Evidence map›Paper›PMID 25193093›Full record

ArticleToxicology2014

Differential Fmo3 gene expression in various liver injury models involving hepatic oxidative stress in mice.

Swetha Rudraiah, Jamie E Moscovitz, Ajay C Donepudi, Sarah N Campion, Angela L Slitt, Lauren M Aleksunes, José E Manautou

Open access · greenAbstract readComparative Study
In one paragraph

Article in Toxicology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.9field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Protective Effects of Peroxiredoxin 4 (PRDX4) on Cholestatic Liver Injury.International journal of molecular sciences · 2018
    Article
  7. Article
  8. Review
  9. 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

7 authors at 4 institutions in 1 country.

Swetha RudraiahDepartment of Pharmaceutical Sciences, University of Connecticut, Storrs, CT, USA. Electronic address: swetha.rudraiah@uconn.edu.
Jamie E MoscovitzDepartment of Pharmacology and Toxicology, Rutgers University Ernest Mario School of Pharmacy, Piscataway, NJ, USA. Electronic address: jamie.moscovitz@rutgers.edu.
Ajay C DonepudiDepartment of Biomedical and Pharmaceutical Sciences, University of Rhode Island, Kingston, RI, USA. Electronic address: ajaydonepudi@gmail.com.
Sarah N CampionDrug Safety Research and Development, Pfizer Inc., Groton, USA. Electronic address: sarah.campion@pfizer.com.
Angela L SlittDepartment of Biomedical and Pharmaceutical Sciences, University of Rhode Island, Kingston, RI, USA. Electronic address: angela_slitt@ds.uri.edu.
Lauren M AleksunesDepartment of Pharmacology and Toxicology, Rutgers University Ernest Mario School of Pharmacy, Piscataway, NJ, USA. Electronic address: aleksunes@eohsi.rutgers.edu.
José E ManautouDepartment of Pharmaceutical Sciences, University of Connecticut, Storrs, CT, USA. Electronic address: jose.manautou@uconn.edu.
Rutgers, The State University of New Jersey · USUniversity of Connecticut · USUniversity of Rhode Island · USPfizer (United States) · US

Funding

Translational Research Support CoreP30ES005022 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Emily S Barrett · 1988 to 2026
$47.4M
TRAINING IN EVIRONMENTAL TOXICOLOGYT32ES007148 · NIEHS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI Lauren M Aleksunes · 1987 to 2026
$11.4M
Transporter Expression in Response to HepatotoxicantsR01DK069557 · NIDDK · UNIVERSITY OF CONNECTICUT STORRS · PI MANAUTOU, JOSE E · 2005 to 2013
$2.4M
NIDDK NIH HHS DK069557NIDDK NIH HHS R01 DK069557NIEHS NIH HHS P30 ES005022NIEHS NIH HHS T32 ES007148
6 · The paper itself

Abstract

Flavin-containing monooxygenase-3 (FMO3) catalyzes metabolic reactions similar to cytochrome P450 monooxygenase, however, most metabolites of FMO3 are considered non-toxic. Recent findings in our laboratory demonstrated Fmo3 gene induction following toxic acetaminophen (APAP) treatment in mice. The goal of this study was to evaluate Fmo3 gene expression in other diverse mouse models of hepatic oxidative stress and injury. Fmo3 gene regulation by Nrf2 was also investigated using Nrf2 knockout (Nrf2 KO) mice. In our studies, male C57BL/6J mice were treated with toxic doses of hepatotoxicants or underwent bile duct ligation (BDL, 10 days). Hepatotoxicants included APAP (400 mg/kg, 24-72 h), alpha-naphthyl isothiocyanate (ANIT; 50 mg/kg, 2-48 h), carbon tetrachloride (CCl4; 10 or 30 μL/kg, 24 and 48 h) and allyl alcohol (AlOH; 30 or 60 mg/kg, 6 and 24 h). Because oxidative stress activates nuclear factor (erythroid-derived 2)-like 2 (Nrf2), additional studies investigated Fmo3 gene regulation by Nrf2 using Nrf2 knockout (Nrf2 KO) mice. At appropriate time-points, blood and liver samples were collected for assessment of plasma alanine aminotransferase (ALT) activity, plasma and hepatic bile acid levels, as well as liver Fmo3 mRNA and protein expression. Fmo3 mRNA expression increased significantly by 43-fold at 12 h after ANIT treatment, and this increase translates to a 4-fold change in protein levels. BDL also increased Fmo3 mRNA expression by 1899-fold, but with no change in protein levels. Treatment of mice with CCl4 decreased liver Fmo3 gene expression, while no change in expression was detected with AlOH treatment. Nrf2 KO mice are more susceptible to APAP (400mg/kg, 72 h) treatment compared to their wild-type (WT) counterparts, which is evidenced by greater plasma ALT activity. The Fmo3 mRNA and protein expression increased in Nrf2 KO mice after APAP treatment. Collectively, not all hepatotoxicants that produce oxidative stress alter Fmo3 gene expression. Along with APAP, toxic ANIT treatment in mice markedly increased Fmo3 gene expression. While BDL increased the Fmo3 mRNA expression, the protein level did not change. The discrepancy with Fmo3 induction in cholestatic models, ANIT and BDL, is not entirely clear. Results from Nrf2 KO mice with APAP suggest that the transcriptional regulation of Fmo3 during liver injury may not involve Nrf2.

Indexed as

Oxidative StressAlanine TransaminaseAnimalsBile Acids and SaltsBile DuctsBiomarkersChemical and Drug Induced Liver InjuryCholestasisDisease Models, AnimalGene Expression Regulation, EnzymologicLigationLiverMaleMice, Inbred C57BLMice, KnockoutNF-E2-Related Factor 2Alanine TransaminaseBile Acids and SaltsBiomarkersdimethylaniline monooxygenase (N-oxide forming)Nfe2l2 protein, mouseNF-E2-Related Factor 2OxygenasesRNA, MessengerAcetaminophenAllyl alcoholAlpha-naphthyl isothiocyanateBile duct ligationCarbon tetrachlorideFlavin-containing monoxygenase-3HepatotoxicantsNrf2Oxidative stress

Identifiers

PMID25193093
PMCPMC4428328
OpenAlexW2001086970

What OpenQuestion holds

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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.