Evidence map›Paper›PMID 23804489›Full record

ArticleObesity (Silver Spring, Md.)2014

CRF type 2 receptors mediate the metabolic effects of ghrelin in C2C12 cells.

Eran Gershon, Wylie W Vale

Open access · bronzeAbstract read
In one paragraph

Article in Obesity (Silver Spring, Md.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Article
  6. Article
  7. Protective Effects of Ghrelin on Fasting-Induced Muscle Atrophy in Aging Mice.The journals of gerontology. Series A, Biological sciences and medical sciences · 2020
    Article
  8. Article
  9. Review
  10. Article
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  13. 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

2 authors at 1 institution in 1 country.

Eran GershonClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, North Torrey Pines Road, La Jolla, California, 10010, USA.
Wylie W Vale
Salk Institute for Biological Studies · US

Funding

TARGETED DISRUPTION OF NEUROENDOCRINE GENESP01DK026741 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI ZORRILLA, ERIC P, ZORRILLA, ERIC P · 1986 to 2014
$31.6M
NIDDK NIH HHS DK026741NIDDK NIH HHS DK 026741-33NIDDK NIH HHS P01 DK026741
6 · The paper itself

Abstract

objectiveGhrelin is known to regulate appetite control and cellular metabolism. The corticotropin-releasing factor (CRF) family is also known to regulate energy balance. In this study, the links between ghrelin and the CRF family in C2C12 cells, a mouse myoblast cell line was investigated. DESIGN AND

methodsC2C12 cells were treated with ghrelin in the presence or absence of CRF receptor antagonists and then subjected to different metabolic analyses.

resultsGhrelin enhanced glucose uptake by C2C12 cells, induced GLUT4 translocation to the cell surface and decreased RBP4 expression. A CRF-R2 selective antagonist, anti-sauvagine-30, blocked ghrelin-induced glucose uptake, Ghrelin upregulated CRF-R2 but not CRF-R1 levels. Moreover, ghrelin-treated C2C12 cells displayed a cAMP and pERK activation in response to Ucn3, a CRF-R2 specific ligand, but not in response to CRF or stressin, CRF-R1 specific ligands. Ghrelin also induced UCP2 and UCP3 expression, which were blocked by anti- sauvagine-30. Ghrelin did not induce fatty acids uptake by C2C12 cells or ACC expression. Even though C2C12 cells clearly exhibited responses to ghrelin, the known ghrelin receptor, GHSR1a, was not detectable in C2C12 cells.

conclusionThe results suggest that, ghrelin plays a role in regulating muscle glucose and, raise the possibility that suppression of the CRF-R2 pathway might provide benefits in high ghrelin states.

Indexed as

Gene Expression RegulationSignal TransductionAnimalsAntibodies, BlockingBiological TransportCell LineCell MembraneCRF Receptor, Type 1GhrelinGlucoseGlucose Transporter Type 4Ion ChannelsMiceMitochondrial ProteinsMyoblastsProtein TransportantalarminAntibodies, BlockingCRF Receptor, Type 1CRF receptor type 2GhrelinGhsr protein, MouseGlucoseGlucose Transporter Type 4Ion ChannelsMitochondrial ProteinsPyrimidinesPyrrolesRbp4 protein, mouseReceptors, Corticotropin-Releasing HormoneReceptors, GhrelinRetinol-Binding Proteins, PlasmaSlc2a4 protein, mouseUcp2 protein, mouseUcp3 protein, mouseUncoupling Protein 2Uncoupling Protein 3urocortin 3 protein, mouseUrocortins

Identifiers

PMID23804489
PMCPMC4170921
OpenAlexW1906600793

What OpenQuestion holds

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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.