Literature DB >> 6262518

Further investigations of the capacity of polynuclear aromatic hydrocarbons to elicit atherosclerotic lesions.

J A Bond, A M Gown, H L Yang, E P Benditt, M R Juchau.   

Abstract

Treatment of chickens for up to 20 wk with varying doses (0.1-10 mg/kg) of benzo[a]pyrene (BaP) or 7,12-dimethylbenz[a]anthracene (DMBA) resulted in significant increases in incidence and size of atherosclerotic lesions at the two higher doses utilized (1 and 10 mg/kg). Maximal lesion formation for birds treated chronically with BaP occurred at 1 mg/kg, while development of lesions in birds treated with DMBA was roughly linear over the dose range tested. The largest doses of BaP or DMBA (10 mg/kg for 20 wk) produced the highest percentage of chickens with detectable lesions (75 and 89%, respectively). Lower doses of BaP or DMBA resulted in a smaller percentage of birds (per group) with lesions, and the lowest dose (0.1 mg/kg) produced no statistical increase in lesion incidence. At approximately equimolar doses, DMBA appeared to be more potent than BaP in enhancing the development of lesions in the chickens. Administration of a single dose of BaP or DMBA followed by weekly doses of the tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA) for 20 wk did not result in enhancement of lesion formation over the respective controls. Blood cholesterol was not significantly altered after treatment of chickens with DMBA, BaP, or TPA.

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Year:  1981        PMID: 6262518     DOI: 10.1080/15287398109529983

Source DB:  PubMed          Journal:  J Toxicol Environ Health        ISSN: 0098-4108


  12 in total

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Review 3.  Passively inhaled tobacco smoke: a challenge to toxicology and preventive medicine.

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Journal:  Arch Toxicol       Date:  1987-12       Impact factor: 5.153

4.  Benzo[a]pyrene potentiates the pathogenesis of abdominal aortic aneurysms in apolipoprotein E knockout mice.

Authors:  Petra A Prins; Prudhvidhar R Perati; Valentina Kon; Zhongmao Guo; Aramandla Ramesh; MacRae F Linton; Sergio Fazio; Uchechukwu K Sampson
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5.  Inherent and benzo[a]pyrene-induced differential aryl hydrocarbon receptor signaling greatly affects life span, atherosclerosis, cardiac gene expression, and body and heart growth in mice.

Authors:  Joanna S Kerley-Hamilton; Heidi W Trask; Christian J A Ridley; Eric Dufour; Corina Lesseur; Carol S Ringelberg; Karen L Moodie; Samantha L Shipman; Murray Korc; Jiang Gui; Nicholas W Shworak; Craig R Tomlinson
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6.  An ultrastructural comparison of carcinogen-associated and spontaneous aortic lesions in the cockerel.

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7.  Excess mortality among Swedish chimney sweeps.

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8.  Overexpression of antioxidant enzymes in ApoE-deficient mice suppresses benzo(a)pyrene-accelerated atherosclerosis.

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9.  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

10.  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
Journal:  Am J Pathol       Date:  2004-01       Impact factor: 4.307

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