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Maternal exposure to nanosized titanium dioxide suppresses embryonic development in mice

Authors Hong F, Zhou Y, Zhao X, Sheng L, Wang L

Received 9 June 2017

Accepted for publication 8 August 2017

Published 24 August 2017 Volume 2017:12 Pages 6197—6204

DOI https://doi.org/10.2147/IJN.S143598

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Alexander Kharlamov

Peer reviewer comments 2

Editor who approved publication: Dr Linlin Sun


Fashui Hong,1–4 Yingjun Zhou,1–4 Xiaoyang Zhao,5 Lei Sheng,5 Ling Wang6

1Jiangsu Collaborative Innovation Center of Regional Modern Agriculture and Environmental Protection, 2Jiangsu Key Laboratory for Food Safety and Nutritional Function, 3Jiangsu Key Laboratory for Eco-Agricultural Biotechnology around Hongze Lake, 4School of Life Sciences, Huaiyin Normal University, Huaian, 5Medical College of Soochow University, Suzhou, 6Library of Soochow University, Suzhou, Jiangsu, China

Abstract: Although nanoscale titanium dioxide (nano-TiO2) has been extensively used in industrial food applications and daily products for pregnant women, infants, and children, its potential toxicity on fetal development has been rarely studied. The main objective of this investigation was to establish the effects of maternal exposure of nano-TiO2 on developing embryos. Female imprinting control region mice were orally administered nano-TiO2 from gestational day 0 to 17. Our findings showed that Ti concentrations in maternal serum, placenta, and fetus were increased in nano-TiO2-exposed mice when compared to controls, which resulted in reductions in the contents of calcium and zinc in maternal serum, placenta, and fetus, maternal weight gain, placental weight, fetal weight, number of live fetuses, and fetal crown–rump length as well as cauda length, and caused an increase in the number of both dead fetuses and resorptions. Furthermore, maternal nano-TiO2 exposure inhibited development of the fetal skeleton, suggesting a significant absence of cartilage, reduced or absent ossification, and an increase in the number of fetuses with dysplasia, including exencephaly, spina bifida, coiled tail, scoliosis, rib absence, and sternum absence. These findings indicated that nano-TiO2 can cross the blood–fetal barrier and placental barrier, thereby delaying the development of fetal mice and inducing skeletal malformation. These factors may be associated with reductions in both calcium and zinc in maternal serum and the fetus, and both the placenta and embryos may be major targets of developmental toxicity following maternal exposure to nano-TiO2 during the prenatal period. Therefore, the application of nano-TiO2 should be carried out with caution.

Keywords: nanosized titanium dioxide, maternal exposure, embryonic toxicity, skeleton developmental suppression

Introduction

Nanoscale titanium dioxide (nano-TiO2) is widely used in various applications, including industry, medicine, and in consumer products such as cosmetics, sunscreens, food products, toothpaste, and sterilization and environmental control measures.16 Initially, nano-TiO2 was thought to exhibit relatively low toxicity as compared with other nanomaterials.710 However, numerous studies have suggested that following exposure via various routes including inhalation, injection, dermal deposition, and gastrointestinal tract absorption, nano-TiO2 can be found in various organs including the lung, liver, kidney, spleen, thymus, heart, stomach, brain, ovary, and testis potentially inducing toxic effects.1113 Thus, based on a recent assessment, the International Agency for Research on Cancer has classified TiO2 as a human group 2B carcinogen.14 Despite the fact that increased use and production of nano-TiO2 may result in health impacts due to its various uses, there is still a lack of knowledge regarding the adverse effects of nano-TiO2 on pregnant dams and embryo–fetal development.

