Evidence map›Paper›PMID 31532247›Full record

ArticleEnvironmental health perspectives2019

Lipid and Cholesterol Homeostasis after Arsenic Exposure and Antibiotic Treatment in Mice: Potential Role of the Microbiota.

Liang Chi, Yunjia Lai, Pengcheng Tu, Chih-Wei Liu, Jingchuan Xue, Hongyu Ru, Kun Lu

Open access · diamondAbstract read
In one paragraph

Article in Environmental health perspectives, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
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  7. Sex-specific effects of gut microbiome on shaping bile acid metabolism.bioRxiv : the preprint server for biology · 2024
    Article
  8. Review
  9. Metabolic Derangement by Arsenic: a Review of the Mechanisms.Biological trace element research · 2024
    Review
  10. Influence of heavy metal exposure on gut microbiota: Recent advances.Journal of biochemical and molecular toxicology · 2023
    Review
  11. Article
  12. Review
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  14. Article
  15. Article
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  17. Review
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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

7 authors at 2 institutions in 1 country.

Liang ChiDepartment of Environmental Sciences and Engineering, University of North Carolina at Chapel Hill, North Carolina, USA.
Yunjia LaiDepartment of Environmental Sciences and Engineering, University of North Carolina at Chapel Hill, North Carolina, USA.
Pengcheng TuDepartment of Environmental Sciences and Engineering, University of North Carolina at Chapel Hill, North Carolina, USA.
Chih-Wei LiuDepartment of Environmental Sciences and Engineering, University of North Carolina at Chapel Hill, North Carolina, USA.
Jingchuan XueDepartment of Environmental Sciences and Engineering, University of North Carolina at Chapel Hill, North Carolina, USA.
Hongyu RuDepartment of Population Health and Pathobiology, North Carolina State University, Raleigh, North Carolina, USA.
Kun LuDepartment of Environmental Sciences and Engineering, University of North Carolina at Chapel Hill, North Carolina, USA.
University of North Carolina at Chapel Hill · USNorth Carolina State University · US

Funding

UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Melissa A. Troester · 2001 to 2026
$36.3M
Functional interaction between the gut microbiome and arsenic exposureR01ES024950 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LU, KUN · 2015 to 2019
$2.5M
NIEHS NIH HHS P30 ES010126NIEHS NIH HHS R01 ES024950
6 · The paper itself

Abstract

backgroundArsenic-induced liver X receptor/retinoid X receptor (LXR/RXR) signaling inhibition is a potential mechanism underlying the cardiovascular effects caused by arsenic. The gut microbiota can influence arsenic toxic effects.

objectiveWe aimed to explore whether gut microbiota play a role in arsenic-induced LXR/RXR signaling inhibition and the subsequent lipid and cholesterol dysbiosis.

methodsConventional and antibiotic-treated mice (AB-treated mice) were exposed to

resultsPathway analysis indicated that arsenic exposure differentially influenced the hepatic signaling pathways in conventional and AB-treated mice. The expression of sterol regulatory element-binding protein 1 (

conclusionsOur results suggest that in mice, the gut microbiota may be a critical factor regulating arsenic-induced LXR/RXR signaling perturbation, suggesting that modulation of the gut microbiota might be an intervention strategy to reduce the toxic effects of arsenic on lipid and cholesterol homeostasis. https://doi.org/10.1289/EHP4415.

Indexed as

AnimalsAnti-Bacterial AgentsArsenicCholesterolGastrointestinal MicrobiomeHomeostasisLipid MetabolismMiceAnti-Bacterial AgentsArsenicCholesterol

Identifiers

PMID31532247
PMCPMC6792374
OpenAlexW2974649071

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.