Evidence map›Paper›PMID 25200869›Full record

ArticleDrug metabolism and disposition: the biological fate of chemicals2014

UDP-glucuronosyltransferase 1a enzymes are present and active in the mouse blastocyst.

Abby C Collier, Yasuhiro Yamauchi, Brittany L M Sato, Luc R A Rougée, Monika A Ward

Open access · bronzeAbstract read
In one paragraph

Article in Drug metabolism and disposition: the biological fate of chemicals, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

5 authors at 3 institutions in 2 countries.

Abby C CollierFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada (A.C.C.); Department of Tropical Medicine, Medical Microbiology, and Pharmacology (A.C.C., B.L.M.S., L.R.A.R.), and Institute for Biogenesis Research (Y.Y., M.A.W.), John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii; and Natural Sciences and Mathematics, Chaminade University of Honolulu, Honolulu, Hawaii (B.L.M.S.) abby.collier@ubc.ca.
Yasuhiro YamauchiFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada (A.C.C.); Department of Tropical Medicine, Medical Microbiology, and Pharmacology (A.C.C., B.L.M.S., L.R.A.R.), and Institute for Biogenesis Research (Y.Y., M.A.W.), John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii; and Natural Sciences and Mathematics, Chaminade University of Honolulu, Honolulu, Hawaii (B.L.M.S.).
Brittany L M SatoFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada (A.C.C.); Department of Tropical Medicine, Medical Microbiology, and Pharmacology (A.C.C., B.L.M.S., L.R.A.R.), and Institute for Biogenesis Research (Y.Y., M.A.W.), John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii; and Natural Sciences and Mathematics, Chaminade University of Honolulu, Honolulu, Hawaii (B.L.M.S.).
Luc R A RougéeFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada (A.C.C.); Department of Tropical Medicine, Medical Microbiology, and Pharmacology (A.C.C., B.L.M.S., L.R.A.R.), and Institute for Biogenesis Research (Y.Y., M.A.W.), John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii; and Natural Sciences and Mathematics, Chaminade University of Honolulu, Honolulu, Hawaii (B.L.M.S.).
Monika A WardFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada (A.C.C.); Department of Tropical Medicine, Medical Microbiology, and Pharmacology (A.C.C., B.L.M.S., L.R.A.R.), and Institute for Biogenesis Research (Y.Y., M.A.W.), John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii; and Natural Sciences and Mathematics, Chaminade University of Honolulu, Honolulu, Hawaii (B.L.M.S.).
University of Hawaiʻi at Mānoa · USUniversity of Hawaii System · USUniversity of British Columbia · CA

Funding

UH Hilo COP A&RP20GM103466 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI Peter R Hoffmann · 2012 to 2026
$60.3M
RESEARCH DESIGN, BIOSTATISTICS AND RESEARCH ETHICS COREG12MD007601 · NIMHD · UNIVERSITY OF HAWAII AT MANOA · PI BERRY, MARLA J · 2012 to 2016
$13.0M
Transgenic Mouse, ICSI and IVF CoreP20GM103457 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI WARD, WILLIAM S · 2012 to 2018
$12.9M
Do we need Y chromosome for successful reproduction?R01HD072380 · NICHD · UNIVERSITY OF HAWAII AT MANOA · PI WARD, MONIKA A · 2012 to 2022
$3.7M
NICHD NIH HHS R01 HD072380NICHD NIH HHS R01-HD072380NIGMS NIH HHS P20 GM103457NIGMS NIH HHS P20-GM103457NIGMS NIH HHS P20 GM103466NIMHD NIH HHS G12 MD007601NIMHD NIH HHS G12-MD007601
6 · The paper itself

Abstract

The UDP-glucuronosyltransferase (UGT) enzymes are critical for regulating nutrients, hormones, and endobiotics, as well as for detoxifying xenobiotics. Human and murine fetuses are known to express glucuronidation enzymes, but there are currently no data prior to implantation. Here we addressed this gap in knowledge and tested whether Ugt enzymes are already present in preimplantation-stage embryos. Blastocysts were obtained after in vitro fertilization with gametes from B6D2F1 hybrid mice and from embryo culture. Protein expression and localization were determined using pan-specific UGT1A and UGT2B, as well as anti-human isoform-specific antibodies. Immunofluorescence analysis showed that blastocysts expressed Ugt1a globally, in the cytoplasm and nuclei of all of the cells. Western blots demonstrated the presence of Ugt1a6 but not Ugt1a1, Ugt1a3, Ugt1a4, or Ugt1a9. The Ugt2b proteins were not detected by either assay. The level of Ugt activity in murine blastocysts was comparable with that of the adult human liver (per milligram of protein), but the activity of β-glucuronidase, an Ugt-partnering enzyme responsible for substrate regeneration, was lower. Altogether, these data confirm that Ugt1a proteins are present and active in preimplantation murine embryos and point to a potential role for these proteins in implantation and early embryonic and fetal development.

Indexed as

AnimalsBlastocystBlotting, WesternFluorescent Antibody TechniqueGlucuronidaseGlucuronosyltransferaseMiceUGT1A1 EnzymeGlucuronidaseGlucuronosyltransferaseUGT1A1 Enzyme

Identifiers

PMID25200869
PMCPMC4201130
OpenAlexW2106219747

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.