Arsenic (As) exposure is a significant worldwide environmental health concern. Chronic exposure via contaminated drinking water has been associated with an increased incidence of a number of diseases, including reproductive and developmental effects. The goal of this study was to identify adverse outcomes in a mouse model of early life exposure to low-dose drinking water As (10 ppb, current U.S. EPA Maximum Contaminant Level).
Methodology and Findings
C57B6/J pups were exposed to 10 ppb As, via the dam in her drinking water, either in utero and/or during the postnatal period. Birth outcomes, the growth of the F1 offspring, and health of the dams were assessed by a variety of measurements. Birth outcomes including litter weight, number of pups, and gestational length were unaffected. However, exposure during the in utero and postnatal period resulted in significant growth deficits in the offspring after birth, which was principally a result of decreased nutrients in the dam's breast milk. Cross-fostering of the pups reversed the growth deficit. Arsenic exposed dams displayed altered liver and breast milk triglyceride levels and serum profiles during pregnancy and lactation. The growth deficits in the F1 offspring resolved following separation from the dam and cessation of exposure in male mice, but did not resolve in female mice up to six weeks of age.
Citation: Kozul-Horvath CD, Zandbergen F, Jackson BP, Enelow RI, Hamilton JW (2012) Effects of Low-Dose Drinking Water Arsenic on Mouse Fetal and Postnatal Growth and Development. PLoS ONE7(5): e38249. https://doi.org/10.1371/journal.pone.0038249
Editor: Silvana Gaetani, Sapienza University of Rome, Italy
Received: August 8, 2011; Accepted: May 4, 2012; Published: May 31, 2012
Copyright: © 2012 Kozul-Horvath et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by National Institute of Environmental Health Sciences at the National Institutes of Health grants 1F32 ES019070 (CDK-H) and P42 ES007373 (BPJ, JWH, RIE and CDK-H, Dartmouth Superfund Research Program Project Grant, Project 2 and Pilot Project). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Chronic exposure to arsenic (As), by contamination of drinking water from natural geological sources, is a significant worldwide environmental health concern , . As many as 25 million people in the United States are exposed to As at levels above the current EPA standard from private, unregulated wells, and worldwide the estimated exposure is several hundreds of millions of people. Chronic exposure to such elevated levels has been associated with a variety of adverse health impacts in human epidemiology studies, including various cancers, cardiovascular disease, diabetes and developmental/reproductive effects , , . The mechanism(s) by which arsenic can induce or contribute to such a wide array of adverse health impacts, over a wide range of exposures, have yet to be elucidated.
Exposure events during critical windows of fetal and postnatal (PN) development pose a serious risk for adverse health outcomes later in life . An increasing number of animal and human epidemiological studies have indicated an association between As exposure and adverse reproductive and developmental outcomes. Arsenic readily crosses the placenta , , but it has been shown that As transfer via the breast milk is limited . Prenatal exposure to high levels of As (ppm range) in mouse models has been reported to result in a variety of adverse effects including placental dysplasia and loss of fecundity , transplacental carcinogenicity , early onset of atherosclerosis , and neural tube defects . Prenatal exposure of mice to lower doses of As (50 ppb) has been shown to result in learning deficits  and alterations in lung structure and function .
Epidemiology studies have shown that exposure to As during gestation is associated with a number of adverse effects on the fetus, including low birth weight, survival, and spontaneous abortion , , , , . However, most of this work has been conducted in areas with relatively high exposures (several hundred ppb), such as Bangladesh and Taiwan. A number of studies have identified adverse immunological outcomes following early life As exposure, including decreased infant thymic development, decreased immune factors in breast milk, increased acute respiratory infections in offspring, and the activation of inflammation in the placenta and cord blood , , , . Early life As exposure has also been associated with an increased incidence of cancer and bronchiectasis in adulthood, even several decades after cessation of exposure . Interestingly, in Bangladesh, no effects have been observed on infant development at 7 or 18 months , .
Based on cancer evidence, the U.S. EPA's current Maximum Contaminant Level (MCL) for As in public drinking water supplies is 10 ppb (0.13 µM) , which was recently revised from 50 ppb. Since that regulatory change, a number of studies have reported significant effects of As exposure at or below 10 ppb in experimental model systems , , , . The effects of low dose As at the current EPA standard on susceptible populations, such as pregnant women and infants, have been largely unexplored. Our goal was to develop a mouse model of early life As exposure through which we could identify critical windows of exposure that might result in adverse impacts on the development of the immune system later in life. However, following the development of our model, we unexpectedly observed that gestational and post natal As exposure at 10 ppb caused immediate effects on the rate of body weight gain of the F1 offspring. Thus, the studies presented here were designed to further explore the developmental outcomes following low dose As exposure during gestation and lactation.
The experimental model of exposure is detailed in Figure 1 and the Methods section. Differences were not observed in any birth outcome (n = 14–17 dams per exposure), such as litter size (control: 7.5 (±0.3) pups; arsenic: 7.4 (±0.3) pups), gestational length (control: 20.2 (±0.33) days; arsenic: 19.6 (±0.38) days), the average weight of the litter or the survival of the pups (control: 1.28 (±0.01) grams; arsenic: 1.26 (±0.02) grams).
Following the detection of cervical plugs, mated females were exposed to control water or 10 ppb As in drinking water through the gestational period. At the birth of their pups, dams in each exposure group were further divided into sub-groups receiving control water or 10 ppb As in drinking water through 30 days of age (n = 14–17 dams per exposure). Weaning from the dam took place at day 21 PN (or later if a pup did not reach the 7 gram weight cut-off). This resulted in 4 overall exposure groups: 1. Control (no As drinking water exposure; 2. Postnatal (PN, offspring receiving 10 ppb As from PN days 1–30); 3. In utero (IU, offspring receiving 10 ppb As from gestational day 1 through birth); 4. In utero & postnatal (IU&PN, offspring receiving 10 ppb As from gestational day 1 through day 30 PN) At day 30 PN, all offspring were placed on control drinking water and growth was assessed until 6 weeks PN.
