Evidence map›Paper›PMID 21730012›Full record

ArticleThe Journal of pharmacology and experimental therapeutics2011

Generation and characterization of a Cyp2f2-null mouse and studies on the role of CYP2F2 in naphthalene-induced toxicity in the lung and nasal olfactory mucosa.

Lei Li, Yuan Wei, Laura Van Winkle, Qing-Yu Zhang, Xin Zhou, Jinping Hu, Fang Xie, Kerri Kluetzman, Xinxin Ding

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of pharmacology and experimental therapeutics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
10.9field-weighted citation impact, top 2% 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

49 citing papers in PubMed, 85 citations in OpenAlex.

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  16. Assessing cytochrome P450 function using genetically engineered mouse models.Advances in pharmacology (San Diego, Calif.) · 2022
    Review
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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

9 authors at 1 institution in 1 country.

Lei LiWadsworth Center, New York State Department of Health, and School of Public Health, State University of New York at Albany, Albany, New York 12201-0509, USA.
Yuan Wei
Laura Van Winkle
Qing-Yu Zhang
Xin Zhou
Jinping Hu
Fang Xie
Kerri Kluetzman
Xinxin Ding
University at Albany, State University of New York · US

Funding

Human CYP2A and respiratory tract xenobiotic toxicityR01CA092596 · NCI · WADSWORTH CENTER · PI DING, XINXIN · 2003 to 2020
$6.1M
OLFACTORY TOXICITY OF ENVIRONMENTAL AGENTSR01ES007462 · NIEHS · WADSWORTH CENTER · PI DING, XINXIN · 1994 to 2010
$3.3M
Intestinal P450 and Xenobiotic MetabolismR01GM082978 · NIGMS · WADSWORTH CENTER · PI ZHANG, QING-YU · 2008 to 2018
$3.3M
MECHANISMS OF LUNG INJURY BY NAPTHALENESR01ES004311 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI BUCKPITT, ALAN R · 1987 to 2009
$2.9M
Gonadal vs. Genomic Influences on Xenobiotic MetabolismR01ES012720 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI VAN WINKLE, LAURA S · 2005 to 2008
$969k
NCI NIH HHS CA092596NCI NIH HHS R01 CA092596NIEHS NIH HHS ES004311NIEHS NIH HHS ES007462NIEHS NIH HHS ES012720NIEHS NIH HHS R01 ES004311NIEHS NIH HHS R01 ES007462NIEHS NIH HHS R01 ES012720NIGMS NIH HHS GM082978NIGMS NIH HHS R01 GM082978
6 · The paper itself

Abstract

The CYP2F enzymes, abundantly expressed in the respiratory tract, are active toward many xenobiotic compounds, including naphthalene (NA). However, the precise roles of these enzymes in tissue-selective chemical toxicity have been difficult to resolve. A Cyp2f2-null mouse was generated in this study by disrupting the Cyp2f2 fourth exon. Homozygous Cyp2f2-null mice, which had no CYP2F2 expression and showed no changes in the expression of other P450 genes examined, were viable and fertile and had no in utero lethality or developmental deficits. The loss of CYP2F2 expression led to substantial decreases in the in vitro catalytic efficiency of microsomal NA epoxygenases in lung (up to ~160-fold), liver (~3-fold), and nasal olfactory mucosa (OM; up to ~16-fold), and significant decreases in rates of systemic NA (300 mg/kg i.p.) clearance. The Cyp2f2-null mice were largely resistant to NA-induced cytotoxicity, when examined at 24 h after NA dosing (at 300 mg/kg i.p.), and to NA-induced depletion of total nonprotein sulfhydryl (NPSH), examined at 2 h after dosing, in the lungs. In contrast, the loss of CYP2F2 expression did not alleviate NA-induced NPSH depletion or tissue toxicity in the OM. Mouse CYP2F2 clearly plays an essential role in the bioactivation and toxicity of NA in the lung but not in the OM. The Cyp2f2-null mouse should be valuable for studies on the role of CYP2F2 in the metabolism and toxicity of numerous other xenobiotic compounds and for future production of a CYP2F1-humanized mouse.

Indexed as

AnimalsBiotransformationBlotting, WesternCytochrome P-450 Enzyme SystemEmbryonic Stem CellsFemaleGlutathioneImmunohistochemistryLiverLung DiseasesMiceMice, Inbred CBAMice, KnockoutMicrosomesNaphthalenesNose DiseasesCyp2f2 protein, mouseCytochrome P-450 Enzyme SystemGlutathionenaphthaleneNaphthalenesSulfhydryl Compounds

Identifiers

PMID21730012
PMCPMC3186285
OpenAlexW2142971789

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.