Evidence map›Paper›PMID 32627017›Full record

ArticleMolecular medicine reports2020

The gonadal expression pattern of lipocalin‑2 and 24p3 receptor is modified in the gonads of the offspring of obese rats.

Elsa De La Chesnaye, Leticia Manuel-Apolinar, Leticia Damasio, Edgar Castrejón, Rebeca López-Ballesteros, María Cristina Revilla-Monsalve, Juan Pablo Méndez

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 90% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

7 authors at 3 institutions in 1 country.

Elsa De La ChesnayeCardiovascular and Metabolic Diseases Research Unit, Mexican Social Security Institute, Mexico City 06720, Mexico.
Leticia Manuel-ApolinarEndocrine Research Unit, National Medical Center, Mexican Social Security Institute, Mexico City 06720, Mexico.
Leticia DamasioEndocrine Research Unit, National Medical Center, Mexican Social Security Institute, Mexico City 06720, Mexico.
Edgar CastrejónDepartment of Biochemistry Diagnostics, Faculty of Higher Education, Cuautitlán Izcalli Campus, National Autonomous University of Mexico, State of Mexico 54714, Mexico.
Rebeca López-BallesterosDepartment of Biochemistry Diagnostics, Faculty of Higher Education, Cuautitlán Izcalli Campus, National Autonomous University of Mexico, State of Mexico 54714, Mexico.
María Cristina Revilla-MonsalveCardiovascular and Metabolic Diseases Research Unit, Mexican Social Security Institute, Mexico City 06720, Mexico.
Juan Pablo MéndezPeripheral Obesity Research Unit, Faculty of Medicine, National Autonomous University of Mexico, Mexico City 14000, Mexico.
Mexican Social Security Institute · MXUniversidad Autónoma del Estado de México · MXUniversidad Nacional Autónoma de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity represents a global health and economic burden, affecting millions of individuals worldwide. This pathology is associated with a chronic low‑grade inflammatory state that is partially responsible for the development of other cardiometabolic complications. Clinical studies have reported an association between high circulating levels of lipocalin‑2 (Lcn2) and increased body weight. Additionally, there is scientific evidence demonstrating the impact of maternal obesity on fetal programming. The latter and the fact that the authors previously found that Lcn2 and its receptor (24p3R) are expressed in the gonads of wild‑type rats, led to the analysis of their mRNA profile and cellular localization in gonads collected from the offspring of obese rats at 21 days postconception (dpc), and 0, 2, 4, 6, 12, 20 and 30 days postnatal (dpn) in the present study. Semi‑quantitative PCR revealed a statistically significant downregulation of Lcn2 and 24p3R mRNA at 21 dpc in the ovaries (P<0.01) and testicles (P<0.001) of the offspring of obese mothers. At 30 dpn, the relative expression of Lcn2 mRNA decreased significantly in the ovaries of the experimental group (P<0.05), while Lcn2 mRNA expression was not detectable in testicles. Regarding 24p3R, its mRNA was only significantly decreased at 21 dpc in ovaries of pups of obese mothers. At 30 dpn, the change in females was not significant. Conversely, in testicles, 24p3R mRNA levels increased slightly in the experimental group at 30 dpn. The Lcn2 protein signal was less intense in gonadal tissue sections from 30 dpn offspring of obese rats (P<0.001), whereas the 24p3R signal was downregulated in ovaries (P<0.001) and slightly upregulated in testicles. It was concluded that maternal obesity changes the expression of Lcn2 and 24p3R in the gonads of the offspring of obese rats, possibly through fetal programming. The consequences of this dysregulation for the offspring's gonadal function remains to be determined.

Indexed as

Fetal DevelopmentAnimalsAnimals, NewbornFemaleFetusGonadsLipocalin-2MalePregnancyPregnancy in ObesityPrenatal Exposure Delayed EffectsRatsRats, Sprague-DawleyReceptors, Cell Surface24p3R receptor, ratLcn2 protein, ratLipocalin-2Receptors, Cell Surface24p3 receptoradipokinesfetal programminggonadal expressionlipocalin-2obesity

Identifiers

PMID32627017
PMCPMC7339820
OpenAlexW3034418157

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.