Evidence map›Paper›PMID 31666353›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2019

Synaptic Inputs to the Mouse Dorsal Vagal Complex and Its Resident Preproglucagon Neurons.

Marie K Holt, Lisa E Pomeranz, Kevin T Beier, Frank Reimann, Fiona M Gribble, Linda Rinaman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.9field-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

38 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Review
  3. The critical role of gut-brain signalling in eating behaviour and obesity.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  4. Review
  5. Article
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  7. Cellular coding of ingestion in the caudal brainstem.bioRxiv : the preprint server for biology · 2026
    Article
  8. Review
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  12. Review
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  15. Article
  16. Molecular Ontology of the Nucleus of Solitary Tract.The Journal of comparative neurology · 2024
    Article
  17. Review
  18. Article
  19. Review
  20. 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 4 institutions in 2 countries.

Marie K HoltFlorida State University, Department of Psychology and Program in Neuroscience, Tallahassee, Florida 32306-4301.ORCID 0000-0002-7104-206X
Lisa E PomeranzLaboratory of Molecular Genetics, Howard Hughes Medical Institute, Rockefeller University, New York, New York 10065.
Kevin T BeierUniversity of California at Irvine, Department of Physiology and Biophysics, Irvine, California 92697, and.ORCID 0000-0002-4934-1338
Frank ReimannInstitute of Metabolic Science, Metabolic Research Laboratories, University of Cambridge, Cambridge, United Kingdom CB2 0QQ.
Fiona M GribbleInstitute of Metabolic Science, Metabolic Research Laboratories, University of Cambridge, Cambridge, United Kingdom CB2 0QQ.
Linda RinamanFlorida State University, Department of Psychology and Program in Neuroscience, Tallahassee, Florida 32306-4301, Rinaman@psy.fsu.edu.ORCID 0000-0001-5999-8811
Florida State University · USUniversity of Cambridge · GBHoward Hughes Medical Institute · USUniversity of California, Irvine · US

Funding

POSTNATAL DEVELOPMENT OF VAGAL-HYPOTHALAMIC CONNECTIONSR01MH059911 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RINAMAN, LINDA M · 1999 to 2024
$7.3M
Brainstem Satiety Circuits and High Fat Diet HyperphagiaR01DK100685 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RINAMAN, LINDA M · 2014 to 2018
$1.6M
Remote Modulation of the Peripheral Nervous SystemOT2OD024912 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI STANLEY, SARAH AMY · 2017 to 2019
$1.1M
INVESTIGATING FUNCTION OF NOVEL DRUG-INDUCED SYNAPTIC CHANGES IN THE VTAR00DA041445 · NIDA · UNIVERSITY OF CALIFORNIA-IRVINE · PI BEIER, KEVIN T · 2018 to 2020
$747k
Investigating function of novel drug-induced synaptic changes in the VTAK99DA041445 · NIDA · STANFORD UNIVERSITY · PI BEIER, KEVIN T · 2016 to 2017
$362k
Medical Research Council MC_UU_00014/3Medical Research Council MC_UU_00014/5Medical Research Council MC_UU_12012/3NIDA NIH HHS K99 DA041445NIDA NIH HHS R00 DA041445NIDDK NIH HHS R01 DK100685NIH HHS OT2 OD024912NIMH NIH HHS R01 MH059911Wellcome TrustWellcome Trust 106262/Z/14/ZWellcome Trust 106263/Z/14/Z
6 · The paper itself

Abstract

Stress responses are coordinated by widespread neural circuits. Homeostatic and psychogenic stressors activate preproglucagon (PPG) neurons in the caudal nucleus of the solitary tract (cNTS) that produce glucagon-like peptide-1; published work in rodents indicates that these neurons play a crucial role in stress responses. While the axonal targets of PPG neurons are well established, their afferent inputs are unknown. Here we use retrograde tracing with cholera toxin subunit b to show that the cNTS in male and female mice receives axonal inputs similar to those reported in rats. Monosynaptic and polysynaptic inputs specific to cNTS PPG neurons were revealed using Cre-conditional pseudorabies and rabies viruses. The most prominent sources of PPG monosynaptic input include the lateral (LH) and paraventricular (PVN) nuclei of the hypothalamus, parasubthalamic nucleus, lateral division of the central amygdala, and Barrington's nucleus (Bar). Additionally, PPG neurons receive monosynaptic vagal sensory input from the nodose ganglia and spinal sensory input from the dorsal horn. Sources of polysynaptic input to cNTS PPG neurons include the hippocampal formation, paraventricular thalamus, and prefrontal cortex. Finally, cNTS-projecting neurons within PVN, LH, and Bar express the activation marker cFOS in mice after restraint stress, identifying them as potential sources of neurogenic stress-induced recruitment of PPG neurons. In summary, cNTS PPG neurons in mice receive widespread monosynaptic and polysynaptic input from brain regions implicated in coordinating behavioral and physiological stress responses, as well as from vagal and spinal sensory neurons. Thus, PPG neurons are optimally positioned to integrate signals of homeostatic and psychogenic stress.

Indexed as

AnimalsAxonsFemaleHypothalamusMaleMiceMice, Inbred C57BLNeural PathwaysNeuronsNeurons, AfferentPosterior Horn CellsProglucagonReflex, MonosynapticRestraint, PhysicalSolitary NucleusStress, PsychologicalProglucagonGLP1nodose ganglionpseudorabiesrabiesstressviral tracing

Identifiers

PMID31666353
PMCPMC6891065
OpenAlexW2982442142

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.