Evidence map›Paper›PMID 34544755›Full record

ArticleeNeuro

Intrauterine Growth Restriction Causes Abnormal Embryonic Dentate Gyrus Neurogenesis in Mouse Offspring That Leads to Adult Learning and Memory Deficits.

Ashley S Brown, Matthew Wieben, Shelby Murdock, Jill Chang, Maria L V Dizon, Mark St Pierre, Raul Chavez-Valdez, Richard I Dorsky, Camille M Fung

Open access · goldAbstract read
In one paragraph

Article in eNeuro. 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
5.0field-weighted citation impact, top 5% 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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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

9 authors at 3 institutions in 1 country.

Ashley S BrownDivision of Neonatology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah 84158.
Matthew WiebenUniversity of Utah, Salt Lake City, Utah 84108.
Shelby MurdockUniversity of Utah, Salt Lake City, Utah 84108.
Jill ChangDivision of Neonatology, Department of Pediatrics, Northwestern University, Chicago, Illinois 60611.ORCID 0000-0003-4702-8302
Maria L V DizonDivision of Neonatology, Department of Pediatrics, Northwestern University, Chicago, Illinois 60611.
Mark St PierreDivision of Neonatology, Department of Pediatrics, Johns Hopkins University, Baltimore, Maryland 21287.
Raul Chavez-ValdezDivision of Neonatology, Department of Pediatrics, Johns Hopkins University, Baltimore, Maryland 21287.
Richard I DorskyDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, Utah 84108.
Camille M FungDivision of Neonatology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah 84158 camille.fung@hsc.utah.edu.ORCID 0000-0001-7564-8395
University of Utah · USJohns Hopkins University · USNorthwestern University · US

Funding

MicroRNAs and Perinatal Hypoxia-IschemiaR01NS086945 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DIZON, MARIA LUZ VALDECANAS · 2015 to 2019
$1.7M
Injury of Hippocampal Interneurons following Neonatal Hypoxia-Ischemia and Therapeutic HypothermiaK08NS096115 · NINDS · JOHNS HOPKINS UNIVERSITY · PI CHAVEZ-VALDEZ, RAUL · 2017 to 2021
$1.2M
NINDS NIH HHS K08 NS096115NINDS NIH HHS R01 NS086945
6 · The paper itself

Abstract

Human infants who suffer from intrauterine growth restriction (IUGR), which is a failure to attain their genetically predetermined weight, are at increased risk for postnatal learning and memory deficits. Hippocampal dentate gyrus (DG) granule neurons play an important role in memory formation; however, it is unknown whether IUGR affects embryonic DG neurogenesis, which could provide a potential mechanism underlying abnormal postnatal learning and memory function. Using a mouse model of the most common cause of IUGR, induced by hypertensive disease of pregnancy, we first assessed adult learning and memory function. We quantified the percentages of embryonic hippocampal DG neural stem cells (NSCs) and progenitor cells and developing glutamatergic granule neurons, as well as hippocampal volumes and neuron cell count and morphology 18 and 40 d after delivery. We characterized the differential embryonic hippocampal transcriptomic pathways between appropriately grown and IUGR mouse offspring. We found that IUGR offspring of both sexes had short-term adult learning and memory deficits. Prenatally, we found that IUGR caused accelerated embryonic DG neurogenesis and Sox2

Indexed as

Dentate GyrusNeural Stem CellsFemaleFetal Growth RetardationHippocampusHumansMaleMemory DisordersNeurogenesisPregnancyembryonic dentate gyrus neurogenesisfetal growth restrictionhypertensive disease of pregnancyintrauterine growth restrictionlearning and memoryneural stem cell

Identifiers

PMID34544755
PMCPMC8503959
OpenAlexW3198925684

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.