- Open Access
Effects of prenatal exposure to diesel exhaust particles on postnatal development, behavior, genotoxicity and inflammation in mice
© Hougaard et al; licensee BioMed Central Ltd. 2008
- Received: 13 July 2007
- Accepted: 11 March 2008
- Published: 11 March 2008
Results from epidemiological studies indicate that particulate air pollution constitutes a hazard for human health. Recent studies suggest that diesel exhaust possesses endocrine activity and therefore may affect reproductive outcome. This study in mice aimed to investigate whether exposure to diesel exhaust particles (DEP; NIST 2975) would affect gestation, postnatal development, activity, learning and memory, and biomarkers of transplacental toxicity. Pregnant mice (C57BL/6; BomTac) were exposed to 19 mg/m3 DEP (~1·106 particles/cm3; mass median diameter ≅ 240 nm) on gestational days 9–19, for 1 h/day.
Gestational parameters were similar in control and diesel groups. Shortly after birth, body weights of DEP offspring were slightly lower than in controls. This difference increased during lactation, so by weaning the DEP exposed offspring weighed significantly less than the control progeny. Only slight effects of exposure were observed on cognitive function in female DEP offspring and on biomarkers of exposure to particles or genotoxic substances.
In utero exposure to DEP decreased weight gain during lactation. Cognitive function and levels of biomarkers of exposure to particles or to genotoxic substances were generally similar in exposed and control offspring. The particle size and chemical composition of the DEP and differences in exposure methods (fresh, whole exhaust versus aged, resuspended DEP) may play a significant role on the biological effects observed in this compared to other studies.
- Diesel Engine
- Comet Assay
- Morris Water Maze
- Diesel Exhaust
- Prenatal Exposure
Results from epidemiological studies indicate that particulate air pollution constitutes a hazard for human health, by increasing the prevalence of e.g., cardiovascular and lung disease . Air pollution has also been associated with adverse reproductive outcomes in humans, although further studies are needed for most endpoints to confirm causal relationships and the role of different air pollutant sources .
Overview of animal studies with maternal inhalation exposure to whole diesel exhaust
Diesel particulate in air (mg/m 3 )
Exposure period (GD)
Maternal measures (n)
Offspring endpoints (n)
-inflammatory cytokines [↑0.3, 3.0]
Fetal weight [↓3.0]
Rate of abnormal fetuses
From four months before gestation to mating
Nest construction [↓all]
Weight, PND11 [♂↑0.3], 14, 21 [♀↓3.0], 28 [↓3.0], 35 [↓3.0], 42 [↓0.1, 3.0], 49 [↓0.1♂, 3.0], 56 [↓1.0, 3.0], 63 [↓1.0♀, 3.0], 70 [↓3.0]
Vaginal opening [↓0.3, 1.0]
Anogenital distance PND28 [♂↓0.3], 70 [♂↓3.0]
♀ Weights, PND28
♀ Weights, PND70
-thymus [↓0.3, 1.0]
♂ Weights, PND 70
-seminal vesicles [↓1.0]
Total placental weight
Total fetal weight
Bone morphogenetic protein 15[↓]
0.17 (Filtered, pore size estimated to 0.1–0.2 μm)
Weight, PND 96:
Daily sperm production [↓]
Sertoli cells [↓]
Spermatids/Sertoli cell [↓]
Filtered (pore size 0.05 μm)
90% < 0.5 μm
-placenta [↓, non-filtered]
-adrenal gland [↓, filtered]
Corpora lutea [smaller]
Estradiol [↓, filtered]
LH [↓, filtered]
Fetal weight [females↑]
Anogenital distance [↑]
Thymus weight [↓]
Testis differentiation [↓]
Ovary differentation [↓]
Thymus differentiation [↓]
Filtered (pore size 0.05 μm)
90% < 0.5 μm
(6–20, males only)
Weight PND 4, 49
Organ weights, PND 4, 49, 82:
-Testosterone, PND 4, 23 [↑]
-Estrogen, PND 4, 23
-four immunizations [↑]
~90% < 1 μ
~50% < 0.3 μ
Corpora luetea [↓]
~90% < 1 μ
~50% < 0.3 μ
(7–14, males only)
Weight, PND 28 [↑1.0, 3.0]
Organ weights, PND 28
-testes [↑1.0, 3.0]
-accessory glands [↑1.0, 3.0]
Weight, PND 8 [↓], 16(↓), 21(↓), 35 [↓], 84:
-seminal vesicle [↑, PND8+16]
Sperm counts [↓PND35+84]
Testis morphology [↑Multinucl. cells PND84]
Testosterone [↓PND21,(↓)PND35, ↑PND84]
-steroidogen acute regul protein [↑PND84]
-cytochrome P-450 side-chain cleavage
-cytochrome P-450 aromatase
The inhalation exposure was performed on a daily basis on 13 successive days for both DEP and control air, each organized in two groups. The DEP mass concentration was controlled by filter sampling and showed the mean mass concentration in the exposure chamber was 19.1 ± 1.13 (SEM) mg/m3DEP.
