Evidence map›Paper›PMID 20158385›Full record

ArticleToxicology mechanisms and methods2010

Effect of benzo(a)pyrene exposure on fluoranthene metabolism by mouse adipose tissue microsomes.

Ashley C Huderson, Deacqunita L Harris, Mohammad S Niaz, Aramandla Ramesh

Abstract read
In one paragraph

Article in Toxicology mechanisms and methods, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Tumor microsomal metabolism of the food toxicant, benzo(a)pyrene, in ApcMin mouse model of colon cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2012
    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

4 authors at 1 institution in 1 country.

Ashley C HudersonDepartment of Biochemistry & Cancer Biology, Meharry Medical College, 1005 D.B. Todd Blvd., Nashville, TN 37208, USA.
Deacqunita L Harris
Mohammad S Niaz
Aramandla Ramesh
Meharry Medical College · US

Funding

Technologies and Resources CoreU54MD007593 · NIMHD · MEHARRY MEDICAL COLLEGE · PI ADUNYAH, SAMUEL EVANS · 2012 to 2018
$24.7M
RESEARCH PROJECT: "Mechanisms of B(a)P Induced Neurotoxicity"S11ES014156 · NIEHS · MEHARRY MEDICAL COLLEGE · PI HOOD, DARRYL BRICE · 2006 to 2010
$3.8M
Minority Institution Research Training ProgramT32HL007735 · NHLBI · MEHARRY MEDICAL COLLEGE · PI ADUNYAH, SAMUEL EVANS · 1992 to 2014
$2.9M
Mechanisms for Benzo(a)pyrene-Induced Colon Cancer Exacerbation by Dietary FatR01CA142845 · NCI · MEHARRY MEDICAL COLLEGE · PI RAMESH, ARAMANDLA · 2010 to 2013
$1.2M
Chemoprevention of colon cancer via neonatal imprintingR03CA130112 · NCI · MEHARRY MEDICAL COLLEGE · PI RAMESH, ARAMANDLA · 2007 to 2008
$147k
The Effect of Dietary Fat on Benzo(a)pyrene Induced Colon Cancer in Apc Min MiceF31ES017391 · NIEHS · MEHARRY MEDICAL COLLEGE · PI DIGGS, DEACQUNITA LAQUADE · 2009 to 2010
$72k
NCI NIH HHS 1R03CA130112-01NCI NIH HHS R01 CA142845NCI NIH HHS R03 CA130112NHLBI NIH HHS 5T32HL007735-12NHLBI NIH HHS T32 HL007735NIEHS NIH HHS 1F31ES017391-01NIEHS NIH HHS 1S11ES014156-01A1NIEHS NIH HHS F31 ES017391NIEHS NIH HHS S11 ES014156NIMHD NIH HHS U54 MD007593
6 · The paper itself

Abstract

The present study has been undertaken to examine whether exposure to benzo(a)pyrene (BaP), a polycyclic aromatic hydrocarbon (PAH) compound, influences the metabolism of fluoranthene (FLA), another PAH compound. Microsomes were isolated from the adipose tissue of mice that received 50 microg/kg BaP and incubated with FLA (3 microM) alone; FLA in combination with BaP at equimolar concentrations, and a control group that received nothing. Post-incubation, samples were extracted with ethyl acetate and analyzed for FLA metabolites by reverse-phase HPLC with fluorescence detection. The rate of FLA metabolism (pmol of metabolite/min/mg protein) was increased when microsomes from BaP-treated mice were exposed to FLA alone and FLA in combination with BaP, compared to controls. On the other hand, the difference in FLA metabolic rate between microsomes that were exposed to FLA + BaP was higher than the ones that received FLA. The microsomes from BaP-pre-treated mice produced a considerably higher proportion of FLA 2, 3-diol, and 2, 3 D FLA when microsomes were incubated with FLA. There were no differences in the FLA metabolite types formed when BaP-pre-treated mice were co-incubated with BaP and FLA than with FLA alone. The enhanced biotransformation of FLA as a result of prior and concomitant exposure to BaP may have implications for assessment of risks arising from human exposure to PAH mixtures.

Indexed as

Adipose TissueAdministration, OralAnimalsBenzo(a)pyreneBiotransformationChromatography, High Pressure LiquidChromatography, Reverse-PhaseEnvironmental PollutantsFluorenesGenes, APCMaleMiceMice, Mutant StrainsMicrosomesRisk AssessmentSpectrometry, FluorescenceBenzo(a)pyreneEnvironmental PollutantsfluorantheneFluorenes

Identifiers

PMID20158385
PMCPMC2826120
OpenAlexW1964994368

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.