Evidence map›Paper›PMID 33711049›Full record

ArticlePloS one2021

Key hepatic metabolic pathways are altered in germ-free mice during pregnancy.

Lyrialle W Han, Yuanyuan Shi, Alison Paquette, Lu Wang, Theo K Bammler, Qingcheng Mao

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. 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
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

11 citing papers in PubMed, 15 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

6 authors at 2 institutions in 1 country.

Lyrialle W HanDepartment of Pharmaceutics, School of Pharmacy, University of Washington, Seattle, Washington, United States of America.
Yuanyuan ShiDepartment of Medicinal Chemistry, School of Pharmacy, University of Washington, Seattle, Washington, United States of America.
Alison PaquetteCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, and Department of Pediatrics, University of Washington, Seattle, Washington, United States of America.
Lu WangDepartment of Environmental and Occupational Health Sciences, School of Public Health, University of Washington, Seattle, Washington, United States of America.
Theo K BammlerDepartment of Environmental and Occupational Health Sciences, School of Public Health, University of Washington, Seattle, Washington, United States of America.
Qingcheng MaoDepartment of Pharmaceutics, School of Pharmacy, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0002-0830-7627
University of Washington · USSeattle Children's Hospital · US

Funding

XENOBIOTIC BIOTRANSFORMATION AND DISPOSITIONP30ES007033 · NIEHS · UNIVERSITY OF WASHINGTON · PI Sheela Sathyanarayana · 1995 to 2026
$42.5M
Understanding Fetal Exposure to Cannabinoids Through In Vitro and In Vivo StudiesP01DA032507 · NIDA · UNIVERSITY OF WASHINGTON · PI UNADKAT, JASHVANT D · 2013 to 2023
$12.4M
Institute of Translational Health SciencesTL1TR000422 · NCATS · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2012 to 2016
$2.1M
The role of Corticotrophin Releasing Hormone on placental transcriptional networks and birth timingK99HD096112 · NICHD · INSTITUTE FOR SYSTEMS BIOLOGY · PI PAQUETTE, ALISON GENEVIEVE · 2018 to 2019
$258k
NCATS NIH HHS TL1 TR000422NICHD NIH HHS K99 HD096112NIDA NIH HHS P01 DA032507NIEHS NIH HHS P30 ES007033
6 · The paper itself

Abstract

Pregnancy is associated with metabolic changes to accommodate the mother and her growing fetus. The microbiome has been shown to modulate host metabolism of endogenous and exogenous substances. However, the combined effects of pregnancy and the microbiome on host metabolism have not been investigated. The objective of this study was to investigate how the microbiome affects overall hepatic metabolic processes during pregnancy. We assessed these changes within 4 groups of C57BL/6 mice: conventional non-pregnant, conventional pregnant, germ-free non-pregnant, and germ-free pregnant mice. We performed RNA-seq analysis on liver tissues and LC-MS/MS analysis of the plasma to assess the effects of pregnancy and the microbiome on hepatic transcriptome and untargeted plasma metabolome to describe metabolic changes as results of both pregnancy and lack of microbiome. By integrating transcriptomics and metabolomics data, we identified eight metabolic pathways that were significantly enriched for differentially expressed genes associated with pregnancy in both conventional and germ-free mice. Notably, of the eight pathways, 4 pathways (retinol metabolism, arachidonic acid metabolism, linoleic acid metabolism, and steroid hormone biosynthesis) which are all critical for normal pregnancy and fetal development were affected by the germ-free status in pregnant mice, but not at all in non-pregnant mice, indicating that the alterations in these four pathways caused by the lack of microbiome are unique for pregnancy. These results provide novel insight into the role of the microbiome in modulating host metabolic processes critical for maternal health and fetal development during pregnancy.

Indexed as

Fetal DevelopmentGerm-Free LifeMetabolic Networks and PathwaysRNA-SeqAnimalsFemaleLiverMicePregnancy

Identifiers

PMID33711049
PMCPMC7954286
OpenAlexW3134602116

What OpenQuestion holds

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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.