Evidence map›Paper›PMID 22684939›Full record

ArticleThe Journal of comparative neurology2012

Spatiotemporal distribution of vasoactive intestinal polypeptide receptor 2 in mouse suprachiasmatic nucleus.

Sungwon An, Connie Tsai, Julie Ronecker, Alison Bayly, Erik D Herzog

Abstract read
In one paragraph

Article in The Journal of comparative neurology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

44 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
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  6. Identification ofFrontiers in molecular neuroscience · 2023
    Article
  7. Circadian Responses to Light in the BTBR Mouse.Journal of biological rhythms · 2022
    Article
  8. Anatomical Methods to Study the Suprachiasmatic Nucleus.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  9. Article
  10. Article
  11. Probing theFrontiers in neuroscience · 2021
    Review
  12. Article
  13. Article
  14. Time-Restricted G-Protein Signaling Pathways via GPR176, GInternational journal of molecular sciences · 2020
    Review
  15. Article
  16. Article
  17. SCN VIP Neurons Are Essential for Normal Light-Mediated Resetting of the Circadian System.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  18. Article
  19. Article
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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.

Sungwon AnDepartment of Biology, Washington University, Saint Louis, Missouri 63130, USA.
Connie Tsai
Julie Ronecker
Alison Bayly
Erik D Herzog
Washington University in St. Louis · US

Funding

Washington University Center for Translational NeuroscienceP30NS057105 · NINDS · WASHINGTON UNIVERSITY · PI HOLTZMAN, DAVID M. · 2006 to 2011
$8.7M
CELLULAR BASIS OF CIRCADIAN RHYTHMS IN MAMMALSR01MH063104 · NIMH · WASHINGTON UNIVERSITY · PI HERZOG, ERIK · 2000 to 2013
$4.2M
MECHANISMS AND MODELING OF NETWORKED CIRCADIAN PACEMAKER SYNCHRONIZATIONR01GM096873 · NIGMS · WASHINGTON UNIVERSITY · PI DOYLE, FRANCIS J, HENSON, MICHAEL · 2011 to 2014
$1.1M
21st-Century Imaging Sciences: Undergraduate and Graduate Student TrainingT90DA022871 · NIDA · WASHINGTON UNIVERSITY · PI ANDERSON, CAROLYN J. · 2006 to 2009
$723k
NIDA NIH HHS T90 DA022871NIGMS NIH HHS R01 GM096873NIMH NIH HHS R01 MH063104NINDS NIH HHS P30 NS057105
6 · The paper itself

Abstract

Vasoactive intestinal polypeptide (VIP) signaling is critical for circadian rhythms. For example, the expression of VIP and its main receptor, VPAC2R, is necessary for maintaining synchronous daily rhythms among neurons in the suprachiasmatic nucleus (SCN), a master circadian pacemaker in animals. Where and when VPAC2R protein is expressed in the SCN and other brain areas has not been examined. Using immunohistochemistry, we characterized a new antibody and found that VPAC2R was highly enriched in the SCN and detectable at low levels in many brain areas. Within the SCN, VPAC2R was circadian, peaking in the subjective morning, and abundantly expressed from the rostral to caudal margins with more in the dorsomedial than ventrolateral area. VPAC2R was found in nearly all SCN cells including neurons expressing either VIP or vasopressin (AVP). SCN neurons mainly expressed VPAC2R in their somata and dendrites, not axons. Finally, constant light increased VIP and AVP expression, but not VPAC2R. We conclude that the circadian clock, not the ambient light level, regulates VPAC2R protein localization. These results are consistent with VPAC2R playing a role in VIP signaling at all times of day, broadly throughout the brain and in all SCN cells.

Indexed as

AnimalsCells, CulturedCircadian RhythmMaleMiceMice, Inbred C57BLNeuronsOrgan Culture TechniquesReceptors, Vasoactive Intestinal Peptide, Type IISignal TransductionSuprachiasmatic NucleusReceptors, Vasoactive Intestinal Peptide, Type IIVipr2 protein, mouse

Identifiers

PMID22684939
PMCPMC3961765
OpenAlexW2052563879

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.