Growth of F1 offspring
Following birth, pups were monitored daily to assess survival and development. Survival and developmental milestones (eye opening, pinna unfolding, appearance of fur) was not differentially affected by the As exposure paradigm. As early as day 10 post natal, offspring exposed to As displayed significant decreases in growth (evidenced by total body weight), regardless of the timing of As exposure (Figure 2A). At the time of weaning (day 21 post natal) many of the As-exposed offspring were so small that it was not feasible to separate the offspring from the dams at the day of weaning. All pups were maintained with the dam until they reached a weight standard for separation of 7 grams. At weaning, mean weight values for IU, PN and IU&PN As exposed offspring were 7.5, 7.6 and 7.1 grams, respectively. The mean control weight was 9.2 grams. Given this cutoff for separation from the dam, percentages of mice requiring a delayed wean for control, IU, PN and IU&PN exposures were as follows: 0%, 33%, 25% and 46%, respectively. This growth deficit persisted through day 28 PN, regardless of whether or not a delayed wean was required. At day 42 PN, the growth deficit was still apparent in female but not in male mice (Figure 2B). Prior to this time point, both genders of mice were equally affected (Figure S1).
(A). The weight (grams) of offspring was monitored over the course of development and is shown across all four exposure groups at birth, day 10, 21, and day 28 PN. Male and female mice are included. Birth, n = 21–25; Day 10, n = 17–21; Day 21, n = 65–71; Day 28, n = 44–52. One Way ANOVA, compared to control for each respective time point (B.) Mouse weights separated by gender at day 42 PN across all four exposure groups; n = 49–54. Male mice in all exposure groups are represented with open shapes and female mice with closed shapes. One Way ANOVA for female mice, compared to unexposed female mice. Asterisks indicate statistical significance, * p<0.05, ** p<0.01*** p<0.001, ****p<0.0001. Error bars represent mean ± SEM.
Arsenic tissue concentrations
To assess the direct exposure of the F1 offspring to As, total As levels in the placenta, dam's breast milk, pup stomach content (day 10 and 21 PN), and urine were measured by ICP-MS across all exposure groups at various time points pre-, during and post-pregnancy. Arsenic levels in the placentas, dam's milk and pup stomachs were near the limits of detection in all exposure groups. There was no observable increase in the As concentrations in the placenta or milk, but there was a significant increase in the stomach As contents of the pups that received As exposure IU and IU&PN compared to control offspring. This increase in stomach As levels was observed at day 10 PN, during which time the offspring would be primarily consuming breast milk, as opposed to drinking from the water bottle source of As. By day 21 PN, no differences in As levels were detected in the stomach contents of the pups. As expected, urinary excretion of As significantly increased in the As exposure groups. Interestingly, while all mice in the exposure groups received the same level of As (10 ppb), excretion values decreased in the pregnant and lactating As-exposed mice, when compared to As-exposed virgin mice. Mice that were exposed to As only IU no longer excreted significant levels of As during the postpartum period. Urinary As excretion was primarily in the form of dimethylarsenate (DMA). Values are represented in Table 1. Intake of water and excretion of urine displayed a trending, but not significant, increase across the exposure groups (Table S1).
Alterations in breast milk nutrition
Given that the growth deficit manifested during the postnatal period (as early as day 10) and there was not a significant increase in the exposure of the pups to As via the breast milk, we hypothesized that other alterations in the dam's milk were at least partially responsible. Obvious differences in the rearing of the pups by the dams in different exposure groups were not observed. By day 1 PN, all pups displayed prominent milk spots and by day 10 PN, no significant difference was observed in the weight of the stomach contents of the pups, which confirmed that the offspring in all exposure groups were being fed and general milk production was intact. The milk of the dams in all exposure groups was assessed for total protein and triglyceride (TG) concentrations. Protein concentrations were not significantly different (Figure 3A), but TG concentrations displayed a significant decrease in all As exposure groups compared to control (Figure 3B). No differences were observed in the amount of milk collected in the different exposure groups.
Breast milk was collected between day 10–12 PN. Breast milk was analyzed for (A.) total protein concentrations and (B.) total TG concentrations. Asterisks indicate statistical significance, ** p<0.01, *** p<0.001, One Way ANOVA compared to control. Error bars equal mean ± SEM (n = 8–9 mice per exposure).
Triglyceride levels in the dams
We were interested to assess how exposure to As might alter lipid metabolism in the dams during the course of pregnancy and lactation. Unexpectedly, we found a significant increase in the incidence of liver steatosis in the As-exposed dams at day 15.5 gestation. None of the control dams displayed gross liver steatosis at day 15.5 gestation, while 55.5% (5/9) of the As exposure dams displayed gross liver steatosis (* p<0.05, compared to control, Fisher's exact probability test). Liver steatosis was confirmed at the histological level (Figure 4 A–F). Maternal weight gain was not altered by As exposure (Figure S2). Gross liver steatosis was not observed at day 21 PN in any of the exposure groups, indicating that the effects are transient. The total TG levels in the serum and livers of pregnant (gestational day 15.5) and lactating mice (PN day 15–18) were also measured (Table 2). Significant decreases were observed in the levels of total serum TG during pregnancy and lactation for mice receiving As in all exposure paradigms. Liver TG were significantly increased in mice exposed to As during gestation, as expected, given the gross liver steatosis. However, liver TG levels displayed a trending, but not significant, increase in As exposure groups during the lactation period.
Dams were sacrificed at gestation day 15.5. (A, B.) Detection of liver steatosis at the gross level was observed in a significant percentage of the As exposed mice (C–F.) Histological hematoxylin and eosin staining in (C.,E.) control and (D., F.) As-exposed dams. Scale bars indicate magnification.