No clinical signs of toxicity were observed in the dams during the exposure period and the number of females presenting offspring was similar in the two groups. DEP females tended to gain more weight during gestation than did controls [DEP weight gain 14.73 ± 0.59 g (SEM) vs. weight gain in controls: 12.98 ± 0.66 g (SEM), p = 0.05], but lactational body weights and absolute and relative maternal organ weights at weaning were similar in control and DEP dams.
Inflammatory and genotoxic endpoints
Thyroid hormone analysis
In the Open field, there was a tendency towards increased activity in female DEP offspring [Control 9.77 ± 1.0 m (SEM) vs. DEP 13.5 ± 2.1 m (SEM), (p < 0.1)], whereas male offspring from the two groups behaved similarly [Control 14.9 ± 2.4 m (SEM) vs. DEP 15.5 ± 2.5 m (SEM)].
The present study assessed the effects of prenatal exposure to resuspended diesel exhaust particles on gestation, postnatal development, behavior, and biomarkers of prenatal exposure to particles and genotoxic substances. Cognitive function and selected biomarkers only differed slightly between prenatal exposure groups, whereas body weight gain differed between offspring from control and DEP exposed dams, particularly during the latter half of the nursing period. Thus, statistically body weight of DEP pups differed significantly from controls on the day of weaning and rate of weight gain was significantly reduced during the latter half of lactation, i.e. from PND 9 to PND 22.
Growth restriction is a common effect of chemical exposure, also when exposure occurs during fetal life. Thus, chemical exposure of the mother during gestation may be associated with prenatal growth restriction and thus reduced birth weight. When maternal exposure is discontinued at birth, group differences in birth weight may fade with time [17, 18]. In the present study, body weights of DEP offspring were slightly, but insignificantly, lower than weights of controls a few days after birth. This difference increased during lactation and body weight was especially affected during the latter part of the period, even if DEP exposure was terminated just prior to birth.
Other studies report effects of diesel exposure during perinatal life on perinatal growth, all using direct exposure to newly generated diesel exhaust (Table 1). Ono et al. observed statistically significantly decreased weight of offspring from ICR mice exposed continuously to whole diesel engine exhaust with 1.0 mg/m3 DEP during gestation day (GD) 2–16, compared to controls at PND 8 and 35 (body weights lower in DEP offspring by 16.4% and 9.5%, respectively). Weights were also lower at GD 16 (by 14.6%) and 21 (by 22.6%), although not significantly so . Since body weights were not recorded prior to PND 8, it is not possible to assess whether diesel exhaust exposure lowered offspring body weights already from birth. In another study, female C57B1 mice were exposed to diesel engine exhaust with 0.3, 1.0, or 3.0 mg/m3 DEP for 12 h/day for four months, terminated at initiation of mating. At the lowest dose levels, the body weights were increased in male diesel pups at PND 11 compared to controls, but no differences were observed later in life for this group. In the highest dose-group body weights were decreased from postnatal week 3 to 10, whereas the middle dose was associated with decreased body weights during postnatal week 6 to 9 . Male offspring from pregnant ICR mice exposed to diesel exhaust with 1.0 or 3.0 mg/m3 DEP 12 h/day during GD 2–16 exhibited increased body weights on PND 28, the only time point measured, but no effect was observed at 0.3 mg/m3 (no data for female offspring). Several studies have measured fetal weights in late gestation after prenatal exposure to whole diesel exhaust, and observed decreased , increased (females only ) or no effect [6, 20] on fetal weight in mice, rabbits or mice.
