Evidence map›Paper›PMID 24303008›Full record

ArticlePloS one2013

The gastric CB1 receptor modulates ghrelin production through the mTOR pathway to regulate food intake.

Lucia L Senin, Omar Al-Massadi, Cintia Folgueira, Cecilia Castelao, Maria Pardo, Silvia Barja-Fernandez, Arturo Roca-Rivada, Maria Amil, Ana B Crujeiras, Tomas Garcia-Caballero and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Ghrelin Recruits the Endocannabinoid System to Modulate Food Reward.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. The Peripheral Cannabinoid Receptor Type 1 (CBMolecules (Basel, Switzerland) · 2021
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Ghrelin and liver disease.Reviews in endocrine & metabolic disorders · 2020
    Review
  18. Article
  19. Targeting Peripheral CBCell metabolism · 2019
    Article
  20. Cannabinoid CBFrontiers in physiology · 2019
    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

16 authors at 5 institutions in 2 countries.

Lucia L SeninGrupo Fisiopatologia Endocrina, Instituto de Investigacion Sanitaria de Santiago de Compostela (IDIS), Complexo Hospitalario Universitario de Santiago (CHUS/SERGAS), Santiago de Compostela, Spain ; CIBER Fisiopatologia Obesidad y Nutricion (CB06/03), Instituto de Salud Carlos III, Santiago de Compostela, Spain.
Omar Al-Massadi
Cintia Folgueira
Cecilia Castelao
Maria Pardo
Silvia Barja-Fernandez
Arturo Roca-Rivada
Maria Amil
Ana B Crujeiras
Tomas Garcia-Caballero
Enrico Gabellieri
Rosaura Leis
Carlos Dieguez
Uberto Pagotto
Felipe F Casanueva
Luisa M Seoane
Instituto de Investigación Sanitaria de Santiago · ESServicio Gallego de Salud · ESInstituto de Salud Carlos III · ESPoliclinico S.Orsola-Malpighi · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the years, the knowledge regarding the relevance of the cannabinoid system to the regulation of metabolism has grown steadily. A central interaction between the cannabinoid system and ghrelin has been suggested to regulate food intake. Although the stomach is the main source of ghrelin and CB1 receptor expression in the stomach has been described, little information is available regarding the possible interaction between the gastric cannabinoid and ghrelin systems in the integrated control of energy homeostasis. The main objective of the present work was to assess the functional interaction between these two systems in terms of food intake using a combination of in vivo and in vitro approaches. The present work demonstrates that the peripheral blockade of the CB1 receptor by rimonabant treatment decreased food intake but only in food-deprived animals. This anorexigenic effect is likely a consequence of decreases in gastric ghrelin secretion induced by the activation of the mTOR/S6K1 intracellular pathway in the stomach following treatment with rimonabant. In support of this supposition, animals in which the mTOR/S6K1 intracellular pathway was blocked by chronic rapamycin treatment, rimonabant had no effect on ghrelin secretion. Vagal communication may also be involved because rimonabant treatment was no longer effective when administered to animals that had undergone surgical vagotomy. In conclusion, to the best of our knowledge, the present work is the first to describe a CB1 receptor-mediated mechanism that influences gastric ghrelin secretion and food intake through the mTOR pathway.

Indexed as

Feeding BehaviorSignal TransductionAnimalsCannabinoidsGastric MucosaGene ExpressionGhrelinImmunohistochemistryMalePiperidinesPyrazolesRatsReceptor, Cannabinoid, CB1RimonabantTOR Serine-Threonine KinasesCannabinoidsGhrelinPiperidinesPyrazolesReceptor, Cannabinoid, CB1RimonabantTOR Serine-Threonine Kinases

Identifiers

PMID24303008
PMCPMC3841176
OpenAlexW1999709879

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.