It is known that the development of humans and animals, in particular developing embryos, is significantly influenced by environmental factors.15,16 The ability to scavenge toxins in the body is low as the developing embryo lacks the feedback protection mechanism,17,18 and may be more sensitive to the effects of nano-TiO2 compared with mature organisms. Recently, maternal exposure to manufactured nanoparticles (NPs) which induced toxicity during embryo development has attracted considerable attention.19,20 It was reported that maternal exposure to a variety of manufactured NPs was associated with harmful effects on mouse and rat embryos.2125 NPs were detected in prenatally exposed offspring thereby indicating that NPs were transferred to the developing conceptus across the placenta. However, nano-CdO was detected in the placenta and maternal organs of treated mice but not in their fetuses.2628 Exposure of pregnant female mice or rats to different types of NPs may result in a variety of adverse pregnancy outcomes such as embryo mortality, intrauterine growth retardation, and structural anomalies in the prenatally exposed offspring,19 as developmentally toxic NPs crossed the placenta, embryos were directly exposed, and the embryotoxic effects of NPs seemed to have been secondary to maternal and/or placental toxicity.24 Philbrook et al indicated that the intragastric administration of hydroxyl-modified single-walled carbon nanotubes to pregnant mice resulted in increased skeletal defects, such as forked cervical vertebrae, reduced ossification of sternebrae and phalanges, and morphological abnormalities.29 It was proved that exposure to nanosilica (70 nm) led to fetal resorption and inhibition of fetal growth.30 Pregnant female rats were orally treated with nano zinc oxide (ZnO) for 15 days, during gestational days (GDs) 5–19, at doses of 100, 200, and 400 mg/kg/day, and it was found that nano ZnO had no impact on embryo–fetal development in rats.31 Following maternal exposure to nano-TiO2, it was demonstrated that nano-TiO2 migrated into the uterus, affected the embryo, and caused abortion; for example, 500 mg/kg led to significant decreases in the total length of limb buds, arm skin thickness, number of proliferating chondrocytes in the arm, red blood cells in the fingers, and mesenchymal cells in the palm and wrist.32,33 Maternal exposure to nano-TiO2 was also reported to affect the development and function of the central nervous system in mouse and rat offspring.3440 Therefore, we hypothesized that maternal exposure to nano-TiO2 may lead to disorders in embryo–fetal development, especially fetal bone development.

Accordingly, we determined whether mouse embryonic development was influenced by the toxic effects of nano-TiO2 as there is evidence to suggest that fetuses are affected more than adults by a variety of environmental toxins, due to physiological immaturity. Female imprinting control region (ICR) mice were selected as the experimental model and exposed to nano-TiO2 via oral (gavage) administration from GD 0 to 17. After the 18-day gestational period, Ti, Ca, and Zn contents in maternal serum, placenta, and fetus, maternal weight gain, fetal crown–rump and cauda length, body weight (BW) and placental weight, and numbers of live fetuses, dead fetuses, and resorption sites as well as fetal bone development were examined following maternal nano-TiO2 exposure, with a view to clarifying its toxic effects on developing mouse embryos.

Methods

Chemicals

Nanoparticulate TiO2 was prepared by controlled hydrolysis of titanium tetrabutoxide. Details of the synthesis and characterization of nano-TiO2 are described in a previous report by our group.41 NP characteristics were as follows: anatase phase, 6.5 nm particle size, mainly 294 nm hydrodynamic diameter, 174.8 m2/g surface area, and 7.57 mV zeta potential.41

Ethics approval

All animal experiments were conducted during the light phase of the light-dark cycle and approved by the Animal Experimental Committee of Soochow University (grant 2111270). Procedures were performed in accordance with the National Institutes of Health Guidelines for the Care and Use of Laboratory Animals.