The report from Tsukue et al.  documents effects in the offspring even if exposure to diesel engine exhaust took place during the period preceding mating, indicating that exposure to diesel exhaust do not need to take place concurrently with fetal development for effects to appear . This is possibly owing to gradual release of chemicals attached to diesel particles deposited in maternal lungs, extending the period of internal exposure and thus of induction of effects beyond the period of dosing. Furthermore, substances may be secreted into milk. Pregnant rats were exposed to whole diesel exhaust on GD 7–20, or during the two last weeks of prenatal and two first weeks of postnatal life. Polycyclic aromatic hydrocarbons (PAHs) were measured in fetuses and maternal blood at GD 20, and in breast milk at PND 14. Exposure increased PAH levels in fetal tissues and maternal milk, indicating that PAHs from particles inhaled by the mother transfer to the offspring via the placenta and breast milk . If the effects of DEP are due to soluble compounds leaching from these particles, the blood levels of these compounds may even increase very slowly, and thus the biological effect may be delayed compared to the period of exposure . Finally, chemical substances transferred from mother to fetus may act as toxicants later in life, even if diesel particles were inhaled only during gestation ("programming") [22, 23].
Some chemical compounds have been shown to reduce levels of circulating thyroid hormones in developing animals. As a consequence postnatal growth diminishes, because thyroid hormone is a prerequisite for normal growth and development [24, 25]. This is for example the case for some polyhalogenated aromatic hydrocarbons [26, 27]. It was therefore possible, that toxic agents from the diesel particles had been secreted into maternal milk and ingested by the offspring, where the compounds interfered with the pituitary-thyroid axis and thereby growth, or prenatally transferred substances acted as thyrotoxicants during postnatal life . To pursue this hypothesis, thyroxine (T4), the dominating thyroid hormone, was measured in plasma from both dams and offspring. However, T4 was similar in exposed and control animals at weaning, the time of maximum observed difference in body weights between control and diesel litters. Thyroid disruption does therefore not seem to be involved in the postnatal growth restriction observed in the present study.
Some animal studies indicate that perinatal exposure to diesel exhaust restricts postnatal growth, whereas other studies report the opposite. Diesel exhaust is produced by the combustion of diesel fuel, which yields a complex mixture of compounds. Therefore the composition varies with fuel type, engine model and tuning, load, age of exhaust etc . In the present study, the animals were exposed to aged resuspended diesel engine exhaust particles that was collected in a bag-filter during operation of a heavy duty fork-lift, i.e. NIST SRM 2975. Most previous studies employed freshly generated diesel exhaust, also including gases, however from a range of different vehicle engines [4, 8, 9]. These different diesel exhaust sources and methods may result in very different physico-chemical exposures. First, the role of volatile species can only be tested by direct exposure to fresh diesel engine exhausts and aged DEP may contain much lower concentrations of semivolatile compounds than achieved by direct exposure due to thermal, chemical and light-induced degradation. Second, the particle size distribution of resuspended DEP is coarser than the DEP emitted directly from a diesel engine. Here we observe a concentration maximum at approximately 145 nm and a mass median diameter of approximately 240 nm. When measured in exhaust directly from a diesel engine, diesel soot particles form both primary particles of up to 40 nm in size and the more abundant agglomeration (accumulation mode) particles. The fresh DEP soot mode is generally below 100 nm in seize, and a peak number in concentration of the carbonaceous soot occurs at approximately 60 nm [29, 30]. Heavy duty diesel engines may show coarser size distributions than smaller engines. Kittelson et al. reported geometric volume mean diameters of around 125 nm for accumulation mode DEP particles . Such differences in size may result in different deposition and translocation efficiencies as well as different toxicological mechanisms. Third, the chemical composition of the pure DEP will vary as function of trace metals in the fuel, additives, and lubricating oils. These factors may result in a highly abundant formation of inorganic particles in DEP exhaust [30, 32] which is observed in ambient