Profiling of serum lipoproteins using Fast Protein Liquid Chromatography revealed no clear differences between the control and As-exposed dams for cholesterol levels in the lipoprotein fractions, indicating that 10 ppb As does not substantially affect the number of lipoprotein particles for any of the fractions (Figure 5). Interestingly, the distribution of TG over the fractions was markedly affected. The very low density lipoprotein (VLDL) fractions of the As-treated mice contained more TG and its distribution was shifted to larger VLDL particles. The low, intermediate, and high density lipoprotein fractions (LDL, IDL, and HDL, respectively), all showed a decreased TG level for the As-treated dams. In accordance with the results from Table 2, the area under the curve for TG was smaller for the As-treated mice (Figure 5).
Dams were fasted for 6 hours on PN day 21 and pooled serum of 4 As (IU&PN) treated dams (open triangles) and 3 controls (black circles) was used for lipoprotein profiling by FPLC. Fractions were assayed for TG (top panel) and total cholesterol levels (bottom panel).
Cross-fostering of F1 offspring
To assess the level to which decreased milk nutrients contributed to the growth deficit, we designed a series of cross-fostering experiments. In these experiments, offspring from opposing gestational exposure groups (control or gestational As) were exchanged and fostered. We observed that we could reverse the growth phenotype by simply exchanging the litters and dams from opposing exposure groups (Figure 6, Column C and D). Fostering within the exposure group recapitulated the original phenotype (Figure 6, Column E and F).
The average litter weight (grams) of offspring at weaning (day 21 PN) was assessed following fostering. Immediately following birth, all dams were placed on control drinking water through the weaning period. Groups were as follows: (A.) Control offspring remaining with biological mom through weaning/not fostered (n = 11 litters); (B.) 10 ppb IU As exposed mice remaining with biological mom/not fostered (n = 11 litters); (C.) Control offspring fostered by 10 ppb IU As mom (n = 5 litters); (D.) 10 ppb IU As offspring fostered by control mom (n = 5 litters); (E.) Control offspring fostered by a non-biological control mom (n = 3 litters); (F.) 10 ppb IU As offspring fostered by a non-biological 10 ppb IU As mom (n = 3 litters). Asterisks indicate statistical significance, * p<0.05, **** p<0.0001, One Way ANOVA compared to control mice remaining with biological mom (column A). Error bars represent mean ± SEM.
In the conduct of an experiment designed to examine immune effects later in life from in utero exposure to As at the current U.S. EPA drinking water standard, we were surprised to observe significant short-term effects of these exposures on the F1 offspring and the dams. Specific effects included decreased growth of the F1 offspring and altered TG levels and profiles in the dams. Decreases in the nutrient content of the dam's breast milk, specifically TGs, appear to play a role in the growth deficits observed in the F1 offspring. The growth deficit was reversed by cross-fostering of the pups.
Arsenic concentrations were measured in the dam's milk, pup stomachs, placentas, and dam's urine, which confirmed that As was not transferred via the breast milk. In two exposure groups (IU and PN), we observed a trend towards decreased As levels in the milk, which was also recently reported in a similar mouse study with much higher doses of exposure . These results are consistent with published reports of healthy lactating women exposed to As . We did not detect significant increases in the levels of As in the placentas of the exposed mice compared to control mice. It is possible that As transfers through the placenta at a greater level in the exposed mice, but the low level of As used in this model and the detection limits of the ICP-MS impair our ability to measure it. Arsenic has been shown to transfer through the placenta in human models of exposure and in mouse models with higher levels of exposure , , . Given the dramatic effect on growth in the offspring, we were concerned that the pups may be acquiring exposure to As from another external source, such as the dam's urine. To assess such exposure, we also measured the stomach content of the pups. While we did not see a significant increase in the As levels in the milk, we did see a significant increase in the As levels the pup stomachs in two exposure groups: IU and IU&PN at day 10 PN. However, it is unlikely that these elevated levels are a result of external exposure, via the urine or some other source, given that we did not observe such increases in the PN group. The dams in the PN exposure group excreted a significantly higher level of As in the urine compared to the IU group during the postnatal period. Thus, the basis for this increase in stomach As in these two groups is unclear. The overall levels of As in the stomachs at day 21 were increased compared to day 10 PN. This was likely a result of the pup's consumption of chow at this time point.
Interestingly, we also observed significant decreases in As excretion by the dams in all As exposure groups during the gestational and postnatal period, compared to virgin mice ingesting the same level of As. There was a trend towards increased water consumption and urine output in the As-exposed mice during pregnancy (and across all groups during the lactational period), but given the magnitude of these trends, the changes in water consumption and urine output are unlikely to account entirely for the significant decrease in urinary As output. Recent epidemiological data has shown that pregnancy can significantly alter the metabolism of As , but one challenge in the field has been extrapolating animal model studies of As exposure to human studies because mice are very efficient at metabolizing As . Further research in this area is needed, but these data suggest that urinary As levels in pregnant mice may not be an accurate marker of the level of drinking water exposure.
The impeded growth of As-exposed offspring observed in this study was unexpected, given the low dose (10 ppb) of As used. Similar growth deficits have been observed in a high dose [10, 50 and 100 mg/L] IU exposure model of rats . Other studies have used similar models of exposure (ppb and ppm levels of As during gestation and lactation), but have not reported changes in body weight gain early in life , , . It has become clear in comparing different experiments that the dose of As is very important, as well as understanding and controlling the background concentrations of As in the diet and bedding . Moreover, arsenic has been shown to display complicated, multi-phasic dose response curves over a broad range that suggest different physiological effects at different dose ranges , so in retrospect it is not surprising to observe a different effect at these lower exposures, which might then be superseded by other effects at higher doses. We also recognize that many of these effects appear to be transient and can be experimentally ameliorated, suggesting that differences in the timing of exposure and in the experiment endpoints between this study and other studies using similar models could influence the observed results. It is also interesting that we did not observe greater effects in the groups with the combined exposure period (i.e., IU+PN) versus groups with only one or the other period of exposure (IU or PN). We cannot rule out the possibility that there is some capability to adapt to such low level exposures. Clearly, the response curves of As exposure, particularly at low levels, are complex, but these unexpected low-level effects on fetal growth warrant further investigation.