Animals and treatment

Female CD-1 (ICR) mice (20±1.5 g) and male mice (23±2 g) were purchased from the Animal Center of Soochow University (China). All mice were housed in stainless steel cages in a ventilated animal room. The room temperature of the housing facility was maintained at 20°C–25°C with a relative humidity of 45%–55% and a 12-hour light/dark cycle. Distilled water and sterilized food were available ad libitum. Prior to dosing, the mice were acclimated to the environment for 5 days. Mice were kept in cages at a ratio of 2:1 (female:male) from 18:00 every evening, and the vaginal suppository of female mice was checked the next morning at 06:00–08:00. Female mice were considered pregnant when the vaginal suppository was found (day 0). Twenty pregnant mice were randomly divided into four subgroups (n=5 per group), including a control group treated with 0.5% w/v hydroxypropylmethylcellulose (Sigma-Aldrich Co., St Louis, MO, USA) and three experimental groups treated with 25, 50, and 100 mg/kg BW nano-TiO2. For appropriate dose selection, previous reports were consulted.42,43 A report by the World Health Organization from 1969 was also consulted, and according to this report, the lethal dose 50 of TiO2 for rats was found to be >12 g/kg BW after oral administration. In addition, US Food and Drug Administration states that the quantity of nano-TiO2 should not exceed 1% by weight of the food. Animals received 25, 50, and 100 mg/kg BW nano-TiO2 orally (gavage) from GD 0 to 17 in an isolated animal room under specific pathogen-free conditions. After the 18-day gestational period, all pregnant mice were weighed and then sacrificed after being anesthetized with ether. Blood samples were collected from the eye vein by rapidly removing the eyeball. Serum was collected by centrifuging blood at 1,200× g for 10 minutes. The uterus was quickly removed, the numbers of live fetuses, dead fetuses, and resorption sites were counted and recorded for each litter, the weight of live fetuses in each litter was recorded, and the length of the fetal crown–rump and cauda were measured. Every effort was made to minimize animal suffering. All experiments were performed in accordance with the National Institutes of Health Guidelines for the Care and Use of Laboratory Animals.

Element content analysis

Two milliliters of maternal sera and ~0.1 g of the placenta and the fetuses were digested, and analyzed for element contents. Inductively coupled plasma-mass spectrometry (Thermo Elemental X7; Thermo Electron Co, Waltham, MA, USA) was used to analyze the Ti, Ca, and Zn concentrations in the samples.42,43 An indium concentration of 20 ng/mL was used as an internal standard, and the detection limit of Ti was 0.074 ng/mL.

Evaluation of fetal skeleton development

The skeletal development of fetuses was evaluated using Menegola’s method.44 The selected fetal mice were soaked in hot water at 80°C for 10 seconds, the skin and viscera were carefully removed with eye forceps and scissors, and stained with alcian blue dye solution for 48 hours. The cartilage in the specimen appeared blue (slightly deeper than the color of the stain solution) when viewed with a stereo microscope (Olympus SZ61; Olympus Corporation, Tokyo, Japan) during the staining period; the specimen was then rinsed 2–3 times with tap water, immersed in alizarin red dye solution for 36–48 hours; the solution was renewed every 12 hours until the bone was purple, and thereafter again the specimen was gently rinsed 2–3 times with tap water. The double stained fetuses were placed in a new transparent solution containing 1% potassium hydroxide for 36–48 hours.45,46 The blue embryonic cartilage and purplish red skeletal ossification were observed under the stereo microscope.

Statistical analysis

Data were analyzed using Statistical Analysis Software (SAS 9.1) (Chicago, IL, USA). The significance of the differential expression between groups was assessed using one-way analysis of variance (ANOVA) followed by Tukey’s honestly significant difference post hoc test, and the results are presented as means ± standard deviation. Differences were considered statistically significant at p<0.05.

Results

Element contents in maternal serum and fetuses

In order to confirm whether nano-TiO2 entered the blood circulation in pregnant mice and crossed the blood–fetal barrier to enter the fetus, we observed and found significant increases in the Ti contents in the maternal serum, placenta, and fetus (Table 1, p<0.05). Furthermore, to confirm the effects of maternal exposure to nano-TiO2 on embryonic development, we also examined the changes in Ca and Zn contents in maternal serum, placenta, and fetus, and found that the contents of Ca and Zn decreased significantly in the high dose nano-TiO2-treated groups (Table 1, p<0.05).

Table 1 Effects of nano-TiO2 on element contents in maternal serum, placenta, and fetus
Notes: Results marked with an asterisk, double asterisks, or three asterisks mean they are significantly different from the control (no nano-TiO2) at the p<0.05, p<0.01, and p<0.001 confidence level, respectively. Values represent mean ± SD (n=5).
Abbreviations: nano-TiO2, nanoscale titanium dioxide; BW, body weight; SD, standard deviation.

