Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 37
Filter
1.
J Epidemiol ; 32(5): 228-236, 2022 05 05.
Article in English | MEDLINE | ID: mdl-33390465

ABSTRACT

BACKGROUND: The Japan Environment and Children's Study (JECS) is a nationwide birth cohort study investigating environmental effects on children's health and development. A Sub-Cohort Study has begun, conducting extended exposure and outcome measurements by targeting a subgroup randomly selected from the JECS Main Study. We report the Sub-Cohort Study methodology and participants' baseline profiles. METHODS: Of 100,148 children in the JECS Main Study, children born after April 1, 2013 who met eligibility criteria ([1] all questionnaire and medical record data from children and their mothers collected from the first trimester to 6 months of age, [2] biospecimens [except umbilical cord blood] from children and their mothers collected at first to second/third trimester and delivery) were randomly selected for each Regional Centre at regular intervals. Face-to-face assessment of neuropsychiatric development, body measurement, paediatrician's examination, blood/urine collection for clinical testing and chemical analysis, and home visits (ambient and indoor air measurement and dust collection) are conducted. Participants are followed up at 1.5 and 3 years old for home visits, and 2, 4, 6, and 8 years old for developmental/medical examination. The details of protocols after age 10 are under discussion. RESULTS: Of 10,302 selected children, 5,017 participated. The profiles of the participating mothers, fathers and children did not substantially differ between the Main Study and Sub-Cohort Study. CONCLUSION: The JECS Sub-Cohort Study offers a platform for investigating associations between environmental exposure and outcomes.


Subject(s)
Child Health , Environmental Exposure , Child , Child, Preschool , Cohort Studies , Female , Humans , Infant , Japan , Mothers
2.
Br J Nutr ; 121(1): 100-108, 2019 01.
Article in English | MEDLINE | ID: mdl-30370875

ABSTRACT

Current evidence suggests that the aetiology of congenital gastrointestinal (GI) tract atresia is multifactorial, and not based solely on genetic factors. However, there are no established modifiable risk factors for congenital GI tract atresia. We used data from a Japanese nationwide birth cohort study launched in 2011, and examined whether fish consumption in early pregnancy was associated with congenital GI tract atresia. We analysed data of 89 495 women (mean age at delivery=31·2 years) who delivered singleton live births without chromosomal anomalies. Based on the results of the FFQ, we estimated the daily intake of fish and n-3 PUFA consumption in early pregnancy. We defined a composite outcome (oesophageal atresia, duodenal atresia, jejunoileal atresia and/or anorectal malformation) as congenital GI tract atresia. In this population, median fish intake was 31·9 g/d, and seventy-four cases of congenital GI tract atresia were identified. Fish consumption in early pregnancy was inversely associated with the composite outcome (multivariable-adjusted OR for the high v. low consumption category=0·5, 95 % CI 0·3, 1·0). For all the specific types of atresia, decreased OR were observed in the high consumption category, although not statistically significant. Reduced atresia occurrence was observed even beyond the US Food and Drug Administration's recommended consumption of no more than 340 g/week. Also, n-3 PUFA-rich fish and n-3 PUFA consumptions tended to be inversely associated with atresia. Fish consumption in early pregnancy may be a preventive factor for congenital GI tract atresia.


Subject(s)
Diet , Fatty Acids, Omega-3/administration & dosage , Fishes , Intestinal Atresia/epidemiology , Intestinal Atresia/prevention & control , Maternal Nutritional Physiological Phenomena , Adult , Animals , Anorectal Malformations/epidemiology , Anorectal Malformations/prevention & control , Female , Gestational Age , Humans , Japan/epidemiology , Odds Ratio , Pregnancy
3.
Urology ; 124: 229-236, 2019 02.
Article in English | MEDLINE | ID: mdl-30447265