Based on our results, it is clear that As effects on the dam play a major role in the growth deficit of the offspring. The results of the fostering experiments suggest that the milk is the major contributor to the effects we have observed. However, we cannot definitively rule out that small behavioral changes in the dams rearing of the pups did not play a role in the growth deficit. Breastfeeding of infants in human populations with As exposure has been shown to be protective against increased As exposure to the infant . Our results suggest that As exposure can impact the composition and quality of breast milk, even when As is not being directly transferred via the breastmilk. We also observed an interesting gender-specific effect. These results suggest that female mice are more vulnerable to early life As exposure, compared to their male siblings, implying a hormonal contribution. Arsenic is a well-documented endocrine disruptor and this could represent yet another example of such actions in vivo , , , .
We have previously reported that a combined exposure of adult mice to As followed by a sublethal infection with influenza significantly increased the severity of respiratory infection . Based on our previous studies, we have hypothesized that exposure to low levels of As may act as a predisposing factor, in which a secondary stress is needed to induce the adverse health effects we have observed. In the results reported in this study, we believe that pregnancy/lactation can act as such a secondary stress in the dams. Under conditions of physiological stress, such as during pregnancy and lactation, small alterations in lipid metabolism may be exacerbated, leading to the measureable decreases in the TG concentration of the breast milk, altered lipid profliles and the liver steatosis we observed in this study. The shift to increased VLDL size in As-treated dams, as indicated by FPLC analysis, may reflect an increase in hepatic de novo lipogenesis , which would be in agreement with the fatty livers observed in a significant number of the As-exposed dams. Alternatively, As exposure may result in impaired VLDL-TG catabolism, but this would be expected to result in elevated serum TG levels. It is conceivable that As affects serum lipid metabolism via multiple mechanisms with lower TG levels as the ultimate effect. An elevated serum TG by increased production or decreased catabolism of VLDL-TG may for instance be compensated by increased hepatic clearance of IDL/LDL triglycerides, which would be supported by the lower TG levels in the corresponding fractions from the As-exposed dams. Regardless, the lower serum TG levels would potentially reduce availability of lipids in peripheral tissues, including mammary glands. Acute fatty liver of pregnancy (AFLP) is a specific clinical disease reported in a small percentage of human pregnancies . It is interesting to speculate that such a background of altered lipid metabolism, itself elaborated by the physiological stress of pregnancy, may be further altered by As.
Overall, this study indicates that low-level As exposure during the IU or PN period results in a number of immediate adverse effects, including altered TG levels and profiles and growth deficits in the F1 offspring. Many of these outcomes were direct effects on the dam, which manifested as adverse outcomes in the F1 offspring. The results suggest that exposure of vulnerable populations to As, perhaps at levels as low as the current MCL of 10 ppb, may induce a significant increase in adverse health outcomes, which has been previously unrecognized. It is well documented that exposure to chemicals and environmental toxicants during the developmental period can have both immediate and long-term health problems. The goal of our future research will be to address the impact of early-life As exposure on the development and relative adverse health risks of these F1 individuals as adults, and on their F2 offspring.
All animal studies were conducted in accordance with Association for Assessment and Accreditation of Laboratory Animal Care (AALAC)-approved guidelines using a protocol approved by the Dartmouth Institutional Animal Care and Use Committee (IACUC). Approval protocol number for Dartmouth IACUC was 10-10-02. All animals were treated humanely and with regard for alleviation of suffering. C57BL/6J mice (Jackson Labs, Bar Harbor, ME) were housed in ventilated cages with AIN-76A chow (Harlan Teklad, Madison, WI, ad lib) and corncob and carefresh bedding (Scott's Distributing, Hudson, NH). Background As concentrations in the diet were less than 20 ppb, which is a level too low to speciate. We have demonstrated in previous studies that the bioavailable fraction of inorganic arsenic in this diet is low and that we can clearly distinguish an experimental signal as compared to control by exposing animals to drinking water As at 10 ppb .
Mated mice were acclimated on the AIN-76A diet for 2 weeks prior to mating. In this model, following the detection of cervical plugs, naïve pregnant mice were exposed to control or 10 ppb As in drinking water through the gestational and weaning period. Males were not exposed to As prior to mating. At birth, dams in control and As exposure groups were further split into groups receiving control or 10 ppb As in drinking water, which resulted in 4 overall exposure groups: 1. Control (no As drinking water exposure); 2. Postnatal (PN, offspring receiving 10 ppb As from PN days 1–30); 3. In utero (IU, offspring receiving 10 ppb As from gestational day 1 through birth); 4. In utero & postnatal (IU&PN, offspring receiving 10 ppb As from gestational day 1 through day 30 PN). (Figure 1). Starting at day 18 gestation, cages were monitored twice daily for the birth of pups. Litters were not culled. Litters were monitored for developmental milestones, such as eye opening, pinna unfolding and the appearance of fur. Offspring were weaned from the mothers at day 21 PN and continued with their designated drinking water exposure through day 30 PN. From days 30–42 PN, all offspring were maintained on deionized distilled water ddH2O (no As). In all instances (dams and offspring), mice not being exposed to As during specified time frames, were given ddH2O. Background As levels in the ddH20 were below 1 ppb. Animals were euthanized with carbon dioxide. Maternal necropsies were conducted at day 15.5 gestation or at various time points during lactation. F1 offspring necropsies were conducted at day 10, 21 and 42 PN. No gross lesions or visceral internal malformations (observed by gross physical observation at necropsy) were noted in the FI offspring at any time point up to the termination of the study at day 42 postnatal. A subset of dams and virgin mice from each exposure group (n = 3–6) was placed in metabolic cages (Nalgene) for a period of 24 hours at indicated time points to facilitate collection of urine and measurement of drinking water intake (Table S1).
