Evidence map›Paper›PMID 25673501›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2015

Supplementation with vitamin D3 during pregnancy protects against lipopolysaccharide-induced neural tube defects through improving placental folate transportation.

Yuan-Hua Chen, Zhen Yu, Lin Fu, Mi-Zhen Xia, Mei Zhao, Hua Wang, Cheng Zhang, Yong-Fang Hu, Fang-Biao Tao, De-Xiang Xu

Open access · bronzeAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.5field-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

9 citing papers in PubMed, 31 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

10 authors at 1 institution in 1 country.

Yuan-Hua Chen*Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China *Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China *Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China.
Zhen Yu*Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China *Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China.
Lin Fu*Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China.
Mi-Zhen Xia*Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China.
Mei Zhao*Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China.
Hua Wang*Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China *Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China.
Cheng Zhang*Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China.
Yong-Fang Hu*Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China.
Fang-Biao Tao*Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China xudex@126.com.
De-Xiang Xu*Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China *Department of Toxicology, Anhui Provincial Key Laboratory of Population Health & Aristogenics, School of Basic Medical Science and School of Life Science, Anhui Medical University, Hefei 230032, China xudex@126.com.
Anhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several reports demonstrated that maternal lipopolysaccharide (LPS) exposure at middle gestational stage caused neural tube defects (NTDs). This study investigated the effects of supplementation with vitamin D3 (VitD3) during pregnancy on LPS-induced NTDs. Pregnant mice except controls were ip injected with LPS (25 μg/kg) daily from gestational day (GD)8 to GD12. In LPS+VitD3 group, pregnant mice were orally administered with VitD3 (25 μg/kg) before LPS injection. As expected, a 5-day LPS injection resulted in 62.5% (10/16) of dams and 20.3% of fetuses with NTDs. Additional experiment showed that a 5-day LPS injection downregulated placental proton-coupled folate transporter (pcft) and reduced folate carrier 1 (rfc1), 2 major folate transporters in placentas. Consistent with downregulation of placental folate transporters, folate transport from maternal circulation into embryos was disturbed in LPS-treated mice. Interestingly, VitD3 not only inhibited placental inflammation but also attenuated LPS-induced downregulation of placental folate transporters. Correspondingly, VitD3 markedly improved folate transport from maternal circulation into the embryos. Importantly, supplementation with VitD3 during pregnancy protected mice from LPS-induced NTDs. Taken together, these results suggest that supplementation with VitD3 during pregnancy prevents LPS-induced NTDs through inhibiting placental inflammation and improving folate transport from maternal circulation into the embryos.

Indexed as

Dietary SupplementsAnimalsChemokinesCholecalciferolCytokinesFemaleFolic AcidLipopolysaccharidesMaternal-Fetal ExchangeMiceMice, Inbred ICRNeural Tube DefectsPlacentaPregnancyUp-RegulationChemokinesCholecalciferolCytokinesFolic AcidLipopolysaccharidesfolic acidlipopolysaccharideneural tube defectsproton-coupled folate transporterreduced folate carriervitamin D3

Identifiers

PMID25673501
PMCPMC4833037
OpenAlexW2146922899

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.