air . Engine wear and corrosion can also affect the composition of the DEP exhaust dramatically . Current analysis of the chemistry and water solubility of elements in SRM 2975 has shown that the total concentration of inorganic elements were in the order of only 0.3 wt%. Approximately 50 wt% of the elements were water soluble and dominated by Na, Mg, K, Ca, Si, P and Zn [Jensen, KA, in preparation]. The individual concentrations of other water-soluble well-known toxic trace elements were <30 ng/mg. The concentration of the 12 (phenanthrene to indeno(1,2,3-cd)pyrene) of the 16 US-EPA target PAHs were also relatively low making a total of 75.8 ± 6.3 ng/mg [35, 36]. For comparison, a typical driving cycle for heavy duty diesel engines results in approximately 40 wt% carbonaceous soot, 13 wt% ash and other, 14 wt% sulphate and water, as well as 7 and 25 wt% unburned fuel and oil, respectively . Docekal et al.  report 0.5 to 4 wt% in exhaust from a new diesel engine for passenger cars depending on engine load. It is evident that such differences in the exposure type offer a highly plausible explanation for the incongruent findings, i.e. different atmospheres exert different effects. It is crucial that these parameters are well-characterized in future DEP exposure studies to enable a future understanding of causal relationships between exposure and effects.
Besides the potential exposure, several other factors influence pup growth, alterations in growth may also be caused by e.g. changes in milk palatability, reduced milk availability, maternal behavior, or poor sucking ability in the pup . Cross fostering and/or observation of interactions between the dam and her pups may help elucidate whether the observed effect is in fact an indirect (maternal) effect or a direct consequence of the DEP exposure.
The genotoxic effects of particles can be particle- or inflammation driven due to either the chemical composition, surface properties of the particles themselves, or induction of an inflammatory response. These mechanisms may generate reactive oxygen and nitrogen species with genotoxic effects as the result . Both genotoxic and inflammatory effects of prenatal DEP exposure were pursued in the present study. DNA damage was evaluated by means of the comet assay, which is a sensitive and reliable method for detection of DNA strand breaks . Besides directly induced DNA strand breaks, also breaks that are transiently present during repair of DNA lesions such as oxidative DNA damage, will be detected. DNA damage was furthermore evaluated by mRNA expression of HO-1, which is expressed during oxidative stress, as well as OGG1 and ERCC1, which are genes expressed during DNA repair. Elevated expression levels of HO-1, OGG1, and ERCC1 have previously been demonstrated in adult rats and mice after DEP exposure, together with an increased level of DNA strand breaks when evaluated by the comet assay [41, 42]. DNA damage was not detected by the comet assay or by mRNA gene expression of defense genes in the present study, suggesting that DNA damage was not induced in the DEP exposed offspring. Prenatal exposure to DEP has previously been associated with genotoxic effects. An increased level of DNA deletions was observed in the offspring of mice orally exposed on day 10.5 to 15.5 of gestation to various doses of DEP (generated by a light-duty, four-cylinder passenger car) . However, the transplacental exposure did not cause oxidative DNA damage in the embryo tissue, which is consistent with the observed results in the present study. Low induction of DNA-damage is expected from the relatively low concentration of PAHs and transition metals in SRM 2975 . SRM 2975 also induce modest amounts of OH radicals (316 ± 148 nmol OH radical/mg) as compared to a tail-pipe deposit sample from a VW-1600 GTD (2,133 ± 1,393 nmol OH radical/mg) [Jensen, KA, in preparation]. Hence, the effects may be related to the carbonaceous core of DEP rather than the chemical compounds in this DEP sample. The inflammatory response in offspring exposed to DEP during fetal life was assessed by analyzing mRNA expression of the inflammatory cytokines IL-6, MCP-1, and MIP-2. Although insignificantly, the mean mRNA expression levels of inflammatory cytokines were slightly increased for these cytokines, indicating a tendency of inflammation. Increased mRNA expression levels of inflammatory cytokines have previously been observed in placentas of pregnant mice exposed to diesel exhaust by inhalation at similar concentrations . In this study, the mRNA expression level of IL-6 was elevated approximately 10-fold. Thus, in utero exposure to DEP may be associated with increased inflammation in the offspring as well.
