Evidence map›Paper›PMID 20534729›Full record

ArticleEndocrinology2010

EGR1 Is a target for cooperative interactions between cholecystokinin and leptin, and inhibition by ghrelin, in vagal afferent neurons.

Guillaume de Lartigue, Gyorgy Lur, Rod Dimaline, Andrea Varro, Helen Raybould, Graham J Dockray

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 82 citations in OpenAlex.

  1. The critical role of gut-brain signalling in eating behaviour and obesity.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  2. Review
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  4. Article
  5. Article
  6. Article
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  8. Article
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  11. The metabolic role of vagal afferent innervation.Nature reviews. Gastroenterology & hepatology · 2018
    Review
  12. Review
  13. The vagus neurometabolic interface and clinical disease.International journal of obesity (2005) · 2018
    Review
  14. Article
  15. Anxiety, Depression, and the Microbiome: A Role for Gut Peptides.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2018
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Dorsomedial hypothalamic NPY affects cholecystokinin-induced satiety via modulation of brain stem catecholamine neuronal signaling.American journal of physiology. Regulatory, integrative and comparative physiology · 2016
    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

6 authors at 2 institutions in 2 countries.

Guillaume de LartiguePhysiological Laboratory, School of Biomedical Sciences, University of Liverpool, Liverpool, UK. g.j.dockray@liverpool.ac.uk
Gyorgy Lur
Rod Dimaline
Andrea Varro
Helen Raybould
Graham J Dockray
University of Liverpool · GBUniversity of California, Davis · US

Funding

CHOLECYSTOKININ--ROLE IN POSTPRANDIAL GASTRIC MOTILITYR01DK041004 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RAYBOULD, HELEN E · 1995 to 2019
$5.4M
Biotechnology and Biological Sciences Research CouncilMedical Research Council G8714277NIDDK NIH HHS R01 DK041004
6 · The paper itself

Abstract

Food intake is regulated by signals from peripheral organs, but the way these are integrated remains uncertain. Cholecystokinin (CCK) from the intestine and leptin from adipocytes interact to inhibit food intake. Our aim was to examine the hypothesis that these interactions occur at the level of vagal afferent neurons via control of the immediate early gene EGR1. We now report that CCK stimulates redistribution to the nucleus of early growth response factor-1 (EGR1) in these neurons in vivo and in culture, and these effects are not dependent on EGR1 synthesis. Leptin stimulates EGR1 expression; leptin alone does not stimulate nuclear translocation, but it strongly potentiates the action of CCK. Ghrelin inhibits CCK-stimulated nuclear translocation of EGR1 and leptin-stimulated EGR1 expression. Expression of the gene encoding the satiety peptide cocaine- and amphetamine-regulated transcript (CARTp) is stimulated by CCK via an EGR1-dependent mechanism, and this is strongly potentiated by leptin. Leptin potentiated inhibition of food intake by endogenous CCK in the rat in conditions reflecting changes in EGR1 activation. The data indicate that by separately regulating EGR1 activation and synthesis, CCK and leptin interact cooperatively to define the capacity for satiety signaling by vagal afferent neurons; manipulation of these interactions may be therapeutically beneficial.

Indexed as

AnimalsAppetite RegulationCell NucleusCells, CulturedCholecystokininDown-RegulationDrug AntagonismDrug SynergismEarly Growth Response Protein 1GhrelinLeptinMaleNeurons, AfferentProtein TransportRatsRats, WistarCholecystokininEarly Growth Response Protein 1Egr1 protein, mouseGhrelinLeptin

Identifiers

PMID20534729
PMCPMC2940532
OpenAlexW2041541035

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.