Impact of life stage and duration of exposure on arsenic-induced proliferative lesions and neoplasia in C3H mice

被引:23
作者
Ahlborn, Gene J. [1 ,2 ]
Nelson, Gail M. [1 ]
Grindstaff, Rachel D. [1 ]
Waalkes, Michael P. [3 ]
Diwan, Bhalchandra A. [4 ]
Allen, James W. [1 ]
Kitchin, Kirk T. [1 ]
Preston, R. Julian [1 ]
Hernandez-Zavala, Araceli [5 ]
Adair, Blakely [1 ]
Thomas, David J. [1 ]
Delker, Don A. [1 ]
机构
[1] US EPA, Off Res & Dev, Natl Hlth & Environm Effects Res Lab, Res Triangle Pk, NC 27711 USA
[2] N Carolina State Univ, Coll Vet Med, Dept Mol Biomed Sci, Raleigh, NC USA
[3] NIEHS, NCI, Lab Comparat Carcinogenesis, Res Triangle Pk, NC 27709 USA
[4] SAIC, Basic Res Program, Fredericksburg, MD USA
[5] Univ N Carolina, Ctr Environm Med Asthma & Lung Biol, Chapel Hill, NC USA
关键词
Arsenic; Carcinogenesis; Life stage; Age susceptibility; Urinary bladder; C3H mice; MALE F344 RATS; DRINKING-WATER; DIMETHYLARSINIC ACID; IN-UTERO; INTERNAL CANCERS; LUNG-CANCER; MOUSE SKIN; CARCINOGENESIS; METABOLISM; MORTALITY;
D O I
10.1016/j.tox.2009.05.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Epidemiological studies suggest that chronic exposure to inorganic arsenic is associated with cancer of the skin, urinary bladder and lung as well as the kidney and liver. Previous experimental studies have demonstrated increased incidence of liver, lung, ovary, and uterine tumors in mice exposed to 85 ppm (similar to 8 mg/kg) inorganic arsenic during gestation. To further characterize age susceptibility to arsenic carcinogenesis we administered 85 ppm inorganic arsenic in drinking water to C3H mice during gestation, prior to pubescence and post-pubescence to compare proliferative lesion and tumor outcomes over a one-year exposure period. Inorganic arsenic significantly increased the incidence of hyperplasia in urinary bladder (48%) and oviduct (36%) in female mice exposed prior to pubescence (beginning on postnatal day 21 and extending through one year) compared to control mice (19 and 5%, respectively). Arsenic also increased the incidence of hyperplasia in urinary bladder (28%) of female mice continuously exposed to arsenic (beginning on gestation day 8 and extending though one year) compared to gestation only exposed mice (0%). In contrast, inorganic arsenic significantly decreased the incidence of tumors in liver (0%) and adrenal glands (0%) of male mice continuously exposed from gestation through one year, as compared to levels in control (30 and 65%, respectively) and gestation only (33 and 55%, respectively) exposed mice. Together, these results suggest that continuous inorganic arsenic exposure at 85 ppm from gestation through one year increases the incidence and severity of urogenital proliferative lesions in female mice and decreases the incidence of liver and adrenal tumors in male mice. The paradoxical nature of these effects may be related to altered lipid metabolism, the effective dose in each target organ, and/or the shorter one-year observational period. Published by Elsevier Ireland Ltd.
引用
收藏
页码:106 / 113
页数:8
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