Evidence map›Paper›PMID 30352741›Full record

ArticleMolecular metabolism2018

Overexpression of melanocortin 2 receptor accessory protein 2 (MRAP2) in adult paraventricular MC4R neurons regulates energy intake and expenditure.

Giuseppe Bruschetta, Jung Dae Kim, Sabrina Diano, Li F Chan

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
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  11. Neuronal cilia in energy homeostasis.Frontiers in cell and developmental biology · 2022
    Review
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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

4 authors at 2 institutions in 3 countries.

Giuseppe BruschettaProgram in Integrative Cell Signaling and Neurobiology of Metabolism, Yale University School of Medicine, New Haven, CT, 06520, USA; Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale University School of Medicine, New Haven, CT, 06520, USA.
Jung Dae KimProgram in Integrative Cell Signaling and Neurobiology of Metabolism, Yale University School of Medicine, New Haven, CT, 06520, USA; Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale University School of Medicine, New Haven, CT, 06520, USA.
Sabrina DianoProgram in Integrative Cell Signaling and Neurobiology of Metabolism, Yale University School of Medicine, New Haven, CT, 06520, USA; Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale University School of Medicine, New Haven, CT, 06520, USA; Department of Neuroscience, Yale University School of Medicine, New Haven, CT, 06520, USA; Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT, 06520, USA; Department of Clinical Medicine and Surgery, University of Naples "Federico II", Naples, Italy. Electronic address: sabrina.diano@yale.edu.
Li F ChanCentre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK. Electronic address: l.chan@qmul.ac.uk.
Yale University · USWilliam Harvey Research Institute · GB

Funding

Mitochondrial Dynamics in VMH Neurons Control Glucose MetabolismR01DK107293 · NIDDK · YALE UNIVERSITY · PI DIANO, SABRINA · 2015 to 2022
$3.6M
Role of Peroxisome Proliferation in Leptin ResistanceR01DK097566 · NIDDK · YALE UNIVERSITY · PI DIANO, SABRINA · 2013 to 2020
$3.3M
Intracellular mechanisms of microglia activation in diet-induced obesityR01DK120321 · NIDDK · YALE UNIVERSITY · PI DIANO, SABRINA · 2018 to 2021
$3.2M
Central Prolyl Carboxypeptidase (PRCP) in the Regulation of MetabolismR01DK105571 · NIDDK · YALE UNIVERSITY · PI DIANO, SABRINA · 2016 to 2019
$1.5M
Medical Research Council G0802796NIDDK NIH HHS R01 DK097566NIDDK NIH HHS R01 DK105571NIDDK NIH HHS R01 DK107293NIDDK NIH HHS R01 DK120321
6 · The paper itself

Abstract

objectiveMelanocortin 2 receptor accessory protein 2 (MRAP2) has a critical role in energy homeostasis. Although MRAP2 has been shown to regulates a number of GPCRs involved in metabolism, the key neurons responsible for the phenotype of gross obesity in MRAP2 deficient animals are unclear. Furthermore, to date, all the murine MRAP2 models involve the prenatal deletion of MRAP2.

methodsTo target Melanocortin 4 receptor (MC4R)-expressing neurons in the hypothalamic paraventricular nucleus (PVN), we performed stereotaxic surgery using AAV to selectively overexpress MRAP2 postnatally in adult Mc4r-cre mice. We assessed energy homeostasis, glucose metabolism, core body temperature, and response to MC3R/MC4R agonist MTII.

resultsMc4r-cre

conclusionsOur data indicate a site-specific role for MRAP2 in PVN MC4R-expressing neurons in potentiating MC4R neuronal activation at baseline conditions in the regulation of food intake and energy expenditure.

Indexed as

Energy MetabolismAdaptor Proteins, Signal TransducingAnimalsBody TemperatureDiet, High-FatEatingFemaleMaleMiceMice, Inbred C57BLNeuronsObesityParaventricular Hypothalamic NucleusReceptor Activity-Modifying ProteinsReceptor, Melanocortin, Type 4Adaptor Proteins, Signal TransducingMC4R protein, mouseMRAP2 protein, mouseReceptor Activity-Modifying ProteinsReceptor, Melanocortin, Type 4Energy homeostasisFood intakeMC4RMRAP2Obesity

Identifiers

PMID30352741
PMCPMC6308034
OpenAlexW2895333507

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.