Rodriguez Karina F, Ungewitter Erica K, Crespo-Mejias Yasmin, Liu Chang, Nicol Barbara, Kissling Grace E, Yao Humphrey Hung-Chang
Reproductive Developmental Biology Group, Reproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, North Carolina, USA.
Environ Health Perspect. 2016 Mar;124(3):336-43. doi: 10.1289/ehp.1509703. Epub 2015 Aug 21.
Mice exposed to high levels of arsenic in utero have increased susceptibility to tumors such as hepatic and pulmonary carcinomas when they reach adulthood. However, the effects of in utero arsenic exposure on general physiological functions such as reproduction and metabolism remain unclear.
We evaluated the effects of in utero exposure to inorganic arsenic at the U.S. Environmental Protection Agency (EPA) drinking water standard (10 ppb) and at tumor-inducing levels (42.5 ppm) on reproductive end points and metabolic parameters when the exposed females reached adulthood.
Pregnant CD-1 mice were exposed to sodium arsenite [none (control), 10 ppb, or 42.5 ppm] in drinking water from gestational day 10 to birth, the window of organ formation. At birth, exposed offspring were fostered to unexposed dams. We examined reproductive end points (age at vaginal opening, reproductive hormone levels, estrous cyclicity, and fertility) and metabolic parameters (body weight changes, hormone levels, body fat content, and glucose tolerance) in the exposed females when they reached adulthood.
Arsenic-exposed females (10 ppb and 42.5 ppm) exhibited early onset of vaginal opening. Fertility was not affected when females were exposed to the 10-ppb dose. However, the number of litters per female was decreased in females exposed to 42.5 ppm of arsenic in utero. In both 10-ppb and 42.5-ppm groups, arsenic-exposed females had significantly greater body weight gain, body fat content, and glucose intolerance.
Our findings revealed unexpected effects of in utero exposure to arsenic: exposure to both a human-relevant low dose and a tumor-inducing level led to early onset of vaginal opening and to obesity in female CD-1 mice.
子宫内暴露于高剂量砷的小鼠成年后对肝癌和肺癌等肿瘤的易感性增加。然而,子宫内砷暴露对生殖和代谢等一般生理功能的影响仍不清楚。
我们评估了子宫内暴露于美国环境保护局(EPA)饮用水标准(10 ppb)和致瘤水平(42.5 ppm)的无机砷对成年后暴露雌性小鼠生殖终点和代谢参数的影响。
怀孕的CD-1小鼠在器官形成期(妊娠第10天至出生)饮用含亚砷酸钠[无(对照)、10 ppb或42.5 ppm]的水。出生时,将暴露的后代寄养给未暴露的母鼠。我们检查了成年后暴露雌性小鼠的生殖终点(阴道开口年龄、生殖激素水平、发情周期和生育能力)和代谢参数(体重变化、激素水平、体脂含量和葡萄糖耐量)。
暴露于砷的雌性小鼠(10 ppb和42.5 ppm)阴道开口提前。暴露于10 ppb剂量时,雌性小鼠的生育能力未受影响。然而,子宫内暴露于42.5 ppm砷的雌性小鼠每窝产仔数减少。在10 ppb和42.5 ppm组中,暴露于砷的雌性小鼠体重增加、体脂含量和葡萄糖不耐受程度均显著更高。
我们的研究结果揭示了子宫内暴露于砷的意外影响:暴露于与人类相关的低剂量和致瘤水平均导致雌性CD-1小鼠阴道开口提前和肥胖。