Evidence map›Paper›PMID 26260700›Full record

ArticleReproductive biology and endocrinology : RB&E2015

The rat placental renin-angiotensin system - a gestational gene expression study.

Kanchan Vaswani, Hsiu-Wen Chan, Pali Verma, Marloes Dekker Nitert, Hassendrini N Peiris, Ryan J Wood-Bradley, James A Armitage, Gregory E Rice, Murray D Mitchell

Open access · goldAbstract read
In one paragraph

Article in Reproductive biology and endocrinology : RB&E, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 19 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 4 institutions in 1 country.

Kanchan VaswaniCentre for Clinical Diagnostics, University of Queensland Centre for Clinical Research Royal Brisbane and Women's Hospital Campus, Building 71/918, Royal Brisbane Hospital, Herston, QLD, 4029, Australia. k.vaswani@uq.edu.au.
Hsiu-Wen ChanCentre for Clinical Diagnostics, University of Queensland Centre for Clinical Research Royal Brisbane and Women's Hospital Campus, Building 71/918, Royal Brisbane Hospital, Herston, QLD, 4029, Australia. h.chan4@uq.edu.au.
Pali VermaCentre for Clinical Diagnostics, University of Queensland Centre for Clinical Research Royal Brisbane and Women's Hospital Campus, Building 71/918, Royal Brisbane Hospital, Herston, QLD, 4029, Australia. paliverma@gmail.com.
Marloes Dekker NitertCentre for Clinical Diagnostics, University of Queensland Centre for Clinical Research Royal Brisbane and Women's Hospital Campus, Building 71/918, Royal Brisbane Hospital, Herston, QLD, 4029, Australia. m.dekker@uq.edu.au.
Hassendrini N PeirisCentre for Clinical Diagnostics, University of Queensland Centre for Clinical Research Royal Brisbane and Women's Hospital Campus, Building 71/918, Royal Brisbane Hospital, Herston, QLD, 4029, Australia. h.peiris@uq.edu.au.
Ryan J Wood-BradleyDepartment of Anatomy & Developmental Biology Monash University, Clayton, VIC, 3800, Australia. r.woodbradley@deakin.edu.au.
James A ArmitageDepartment of Anatomy & Developmental Biology Monash University, Clayton, VIC, 3800, Australia. James.Armitage@bakeridi.edu.au.
Gregory E RiceCentre for Clinical Diagnostics, University of Queensland Centre for Clinical Research Royal Brisbane and Women's Hospital Campus, Building 71/918, Royal Brisbane Hospital, Herston, QLD, 4029, Australia. g.rice@uq.edu.au.
Murray D MitchellCentre for Clinical Diagnostics, University of Queensland Centre for Clinical Research Royal Brisbane and Women's Hospital Campus, Building 71/918, Royal Brisbane Hospital, Herston, QLD, 4029, Australia. murray.mitchell@uq.edu.au.
Royal Brisbane and Women's Hospital · AUUniversity of Queensland · AUDeakin University · AUMonash University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe placenta is an essential organ that provides nutrients and oxygen to the developing fetus and removes toxic waste products from the fetal circulation. Maintaining placental blood osmotic pressure and blood flow is crucial for viable offspring. The renin-angiotensin system (RAS) in the placenta is a key player in the regulation of maternal-fetal blood flow during pregnancy. Therefore, the aim of this study was to determine if RAS genes are differentially expressed in mid to late gestation in rat placenta.

methodsWhole placental tissue samples from pregnant Sprague Dawley rats at embryonic (E) days 14.25, 15.25, 17.25 and 20 (n = 6 for each gestational age) were used for genome-wide gene expression by microarray. RAS genes with expression differences of >2 fold were further analyzed. Quantitative Real-Time PCR (qPCR) was performed on independent samples to confirm and validate microarray data. Immunohistochemisty and Western blotting were performed on a differentially expressed novel RAS pathway gene (ANPEP).

resultsSix out of 17 genes of the RAS pathway were differentially expressed at different gestational ages. Gene expression of four genes (Angiotensin converting enzyme (Ace), angiotensin converting enzyme 2 (Ace2), membrane metalloendopeptidase (Mme) and angiotensin II receptor 1A (Agtr1a)) were significantly upregulated at E20 whereas two others (Thimet oligopeptidase 1 (Thop1) and Alanyl aminopeptidase (Anpep)) were downregulated at E20 prior to the onset of labour. These changes were confirmed by qPCR. Western blots revealed no overall differences in ANPEP protein expression in the placentae. Immunohistochemical studies, however, indicated that the localization of ANPEP differed at E17.25 and E20 as ANPEP localization in the giant trophoblast cell of the junctional zone was no longer detectable at E20.

conclusionsThe current study investigated the expression of members of the RAS pathway in rat placentae and observed significantly altered expression of 6 RAS genes at 4 gestational ages. These findings present the need for further comprehensive investigation of RAS genes in normal and complicated pregnancies.

Indexed as

Gene Expression Regulation, DevelopmentalGestational AgeAnimalsFemalePlacentaPregnancyRatsRats, Sprague-DawleyRenin-Angiotensin System

Identifiers

PMID26260700
PMCPMC4532142
OpenAlexW2134722585

What OpenQuestion holds

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LicenceCC BY
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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.