Maternal weight gain

Pregnant mice were exposed to different concentrations of nano-TiO2 from GD 0 to 17, and the weight of pregnant mice at days 0, 3, 9, 12, 15, and 18 during pregnancy is presented in Table 2. It can be seen that maternal weight gain gradually increased with pregnancy duration in the control group and nano-TiO2 groups, whereas maternal weight gain in the nano-TiO2-exposed groups at day 18 was significantly lower than that of the control (Table 2, p<0.05).

Table 2 Effects of nano-TiO2 on maternal weight (g) gain during pregnancy
Notes: Results marked with an asterisk mean that they are significantly different from the control (no nano-TiO2) at the p<0.05 confidence level. Values represent mean ± SD (n=5).
Abbreviations: nano-TiO2, nanoscale titanium dioxide; BW, body weight; SD, standard deviation.

Fetal growth

Pregnant mice were sacrificed at GD 18, and the cesarean section was performed to measure the crown–rump and cauda length, and fetal BW and placental weight of the live fetal mice (Table 3). Compared with the control, both fetal crown–rump and cauda length, and fetal BW and placental weight in the 100 mg/kg nano-TiO2-treated group were markedly lower than that in the control (Table 3, p<0.05).

Table 3 Effects of nano-TiO2 on fetal growth of mice
Notes: Results marked with an asterisk or double asterisks mean they are significantly different from the control (no nano-TiO2) at the p<0.05 and p<0.01 confidence level. Values represent mean ± SD (n=5).
Abbreviations: nano-TiO2, nanoscale titanium dioxide; BW, body weight; SD, standard deviation.

Survival and mortality of fetuses

After GD 18, the numbers of live, dead, and resorption sites were counted and are shown in Table 4. Compared with the control, the number of live fetuses in the 100 mg/kg nano-TiO2-treated group was significantly lower than that in the control, whereas the numbers of dead fetuses and resorption sites were obviously higher than those in the control (Table 4, p<0.05), respectively.

Table 4 Effects of nano-TiO2 on survival and mortality in mouse fetus
Notes: Results marked with an asterisk or double asterisks mean they are significantly different from the control (no nano-TiO2) at the p<0.05 and p<0.01 confidence level. Values represent mean ± SD (n=5).
Abbreviations: nano-TiO2, nanoscale titanium dioxide; BW, body weight; SD, standard deviation.

Fetal skeletal development

Table 5 and Figure 1 show that fetal skeleton development in the 100 mg/kg nano-TiO2-exposed group was significantly slower than that in the control, suggesting the absence of significant cartilage, non-ossification of the sternum and metacarpal bones, or incomplete ossification of the sternum. Following maternal exposure to nano-TiO2, fetal dysplasia was also observed compared with the control; dysplasia included exencephaly, spina bifida, coiled tail, scoliosis, rib absence, and sternum absence.

Table 5 Effects of nano-TiO2 on skeletal ossification in mouse fetuses (n=10)
Abbreviations: nano-TiO2, nanoscale titanium dioxide; BW, body weight.

Figure 1 Maternal exposure to nano-TiO2 induced dysplasia of skeleton in mice embryos at gestational day 18.
Notes: Blue indicates cartilage. Purplish red indicates ossification. Red indicates incomplete ossification.
Abbreviations: nano-TiO2, nanoscale titanium dioxide; BW, body weight.

Discussion

Recently, knowledge on the toxicity of different types of nano-TiO2, including damage to the liver, lung, kidney, spleen, heart, brain, testis, and ovary of mice or rats,11 stomach and thymus of mice,12,13 inflammatory response, membrane injury, and cytotoxicity,11 has increased, resulting in several toxicity studies of nano-TiO2 in different biological systems, such as zebrafish and Caenorhabditis elegans.47,48 However, evidence of developmental toxicity caused by nano-TiO2 in mammals is still limited. It is highly desirable and necessary to have a better understanding of the possible developmental toxicity of nano-TiO2 as humans are often exposed to nano-TiO2 both intentionally and unintentionally.

