Evidence map›Paper›PMID 30670847›Full record

ArticleInternational journal of obesity (2005)2019

Mice exposed to maternal androgen excess and diet-induced obesity have altered phosphorylation of catechol-O-methyltransferase in the placenta and fetal liver.

Romina Fornes, Maria Manti, Xiaojuan Qi, Egor Vorontsov, Carina Sihlbom, Jenny Nyström, Elisabet Jerlhag, Manuel Maliqueo, Angelica Lindén Hirschberg, Mattias Carlström and 2 more

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In one paragraph

Article in International journal of obesity (2005), 2019. 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
5.1field-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, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Maternal Adiponectin Decreases Placenta Nutrient Transport in Mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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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

12 authors at 6 institutions in 3 countries.

Romina FornesDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Maria MantiDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Xiaojuan QiDepartment of Physiology, Qiqihar Medical University, Qiqihar, China.
Egor VorontsovProteomics Core Facility, University of Gothenburg, Gothenburg, Sweden.
Carina SihlbomProteomics Core Facility, University of Gothenburg, Gothenburg, Sweden.
Jenny NyströmDepartment of Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Elisabet JerlhagDepartment of Pharmacology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Manuel MaliqueoEndocrinology and Metabolism, Faculty of Medicine, West division, University of Chile, Santiago, Chile.
Angelica Lindén HirschbergDivision of Obstetrics and Gynecology, Karolinska University Hospital, Solna, Sweden.
Mattias CarlströmDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Anna BenrickDepartment of Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Elisabet Stener-VictorinDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden. elisabet.stener-victorin@ki.se.ORCID http://orcid.org/0000-0002-3424-1502
Karolinska Institutet · SEUniversity of Gothenburg · SEKarolinska University Hospital · SEQiqihar Medical University · CNUniversity of Chile · CLUniversity of Skövde · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesMaternal obesity together with androgen excess in mice negatively affects placental function and maternal and fetal liver function as demonstrated by increased triglyceride content with dysfunctional expression of enzymes and transcription factors involved in de novo lipogenesis and fat storage. To identify changes in molecular pathways that might promote diseases in adulthood, we performed a global proteomic analysis using a liquid-chromatography/mass-spectrometry system to investigate total and phosphorylated proteins in the placenta and fetal liver in a mouse model that combines maternal obesity with maternal androgen excess.

methodsAfter ten weeks on a control diet (CD) or high fat/high sugar-diet, dams were mated with males fed the CD. Between gestational day (GD) 16.5 and GD 18.5, mice were injected with vehicle or dihydrotestosterone (DHT) and sacrificed at GD 18.5 prior to dissection of the placentas and fetal livers. Four pools of female placentas and fetal livers were subjected to a global proteomic analysis. Total and phosphorylated proteins were filtered by ANOVA q < 0.05, and this was followed by two-way ANOVA to determine the effect of maternal obesity and/or androgen exposure.

resultsIn placenta, phosphorylated ATP-citrate synthase was decreased due to maternal obesity, and phosphorylated catechol-O-methyltransferase (COMT) was differentially expressed due to the interaction between maternal diet and DHT exposure. In fetal liver, five total proteins and 48 proteins phosphorylated in one or more sites, were differentially expressed due to maternal obesity or androgen excess. In fetal liver, phosphorylated COMT expression was higher in fetus exposed to maternal obesity.

conclusionThese results suggest a common regulatory mechanism of catecholamine metabolism in the placenta and the fetal liver as demonstrated by higher phosphorylated COMT expression in the placenta and fetal liver from animals exposed to diet-induced maternal obesity and lower expression of phosphorylated COMT in animals exposed to maternal androgen excess.

Indexed as

Catechol O-MethyltransferaseLiverPlacentaAnimalsDietary SugarsDiet, High-FatDihydrotestosteroneFemaleFetusMaleMiceObesityPhosphorylationPregnancyCatechol O-MethyltransferaseDietary SugarsDihydrotestosterone

Identifiers

PMID30670847
OpenAlexW2913432589

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.