Results from several in vivo studies indicate that diesel exhaust exerts hormone like activity [4, 7, 8, 11–13]. Because hormonally mediated events play a central role in the development and function of the central nervous system, it is possible that cognitive effects may arise from developmental exposure to endocrine disruptors . When cognitive function was tested in the Morris water maze, control and exposed offspring performed similarly in learning and memory tasks, but DEP exposed female offspring showed enhanced function during the first trial of the spatial reversal learning task. A similar, although statistically insignificant pattern was observed in male DEP offspring. Prenatal events may under some circumstances facilitate cognition . Thus, prenatal stress improved performance on the reversal task in the Morris water maze , a study of perinatal exposure to dieldrin reported facilitated retention of learning on a symmetrical maze , and prenatal dioxin exposure has been associated with enhanced cognitive function in several studies [46–48]. However, in the latter studies it was also observed that improvement of cognitive function was specific to the 8-arm radial maze . Further, the dioxin exposed rats showed deficits in a non-spatial learning task . It is therefore interesting that the only other published study of cognitive function after prenatal exposure to diesel exhaust reported reduced performance in the passive avoidance learning test in both male and female mice , indicating that also prenatal DEP may affect domains of cognitive function differentially.
In utero exposure to NIST SRM 2975 DEP affected weight gain during lactation. Cognitive function and levels of inflammatory and genotoxic responses were generally similar in exposed and control offspring. The particle size and chemical composition of the DEP and differences in exposure method may play a significant role on the biological effects observed. Of specific interest would be a comparative study of the effects of prenatal exposure to fresh exhaust versus resuspended particles.
time-mated, nulliparous, young adult mice (C57BL/6BomTac, Taconic Europe, Ejby, Denmark) were supplied at GD 3. The animals were, upon arrival, randomly distributed in groups of five and housed in white polypropylene (type III) cages with bedding (Lignocel S8) and enrichment (soft paper wool and small aspen wood blocks, Lillico), under controlled environmental conditions (12 hour light-dark cycles with light starting at 6.00 a.m., temperature 21 ± 2°C, humidity 50 ± 5%, ventilation 13 air changes per hour). Food (Altromin 1324) and tap water were provided ad libitum. The day after arrival, i.e. GD 4, the animals were weighed and assigned to two groups of 20 animals each, with similar weight distributions.
The animal welfare committee, appointed by the Danish Ministry of Justice, granted ethical permission for the studies. All procedures were carried out in compliance with the EC Directive 86/609/EEC and with the Danish law regulating experiments on animals (permission 2006/561-1123).
The diesel exhaust particles were Standard Reference Material 2975 from the National Institute of Standards and Technology (NIST, Gaithersburg, MD, USA). The specific surface area was 90 mg2/g, as determined by multipoint (Brunauer, Emmett, and Teller) nitrogen adsorption (Micromeritics, Gemini 2375), corresponding well to the reported specific area of 90 mg2/g, reported by NIST. Pycnometric particle density was 2.1 g/cm3, measured by an AccuPyc 1330 (Micromeritics). Detailed chemical characterization has recently been conducted by e.g.,  and [Jensen, KA, in preparation].
