Evidence map›Paper›PMID 28134808›Full record

ReviewInternational journal of molecular sciences2017

From Belly to Brain: Targeting the Ghrelin Receptor in Appetite and Food Intake Regulation.

Ken Howick, Brendan T Griffin, John F Cryan, Harriët Schellekens

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 2 pooled it
8.6field-weighted citation impact, top 1% 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

67 citing papers in PubMed, 2 syntheses or guidelines pooled it, 171 citations in OpenAlex.

  1. Pooled it
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  13. Gut-brain axis in health and brain disease.Chinese medical journal · 2026
    Review
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  20. The Potential of DehydratedPharmaceuticals (Basel, Switzerland) · 2024
    Article

7 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Ken HowickDepartment of Anatomy and Neuroscience, University College Cork, Cork, Ireland. brendan.griffin@ucc.ie.
Brendan T GriffinSchool of Pharmacy, University College Cork, Cork, Ireland. brendan.griffin@ucc.ie.
John F CryanDepartment of Anatomy and Neuroscience, University College Cork, Cork, Ireland. j.cryan@ucc.ie.
Harriët SchellekensDepartment of Anatomy and Neuroscience, University College Cork, Cork, Ireland. h.schellekens@ucc.ie.
University College Cork · IEAPC Microbiome Institute · IEFood for Health Ireland · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ghrelin is the only known peripherally-derived orexigenic hormone, increasing appetite and subsequent food intake. The ghrelinergic system has therefore received considerable attention as a therapeutic target to reduce appetite in obesity as well as to stimulate food intake in conditions of anorexia, malnutrition and cachexia. As the therapeutic potential of targeting this hormone becomes clearer, it is apparent that its pleiotropic actions span both the central nervous system and peripheral organs. Despite a wealth of research, a therapeutic compound specifically targeting the ghrelin system for appetite modulation remains elusive although some promising effects on metabolic function are emerging. This is due to many factors, ranging from the complexity of the ghrelin receptor (Growth Hormone Secretagogue Receptor, GHSR-1a) internalisation and heterodimerization, to biased ligand interactions and compensatory neuroendocrine outputs. Not least is the ubiquitous expression of the GHSR-1a, which makes it impossible to modulate centrallymediated appetite regulation without encroaching on the various peripheral functions attributable to ghrelin. It is becoming clear that ghrelin's central signalling is critical for its effects on appetite, body weight regulation and incentive salience of food. Improving the ability of ghrelin ligands to penetrate the blood brain barrier would enhance central delivery to GHSR-1a expressing brain regions, particularly within the mesolimbic reward circuitry.

Indexed as

Appetite RegulationEatingAnimalsBrainGastric MucosaGhrelinHumansReceptors, GhrelinGhrelinReceptors, Ghrelinappetiteblood brain barriercachexiadesacyl-ghrelinfood rewardghrelinGHSR-1amesolimbic reward circuitryobesity

Identifiers

PMID28134808
PMCPMC5343809
OpenAlexW2582620106

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.