Evidence map›Paper›PMID 32193397›Full record

ArticleNature communications2020

Output from VIP cells of the mammalian central clock regulates daily physiological rhythms.

Sarika Paul, Lydia Hanna, Court Harding, Edward A Hayter, Lauren Walmsley, David A Bechtold, Timothy M Brown

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 85 citations in OpenAlex.

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  11. Neuropeptidergic Input from the Lateral Hypothalamus to the Suprachiasmatic Nucleus Alters the Circadian Period in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
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  19. Review
  20. Somatostatin regulates central clock function and circadian responses to light.Proceedings of the National Academy of Sciences of the United States of America · 2023
    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

7 authors at 2 institutions in 1 country.

Sarika PaulCentre for Biological timing, Faculty of Biology Medicine & Health, University of Manchester, Manchester, UK.
Lydia HannaCentre for Biological timing, Faculty of Biology Medicine & Health, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0002-5000-6676
Court HardingCentre for Biological timing, Faculty of Biology Medicine & Health, University of Manchester, Manchester, UK.
Edward A HayterCentre for Biological timing, Faculty of Biology Medicine & Health, University of Manchester, Manchester, UK.
Lauren WalmsleyCentre for Biological timing, Faculty of Biology Medicine & Health, University of Manchester, Manchester, UK.
David A BechtoldCentre for Biological timing, Faculty of Biology Medicine & Health, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0001-8676-8704
Timothy M BrownCentre for Biological timing, Faculty of Biology Medicine & Health, University of Manchester, Manchester, UK. timothy.brown@manchester.ac.uk.
University of Manchester · GBManchester Academic Health Science Centre · GB

Funding

Biotechnology and Biological Sciences Research Council BB/N007115/1Medical Research Council MR/P00279X/1
6 · The paper itself

Abstract

The suprachiasmatic nucleus (SCN) circadian clock is critical for optimising daily cycles in mammalian physiology and behaviour. The roles of the various SCN cell types in communicating timing information to downstream physiological systems remain incompletely understood, however. In particular, while vasoactive intestinal polypeptide (VIP) signalling is essential for SCN function and whole animal circadian rhythmicity, the specific contributions of VIP cell output to physiological control remains uncertain. Here we reveal a key role for SCN VIP cells in central clock output. Using multielectrode recording and optogenetic manipulations, we show that VIP neurons provide coordinated daily waves of GABAergic input to target cells across the paraventricular hypothalamus and ventral thalamus, supressing their activity during the mid to late day. Using chemogenetic manipulation, we further demonstrate specific roles for this circuitry in the daily control of heart rate and corticosterone secretion, collectively establishing SCN VIP cells as influential regulators of physiological timing.

Indexed as

Action PotentialsAnimalsBicucullineChannelrhodopsinsCircadian ClocksCircadian RhythmCorticosteroneElectrodes, ImplantedFemaleGABA-A Receptor AntagonistsGABAergic NeuronsHeart RateMaleMiceMice, TransgenicModels, AnimalBicucullineChannelrhodopsinsCorticosteroneGABA-A Receptor AntagonistsVasoactive Intestinal Peptide

Identifiers

PMID32193397
PMCPMC7081308
OpenAlexW3009509292

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.