Evidence map›Paper›PMID 26696396›Full record

ArticleJournal of proteome research2016

Antioxidant Drug Tempol Promotes Functional Metabolic Changes in the Gut Microbiota.

Jingwei Cai, Limin Zhang, Richard A Jones, Jared B Correll, Emmanuel Hatzakis, Philip B Smith, Frank J Gonzalez, Andrew D Patterson

Abstract read
In one paragraph

Article in Journal of proteome research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. The Gut Microbiome and Xenobiotics: Identifying Knowledge Gaps.Toxicological sciences : an official journal of the Society of Toxicology · 2020
    Article
  7. Propionate and Alzheimer's Disease.Frontiers in aging neuroscience · 2020
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Orthogonal Comparison of GC-MS andAnalytical chemistry · 2017
    Article
  13. 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

8 authors at 2 institutions in 2 countries.

Jingwei CaiCenter for Molecular Toxicology and Carcinogenesis, Department of Veterinary and Biomedical Sciences, Pennsylvania State University , University Park, State College, Pennsylvania 16802, United States.
Limin ZhangCenter for Molecular Toxicology and Carcinogenesis, Department of Veterinary and Biomedical Sciences, Pennsylvania State University , University Park, State College, Pennsylvania 16802, United States.
Richard A JonesCenter for Molecular Toxicology and Carcinogenesis, Department of Veterinary and Biomedical Sciences, Pennsylvania State University , University Park, State College, Pennsylvania 16802, United States.
Jared B CorrellCenter for Molecular Toxicology and Carcinogenesis, Department of Veterinary and Biomedical Sciences, Pennsylvania State University , University Park, State College, Pennsylvania 16802, United States.
Emmanuel HatzakisDepartment of Chemistry, Pennsylvania State University , University Park, State College, Pennsylvania 16802, United States.
Philip B SmithMetabolomics Facility, Huck Institutes of Life Sciences, Pennsylvania State University , University Park, State College, Pennsylvania 16802, United States.
Frank J GonzalezLaboratory of Metabolism, National Cancer Institute, NIH , Bethesda, Maryland 20892, United States.
Andrew D PattersonCenter for Molecular Toxicology and Carcinogenesis, Department of Veterinary and Biomedical Sciences, Pennsylvania State University , University Park, State College, Pennsylvania 16802, United States.
Pennsylvania State University · USNational Cancer Institute · US

Funding

Xenobiotic receptorsZIABC005562 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GONZALEZ, FRANK J · 2009 to 2025
$26.9M
Optimized Metabolite Extraction, Separation, and Identification for MetabolomicsR01ES022186 · NIEHS · PENNSYLVANIA STATE UNIVERSITY, THE · PI PATTERSON, ANDREW · 2012 to 2016
$2.0M
NIEHS NIH HHS ES022186NIEHS NIH HHS R01 ES022186
6 · The paper itself

Abstract

Recent studies have identified the important role of the gut microbiota in the pathogenesis and progression of obesity and related metabolic disorders. The antioxidant tempol was shown to prevent or reduce weight gain and modulate the gut microbiota community in mice; however, the mechanism by which tempol modulates weight gain/loss with respect to the host and gut microbiota has not been clearly established. Here we show that tempol (0, 1, 10, and 50 mg/kg p.o. for 5 days) decreased cecal bacterial fermentation and increased fecal energy excretion in a dose-dependent manner. Liver (1)H NMR-based metabolomics identified a dose-dependent decrease in glycogen and glucose, enhanced glucogenic and ketogenic activity (tyrosine and phenylalanine), and increased activation of the glycolysis pathway. Serum (1)H NMR-based metabolomics indicated that tempol promotes enhanced glucose catabolism. Hepatic gene expression was significantly altered as demonstrated by an increase in Pepck and G6pase and a decrease in Hnf4a, ChREBP, Fabp1, and Cd36 mRNAs. No significant change in the liver and serum metabolomic profiles was observed in germ-free mice, thus establishing a significant role for the gut microbiota in mediating the beneficial metabolic effects of tempol. These results demonstrate that tempol modulates the gut microbial community and its function, resulting in reduced host energy availability and a significant shift in liver metabolism toward a more catabolic state.

Indexed as

AnimalsAntioxidantsCyclic N-OxidesDose-Response Relationship, DrugEnergy MetabolismGas Chromatography-Mass SpectrometryGastrointestinal MicrobiomeGastrointestinal TractGene ExpressionHost-Pathogen InteractionsLiverMaleMetabolomeMetabolomicsMice, Inbred BALB CReverse Transcriptase Polymerase Chain ReactionAntioxidantsCyclic N-OxidesSpin Labelstempolbomb calorimetryGC−MSmetabolomicsNMRobesitySCFAstempol

Identifiers

PMID26696396
PMCPMC4847541
OpenAlexW2235841811

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.