Evidence map›Paper›PMID 33831110›Full record

ArticlePloS one2021

Maternal nutrient restriction in late pregnancy programs postnatal metabolism and pituitary development in beef heifers.

John M Long, Levi A Trubenbach, Kenneth C Hobbs, Andrew E Poletti, Chelsie B Steinhauser, Jane H Pryor, Charles R Long, Tryon A Wickersham, Jason E Sawyer, Rhonda K Miller and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. 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
4.7field-weighted citation impact, top 6% 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.

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  10. Developmental Programming of Fertility in Cattle-Is It a Cause for Concern?Animals : an open access journal from MDPI · 2022
    Review
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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

12 authors at 2 institutions in 1 country.

John M LongDepartment of Animal Science, Texas A&M University, College Station, Texas, United States of America.
Levi A TrubenbachDepartment of Animal Science, Texas A&M University, College Station, Texas, United States of America.
Kenneth C HobbsDepartment of Animal Science, Texas A&M University, College Station, Texas, United States of America.
Andrew E PolettiDepartment of Animal Science, Texas A&M University, College Station, Texas, United States of America.
Chelsie B SteinhauserDepartment of Animal Science, Texas A&M University, College Station, Texas, United States of America.
Jane H PryorDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, Texas, United States of America.
Charles R LongDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, Texas, United States of America.
Tryon A WickershamDepartment of Animal Science, Texas A&M University, College Station, Texas, United States of America.
Jason E SawyerDepartment of Animal Science, Texas A&M University, College Station, Texas, United States of America.ORCID 0000-0003-2669-0567
Rhonda K MillerDepartment of Animal Science, Texas A&M University, College Station, Texas, United States of America.
Rodolfo C CardosoDepartment of Animal Science, Texas A&M University, College Station, Texas, United States of America.ORCID 0000-0002-2466-5205
Michael Carey SatterfieldDepartment of Animal Science, Texas A&M University, College Station, Texas, United States of America.ORCID 0000-0002-9819-141X
Texas A&M University · USTexas A&M University – Kingsville · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Maternal undernutrition during pregnancy followed by ad libitum access to nutrients during postnatal life induces postnatal metabolic disruptions in multiple species. Therefore, an experiment was conducted to evaluate postnatal growth, metabolism, and development of beef heifers exposed to late gestation maternal nutrient restriction. Pregnancies were generated via transfer of in vitro embryos produced using X-bearing sperm from a single Angus sire. Pregnant dams were randomly assigned to receive either 100% (control; n = 9) or 70% (restricted; n = 9) of their total energy requirements from gestational day 158 to parturition. From post-natal day (PND) 301 until slaughter (PND485), heifers were individually fed ad libitum in a Calan gate facility. Calves from restricted dams were lighter than controls at birth (P<0.05) through PND70 (P<0.05) with no difference in body weight from PND105 through PND485 (P>0.10). To assess pancreatic function, glucose tolerance tests were performed on PND315 and PND482 and a diet effect was seen with glucose area under the curve being greater (P<0.05) in calves born to restricted dams compared to controls. At slaughter, total internal fat was greater (P<0.05) in heifers born to restricted dams, while whole pituitary weight was lighter (P<0.05). Heifers from restricted dams had fewer growth hormone-positive cells (somatotrophs) compared to controls (P<0.05). Results demonstrate an impaired ability to clear peripheral glucose in heifers born to restricted dams leading to increased deposition of internal fat. A reduction in the number of somatotrophs may contribute to the adipogenic phenotype of heifers born to restricted dams due to growth hormone's known anabolic roles in growth, lipolysis, and pancreatic islet function.

Indexed as

Food DeprivationAnimalsAnimals, NewbornBody WeightCattleDietEnergy MetabolismFemaleGlucose Tolerance TestGrowth HormonePituitary GlandPregnancyPrenatal Exposure Delayed EffectsRandom AllocationSomatotrophsGrowth Hormone

Identifiers

PMID33831110
PMCPMC8031383
OpenAlexW3149406535

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.