Suprachiasmatic Clock Neuron Excitability.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  12. Article
  13. Synchronous circadian voltage rhythms with asynchronous calcium rhythms in the suprachiasmatic nucleus.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. The Neurobiology of Circadian Rhythms.The Psychiatric clinics of North America · 2015
    Review
  18. Article
  19. Distinct roles for GABA across multiple timescales in mammalian circadian timekeeping.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  20. GABA-mediated repulsive coupling between circadian clock neurons in the SCN encodes seasonal time.Proceedings of the National Academy of Sciences of the United States of America · 2015
    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

6 authors at 4 institutions in 2 countries.

Casey O DiekmanDepartment of Mathematical Sciences, New Jersey Institute of Technology, Newark, New Jersey, United States of America.
Mino D C Belle
Robert P Irwin
Charles N Allen
Hugh D Piggins
Daniel B Forger
Oregon Health & Science University · USUniversity of Manchester · GBNew Jersey Institute of Technology · USUniversity of Michigan–Ann Arbor · US

Funding

Calcium Signaling in Suprachiasmatic Nucleus NeuronsR01GM096972 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI ALLEN, CHARLES N · 2011 to 2014
$1.3M
NIGMS NIH HHS GM096972NIGMS NIH HHS R01 GM096972Wellcome Trust
6 · The paper itself

Abstract

Hyperexcited states, including depolarization block and depolarized low amplitude membrane oscillations (DLAMOs), have been observed in neurons of the suprachiasmatic nuclei (SCN), the site of the central mammalian circadian (~24-hour) clock. The causes and consequences of this hyperexcitation have not yet been determined. Here, we explore how individual ionic currents contribute to these hyperexcited states, and how hyperexcitation can then influence molecular circadian timekeeping within SCN neurons. We developed a mathematical model of the electrical activity of SCN neurons, and experimentally verified its prediction that DLAMOs depend on post-synaptic L-type calcium current. The model predicts that hyperexcited states cause high intracellular calcium concentrations, which could trigger transcription of clock genes. The model also predicts that circadian control of certain ionic currents can induce hyperexcited states. Putting it all together into an integrative model, we show how membrane potential and calcium concentration provide a fast feedback that can enhance rhythmicity of the intracellular circadian clock. This work puts forward a novel role for electrical activity in circadian timekeeping, and suggests that hyperexcited states provide a general mechanism for linking membrane electrical dynamics to transcription activation in the nucleus.

Indexed as

Models, NeurologicalAnimalsCalciumCalcium Channels, L-TypeCircadian RhythmCLOCK ProteinsComputer SimulationFeedback, PhysiologicalFemaleIntracellular SpaceMaleMiceNeuronsPatch-Clamp TechniquesReproducibility of ResultsSuprachiasmatic NucleusCalciumCalcium Channels, L-TypeCLOCK Proteins

Identifiers

PMID23990770
PMCPMC3749949
OpenAlexW2007321452

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.