Evidence map›Paper›PMID 32285754›Full record

ArticleJournal of biological rhythms2020

Astrocytic Modulation of Neuronal Activity in the Suprachiasmatic Nucleus: Insights from Mathematical Modeling.

Natthapong Sueviriyapan, Chak Foon Tso, Erik D Herzog, Michael A Henson

Open access · greenAbstract read
In one paragraph

Article in Journal of biological rhythms, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 41% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. 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.

Natthapong SueviriyapanDepartment of Chemical Engineering and the Institute for Applied Life Sciences, University of Massachusetts, Amherst, Massachusetts.ORCID 0000-0001-8001-1532
Chak Foon TsoDepartment of Biology, Washington University in St. Louis, Saint Louis, Missouri.
Erik D HerzogDepartment of Biology, Washington University in St. Louis, Saint Louis, Missouri.
Michael A HensonDepartment of Chemical Engineering and the Institute for Applied Life Sciences, University of Massachusetts, Amherst, Massachusetts.
University of Massachusetts Amherst · USWashington University in St. Louis · US

Funding

Multiscale Modeling of the Mammalian Circadian Clock: The Role of GABA SignalingU01EB021956 · NIBIB · UNIVERSITY OF MASSACHUSETTS AMHERST · PI HENSON, MICHAEL, HERZOG, ERIK · 2016 to 2019
$1.8M
NIBIB NIH HHS U01 EB021956
6 · The paper itself

Abstract

The suprachiasmatic nucleus (SCN) of the hypothalamus consists of a highly heterogeneous neuronal population networked together to allow precise and robust circadian timekeeping in mammals. While the critical importance of SCN neurons in regulating circadian rhythms has been extensively studied, the roles of SCN astrocytes in circadian system function are not well understood. Recent experiments have demonstrated that SCN astrocytes are circadian oscillators with the same functional clock genes as SCN neurons. Astrocytes generate rhythmic outputs that are thought to modulate neuronal activity through pre- and postsynaptic interactions. In this study, we developed an in silico multicellular model of the SCN clock to investigate the impact of astrocytes in modulating neuronal activity and affecting key clock properties such as circadian rhythmicity, period, and synchronization. The model predicted that astrocytes could alter the rhythmic activity of neurons via bidirectional interactions at tripartite synapses. Specifically, astrocyte-regulated extracellular glutamate was predicted to increase neuropeptide signaling from neurons. Consistent with experimental results, we found that astrocytes could increase the circadian period and enhance neural synchronization according to their endogenous circadian period. The impact of astrocytic modulation of circadian rhythm amplitude, period, and synchronization was predicted to be strongest when astrocytes had periods between 0 and 2 h longer than neurons. Increasing the number of neurons coupled to the astrocyte also increased its impact on period modulation and synchrony. These computational results suggest that signals that modulate astrocytic rhythms or signaling (e.g., as a function of season, age, or treatment) could cause disruptions in circadian rhythm or serve as putative therapeutic targets.

Indexed as

Models, TheoreticalAnimalsAstrocytesCircadian ClocksCircadian RhythmMammalsNeuronsSuprachiasmatic Nucleusastrocytescircadian rhythmsmathematical modelingneuronal couplingsuprachiasmatic nucleus

Identifiers

PMID32285754
PMCPMC7401727
OpenAlexW3016088522

What OpenQuestion holds

Textmetadata
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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.