Cross-fostering of pups
Litters born to a control dam or a gestationally As-exposed dam within 12 hours of each other were eligible for cross-fostering. Fostering of litters always occurred within 12 hours of birth. All biological offspring were removed, the litters were culled to seven pups, and they were transferred, as a group, to the cage of the foster dam. The behavior of the dam was monitored for one hour post-fostering to ensure acceptance of the litter. All dams were maintained on deionized distilled water ddH2O (no As) following birth. Weight (grams) of fostered offspring was assessed at day 21 PN.
Sodium arsenite (Sigma Aldrich, St. Louis, MO) was prepared from stock solution in ddH2O to yield a 10 ppb (µg/L) concentration of drinking water. The arsenic concentration in the final solution was confirmed by induction-coupled plasma mass spectrometry (ICP-MS) metal analysis at Dartmouth's Trace Elements Analysis Core Facility. Drinking water was changed twice weekly.
At birth, the gestational length, number of pups, average litter weight (weight of individual pups/number of pups in litter), number of dead pups, and number of pups with malformations were recorded. Weight (grams) was recorded for offspring at birth, day 10, day 21, day 28 and day 42 PN.
Liver steatosis in the dams was observed at the gross observational level. For histological confirmation, livers were removed and fixed in formaldehyde, paraffin embedded, sliced and stained with hematoxylin and eosin.
Collection of breast milk
Dams (day 10–12 postnatal) were separated from pups for 6 hours to allow for milk accumulation. Dams were lightly anesthetized (i.p.) with 9∶1 ketamine∶xylazine mix at 0.1 ml/30 g body weight and injected (i.p.) with 2 IU (100 uL) of oxytocin (Sigma-Aldrich, St. Louis, MO). Dams were milked by gentle manual stimulation of the teat and collection with a pipette. Milk was stored at −20 degrees C.
Analysis of protein levels
Milk samples were diluted in PBS and assayed for protein (1∶400 dilution). Protein concentrations were determined by BCA Protein Assay (Pierce, Rockford, IL), according to manufacturer's instructions.
Collection of serum and livers
Dams were fasted for 6 hours. Blood was collected from the vena cava and livers were collected and snap frozen. Liver tissue (∼150 mg) was homogenized in PBS using the Bullet Blender Homogenizer (Next Advance, Cambridge, MA).
Analysis of triglycerides
Triglyceride concentrations were determined in the dam's breast milk (1∶160 dilution), liver tissue (1∶20 dilution) and serum (1∶2 dilution) samples from pregnant and lactating dams across all exposure groups, using Wako L-type triglyceride (Wako Diagnostics, Richmond, VA), according to manufacturer's instructions.
Lipoproteins were separated using fast protein liquid chromatography (FPLC). 0.2 mL of pooled mouse plasma was injected onto a Superose 6B 10/30 column (GE Healthcare Life Sciences, Piscataway, NJ) and eluted at a constant flow of 0.2 mL/minute with phosphate buffered saline (pH 7.4). The effluent was collected in 0.2 mL fractions and triglyceride and cholesterol levels were determined for each fraction using L-type and Cholesterol E kits from Wako Diagnostics (Richmond, VA).
ICP-MS metal analysis
Total concentrations of trace metals in the breast milk (n = 4–5), pup stomachs (n = 6), maternal urine (n = 3) and placentas (n = 3) were measured by ICP-MS. Placenta, stomach and milk samples were digested with 0.3–0.5 ml optima HNO3 at 70°C followed by addition of 0.05–0.1 ml of H2O2. The digested samples were then diluted to 3 ml (stomach and milk) or 5 ml (placenta) final volume. These samples were then analyzed by ICP-MS (7700x, Agilent, Santa Clara, CA) using He as a collision gas for As determination. Quality control included sample analysis duplicates and spikes. Urine was diluted 10-fold with 1% optima HNO3 and analyzed for As by ICP-MS as above.
Effects of in utero and postnatal arsenic exposure on the gender specific growth of offspring. Mouse weights separated by gender at (A.) day 21 and (B.) day 28 across all four exposure groups. No significant differences are observed when comparing male vs female mice within the same exposure group. n = 24–32.
Gestational As exposure does not affect weight gain in dams. Maternal weight gain (n = 9) was not affected by As exposure (solid lines). The growth of virgin female mice was also not affected by As exposure (dotted lines). Error bars represent mean ± SEM.
The authors thank Dr. Radu Stan for use of metabolic cages and Roxanna Barnaby for animal breeding and husbandry.
Conceived and designed the experiments: CDK-H FZ RIE JWH. Performed the experiments: CDK-H FZ BPJ. Analyzed the data: CDK-H FZ BPJ. Contributed reagents/materials/analysis tools: BPJ. Wrote the paper: CDK-H.
