Evidence map›Paper›PMID 32166324›Full record

ArticleEndocrinology2020

Neurochemical Characterization of Brainstem Pro-Opiomelanocortin Cells.

Teodora Georgescu, David Lyons, Barbora Doslikova, Ana Paula Garcia, Oliver Marston, Luke K Burke, Raffaella Chianese, Brian Y H Lam, Giles S H Yeo, Justin J Rochford and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Endocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

11 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Homeostatic Regulation of Glucose Metabolism by the Central Nervous System.Endocrinology and metabolism (Seoul, Korea) · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. 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

12 authors at 2 institutions in 2 countries.

Teodora GeorgescuRowett Institute, University of Aberdeen, Foresterhill, Aberdeen, UK.
David LyonsRowett Institute, University of Aberdeen, Foresterhill, Aberdeen, UK.
Barbora DoslikovaDepartment of Pharmacology, University of Cambridge, Cambridge, UK.
Ana Paula GarciaDepartment of Pharmacology, University of Cambridge, Cambridge, UK.
Oliver MarstonDepartment of Pharmacology, University of Cambridge, Cambridge, UK.
Luke K BurkeDepartment of Pharmacology, University of Cambridge, Cambridge, UK.
Raffaella ChianeseRowett Institute, University of Aberdeen, Foresterhill, Aberdeen, UK.
Brian Y H LamMRC Metabolic Diseases Unit, University of Cambridge Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, UK.
Giles S H YeoMRC Metabolic Diseases Unit, University of Cambridge Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, UK.
Justin J RochfordDepartment of Pharmacology, University of Cambridge, Cambridge, UK.
Alastair S GarfieldDepartment of Pharmacology, University of Cambridge, Cambridge, UK.
Lora K HeislerRowett Institute, University of Aberdeen, Foresterhill, Aberdeen, UK.
University of Cambridge · GBUniversity of Aberdeen · GB

Funding

Biotechnology and Biological Sciences Research Council BB/K001418/1Biotechnology and Biological Sciences Research Council BB/NO17838/1Medical Research Council MC/PC/15077Medical Research Council MC_UU_00014/5Medical Research Council MC_UU_12012/5Medical Research Council MRC_MC_UU_12012/5Wellcome TrustWellcome Trust 093566/Z/10/AWellcome Trust 100574/Z/12/ZWellcome Trust 204815/Z/16/ZWellcome Trust WT081713Wellcome Trust WT098012
6 · The paper itself

Abstract

Genetic research has revealed pro-opiomelanocortin (POMC) to be a fundamental regulator of energy balance and body weight in mammals. Within the brain, POMC is primarily expressed in the arcuate nucleus of the hypothalamus (ARC), while a smaller population exists in the brainstem nucleus of the solitary tract (POMCNTS). We performed a neurochemical characterization of this understudied population of POMC cells using transgenic mice expressing green fluorescent protein (eGFP) under the control of a POMC promoter/enhancer (PomceGFP). Expression of endogenous Pomc mRNA in the nucleus of the solitary tract (NTS) PomceGFP cells was confirmed using fluorescence-activating cell sorting (FACS) followed by quantitative PCR. In situ hybridization histochemistry of endogenous Pomc mRNA and immunohistochemical analysis of eGFP revealed that POMC is primarily localized within the caudal NTS. Neurochemical analysis indicated that POMCNTS is not co-expressed with tyrosine hydroxylase (TH), glucagon-like peptide 1 (GLP-1), cholecystokinin (CCK), brain-derived neurotrophic factor (BDNF), nesfatin, nitric oxide synthase 1 (nNOS), seipin, or choline acetyltransferase (ChAT) cells, whereas 100% of POMCNTS is co-expressed with transcription factor paired-like homeobox2b (Phox2b). We observed that 20% of POMCNTS cells express receptors for adipocyte hormone leptin (LepRbs) using a PomceGFP:LepRbCre:tdTOM double-reporter line. Elevations in endogenous or exogenous leptin levels increased the in vivo activity (c-FOS) of a small subset of POMCNTS cells. Using ex vivo slice electrophysiology, we observed that this effect of leptin on POMCNTS cell activity is postsynaptic. These findings reveal that a subset of POMCNTS cells are responsive to both changes in energy status and the adipocyte hormone leptin, findings of relevance to the neurobiology of obesity.

Indexed as

AnimalsBrain-Derived Neurotrophic FactorBrain StemCholecystokininCholine O-AcetyltransferaseGlucagon-Like Peptide 1Green Fluorescent ProteinsGTP-Binding Protein gamma SubunitsMiceMice, TransgenicNeuronsNitric Oxide Synthase Type INucleobindinsPromoter Regions, GeneticPro-OpiomelanocortinReceptors, LeptinBrain-Derived Neurotrophic FactorBscl2 protein, mouseCholecystokininCholine O-AcetyltransferaseGlucagon-Like Peptide 1Green Fluorescent ProteinsGTP-Binding Protein gamma SubunitsNitric Oxide Synthase Type INUCB2 protein, humanNucleobindinsPro-OpiomelanocortinReceptors, LeptinTyrosine 3-Monooxygenaseleptin receptorNTSobesityPomc

Identifiers

PMID32166324
PMCPMC7102873
OpenAlexW3012482533

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.