Evidence map›Paper›PMID 26076986›Full record

ArticleJournal of proteome research2015

NMR Metabolomics Show Evidence for Mitochondrial Oxidative Stress in a Mouse Model of Polycystic Ovary Syndrome.

Ebru Selin Selen, Zeinab Bolandnazar, Marco Tonelli, Daniel E Bütz, Julia A Haviland, Warren P Porter, Fariba M Assadi-Porter

Abstract read
In one paragraph

Article in Journal of proteome research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.0field-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

14 citing papers in PubMed, 29 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

7 authors at 1 institution in 1 country.

Ebru Selin Selen†Department of Zoology, ‡Magnetic Resonance Facility at Madison, and §Department of Animal Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.
Zeinab Bolandnazar†Department of Zoology, ‡Magnetic Resonance Facility at Madison, and §Department of Animal Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.
Marco Tonelli†Department of Zoology, ‡Magnetic Resonance Facility at Madison, and §Department of Animal Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.
Daniel E Bütz†Department of Zoology, ‡Magnetic Resonance Facility at Madison, and §Department of Animal Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.
Julia A Haviland†Department of Zoology, ‡Magnetic Resonance Facility at Madison, and §Department of Animal Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.
Warren P Porter†Department of Zoology, ‡Magnetic Resonance Facility at Madison, and §Department of Animal Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.
Fariba M Assadi-Porter†Department of Zoology, ‡Magnetic Resonance Facility at Madison, and §Department of Animal Sciences, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.
University of Wisconsin–Madison · US

Funding

Integrated Multidisciplinary Strategies for Detection of Diabetic RetinopathiesRC4EY021357 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI ASSADI, AMIR H, ASSADI-PORTER, FARIBA M · 2010 to 2010
$3.2M
The sweet protein brazzein and its interaction with the human taste receptorR01DC009018 · NIDCD · UNIVERSITY OF WISCONSIN-MADISON · PI ASSADI-PORTER, FARIBA M · 2008 to 2012
$1.6M
NEI NIH HHS RC4 EY021357NIDCD NIH HHS R01 DC009018
6 · The paper itself

Abstract

Polycystic ovary syndrome (PCOS) is associated with metabolic and endocrine disorders in women of reproductive age. The etiology of PCOS is still unknown. Mice prenatally treated with glucocorticoids exhibit metabolic disturbances that are similar to those seen in women with PCOS. We used an untargeted nuclear magnetic resonance (NMR)-based metabolomics approach to understand the metabolic changes occurring in the plasma and kidney over time in female glucocorticoid-treated (GC-treated) mice. There are significant changes in plasma amino acid levels (valine, tyrosine, and proline) and their intermediates (2-hydroxybutyrate, 4-aminobutyrate, and taurine), whereas in kidneys, the TCA cycle metabolism (citrate, fumarate, and succinate) and the pentose phosphate (PP) pathway products (inosine and uracil) are significantly altered (p < 0.05) from 8 to 16 weeks of age. Levels of NADH, NAD(+), NAD(+)/NADH, and NADH redox in kidneys indicate increased mitochondrial oxidative stress from 8 to 16 weeks in GC-treated mice. These results indicate that altered metabolic substrates in the plasma and kidneys of treated mice are associated with altered amino acid metabolism, increased cytoplasmic PP, and increased mitochondrial activity, leading to a more oxidized state. This study identifies biomarkers associated with metabolic dysfunction in kidney mitochondria of a prenatal gluococorticoid-treated mouse model of PCOS that may be used as early predictive biomarkers of oxidative stress in the PCOS metabolic disorder in women.

Indexed as

Oxidative StressAmino AcidsAnimalsBiomarkersCitric Acid CycleDisease Models, AnimalFemaleGlucocorticoidsHumansHydroxybutyratesKidneyMagnetic Resonance SpectroscopyMetabolic DiseasesMetabolomeMetabolomicsMice2-hydroxybutyric acidAmino AcidsBiomarkersGlucocorticoidsHydroxybutyratesNADanimal modelmetabolomicsmitochondrianuclear magnetic resonance (NMR)oxidative stresspolycystic ovary syndrome (PCOS)

Identifiers

PMID26076986
PMCPMC6681913
OpenAlexW2401605092

What OpenQuestion holds

Textmetadata
LicenceTDM
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.