Evidence map›Paper›PMID 31408482›Full record

ArticlePloS one2019

Physiological changes of growth hormone during lactation in pup rats artificially reared.

Cesar G Toriz, Angel I Melo, Carmen Solano-Agama, Edgar Giovanhi Gómez-Domínguez, Ma de Los Angeles Martínez-Muñoz, Jorge Castañeda-Obeso, Eunice Vera-Aguilar, Elsa Liliana Aguirre-Benítez, Lucero Romero-Aguilar, Margarita González-Del Pliego and 5 more

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

15 authors.

Cesar G TorizDepartamento de Fisiología, Biofísica y Neurociencias, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Mexico City, Mexico.ORCID 0000-0002-9691-8435
Angel I MeloCentro de Investigación en Reproducción Animal, CINVESTAV-IPN -Universidad Autónoma de Tlaxcala, Ixtacuixtla, Tlaxcala, Mexico.
Carmen Solano-AgamaDepartamento de Fisiología, Biofísica y Neurociencias, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Mexico City, Mexico.
Edgar Giovanhi Gómez-DomínguezDepartamento de Fisiología, Biofísica y Neurociencias, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Mexico City, Mexico.
Ma de Los Angeles Martínez-MuñozCentro de Investigación en Reproducción Animal, CINVESTAV-IPN -Universidad Autónoma de Tlaxcala, Ixtacuixtla, Tlaxcala, Mexico.
Jorge Castañeda-ObesoDepartamento de Fisiología, Biofísica y Neurociencias, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Mexico City, Mexico.ORCID 0000-0002-5264-6327
Eunice Vera-AguilarDepartamento de Farmacología, CINVESTAV-IPN, Mexico City, Mexico.
Elsa Liliana Aguirre-BenítezDepartamento de Embriología, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico.
Lucero Romero-AguilarDepartamento de Bioquímica, Facultad de Medicina, UNAM, Mexico City, Mexico.
Margarita González-Del PliegoDepartamento de Embriología, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico.
Ismael Jiménez-EstradaDepartamento de Fisiología, Biofísica y Neurociencias, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Mexico City, Mexico.
Maricela LunaInstituto de Neurobiología, UNAM, Neurobiología Celular y Molecular, Juriquilla, Queretaro, Mexico.
Juan Pablo PardoDepartamento de Bioquímica, Facultad de Medicina, UNAM, Mexico City, Mexico.
Javier CamachoDepartamento de Farmacología, CINVESTAV-IPN, Mexico City, Mexico.
Maria Eugenia Mendoza-GarridoDepartamento de Fisiología, Biofísica y Neurociencias, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Mexico City, Mexico.ORCID 0000-0003-2037-0618

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the lactation period, rat pups are fed by the dam, and the patterns of mother-pup interaction change during this period. Additionally, there are changes in feeding; first, mother´s milk is the only food needed for sustenance, and later, it is combined with solid food and water. GH serum concentrations depend on both maternal-pup interaction and energy metabolism. In the artificial rearing (AR) procedure, pups are deprived of mother-pup interaction, and the feeding pattern is controlled. This rearing paradigm has been used in rats to analyze the effects of maternal deprivation on social behavior. In the present study, we analyzed the variation in GH, acylated ghrelin and IGF-1 serum concentrations throughout the lactation period in AR pups. At pnd7, the maternal rearing (MR) pups responded to a 4 h fast with a drop in GH serum concentration, which is a well-known response to maternal deprivation. GH serum levels in the AR pups did not change, suggesting an adaptation phenomenon. A dopamine inhibitory effect of GH secretion was observed in pnd7 cultured somatotropes, suggesting dopamine regulation of GH secretion at this age. Acylated ghrelin serum levels in the AR pups showed an inverted pattern compared to that in the MR pups, which was related to the artificial feeding pattern. IGF-1 serum levels were lower in the AR pups than in MR pups, which was associated with hepatic GH resistance and with low Igf1 mRNA expression at pnd7. Interestingly, at pnd14, both pup groups showed high hepatic Igf1 mRNA expression but low IGF-1 serum levels, and this was inverted at pnd21. However, serum glucose levels were lower in the AR pups at pnd14 but reached the same levels as the MR pups at pnd21. Moreover, hepatomegaly and higher hepatic GH-receptor levels were observed in the AR pups at pnd21, which was in agreement with an absence of a solid food meal. During AR, the pups lost the maternal interaction-stimulated GH secretion, which correlated with lower IGF-1 serum levels during the first week of postnatal development. Later, the AR pups exhibited hepatic responses, in order to satisfy the metabolic demand for the normal weaning, with low carbohydrates levels in their meal.

Indexed as

AnimalsAnimals, NewbornBlood GlucoseFemaleGhrelinGrowth HormoneInsulin-Like Growth Factor ILactationLiverMaleMaternal DeprivationPituitary GlandRatsRats, WistarReal-Time Polymerase Chain ReactionTibiaBlood GlucoseGhrelinGrowth HormoneInsulin-Like Growth Factor I

Identifiers

PMID31408482
PMCPMC6692037

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LicenceCC BY
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Registered trials

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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.