- 1. NRC (1999) Arsenic in Drinking Water. Washington, DC: National Academy Press. NRC1999Arsenic in Drinking WaterWashington, DCNational Academy Press
- 2. ATSDR (1999) Toxicological Profile for Arsenic (Update). Atlanta: Agency for Toxic Substances and Disease Registry. ATSDR1999Toxicological Profile for Arsenic (Update)AtlantaAgency for Toxic Substances and Disease Registry
- 3. Abernathy CO, Liu YP, Longfellow D, Aposhian HV, Beck B, et al. (1999) Arsenic: health effects, mechanisms of actions, and research issues. Environ Health Perspect 107: 593–597.CO AbernathyYP LiuD. LongfellowHV AposhianB. Beck1999Arsenic: health effects, mechanisms of actions, and research issues.Environ Health Perspect107593597
- 4. Smith AH, Hopenhayn-Rich C, Bates MN, Goeden HM, Hertz-Picciotto I, et al. (1992) Cancer risks from arsenic in drinking water. Environ Health Perspect 97: 259–267.AH SmithC. Hopenhayn-RichMN BatesHM GoedenI. Hertz-Picciotto1992Cancer risks from arsenic in drinking water.Environ Health Perspect97259267
- 5. Barker DJ (2007) The origins of the developmental origins theory. J Intern Med 261: 412–417.DJ Barker2007The origins of the developmental origins theory.J Intern Med261412417
- 6. Concha G, Vogler G, Lezcano D, Nermell B, Vahter M (1998) Exposure to inorganic arsenic metabolites during early human development. Toxicol Sci 44: 185–190.G. ConchaG. VoglerD. LezcanoB. NermellM. Vahter1998Exposure to inorganic arsenic metabolites during early human development.Toxicol Sci44185190
- 7. Ferm VH (1977) Arsenic as a teratogenic agent. Environ Health Perspect 19: 215–217.VH Ferm1977Arsenic as a teratogenic agent.Environ Health Perspect19215217
- 8. Concha G, Vogler G, Nermell B, Vahter M (1998) Low-level arsenic excretion in breast milk of native Andean women exposed to high levels of arsenic in the drinking water. Int Arch Occup Environ Health 71: 42–46.G. ConchaG. VoglerB. NermellM. Vahter1998Low-level arsenic excretion in breast milk of native Andean women exposed to high levels of arsenic in the drinking water.Int Arch Occup Environ Health714246
- 9. He W, Greenwell RJ, Brooks DM, Calderon-Garciduenas L, Beall HD, et al. (2007) Arsenic exposure in pregnant mice disrupts placental vasculogenesis and causes spontaneous abortion. Toxicol Sci 99: 244–253.W. HeRJ GreenwellDM BrooksL. Calderon-GarciduenasHD Beall2007Arsenic exposure in pregnant mice disrupts placental vasculogenesis and causes spontaneous abortion.Toxicol Sci99244253
- 10. Waalkes MP, Ward JM, Liu J, Diwan BA (2003) Transplacental carcinogenicity of inorganic arsenic in the drinking water: induction of hepatic, ovarian, pulmonary, and adrenal tumors in mice. Toxicol Appl Pharmacol 186: 7–17.MP WaalkesJM WardJ. LiuBA Diwan2003Transplacental carcinogenicity of inorganic arsenic in the drinking water: induction of hepatic, ovarian, pulmonary, and adrenal tumors in mice.Toxicol Appl Pharmacol186717
- 11. Srivastava S, D'Souza SE, Sen U, States JC (2007) In utero arsenic exposure induces early onset of atherosclerosis in ApoE−/− mice. Reprod Toxicol 23: 449–456.S. SrivastavaSE D'SouzaU. SenJC States2007In utero arsenic exposure induces early onset of atherosclerosis in ApoE−/− mice.Reprod Toxicol23449456
- 12. Hill DS, Wlodarczyk BJ, Finnell RH (2008) Reproductive consequences of oral arsenate exposure during pregnancy in a mouse model. Birth Defects Res B Dev Reprod Toxicol 83: 40–47.DS HillBJ WlodarczykRH Finnell2008Reproductive consequences of oral arsenate exposure during pregnancy in a mouse model.Birth Defects Res B Dev Reprod Toxicol834047
- 13. Martinez-Finley EJ, Ali AM, Allan AM (2009) Learning deficits in C57BL/6J mice following perinatal arsenic exposure: consequence of lower corticosterone receptor levels? Pharmacol Biochem Behav 94: 271–277.EJ Martinez-FinleyAM AliAM Allan2009Learning deficits in C57BL/6J mice following perinatal arsenic exposure: consequence of lower corticosterone receptor levels?Pharmacol Biochem Behav94271277
- 14. Lantz RC, Chau B, Sarihan P, Witten ML, Pivniouk VI, et al. (2009) In utero and postnatal exposure to arsenic alters pulmonary structure and function. Toxicol Appl Pharmacol 235: 105–113.RC LantzB. ChauP. SarihanML WittenVI Pivniouk2009In utero and postnatal exposure to arsenic alters pulmonary structure and function.Toxicol Appl Pharmacol235105113
- 15. Hopenhayn C, Ferreccio C, Browning SR, Huang B, Peralta C, et al. (2003) Arsenic exposure from drinking water and birth weight. Epidemiology 14: 593–602.C. HopenhaynC. FerreccioSR BrowningB. HuangC. Peralta2003Arsenic exposure from drinking water and birth weight.Epidemiology14593602
