Evidence map›Paper›PMID 28076448›Full record

ArticlePloS one2017

IGF-1 Induces GHRH Neuronal Axon Elongation during Early Postnatal Life in Mice.

Lyvianne Decourtye, Erik Mire, Maud Clemessy, Victor Heurtier, Tatiana Ledent, Iain C Robinson, Patrice Mollard, Jacques Epelbaum, Michael J Meaney, Sonia Garel and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 13% 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, 26 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 2 countries.

Lyvianne DecourtyeSorbonne Universités, UPMC Univ Paris 06, INSERM, UMRS 938, Centre de Recherche St-Antoine (CRSA), Paris, France.
Erik MireSorbonne Universités, UPMC Univ Paris 06, INSERM, UMRS 938, Centre de Recherche St-Antoine (CRSA), Paris, France.
Maud ClemessySorbonne Universités, UPMC Univ Paris 06, INSERM, UMRS 938, Centre de Recherche St-Antoine (CRSA), Paris, France.
Victor HeurtierSorbonne Universités, UPMC Univ Paris 06, INSERM, UMRS 938, Centre de Recherche St-Antoine (CRSA), Paris, France.
Tatiana LedentSorbonne Universités, UPMC Univ Paris 06, INSERM, UMRS 938, Centre de Recherche St-Antoine (CRSA), Paris, France.
Iain C RobinsonMRC, National Institute for Medical Research, Division of Molecular Neuroendocrinology, London, United Kingdom.
Patrice MollardUniversités Montpellier 1 and 2, CNRS, UMR 5203, Institut de Génomique Fonctionnelle, Montpellier, France.
Jacques EpelbaumSorbonne Paris Cité, Université Paris Descartes, INSERM, UMR 894, Centre de Psychiatrie et Neurosciences, Paris, France.
Michael J MeaneyMcGill University, Douglas Mental Health University Institute, Montreal, Canada.
Sonia GarelEcole Normale Supérieure, Institut de Biologie de l'ENS, IBENS, Paris, France.
Yves Le BoucSorbonne Universités, UPMC Univ Paris 06, INSERM, UMRS 938, Centre de Recherche St-Antoine (CRSA), Paris, France.
Laurent KappelerSorbonne Universités, UPMC Univ Paris 06, INSERM, UMRS 938, Centre de Recherche St-Antoine (CRSA), Paris, France.
Centre de Recherche Saint-Antoine · FRInserm · FRSorbonne Université · FRCentre National de la Recherche Scientifique · FRDélégation Paris 5 · FRInstitut de Biologie de l'École Normale Supérieure · FRMcGill University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nutrition during the perinatal period programs body growth. Growth hormone (GH) secretion from the pituitary regulates body growth and is controlled by Growth Hormone Releasing Hormone (GHRH) neurons located in the arcuate nucleus of the hypothalamus. We observed that dietary restriction during the early postnatal period (i.e. lactation) in mice influences postnatal growth by permanently altering the development of the somatotropic axis in the pituitary gland. This alteration may be due to a lack of GHRH signaling during this critical developmental period. Indeed, underfed pups showed decreased insulin-like growth factor I (IGF-I) plasma levels, which are associated with lower innervation of the median eminence by GHRH axons at 10 days of age relative to normally fed pups. IGF-I preferentially stimulated axon elongation of GHRH neurons in in vitro arcuate explant cultures from 7 day-old normally fed pups. This IGF-I stimulating effect was selective since other arcuate neurons visualized concomitantly by neurofilament labeling, or AgRP immunochemistry, did not significantly respond to IGF-I stimulation. Moreover, GHRH neurons in explants from age-matched underfed pups lost the capacity to respond to IGF-I stimulation. Molecular analyses indicated that nutritional restriction was associated with impaired activation of AKT. These results highlight a role for IGF-I in axon elongation that appears to be cell selective and participates in the complex cellular mechanisms that link underfeeding during the early postnatal period with programming of the growth trajectory.

Indexed as

AnimalsAnimals, NewbornAxonsFemaleGrowth and DevelopmentGrowth Hormone-Releasing HormoneInsulin-Like Growth Factor IMaleMiceMice, Inbred C57BLMice, TransgenicNeuronal OutgrowthNeuronsGrowth Hormone-Releasing HormoneInsulin-Like Growth Factor I

Identifiers

PMID28076448
PMCPMC5226784
OpenAlexW2572335422

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.