This study was conducted to examine the maternal and developmental toxic potential of nano-TiO2 orally administered to mice during GD 0–17 of pregnancy. Our findings showed that following maternal exposure, nano-TiO2 crossed the blood–fetal barrier or placental barrier and was deposited in maternal serum, placenta, and fetus, leading to significant decreases in Ca and Zn in the maternal serum, placenta, and fetus. In addition, maternal exposure to 100 mg/kg nano-TiO2 markedly reduced maternal weight gain, placental weight, fetal weight, number of live fetuses, and fetal crown–rump length as well as cauda length, and increased the numbers of both dead fetuses and resorption sites. Skeletal development in fetal mice following maternal exposure to 100 mg/kg nano-TiO2 lagged behind that of the control group, and resulted in absent or reduced ossification, and fetal dysplasia. The main results of the present study are discussed subsequently.

Most of the skeletal system is derived from mesoderm, which is mainly from the ventral and medial mesenchyme of the segment. The critical period of fetal organ development in mice or rats is 7.5–18 days. Therefore, the administration of drugs during this stage can be used to examine their effects on the organs of fetal mice or rats. In the study of embryonic developmental toxicity, evaluation of skeletal deformities is often a major part of the assessment of the effects of external compounds on the body, and bone development is often determined by bone staining. The bones of fetal mice are only partially ossified and cartilage is still present at GD 18. In the present study, we observed that fetal vertebrae, carpal, and metatarsophalangeal bones in the control showed uniform cartilage at GD 18. However, maternal exposure to nano-TiO2 resulted in retardation of skeletal development, for example, cartilage was absent, the ossification centers of some bones were absent, the scale of the ossification center was less than that in the control group, and skeletal deformities (such as scoliosis, vertebral fusion, rib deformity) occurred.