Exposure to DEP was performed in an 18 L inhalation chamber with walls of glass and stainless steel. The airflow in the chamber was dynamic with a flow of 20 L/min and the exposure atmosphere was evenly distributed, with a slightly negative inside pressure. The particles were delivered with a microfeeder and were aerosolized with a dispersion nozzle at a pressure of 5 bar (Frauenhofer Institute für Toxicologie und Aerosolforschung, Germany).
The two groups of mice were exposed to either filtered clean air or approximately 20 mg DEP/m3 on GDs 7–19 for one hour/day. The dose level and exposure period were chosen as not to induce marked maternal toxicity or pup mortality based on published studies of developmental toxicity of diesel exhaust [4, 5, 7]. Results from previous studies in our laboratory confirm that this mode of DEP exposure is associated with detectable effects in adult mice [42, 50, 51]. In observation hereof and to minimize the use of pregnant animals, in addition to the concurrent control group, non-DEP positive control exposures of pregnant mice were not performed.
Exposure took place between 7.30 am and 2.30 p.m. During exposure, the animals were placed singly in the rooms of a cylindrical wire mesh cage (diameter 29 cm, height 9 cm) with radical partitions, holding ten mice at a time ("ten-room-pie"). The females were observed during exposure for signs of toxicity and returned to their cages less than 10 minutes after the end of the one hour exposure period. Body weight was recorded on GD 4, and before exposure on GD 5, 7, 10, 14, 18, and 19.
The DEP mass concentration was controlled by filter sampling and adjusted to maintain an exposure of ~20 mg/m3 total suspended particles. Particle samples were collected at 2 L/min using Millipore cassettes mounted with Millipore Fluoropore filter (φ = 2.5 cm; pore size = 0.45 μm). Each sample was collected for 4 minutes, and weighed using a Sartorius Microscale (Type M3P 000V001) [42, 50]. Before sampling, the filters were equilibrated in an air-conditioned weighing room at 50%RH and 20°C and pre-weighed. After exposure, the gravimetric data were controlled after at least 24 hours re-equilibration in the air-conditioned weighing room.
The fine particle exposure (< 600 nm) was monitored using a GRIMM Sequential (Stepping) Mobility Particle Sizer (SMPS) consisting of a Long Electrostatic Classifier (Model No. 5.521; Serial No. 5LP 10209) connected to a GRIMM Condensation Particle Counter (Model 5.400). The SMPS data sampling and calculations were completed using the GRIMM software 5.477/02 v. 1.34 and operated in the fast scan mode, which allows a full size distribution analysis from 9.8 to 874.8 nm within 3 min and 38 sec. Data were corrected for both Classifier and CPC efficiency using the available software options. Particles were neutralized using a 3.7 MBq Am-241 source (Model No. 5.521). To avoid particle overloading in the SMPS, two impactors with nominal d50 cut-points of 1,185 and 805 nm were mounted externally and internally at the DMA inlet and thoroughly cleaned after each round of exposure. At the measured DEP density (2.1 g/cm3), the lower impactor stage has a d50 at 532 nm. Therefore SMPS data for Dp > 500 nm were excluded in the subsequent data analysis. Similarly particle sizes below the Dp midpoint 12.8 nm midpoint were excluded owing to excess electrical noise during fast scan operation. Coarse particle exposure (0.75 to > 15 μm) was measured using a GRIMM Dust Monitor (Model 1.105) at a resolution of 6 sec. The Dust Monitor particle sizes were subsequently recalculated to geometric means assuming an upper channel cut-point at 20 μm.
