Evidence map›Paper›PMID 39779372›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2025

Ghrelin Recruits the Endocannabinoid System to Modulate Food Reward.

Alexander Edwards, Stephanie DeSante, Carl Duncan Spencer, Lindsay Hyland, Andrea Smith, Aditi S Sankhe, Anett Szilvásy-Szabó, Csaba Fekete, Matthew N Hill, Melissa J Chee and 1 more

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Review
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  4. Review
  5. 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

11 authors.

Alexander EdwardsNeuroscience Department, Carleton University, Ottawa, Ontario K1S5B6, Canada.
Stephanie DeSanteNeuroscience Department, Carleton University, Ottawa, Ontario K1S5B6, Canada.
Carl Duncan SpencerNeuroscience Department, Carleton University, Ottawa, Ontario K1S5B6, Canada.
Lindsay HylandNeuroscience Department, Carleton University, Ottawa, Ontario K1S5B6, Canada.
Andrea SmithNeuroscience Department, Carleton University, Ottawa, Ontario K1S5B6, Canada.
Aditi S SankheNeuroscience Department, Carleton University, Ottawa, Ontario K1S5B6, Canada.
Anett Szilvásy-SzabóLaboratory of Integrative Neuroendocrinology, Institute of Experimental Medicine, Budapest H-1083, Hungary.
Csaba FeketeLaboratory of Integrative Neuroendocrinology, Institute of Experimental Medicine, Budapest H-1083, Hungary.
Matthew N HillHotchkiss Brain Institute, University of Calgary, Calgary, Alberta T2N4T1, Canada.
Melissa J CheeNeuroscience Department, Carleton University, Ottawa, Ontario K1S5B6, Canada.
Alfonso AbizaidNeuroscience Department, Carleton University, Ottawa, Ontario K1S5B6, Canada alfonso_abizaid@carleton.ca.ORCID 0000-0001-9303-3511

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ghrelin enhances feeding by activating the growth hormone secretagogue receptor (GHSR). In the brain, GHSRs are expressed in regions responsible for regulating food motivation including the ventral tegmental area (VTA). Endogenous cannabinoids also promote food-seeking behaviors through the cannabinoid receptor-1 (CB-1Rs) in brain regions including the VTA. It is not known, however, if ghrelin and endocannabinoids interact in the VTA to produce these effects. We therefore examined if GHSR and CB-1R interact within the VTA to enhance food motivation. Results show that GHSR and CB-1R mRNA are expressed in the VTA cells in male and female rats and mice, with the GHSR being expressed in dopamine cells and the CB-1R being expressed primarily in nondopaminergic cells with no obvious sex differences. Ghrelin directly activated and increased excitatory tone onto dopamine cells of male and female mice. Male rats lacking fully functional GHSR signaling showed disrupted gene expression of transcripts important for regulating the synthesis, release, and degradation of endocannabinoids and lowered the levels of 2-arachidonoylglycerol (2-AG) within the VTA. Moreover, pharmacological antagonism of VTA CB-1Rs attenuates the orexigenic and appetitive effects of intra-VTA ghrelin in rats and blocks the ability of ghrelin to promote excitatory drive to VTA dopamine neurons. Finally, blocking the breakdown of cannabinoids in the VTA enhances the effects of ghrelin on food motivation. Together, our data show that ghrelin stimulates VTA dopamine cells and ultimately food motivation in part through a mechanism that involves endocannabinoid signaling at the CB-1R.

Indexed as

EndocannabinoidsFeeding BehaviorGhrelinRewardAnimalsDopaminergic NeuronsFemaleGlyceridesMaleMiceMice, Inbred C57BLMice, KnockoutRatsRats, Sprague-DawleyReceptor, Cannabinoid, CB1Receptors, GhrelinEndocannabinoidsGhrelinGlyceridesReceptor, Cannabinoid, CB1Receptors, Ghrelindopamineelectrophysiologyendocannabinoidsfood rewardghrelinoperant responding

Identifiers

PMID39779372
PMCPMC11867019

What OpenQuestion holds

Textmetadata
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.