Evidence map›Paper›PMID 39737892›Full record

ArticleNature communications2024

Brainstem BDNF neurons are downstream of GFRAL/GLP1R signalling.

Claire H Feetham, Valeria Collabolletta, Amy A Worth, Rosemary Shoop, Sam Groom, Court Harding, Mehdi Boutagouga Boudjadja, Tamer Coskun, Paul J Emmerson, Giuseppe D'Agostino and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Functional segregation of body-brain signals in the area postrema.bioRxiv : the preprint server for biology · 2026
    Article
  5. Review
  6. Article
  7. GLP-1 agonists and exercise: the future of lifestyle prioritization.Frontiers in clinical diabetes and healthcare · 2025
    Review
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.

Claire H Feetham *Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Valeria Collabolletta *Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Amy A WorthFaculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID 0000-0003-2573-7140
Rosemary ShoopFaculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Sam GroomFaculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Court HardingFaculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Mehdi Boutagouga BoudjadjaFaculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Tamer CoskunLilly Research Laboratories, Eli Lilly & Company, Indianapolis, USA.
Paul J EmmersonLilly Research Laboratories, Eli Lilly & Company, Indianapolis, USA.
Giuseppe D'AgostinoFaculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID 0000-0002-3502-4251
Simon M LuckmanFaculty of Biology, Medicine and Health, University of Manchester, Manchester, UK. simon.luckman@manchester.ac.uk.ORCID 0000-0001-5318-5473

Funding

RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/S008098/1RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/Z516405/1RCUK | Medical Research Council (MRC) MR/T032669/1
6 · The paper itself

Abstract

Growth differentiation factor 15, GDF15, and glucagon-like peptide-1 (GLP-1) analogues act through brainstem neurons that co-localise their receptors, GDNF-family receptor α-like (GFRAL) and GLP1R, to reduce food intake and body weight. However, their use as clinical treatments is partially hampered since both can also induce sickness-like behaviours, including aversion, that are mediated through a well-characterised pathway via the exterolateral parabrachial nucleus. Here, in mice, we describe a separate pathway downstream of GFRAL/GLP1R neurons that involves a distinct population of brain-derived neurotrophic factor (BDNF) cells in the medial nucleus of the tractus solitarius. Thus, BDNF

Indexed as

Brain-Derived Neurotrophic FactorBrain StemGlial Cell Line-Derived Neurotrophic Factor ReceptorsGlucagon-Like Peptide-1 ReceptorGrowth Differentiation Factor 15NeuronsSignal TransductionAnimalsBody WeightEatingExenatideGlucagon-Like Peptide 1MaleMiceMice, Inbred C57BLSolitary NucleusBdnf protein, mouseBrain-Derived Neurotrophic FactorExenatideGlial Cell Line-Derived Neurotrophic Factor ReceptorsGlp1r protein, mouseGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorGrowth Differentiation Factor 15

Identifiers

PMID39737892
PMCPMC11685588

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Registered trials

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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.