- 16. Hopenhayn-Rich C, Browning SR, Hertz-Picciotto I, Ferreccio C, Peralta C, et al. (2000) Chronic arsenic exposure and risk of infant mortality in two areas of Chile. Environ Health Perspect 108: 667–673.C. Hopenhayn-RichSR BrowningI. Hertz-PicciottoC. FerreccioC. Peralta2000Chronic arsenic exposure and risk of infant mortality in two areas of Chile.Environ Health Perspect108667673
- 17. Rahman A, Persson LA, Nermell B, El Arifeen S, Ekstrom EC, et al. (2010) Arsenic exposure and risk of spontaneous abortion, stillbirth, and infant mortality. Epidemiology 21: 797–804.A. RahmanLA PerssonB. NermellS. El ArifeenEC Ekstrom2010Arsenic exposure and risk of spontaneous abortion, stillbirth, and infant mortality.Epidemiology21797804
- 18. Ahmad SA, Sayed MH, Barua S, Khan MH, Faruquee MH, et al. (2001) Arsenic in drinking water and pregnancy outcomes. Environ Health Perspect 109: 629–631.SA AhmadMH SayedS. BaruaMH KhanMH Faruquee2001Arsenic in drinking water and pregnancy outcomes.Environ Health Perspect109629631
- 19. Vahter M (2009) Effects of arsenic on maternal and fetal health. Annu Rev Nutr 29: 381–399.M. Vahter2009Effects of arsenic on maternal and fetal health.Annu Rev Nutr29381399
- 20. Moore SE, Prentice AM, Wagatsuma Y, Fulford AJ, Collinson AC, et al. (2009) Early-life nutritional and environmental determinants of thymic size in infants born in rural Bangladesh. Acta Paediatr 98: 1168–1175.SE MooreAM PrenticeY. WagatsumaAJ FulfordAC Collinson2009Early-life nutritional and environmental determinants of thymic size in infants born in rural Bangladesh.Acta Paediatr9811681175
- 21. Raqib R, Ahmed S, Sultana R, Wagatsuma Y, Mondal D, et al. (2009) Effects of in utero arsenic exposure on child immunity and morbidity in rural Bangladesh. Toxicol Lett 185: 197–202.R. RaqibS. AhmedR. SultanaY. WagatsumaD. Mondal2009Effects of in utero arsenic exposure on child immunity and morbidity in rural Bangladesh.Toxicol Lett185197202
- 22. Fry RC, Navasumrit P, Valiathan C, Svensson JP, Hogan BJ, et al. (2007) Activation of inflammation/NF-kappaB signaling in infants born to arsenic-exposed mothers. PLoS Genet 3: e207.RC FryP. NavasumritC. ValiathanJP SvenssonBJ Hogan2007Activation of inflammation/NF-kappaB signaling in infants born to arsenic-exposed mothers.PLoS Genet3e207
- 23. Rahman A, Vahter M, Ekstrom EC, Persson LA (2011) Arsenic Exposure in Pregnancy Increases the Risk of Lower Respiratory Tract Infection and Diarrhea During Infancy in Bangladesh. Environ Health Perspect 719–724.A. RahmanM. VahterEC EkstromLA Persson2011Arsenic Exposure in Pregnancy Increases the Risk of Lower Respiratory Tract Infection and Diarrhea During Infancy in Bangladesh.Environ Health Perspect719724
- 24. Smith AH, Marshall G, Yuan Y, Ferreccio C, Liaw J, et al. (2006) Increased mortality from lung cancer and bronchiectasis in young adults after exposure to arsenic in utero and in early childhood. Environ Health Perspect 114: 1293–1296.AH SmithG. MarshallY. YuanC. FerreccioJ. Liaw2006Increased mortality from lung cancer and bronchiectasis in young adults after exposure to arsenic in utero and in early childhood.Environ Health Perspect11412931296
- 25. Hamadani JD, Grantham-McGregor SM, Tofail F, Nermell B, Fangstrom B, et al. (2010) Pre- and postnatal arsenic exposure and child development at 18 months of age: a cohort study in rural Bangladesh. Int J Epidemiol 39: 1206–1216.JD HamadaniSM Grantham-McGregorF. TofailB. NermellB. Fangstrom2010Pre- and postnatal arsenic exposure and child development at 18 months of age: a cohort study in rural Bangladesh.Int J Epidemiol3912061216
- 26. Tofail F, Vahter M, Hamadani JD, Nermell B, Huda SN, et al. (2009) Effect of arsenic exposure during pregnancy on infant development at 7 months in rural Matlab, Bangladesh. Environ Health Perspect 117: 288–293.F. TofailM. VahterJD HamadaniB. NermellSN Huda2009Effect of arsenic exposure during pregnancy on infant development at 7 months in rural Matlab, Bangladesh.Environ Health Perspect117288293
- 27. EPA (2001) pp. 6975–7066.EPA200169757066National primary drinking water regulations; arsenic and clarifications to compliance and new source contaminants monitoring 40 CFR Parts 9, 141, 142. National primary drinking water regulations; arsenic and clarifications to compliance and new source contaminants monitoring 40 CFR Parts 9, 141, 142.