The suppression of embryonic bone development and skeletal abnormalities in fetuses caused by nano-TiO2 may be related to the following factors. 1) The placenta is one of the target organs of nano-TiO2; thus, nano-TiO2 can affect the normal development of embryos by interfering with placental blood flow, substance transport, and endocrine as well as substance metabolism. In this study, we found that maternal exposure to nano-TiO2 not only caused intrauterine developmental retardation of the fetus, but also affected bone ossification, which may have been due to nano-TiO2 interfering with the permeability of Ca2+ in the placenta. Furthermore, we also observed that nano-TiO2 caused deformities including exencephaly, spina bifida, coiled tail, scoliosis, rib absence, and sternum absence. 2) Nano-TiO2 reduced the levels of Ca in pregnant mice and fetuses, which may be an important aspect of nano-TiO2-induced toxicity. In general, the active transport of Ca by osteoblasts is broadly divided into three stages: firstly, Ca channels are open and Ca2+ enters the cells; secondly, Ca2+ binds to the Ca binding protein in the cytoplasm and rapidly spreads from the free surface side of the cell to the basal surface; finally, the Ca pump on the basal plane uses energy from the hydrolysis of ATP to pump Ca2+ from the cells to the extracellular region.49 Exposure to nano-TiO2 may decrease Ca absorption and increase excretion, leading to a negative Ca balance, and a subsequent reduction in Ca levels in the embryo. Ossification of bone, whether osteogenesis or Ca deposition of endochondral ossification, is an important step in bone formation. Our data suggested that maternal nano-TiO2 exposure interfered with Ca metabolism in embryos (Ca reductions in maternal serum, placenta, and fetus), and thus affected ossification in the fetus. Nano-TiO2 may bind to proteins on the cell membrane, thereby changing membrane function and signal transduction resulting in toxicity. The effects of nano-TiO2 on bone Ca included two aspects: on one hand, the inhibition of bone Ca deposition may lead to the formation of a barrier in the ossification center during bone development;49 on the other hand, damage to osteoblasts and chondrocytes, and increased osteoclast activity may result in an increase in bone Ca dissolution.50,51 3) Nano-TiO2 reduced the levels of Zn in pregnant mice, placenta, and fetuses, which may also be an important aspect of nano-TiO2-induced toxicity. It has been shown that Zn is closely related to bone development, metabolism, and function during normal development of the embryo or fetus.52 Osteoblasts secrete organic substances, such as collagen and proteoglycan, which are called osteoids. Osteoblasts are gradually embedded by osteoids and become osteocytes. Serum phosphatase (AKP) is a marker of osteoblasts, and catalyzes the decomposition of phosphate compounds to produce free phosphates that combine with Ca in the intercellular substance to form Ca phosphate, which is involved in the regulation of calcification. AKP is a Zn-dependent enzyme. Zn can stabilize AKP conformation and maintain AKP activity. When Zn is deficient, the conformation and function of AKP are compromised. Epidemiological findings suggest that Zn deficiency delays growth and bone age in animals and humans; a severe lack of Zn in animals can cause skeletal deformities.53 Nano-TiO2 may play a direct role as a promoter of the metallothionein (MT) gene, and induce MT synthesis in maternal liver, kidney, and in placental trophoblast cells. MT rapidly combines with Zn2+, and then decreases the Zn concentration in maternal blood and impairs placental Zn2+ transport, which results in an insufficient supply of Zn to the embryo, leading to a slow ossification center or incomplete calcification of fetal bones. Exposure to nano-TiO2 has been demonstrated to increase MT level in fish and Daphnia.54,55 A previous study showed that exposure to Cd in pregnant rats caused significant reductions in maternal serum and fetal Zn levels.56 In addition, maternal Zn supplementation during pregnancy significantly decreased fetal malformations and growth retardation in mice caused by Cd.57 In the present study, the levels of Zn, Ca, and Ti in the maternal serum of control mice were determined by the contents of Zn, Ca, and Ti in the diet and drinking water, which were strictly controlled according to the standards of mouse rearing from the Animal Center of Soochow University (China) to meet the needs for growth and development of mice. These findings indicate that reductions of Ca and Zn in the maternal serum may be an important cause of nano-TiO2-induced growth retardation in fetal mice.

The placenta is an important link between the mother and the fetus, and has substance transport, barrier, and endocrine functions. In the current study, placental weight in the nano-TiO2-treated group was lower than that in the control group, suggesting that maternal nano-TiO2 exposure inhibited placental growth, which may be associated with decreases in the relative volume of placental villus space, the relative surface area of fetal capillaries, and the absolute volume of the placenta.58 Furthermore, our data suggested that nano-TiO2 content in the maternal blood was positively correlated with placental and fetal nano-TiO2 levels, and negatively correlated with placental and fetal weight. These findings indicate that placenta and embryo may be the second target organs of nano-TiO2 toxicity, and the abnormal development of placenta may be one of the causes of nano-TiO2-induced fetal growth retardation. Taken together, these findings demonstrate that consecutively maternal exposure to nano-TiO2 could suppress embryonic development in mice; however, the underlying molecular mechanism requires further study.

Conclusion

In this experimental study, exposure to nano-TiO2 in pregnant mice caused fetal growth retardation, which was associated with embryonic toxicity and bone toxicity due to nano-TiO2 accumulation in fetal mice. These effects may be due to the direct role or the indirect role of nano-TiO2 interfering with Ca, Zn, and other metabolic processes, or may be the result of a combination of several factors, which require further investigation in the future. Therefore, the use of nano-TiO2 and exposure to nano-TiO2, especially during pregnancy in humans, should be thoroughly investigated.

Acknowledgments

This work was supported by the National Natural Science Foundation of China (grant nos 31671033, 81473007, 81273036, and 30901218), the National Natural Science Foundation of Jiangsu Province (grant no BK20161306), and the Top-notch Academic Programs Project of Jiangsu Higher Education Institutions (PPZY2015A018).

Disclosure

The authors report no conflicts of interest in this work.


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