Evidence map›Paper›PMID 30694175›Full record

ArticleeLife2019

Long-term consequences of the absence of leptin signaling in early life.

Angela M Ramos-Lobo, Pryscila Ds Teixeira, Isadora C Furigo, Helen M Melo, Natalia de M Lyra E Silva, Fernanda G De Felice, Jose Donato

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  6. Neuroendocrinological and Clinical Aspects of Leptin.Mini reviews in medicinal chemistry · 2024
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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

7 authors at 2 institutions in 2 countries.

Angela M Ramos-LoboDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
Pryscila Ds TeixeiraDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
Isadora C FurigoDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
Helen M MeloInstitute of Medical Biochemistry Leopoldo de Meis, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Natalia de M Lyra E SilvaInstitute of Medical Biochemistry Leopoldo de Meis, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Fernanda G De FeliceInstitute of Medical Biochemistry Leopoldo de Meis, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Jose DonatoDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.ORCID 0000-0002-4166-7608
Universidade de São Paulo · BRUniversidade Federal do Rio de Janeiro · BR

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 14/11752-6Fundação de Amparo à Pesquisa do Estado de São Paulo 15/10992-6Fundação de Amparo à Pesquisa do Estado de São Paulo 16/09679-4
6 · The paper itself

Abstract

Leptin regulates energy balance and also exhibits neurotrophic effects during critical developmental periods. However, the actual role of leptin during development is not yet fully understood. To uncover the importance of leptin in early life, the present study restored leptin signaling either at the fourth or tenth week of age in mice formerly null for the leptin receptor (LepR) gene. We found that some defects previously considered irreversible due to neonatal deficiency of leptin signaling, including the poor development of arcuate nucleus neural projections, were recovered by LepR reactivation in adulthood. However, LepR deficiency in early life led to irreversible obesity via suppression of energy expenditure. LepR reactivation in adulthood also led to persistent reduction in hypothalamic

Indexed as

Gene Expression Regulation, DevelopmentalAgingAgouti-Related ProteinAnimalsAnimals, NewbornArcuate Nucleus of HypothalamusCocaine- and Amphetamine-Regulated Transcript ProteinEnergy MetabolismFemaleGonadsHypothalamusLeptinMaleMiceMice, KnockoutNerve Tissue ProteinsAgouti-Related ProteinAgrp protein, mouseCocaine- and Amphetamine-Regulated Transcript ProteinLeptinleptin receptor, mouseNerve Tissue ProteinsPrlh protein, mouseProlactin-Releasing HormonePro-OpiomelanocortinReceptors, Leptincytokinesdevelopmenthypothalamusmelanocortin systemmetabolic programmingmouseneuroscienceobesity

Identifiers

PMID30694175
PMCPMC6384028
OpenAlexW2913870526

What OpenQuestion holds

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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.