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Acceleration of atherogenesis in ApoE−/− mice exposed to acute or low-dose-rate ionizing radiation
Author(s) -
Mariateresa Mancuso,
Emanuela Pasquali,
Ignacia Braga-Tanaka,
Satoshi Tanaka,
Alessandro Pannicelli,
Paola Giardullo,
Simonetta Pazzaglia,
Soile Tapio,
Michael J. Atkinson,
Anna Saran
Publication year - 2015
Publication title -
oncotarget
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.373
H-Index - 127
ISSN - 1949-2553
DOI - 10.18632/oncotarget.5075
Subject(s) - medicine , ionizing radiation , apolipoprotein e , dose–response relationship , circulatory system , physiology , dose rate , endocrinology , nuclear medicine , urology , irradiation , cardiology , physics , disease , nuclear physics , medical physics
There is epidemiological evidence for increased non-cancer mortality, primarily due to circulatory diseases after radiation exposure above 0.5 Sv. We evaluated the effects of chronic low-dose rate versus acute exposures in a murine model of spontaneous atherogenesis. Female ApoE-/- mice (60 days) were chronically irradiated for 300 days with gamma rays at two different dose rates (1 mGy/day; 20 mGy/day), with total accumulated doses of 0.3 or 6 Gy. For comparison, age-matched ApoE-/- females were acutely exposed to the same doses and sacrificed 300 days post-irradiation. Mice acutely exposed to 0.3 or 6 Gy showed increased atherogenesis compared to age-matched controls, and this effect was persistent. When the same doses were delivered at low dose rate over 300 days, we again observed a significant impact on global development of atherosclerosis, although at 0.3 Gy effects were limited to the descending thoracic aorta. Our data suggest that a moderate dose of 0.3 Gy can have persistent detrimental effects on the cardiovascular system, and that a high dose of 6 Gy poses high risks at both high and low dose rates. Our results were clearly nonlinear with dose, suggesting that lower doses may be more damaging than predicted by a linear dose response.

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