Evidence map›Paper›PMID 20952671›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2011

Circadian regulation of cardiovascular function: a role for vasoactive intestinal peptide.

Analyne Schroeder, Dawn H Loh, Maria C Jordan, Kenneth P Roos, Christopher S Colwell

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2011. 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
1.8field-weighted citation impact, top 16% 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, 38 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. The Circadian Biology of Heart Failure.Circulation research · 2023
    Review
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  7. Article
  8. Article
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  10. Review
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  13. Drosophila DH31 Neuropeptide and PDF Receptor Regulate Night-Onset Temperature Preference.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  14. Review
  15. Review
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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

5 authors at 1 institution in 1 country.

Analyne SchroederDepartment of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, California 90024, USA.
Dawn H Loh
Maria C Jordan
Kenneth P Roos
Christopher S Colwell
University of California, Los Angeles · US

Funding

Training in Molecular, Cellular &Integrative PhysiologyT32GM065823 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TIDBALL, JAMES G · 2003 to 2017
$2.1M
NIGMS NIH HHS T32 GM065823
6 · The paper itself

Abstract

The circadian system, driven by the suprachiasmatic nucleus (SCN), regulates properties of cardiovascular function. The dysfunction of this timing system can result in cardiac pathology. The neuropeptide vasoactive intestinal peptide (VIP) is crucial for circadian rhythms in a number of biological processes including SCN electrical activity and wheel running behavior. Anatomic evidence indicates that SCN neurons expressing VIP are well positioned to drive circadian regulation of cardiac function through interactions with the autonomic centers. In this study, we tested the hypothesis that loss of VIP would result in circadian deficits in heart rate (HR) and clock gene expression in cardiac tissue. We implanted radiotelemetry devices into VIP-deficient mice and wild-type (WT) controls and continuously recorded HR, body temperature, and cage activity in freely moving mice. Under light-dark conditions, VIP-deficient mice displayed weak rhythms in HR, body temperature, and cage activity, with onsets that were advanced in phase compared with WT mice. Similarly, clock gene expression in cardiac tissue was rhythmic but phase advanced in mutant mice. In constant darkness, the normal circadian rhythms in HR were lost in VIP-deficient mice; however, most mutant mice continued to exhibit circadian rhythms of body temperature with shortened free-running period. The loss of VIP altered, but did not abolish, autonomic regulation of HR. Analysis of the echocardiograms did not find any evidence for a loss of cardiac function in VIP-deficient mice, and the size of the hearts did not differ between genotypes. These results demonstrate that VIP is an important regulator of physiological circadian rhythmicity in the heart.

Indexed as

Analysis of VarianceAnimalsARNTL Transcription FactorsBody TemperatureCircadian RhythmEchocardiographyHeart RateMaleMiceMice, KnockoutMotor ActivityMyocardiumNeuronsPeriod Circadian ProteinsReceptors, Vasoactive Intestinal PeptideReverse Transcriptase Polymerase Chain ReactionARNTL Transcription FactorsPer2 protein, mousePeriod Circadian ProteinsReceptors, Vasoactive Intestinal PeptideVasoactive Intestinal Peptide

Identifiers

PMID20952671
PMCPMC4116412
OpenAlexW2114649817

What OpenQuestion holds

Textmetadata
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.