Evidence map›Paper›PMID 29931690›Full record

ArticleThe Journal of comparative neurology2018

Asymmetric vasopressin signaling spatially organizes the master circadian clock.

Joseph L Bedont, Kayla E Rohr, Abhijith Bathini, Samer Hattar, Seth Blackshaw, Amita Sehgal, Jennifer A Evans

Abstract read
In one paragraph

Article in The Journal of comparative neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  9. 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
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  18. Circuit development in the master clock network of mammals.The European journal of neuroscience · 2020
    Review
  19. Vasopressin in circadian function of SCN.Journal of biosciences · 2020
    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

7 authors at 3 institutions in 1 country.

Joseph L BedontDepartment of Neuroscience, Perelman School of Medicine at the University of Pennsylvania.
Kayla E RohrDepartment of Biomedical Sciences, Marquette University, Milwaukee, WI, 53233.
Abhijith BathiniDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, 21218.
Samer HattarDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, 21218.
Seth BlackshawDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, 21218.
Amita SehgalDepartment of Neuroscience, Perelman School of Medicine at the University of Pennsylvania.
Jennifer A EvansDepartment of Biomedical Sciences, Marquette University, Milwaukee, WI, 53233.ORCID 0000-0002-6220-0273
Johns Hopkins University · USMarquette University · USUniversity of Pennsylvania · US

Funding

Section on Light and Circadian RhythmsZIAMH002964 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI HATTAR, SAMER · 2017 to 2025
$24.1M
Inhibitory feedback mechanisms that couple circadian clock neurons in mammalsR01NS091234 · NINDS · MARQUETTE UNIVERSITY · PI EVANS, JENNIFER ANNE · 2015 to 2019
$1.7M
Howard Hughes Medical InstituteNINDS NIH HHS R01 NS091234
6 · The paper itself

Abstract

The suprachiasmatic nucleus (SCN) is the neural network that drives daily rhythms in behavior and physiology. The SCN encodes environmental changes through the phasing of cellular rhythms across its anteroposterior axis, but it remains unknown what signaling mechanisms regulate clock function along this axis. Here we demonstrate that arginine vasopressin (AVP) signaling organizes the SCN into distinct anteroposterior domains. Spatial mapping of SCN gene expression using in situ hybridization delineated anterior and posterior domains for AVP signaling components, including complementary patterns of V1a and V1b expression that suggest different roles for these two AVP receptors. Similarly, anteroposterior patterning of transcripts involved in Vasoactive Intestinal Polypeptide- and Prokineticin2 signaling was evident across the SCN. Using bioluminescence imaging, we then revealed that inhibiting V1A and V1B signaling alters period and phase differentially along the anteroposterior SCN. V1 antagonism lengthened period the most in the anterior SCN, whereas changes in phase were largest in the posterior SCN. Further, separately antagonizing V1A and V1B signaling modulated SCN function in a manner that mapped onto anteroposterior expression patterns. Lastly, V1 antagonism influenced SCN period and phase along the dorsoventral axis, complementing effects on the anteroposterior axis. Together, these results indicate that AVP signaling modulates SCN period and phase in a spatially specific manner, which is expected to influence how the master clock interacts with downstream tissues and responds to environmental changes. More generally, we reveal anteroposterior asymmetry in neuropeptide signaling as a recurrent organizational motif that likely influences neural computations in the SCN clock network.

Indexed as

AnimalsAntidiuretic Hormone Receptor AntagonistsArginine VasopressinBrain MappingCircadian ClocksDose-Response Relationship, DrugGastrointestinal HormonesImmunohistochemistryMiceMice, Inbred C57BLNeuronsNeuropeptidesReceptors, VasopressinSignal TransductionSuprachiasmatic NucleusAntidiuretic Hormone Receptor AntagonistsArginine VasopressinGastrointestinal HormonesNeuropeptidesProk2 protein, mouseReceptors, VasopressinanteroposteriorcircadianRRID: AB_2313978RRID: AB_2340474RRID: AB_2556546RRID: AB_518682RRID: IMSR_JAX:006852spatiotemporalsuprachiasmaticvasopressin

Identifiers

PMID29931690
PMCPMC6158041
OpenAlexW2808934898

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.