Evidence map›Paper›PMID 31052461›Full record

ArticleNutrients2019

A Preterm Rat Model for Immunonutritional Studies.

Blanca Grases-Pintó, Paulina Torres-Castro, Mar Abril-Gil, Margarida Castell, María J Rodríguez-Lagunas, Francisco J Pérez-Cano, Àngels Franch

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Cells · 2020
    Article
  9. Review
  10. Article
  11. Article
  12. 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 1 institution in 1 country.

Blanca Grases-PintóPhysiology Section, Department of Biochemistry and Physiology, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain. blancagrases@ub.edu.ORCID 0000-0003-1071-6195
Paulina Torres-CastroPhysiology Section, Department of Biochemistry and Physiology, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain. mtorreca29@alumnes.ub.edu.
Mar Abril-GilPhysiology Section, Department of Biochemistry and Physiology, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain. mariadelmar.abril@ub.edu.ORCID 0000-0003-0318-6755
Margarida CastellPhysiology Section, Department of Biochemistry and Physiology, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain. margaridacastell@ub.edu.ORCID 0000-0001-5408-0593
María J Rodríguez-LagunasPhysiology Section, Department of Biochemistry and Physiology, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain. mjrodriguez@ub.edu.ORCID 0000-0001-7870-8250
Francisco J Pérez-CanoPhysiology Section, Department of Biochemistry and Physiology, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain. franciscoperez@ub.edu.ORCID 0000-0001-6243-9164
Àngels FranchPhysiology Section, Department of Biochemistry and Physiology, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain. angelsfranch@ub.edu.ORCID 0000-0002-2362-1374
Institute of Agrifood Research and Technology · ES

Funding

Spanish Ministy of Economy, Industry and Competitiveness AGL2013-48459-P
6 · The paper itself

Abstract

Neonates are born with an immature immune system, which develops during the first stages of life. This early immaturity is more acute in preterm newborns. The aim of the present study was to set up a preterm rat model, in which representative biomarkers of innate and adaptive immunity maturation that could be promoted by certain dietary interventions are established. Throughout the study, the body weight was registered. To evaluate the functionality of the intestinal epithelial barrier, in vivo permeability to dextrans was measured and a histomorphometric study was performed. Furthermore, the blood cell count, phagocytic activity of blood leukocytes and plasmatic immunoglobulins (Ig) were determined. Preterm rats showed lower erythrocyte and platelet concentration but a higher count of leukocytes than the term rats. Although there were no changes in the granulocytes' ability to phagocytize, preterm monocytes had lower phagocytic activity. Moreover, lower plasma IgG and IgM concentrations were detected in preterm rats compared to full-term rats, without affecting IgA. Finally, the intestinal study revealed lower permeability in preterm rats and reduced goblet cell size. Here, we characterized a premature rat model, with differential immune system biomarkers, as a useful tool for immunonutritional studies aimed at boosting the development of the immune system.

Indexed as

Models, AnimalAdaptive ImmunityAnimal Nutritional Physiological PhenomenaAnimalsAnimals, NewbornBiomarkersBlood Cell CountCell Membrane PermeabilityFemaleHumansImmune SystemImmunity, InnateInfant, NewbornInfant, PrematureIntestinal MucosaLeukocytesBiomarkersadaptive immunityinnate immunityintestinal permeabilityphagocytosisplasmatic immunoglobulinprematuritysuckling rat

Identifiers

PMID31052461
PMCPMC6566403
OpenAlexW2943466042

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.