Parturition and lactation
After termination of exposure on GD 19, the females were housed alone and were monitored for birth each day, early in the light cycle. The expected day of delivery, GD 20, was designated PND 0 for the pups. Weights of dams and individual pups were recorded on PND 2 and the pups were counted and sexed. On this day one pup with median body weight was removed from litters with at least 5 pups, and the lungs and liver were dissected, weighed, and snap frozen in cryotubes (NUNC) in liquid N2. Pup weights were also recorded on PND 9 and at weaning on PND 22. At weaning, one male and one female with median body weights from each litter were kept for behavioral testing and housed in groups of 5 to 6 mice of the same gender and prenatal exposure status. Thus, the same male and female from each litter took part in all behavioral testing. One male from each litter was allocated to other studies. The females who had not given birth, the dams, and remaining offspring were anaesthetized with a mixture of 1.5 mg/kg hypnorm (Jannsen) and 1.5 mg/kg dormico (Roche) and sacrificed by exanguination (withdrawal of heart blood) on PND 23 or 24. Blood from dams and offspring was stabilized in 72 μL respectively 30 μL 0.17 mol/L K2EDTA and kept on ice until centrifugation (2200 RCF at 4°C for 5 min) within 60 min of collection. The number of uterine implantation sites was determined in the dams, and the thymus, lungs, liver, and spleen were dissected, weighed, and snap frozen in cryotubes (NUNC) in liquid N2. All samples were stored at -80°C until analysis.
Total RNA was purified from liver tissue from two day old mouse pups and DNAse treated by SV Total RNA Isolation System (Promega) as described by the manufacturer. cDNA was synthesized from the RNA using TaqMan® Reverse Transcription Reagents (Applied Biosystems) as described by the manufacturer. mRNA levels of IL-6, MCP-1, MIP-2, HO-1, OGG1, and ERCC1 were quantified by real-time RT-PCR with 18S as a reference gene. For IL-6, MCP-1, and 18S RNA TaqMan predeveloped reaction kits (Applied Biosystems) were applied. For MIP-2, HO-1, OGG1, and ERCC1 probes and primers were designed as described previously for MIP-2  and for HO-1, OGG1, and ERCC1 . The final concentrations of these primers and probes were optimized to concentrations between 100 and 400 nm. mRNA levels of different genes were quantified in separate wells. In all assays, TaqMan® Universal PCR Master Mix from Applied Biosystems was used. Each sample was run in triplicate on the ABI Prism 7300 Sequence Detector System. The target genes were normalized to 18S rRNA by subtracting the threshold cycle (Ct) for 18S (Ct, reference) from the Ct value of the target gene (Ct, target): ΔCt = Ct, target - Ct, reference. The relative expression of the target gene was calculated as 2-ΔCt. The standard deviation of the triplicates was below 15%. Positive and negative mRNA controls were included in each run in the mRNA measurements and the assays were validated to be linear over a 100 fold dilution. Repeated measurements of the same sample (the control) in separate experiments were not allowed to differentiate with more than 30% from the average. If the 18S content fell outside the range in which the PCR had been found to be quantitative, the measurements were excluded.
The Comet assay
DNA strand breaks in liver of pups sacrificed on PND 2 were determined by the Comet assay as previously described in  with minor modifications . Briefly, prepared liver cells are embedded in agarose on a glass microscope slide and lyzed to remove proteins and lipids. During alkaline electrophoresis, pieces of DNA migrate away from the nucleus towards the anode to produce a shape similar to a comet. After staining, the DNA remnants are visualized by fluorescent microscopy. As the smallest DNA strands move fastest, it is possible to evaluate the degree of DNA damage. The level of DNA damage was evaluated by measurements of tail length in 50 randomly selected nuclei from each subject. H2O2 exposed and unexposed A549 cells were included as an internal control of the comet assay.
Total T4 concentrations were analyzed in plasma from dams and offspring at weaning using a modified Delfia T4 Time-resolved fluoroimmunoassay (cat.no. 1244-030, Perkin Elmer, Wallac Oy, Turku, Finland). Instead of the T4 standards and the T4 antibody supplied in the Delfia T4 kit, T4 standards in T4-free rat serum (30041), as well as biotinylated T4 antibody (30039) from Biovian Ltd., Finland were used. The assay was run as outlined in the protocol supplied by Biovian Ltd. using streptavidin microtitration strips 8 × 12 wells (4009-0010) and T4 assay buffer (1244-111) from Perkin Elmer.