- 28. Kozul CD, Hampton TH, Davey JC, Gosse JA, Nomikos AP, et al. (2009) Chronic exposure to arsenic in the drinking water alters the expression of immune response genes in mouse lung. Environ Health Perspect 117: 1108–1115.CD KozulTH HamptonJC DaveyJA GosseAP Nomikos2009Chronic exposure to arsenic in the drinking water alters the expression of immune response genes in mouse lung.Environ Health Perspect11711081115
- 29. Andrew AS, Bernardo V, Warnke LA, Davey JC, Hampton T, et al. (2007) Exposure to arsenic at levels found inU.S. drinking water modifies expression in the mouse lung. Toxicol Sci 100: 75–87.AS AndrewV. BernardoLA WarnkeJC DaveyT. Hampton2007Exposure to arsenic at levels found inU.S. drinking water modifies expression in the mouse lung.Toxicol Sci1007587
- 30. Straub AC, Clark KA, Ross MA, Chandra AG, Li S, et al. (2008) Arsenic-stimulated liver sinusoidal capillarization in mice requires NADPH oxidase-generated superoxide. J Clin Invest 118: 3980–3989.AC StraubKA ClarkMA RossAG ChandraS. Li2008Arsenic-stimulated liver sinusoidal capillarization in mice requires NADPH oxidase-generated superoxide.J Clin Invest11839803989
- 31. Markowski VP, Currie D, Reeve EA, Thompson D, Wise JP Sr (2011) Tissue-Specific and Dose-Related Accumulation of Arsenic in Mouse Offspring Following Maternal Consumption of Arsenic-Contaminated Water. Basic Clin Pharmacol Toxicol 108: 326–332.VP MarkowskiD. CurrieEA ReeveD. ThompsonJP Wise Sr2011Tissue-Specific and Dose-Related Accumulation of Arsenic in Mouse Offspring Following Maternal Consumption of Arsenic-Contaminated Water.Basic Clin Pharmacol Toxicol108326332
- 32. Jin Y, Xi S, Li X, Lu C, Li G, et al. (2006) Arsenic speciation transported through the placenta from mother mice to their newborn pups. Environ Res 101: 349–355.Y. JinS. XiX. LiC. LuG. Li2006Arsenic speciation transported through the placenta from mother mice to their newborn pups.Environ Res101349355
- 33. Gardner RM, Nermell B, Kippler M, Grander M, Li L, et al. (2011) Arsenic methylation efficiency increases during the first trimester of pregnancy independent of folate status. Reprod Toxicol 31: 210–218.RM GardnerB. NermellM. KipplerM. GranderL. Li2011Arsenic methylation efficiency increases during the first trimester of pregnancy independent of folate status.Reprod Toxicol31210218
- 34. Vahter M (1999) Methylation of inorganic arsenic in different mammalian species and population groups. Sci Prog 82(Pt 1): 69–88.M. Vahter1999Methylation of inorganic arsenic in different mammalian species and population groups.Sci Prog82Pt 16988
- 35. Xi S, Jin Y, Lv X, Sun G (2010) Distribution and speciation of arsenic by transplacental and early life exposure to inorganic arsenic in offspring rats. Biol Trace Elem Res 134: 84–97.S. XiY. JinX. LvG. Sun2010Distribution and speciation of arsenic by transplacental and early life exposure to inorganic arsenic in offspring rats.Biol Trace Elem Res1348497
- 36. Kozul CD, Nomikos AP, Hampton TH, Warnke LA, Gosse JA, et al. (2008) Laboratory diet profoundly alters gene expression and confounds genomic analysis in mouse liver and lung. Chem Biol Interact 173: 129–140.CD KozulAP NomikosTH HamptonLA WarnkeJA Gosse2008Laboratory diet profoundly alters gene expression and confounds genomic analysis in mouse liver and lung.Chem Biol Interact173129140
- 37. Bodwell JE, Gosse JA, Nomikos AP, Hamilton JW (2006) Arsenic disruption of steroid receptor gene activation: Complex dose-response effects are shared by several steroid receptors. Chem Res Toxicol 19: 1619–1629.JE BodwellJA GosseAP NomikosJW Hamilton2006Arsenic disruption of steroid receptor gene activation: Complex dose-response effects are shared by several steroid receptors.Chem Res Toxicol1916191629
- 38. Fangstrom B, Moore S, Nermell B, Kuenstl L, Goessler W, et al. (2008) Breast-feeding protects against arsenic exposure in Bangladeshi infants. Environ Health Perspect 116: 963–969.B. FangstromS. MooreB. NermellL. KuenstlW. Goessler2008Breast-feeding protects against arsenic exposure in Bangladeshi infants.Environ Health Perspect116963969
- 39. Davey JC, Nomikos AP, Wungjiranirun M, Sherman JR, Ingram L, et al. (2008) Arsenic as an endocrine disruptor: arsenic disrupts retinoic acid receptor-and thyroid hormone receptor-mediated gene regulation and thyroid hormone-mediated amphibian tail metamorphosis. Environ Health Perspect 116: 165–172.JC DaveyAP NomikosM. WungjiranirunJR ShermanL. Ingram2008Arsenic as an endocrine disruptor: arsenic disrupts retinoic acid receptor-and thyroid hormone receptor-mediated gene regulation and thyroid hormone-mediated amphibian tail metamorphosis.Environ Health Perspect116165172
- 40. Kaltreider RC, Davis AM, Lariviere JP, Hamilton JW (2001) Arsenic alters the function of the glucocorticoid receptor as a transcription factor. Environ Health Perspect 109: 245–251.RC KaltreiderAM DavisJP LariviereJW Hamilton2001Arsenic alters the function of the glucocorticoid receptor as a transcription factor.Environ Health Perspect109245251
- 41. Davey JC, Bodwell JE, Gosse JA, Hamilton JW (2007) Arsenic as an endocrine disruptor: effects of arsenic on estrogen receptor-mediated gene expression in vivo and in cell culture. Toxicol Sci 98: 75–86.JC DaveyJE BodwellJA GosseJW Hamilton2007Arsenic as an endocrine disruptor: effects of arsenic on estrogen receptor-mediated gene expression in vivo and in cell culture.Toxicol Sci987586
- 42. Kozul CD, Ely KH, Enelow RI, Hamilton JW (2009) Low-dose arsenic compromises the immune response to influenza A infection in vivo. Environ Health Perspect 117: 1441–1447.CD KozulKH ElyRI EnelowJW Hamilton2009Low-dose arsenic compromises the immune response to influenza A infection in vivo.Environ Health Perspect11714411447
- 43. Grefhorst A, Elzinga BM, Voshol PJ, Plosch T, Kok T, et al. (2002) Stimulation of lipogenesis by pharmacological activation of the liver X receptor leads to production of large, triglyceride-rich very low density lipoprotein particles. J Biol Chem 277: 34182–34190.A. GrefhorstBM ElzingaPJ VosholT. PloschT. Kok2002Stimulation of lipogenesis by pharmacological activation of the liver X receptor leads to production of large, triglyceride-rich very low density lipoprotein particles.J Biol Chem2773418234190
- 44. Bacq Y (2011) Liver diseases unique to pregnancy: A 2010 update. Clin Res Hepatol Gastroenterol. Y. Bacq2011Liver diseases unique to pregnancy: A 2010 update.Clin Res Hepatol Gastroenterol