Evidence map›Paper›PMID 27190278›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2016

Detection of expressional changes induced by intrauterine growth restriction in the developing rat pancreas.

Lin Zhang, Wei Chen, Yuee Dai, Ziyang Zhu, Qianqi Liu

Open access · greenAbstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Fetal undernutrition, placental insufficiency, and pancreatic β-cell development programming in utero.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    Review
  13. Review
  14. 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

5 authors at 2 institutions in 1 country.

Lin ZhangDepartment of Endocrinology, Nanjing Children's Hospital, Nanjing Medical University, Nanjing 210008, China.
Wei ChenDepartment of Endocrinology, Nanjing Children's Hospital, Nanjing Medical University, Nanjing 210008, China.
Yuee DaiDepartment of Endocrinology, Nanjing Children's Hospital, Nanjing Medical University, Nanjing 210008, China.
Ziyang ZhuDepartment of Endocrinology, Nanjing Children's Hospital, Nanjing Medical University, Nanjing 210008, China ziyangz@126.com.
Qianqi LiuDepartment of Endocrinology, Nanjing Children's Hospital, Nanjing Medical University, Nanjing 210008, China qianqil@163.com.
Nanjing Medical University · CNNanjing Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intrauterine growth retardation (IUGR) is a disorder that can result in permanent changes in the physiology and metabolism of the newborn, which increased the risk of disease in adulthood. Evidence supports IUGR as a risk factor for the development of diabetes mellitus, which could reflect changes in pancreas developmental pathways. We sought to characterize the IUGR-induced alterations of the complex pathways of pancreas development in a rat model of IUGR. We analyzed the pancreases of Sprague Dawley rats after inducing IUGR by feeding a maternal low calorie diet from gestational day 1 until term. IUGR altered the pancreatic structure, islet areas, and islet quantities and resulted in abnormal morphological changes during pancreatic development, as determined by HE staining and light microscopy. We identified multiple differentially expressed genes in the pancreas by RT-PCR. The genes of the insulin/FoxO1/Pdx1/MafA signaling pathway were first expressed at embryonic day 14 (E14). The expressions of insulin and MafA increased as the fetus grew while the expressions of FoxO1 and Pdx1 decreased. Compared with the control rats, the expressions of FoxO1, Pdx1, and MafA were lower in the IUGR rats, whereas insulin levels showed no change. Microarray profiling, in combination with quantitative real-time PCR, uncovered a subset of microRNAs that changed in their degree of expression throughout pancreatic development. In conclusion, our data support the hypothesis that IUGR influences the development of the rat pancreas. We also identified new pathways that appear to be programmed by IUGR.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsBlotting, WesternBody WeightCaloric RestrictionFemaleFetal Growth RetardationForkhead Box Protein O1Homeodomain ProteinsInsulinLectins, C-TypeMaleMembrane GlycoproteinsMicroRNAsNerve Tissue ProteinsOligonucleotide Array Sequence AnalysisForkhead Box Protein O1Foxo1 protein, ratHomeodomain ProteinsInsulinKlrg1 protein, ratLectins, C-TypeMembrane GlycoproteinsMicroRNAsNerve Tissue Proteinspancreatic and duodenal homeobox 1 proteinTrans-Activatorsinsulin/Fox-O1/Pdx1/MafAIntrauterine growth retardationlet-7d*microRNAmiR-21*miR-23a*pancreas development

Identifiers

PMID27190278
PMCPMC4994920
OpenAlexW2401314847

What OpenQuestion holds

Textmetadata
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.