Literature DB >> 6778610

Dose-dependent size increases of aortic lesions following chronic exposure to 7,12-dimethylbenz(a)anthracene.

A Penn, G Batastini, J Soloman, F Burns, R Albert.   

Abstract

The prevalence, size, and patterns of distribution of arterial lesions (plaques) were investigated in cockerels exposed chronically to 7,12-dimethylbenz(a)anthracene (DMBA). Animals, from 5 to 20 weeks of age, received weekly i.m. injections of 5, 10, or 20 mg of DMBA per kg, dissolved in dimethyl sulfoxide. Control animals received weekly injections of dimethyl sulfoxide. All animals were sacrificed at 21 weeks of age. The entire aorta from each animal was cut transversely into 5-mm segments starting at the iliac trifurcation. The cross-sectional area of plaques was determined by light microscopic analysis of sections taken from the face of each segment. Plaque frequency was similar in DMBA-treated and control groups. However, mean plaque cross-sectional area was 7- to 11-fold higher for the treatment groups than for the controls. The distribution of plaque areas in both treated animals and controls was consistent with a log normal distribution. Median cross-sectional area and plaque volume index each increased in a linear fashion with DMBA dose. Small plaques were present in all groups. Large plaques were present only in DMBA-treated animals. Labeling indices of plaques, although low, were 2.3- to 26-fold higher than for underlying medial smooth muscle cells. The data indicate that the primary response to chronic DMBA exposure is a dose-dependent size increase of spontaneous aortic lesions and not the induction of new lesions.

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Year:  1981        PMID: 6778610

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  10 in total

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Review 2.  Passively inhaled tobacco smoke: a challenge to toxicology and preventive medicine.

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3.  An ultrastructural comparison of carcinogen-associated and spontaneous aortic lesions in the cockerel.

Authors:  G Batastini; A Penn
Journal:  Am J Pathol       Date:  1984-03       Impact factor: 4.307

4.  Is preconditioning by nicotine responsible for the better prognosis in smokers with acute myocardial infarction?

Authors:  Y Birnbaum; S L Hale; R A Kloner
Journal:  Basic Res Cardiol       Date:  1996 May-Jun       Impact factor: 17.165

5.  Transforming gene in human atherosclerotic plaque DNA.

Authors:  A Penn; S J Garte; L Warren; D Nesta; B Mindich
Journal:  Proc Natl Acad Sci U S A       Date:  1986-10       Impact factor: 11.205

6.  Focal smooth muscle proliferation in the aortic intima produced by an initiation-promotion sequence.

Authors:  M W Majesky; M A Reidy; E P Benditt; M R Juchau
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

7.  Chronic exposure to the carcinogenic compound benzo[a]pyrene induces larger and phenotypically different atherosclerotic plaques in ApoE-knockout mice.

Authors:  Daniëlle M J Curfs; Esther Lutgens; Marion J J Gijbels; Mark M Kockx; Mat J A P Daemen; Frederik J van Schooten
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8.  Polycyclic aromatic hydrocarbon biomarkers and serum markers of inflammation. A positive association that is more evident in men.

Authors:  Omayma Alshaarawy; Motao Zhu; Alan Ducatman; Baqiyyah Conway; Michael E Andrew
Journal:  Environ Res       Date:  2013-08-22       Impact factor: 6.498

9.  The tar fraction of cigarette smoke does not promote arteriosclerotic plaque development.

Authors:  A Penn; K Keller; C Snyder; A Nadas; L C Chen
Journal:  Environ Health Perspect       Date:  1996-10       Impact factor: 9.031

Review 10.  Molecular alterations critical to the development of arteriosclerotic plaques: a role for environmental agents.

Authors:  A Penn
Journal:  Environ Health Perspect       Date:  1989-05       Impact factor: 9.031

  10 in total

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