Evidence map›Paper›PMID 29520716›Full record

ArticleMolecular neurobiology2018

Rhythmic Diurnal Synthesis and Signaling of Retinoic Acid in the Rat Pineal Gland and Its Action to Rapidly Downregulate ERK Phosphorylation.

Anna Ashton, Patrick N Stoney, Jemma Ransom, Peter McCaffery

Open access · bronzeAbstract read
In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.5field-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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Empowering Melatonin Therapeutics withDiseases (Basel, Switzerland) · 2021
    Review
  9. 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

4 authors at 2 institutions in 2 countries.

Anna AshtonInstitute of Medical Sciences, School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Foresterhill, Aberdeen, Scotland, AB25 2ZD, UK.
Patrick N StoneyCell Signal Unit, Okinawa Institute of Science and Technology, Okinawa, Japan.
Jemma RansomInstitute of Medical Sciences, School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Foresterhill, Aberdeen, Scotland, AB25 2ZD, UK.
Peter McCafferyInstitute of Medical Sciences, School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Foresterhill, Aberdeen, Scotland, AB25 2ZD, UK. peter.mccaffery@abdn.ac.uk.ORCID http://orcid.org/0000-0002-5956-3997
University of Aberdeen · GBOkinawa Institute of Science and Technology Graduate University · JP

Funding

Biotechnology and Biological Sciences Research Council 1438776
6 · The paper itself

Abstract

Vitamin A is important for the circadian timing system; deficiency disrupts daily rhythms in activity and clock gene expression, and reduces the nocturnal peak in melatonin in the pineal gland. However, it is currently unknown how these effects are mediated. Vitamin A primarily acts via the active metabolite, retinoic acid (RA), a transcriptional regulator with emerging non-genomic activities. We investigated whether RA is subject to diurnal variation in synthesis and signaling in the rat pineal gland. Its involvement in two key molecular rhythms in this gland was also examined: kinase activation and induction of Aanat, which encodes the rhythm-generating melatonin synthetic enzyme. We found diurnal changes in expression of several genes required for RA signaling, including a RA receptor and synthetic enzymes. The RA-responsive gene Cyp26a1 was found to change between day and night, suggesting diurnal changes in RA activity. This corresponded to changes in RA synthesis, suggesting rhythmic production of RA. Long-term RA treatment in vitro upregulated Aanat transcription, while short-term treatment had no effect. RA was also found to rapidly downregulate extracellular signal-regulated kinase (ERK) 1/2 phosphorylation, suggesting a rapid non-genomic action which may be involved in driving the molecular rhythm in ERK1/2 activation in this gland. These results demonstrate that there are diurnal changes in RA synthesis and activity in the rat pineal gland which are partially under circadian control. These may be key to the effects of vitamin A on circadian rhythms, therefore providing insight into the molecular link between this nutrient and the circadian system.

Indexed as

Circadian RhythmDown-RegulationSignal TransductionAldehyde Dehydrogenase 1 FamilyAnimalsArylalkylamine N-AcetyltransferaseDarknessEnzyme InductionExtracellular Signal-Regulated MAP KinasesMaleModels, BiologicalNorepinephrinePhosphorylationPineal GlandRats, Sprague-DawleyRetinal DehydrogenaseAanat protein, ratAldehyde Dehydrogenase 1 FamilyAldh1a1 protein, ratArylalkylamine N-AcetyltransferaseExtracellular Signal-Regulated MAP KinasesNorepinephrineRetinal DehydrogenaseRetinoic Acid 4-HydroxylaseRetinoic Acid Receptor alphaTretinoinCircadianERKPineal glandRARgammardh10rdh12Retinoic acidRetinol

Identifiers

PMID29520716
PMCPMC6153719
OpenAlexW2790550825

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.