Evidence map›Paper›PMID 24852945›Full record

ArticlePloS one2014

Unacylated ghrelin suppresses ghrelin-induced neuronal activity in the hypothalamus and brainstem of male rats [corrected].

Darko M Stevanovic, Aldo Grefhorst, Axel P N Themmen, Vera Popovic, Joan Holstege, Elize Haasdijk, Vladimir Trajkovic, Aart-Jan van der Lely, Patric J D Delhanty

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 37 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Melanocortin neurons: Multiple routes to regulation of metabolism.Biochimica et biophysica acta. Molecular basis of disease · 2017
    Review
  12. Review
  13. Ghrelin and motilin receptors as drug targets for gastrointestinal disorders.Nature reviews. Gastroenterology & hepatology · 2016
    Review
  14. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Darko M StevanovicDepartment of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands; Institute of Medical Physiology, School of Medicine, University of Belgrade, Belgrade, Serbia.
Aldo GrefhorstDepartment of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.
Axel P N ThemmenDepartment of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.
Vera PopovicInstitute of Endocrinology, Diabetes and Diseases of Metabolism, School of Medicine, University of Belgrade, Belgrade, Serbia.
Joan HolstegeDepartment of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
Elize HaasdijkDepartment of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
Vladimir TrajkovicInstitute of Microbiology and Immunology, School of Medicine, University of Belgrade, Belgrade, Serbia.
Aart-Jan van der LelyDepartment of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.
Patric J D DelhantyDepartment of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.
Erasmus MC · NLUniversity of Belgrade · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ghrelin, the endogenous growth hormone secretagogue, has an important role in metabolic homeostasis. It exists in two major molecular forms: acylated (AG) and unacylated (UAG). Many studies suggest different roles for these two forms of ghrelin in energy balance regulation. In the present study, we compared the effects of acute intracerebroventricular administration of AG, UAG and their combination (AG+UAG) to young adult Wistar rats on food intake and central melanocortin system modulation. Although UAG did not affect food intake it significantly increased the number of c-Fos positive neurons in the arcuate (ARC), paraventricular (PVN) and solitary tract (NTS) nuclei. In contrast, UAG suppressed AG-induced neuronal activity in PVN and NTS. Central UAG also modulated hypothalamic expression of Mc4r and Bmp8b, which were increased and Mc3r, Pomc, Agrp and Ucp2, which were decreased. Finally, UAG, AG and combination treatments caused activation of c-Fos in POMC expressing neurons in the arcuate, substantiating a physiologic effect of these peptides on the central melanocortin system. Together, these results demonstrate that UAG can act directly to increase neuronal activity in the hypothalamus and is able to counteract AG-induced neuronal activity in the PVN and NTS. UAG also modulates expression of members of the melanocortin signaling system in the hypothalamus. In the absence of an effect on energy intake, these findings indicate that UAG could affect energy homeostasis by modulation of the central melanocortin system.

Indexed as

AcylationAnimalsBase SequenceBrain StemDNA PrimersFeeding BehaviorGene Expression ProfilingGhrelinHypothalamusMaleMiceNeuronsPolymerase Chain ReactionRats, WistarDNA PrimersGhrelin

Identifiers

PMID24852945
PMCPMC4031147
OpenAlexW2022818667

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.