Evidence map›Paper›PMID 24872334›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2015

Prenatal exposure to hypoxia induced Beclin 1 signaling-mediated renal autophagy and altered renal development in rat fetuses.

Shuixiu Xia, Juanxiu Lv, Qinqin Gao, Lingjun Li, Ningjing Chen, Xiaoguang Wei, Jianping Xiao, Jie Chen, Jianying Tao, Miao Sun and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.1field-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

22 citing papers in PubMed, 35 citations in OpenAlex.

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  12. Deletion of theThe Journal of biological chemistry · 2018
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  18. Role of hypoxia during nephrogenesis.Pediatric nephrology (Berlin, Germany) · 2016
    Review
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  20. Article
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

13 authors at 3 institutions in 2 countries.

Shuixiu XiaInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Juanxiu LvInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Qinqin GaoInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Lingjun LiInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Ningjing ChenInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Xiaoguang WeiInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Jianping XiaoInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Jie ChenInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Jianying TaoInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Miao SunInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Caiping MaoInstitute for Fetology, First Hospital of Soochow University, Suzhou, China.
Lubo ZhangInstitute for Fetology, First Hospital of Soochow University, Suzhou, China Center for Perinatal Biology, Loma Linda University, Loma Linda, CA, USA.
Zhice XuInstitute for Fetology, First Hospital of Soochow University, Suzhou, China Center for Perinatal Biology, Loma Linda University, Loma Linda, CA, USA xuzhice@suda.edu.cn.
Soochow University · CNFirst Affiliated Hospital of Soochow University · CNLoma Linda University · US

Funding

Developmental Programming of Ischemic-Sensitive Phenotype in the HeartR01HL118861 · NHLBI · LOMA LINDA UNIVERSITY · PI ZHANG, LUBO · 2014 to 2017
$1.8M
NHLBI NIH HHS R01 HL118861
6 · The paper itself

Abstract

aimsHypoxia has adverse effects on renal development. This study was the first to test hypoxia-induced renal autophagy in rat fetuses.

methodsPregnant rats were exposed to hypoxia or normoxia during pregnancy and fetal kidneys were collected at gestation day 21.

resultsFetal kidney weight and ratio of kidney-body weight were reduced. Histological analysis showed enlargement in Bowman space and wider space between interstitia in the kidneys of fetus exposed to hypoxia. Fetal renal B-cell lymphoma 2 (BCL-2) was decreased accompanied with higher 2'-deoxyuridine 5'-triphosphate nick end-labeling staining and unchanged soluble FAS in the hypoxia group. Hypoxia increased autophagic structures, including autophagosomes and autolysosomes, in fetal kidneys and increased renal APG5L. There was an increase in renal LC3-II, Beclin 1, p-S6, hypoxia inducible factor 1α (HIF-1a), and ratio of LC3-II-LC3-I and a decrease in P62, protein kinase B (AKT), and phosphorylated AKT in the hypoxia group. Both renal mammalian target of rapamycin (mTOR) and Beclin 1 signaling were upregulated.

conclusionHypoxia-affected fetal renal development was associated with renal apoptosis and Beclin 1 signaling-mediated autophagy.

Indexed as

AutophagyAnimalsApoptosis Regulatory ProteinsBeclin-1FemaleGestational AgeHypoxiaHypoxia-Inducible Factor 1, alpha SubunitKidneyMaternal ExposureOrgan SizePhosphorylationPregnancyProto-Oncogene Proteins c-aktRats, Sprague-DawleyRibosomal Protein S6Apoptosis Regulatory ProteinsBeclin-1Becn1 protein, ratHif1a protein, ratHypoxia-Inducible Factor 1, alpha SubunitmTOR protein, ratProto-Oncogene Proteins c-aktRibosomal Protein S6TOR Serine-Threonine Kinasesautophagyhypoxiakidneyrat fetus

Identifiers

PMID24872334
PMCPMC4287595
OpenAlexW2054147765

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.