Postweaning growth and behavioral testing
All investigations were performed during the animals' light cycle, i.e. between 8.00 a.m. and 4.30 p.m. From PND 3, the experimenter was kept unaware as to which group an individual mouse belonged. The same observer was used in any one test. Exposed and control animals were tested alternately. Female and male animals were tested during different weeks. After weaning, the pups were weighed once every month until termination of behavioral tests (19 weeks).
Learning and memory (Morris water maze)
One female and one male per litter were tested. Females were tested at 12 and 16 weeks of age, males at age 13 and 17 weeks as described earlier  with minor modifications. The maze consisted of a circular white plastic pool, with a diameter of 100 cm and a height of 45 cm. The pool was surrounded by many external cues (wall lights, wall decorations of geometric figures in black plastic foil etc.), which were visible from within the pool and could be used by the mouse for spatial orientation. The pool was filled to a depth of 27 cm with water at room temperature. Four points on the rim of the pool, N, E, S and W (not true magnetic directions), were used as starting points and divided the pool into four arbitrary quadrants. A circular transparent platform (diameter 10 cm) was situated on a solid support and submerged 1 cm below the water surface, and thus invisible from water level.
The animals were tested in four daily trials using the four starting points assigned in a pseudo-random sequence. One standard-cage with 5–6 animals was placed near the pool. In each trial, the mouse was gently placed in the water facing the wall at the designated starting position. When the mouse swam to and climbed onto the platform, the trial was completed. If the animal failed to locate the platform within 60 sec, it was led to the platform. All animals were left to sit on the platform for 15 sec, before it was returned to the cage. The latency to reach the platform was measured by stopwatch.
The following scheme was used:
With the platform situated at the center of SW quadrant, the animals were trained until a stable performance was established, i.e. 4 trials for 5 consecutive days.
Three weeks after the learning period, the animals were tested again with the platform still in the SW quadrant of the pool. The animals were given 4 trials on each of 3 consecutive days.
New platform position I (reversal learning)
The day after the memory test, the animals were tested in a reversal procedure with the platform placed opposite the original location, i.e. in the center of the NE quadrant. The animals were tested for 4 trials.
New platform position II (new learning)
The following day, the platform was moved to the center of the pool, and the animals were tested for 4 trials.
Activity (open field)
One female and one male per litter were observed for a 3-min period in circular open field, i.e. the white pool used for learning and memory. The females were tested at the age of 14 weeks and the males at the age of 15 weeks. The mice started each trial in the center of the field, and the location of the animal in the field was registered in real-time with a device developed in our laboratory using contrast-sensitive computer controlled video tracking . The number defecations in the 3-minute observation period were recorded manually. The video-tracking device calculated the total distance the animal moved.
The accepted level of significance was 0.05 and the litter was considered the statistical unit. Post-weaning, one male and one female per litter were evaluated under each test condition and the resulting data analyzed separately. Gestational parameters, mRNA levels of IL-6, MCP-1, MIP-2, and data from the Open field test were analyzed by the Mann-Whitney U-test. The remaining data were analyzed by analyses of variance (ANOVA), when relevant with repeated measures in trials or days (ANOVA). Analyses of co-variance (ANCOVA) were used to test the differences between the groups in lactational weight gain, birth weights, and pre-weaning pup weights while controlling for litter size. ANCOVA was also applied for the post hoc analyses for this endpoint. Analyses were performed in SYSTAT Software Package version 9 and MINITAB 14.
We thank Michael Guldbrandsen and Gitte B. Christiansen for taking good care of the animals and conducting the behavioral tests with great skill, Lourdes Petersen and Birgitte Korsholm are acknowledged for skilled lab instructions. We highly appreciate the assistance from Signe. H. Nielsen for performing the filter weighing and Tina T. Olsen for data transfer and careful quality control the SMPS and Dust Monitor data.
The study and the contributions by technicians and KSH, KAJ, PN, UV, ATS and HW were funded through the Danish Research Council (Air Pollution in a Life Time Health Perspective (AIRPOLIFE), grant no. 2052-03-0016). CT's contributions were supplemented by the National Food Institute.
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