ABSTRACT

OBJECTIVE: To explore the association between isoflavone intake in early pregnancy (the critical window of masculinisation) and hypospadias. Since oestrogen is likely to contribute to the differentiation of male external genitalia, dietary intake of isoflavone, which has a similar structure to human oestrogen, may be associated with the occurrence of hypospadias. However, there has been little evidence of this association. MATERIALS AND METHODS: We used data of a nationwide birth cohort study, which recruited women as early in pregnancy as possible throughout Japan between 2011 and 2014. From the response to a self-administered food-frequency questionnaire, the daily intake of genistein (as a representative for isoflavone) was estimated. Information on hypospadias cases that were diagnosed until the first month after birth was obtained from medical records. Odds ratios (ORs) of hypospadias were estimated using a logistic regression model. RESULTS: Among 41,578 mothers, who delivered singleton live male births, the median genistein intake was 15.3 mg/day, and a total of 51 cases of hypospadias were identified. Compared with mothers in the reference group (genistein intake 11th-89th percentiles), those in the low intake group (≤10th percentile) had an elevated risk of their sons having hypospadias (multivariable-adjusted OR = 2.8, 95% confidence interval = 1.4-5.8). Adverse or beneficial effects of genistein on hypospadias were not observed in the high intake group (≥90th percentile) (OR = 0.9, 95% confidence interval = 0.4-2.4). CONCLUSION: Low maternal intake of isoflavone in early pregnancy was associated with an elevated risk of hypospadias.


Subject(s)
Hypospadias/chemically induced , Isoflavones/adverse effects , Adult , Cohort Studies , Female , Humans , Hypospadias/epidemiology , Infant, Newborn , Japan/epidemiology , Male , Pregnancy
4.
Environ Health Prev Med ; 23(1): 45, 2018 Sep 15.
Article in English | MEDLINE | ID: mdl-30219031

ABSTRACT

BACKGROUND: The Japan Environment and Children's Study (JECS) is a nation-wide birth cohort study investigating environmental effects on children's health and development. In this study, the exposure characteristics of the JECS participating mothers were summarized using two questionnaires administered during pregnancy. METHODS: Women were recruited during the early period of their pregnancy. We intended to administer the questionnaire during the first trimester (MT1) and the second/third trimester (MT2). The total number of registered pregnancies was 103,099. RESULTS: The response rates of the MT1 and MT2 questionnaires were 96.8% and 95.1%, respectively. The mean gestational ages (SDs) at the time of the MT1 and MT2 questionnaire responses were 16.4 (8.0) and 27.9 (6.5) weeks, respectively. The frequency of participants who reported "lifting something weighing more than 20 kg" during pregnancy was 5.3% for MT1 and 3.9% for MT2. The Cohen kappa scores ranged from 0.07 to 0.54 (median 0.31) about the occupational chemical use between MT1 and MT2 questionnaires. Most of the participants (80%) lived in either wooden detached houses or steel-frame collective housing. More than half of the questionnaire respondents answered that they had "mold growing somewhere in the house". Insect repellents and insecticides were used widely in households: about 60% used "moth repellent for clothes in the closet," whereas 32% applied "spray insecticide indoors" or "mosquito coil or an electric mosquito repellent mat." CONCLUSIONS: We summarized the exposure characteristics of the JECS participants using two maternal questionnaires during pregnancy.


Subject(s)
Child Health , Maternal Exposure/statistics & numerical data , Surveys and Questionnaires , Adult , Cohort Studies , Female , Gestational Age , Humans , Japan , Mothers/statistics & numerical data , Pregnancy , Young Adult
5.
J Epidemiol ; 28(2): 99-104, 2018 02 05.
Article in English | MEDLINE | ID: mdl-29093304

ABSTRACT

BACKGROUND: The Japan Environment and Children's Study (JECS), known as Ecochil-Chosa in Japan, is a nationwide birth cohort study investigating the environmental factors that might affect children's health and development. We report the baseline profiles of the participating mothers, fathers, and their children. METHODS: Fifteen Regional Centres located throughout Japan were responsible for recruiting women in early pregnancy living in their respective recruitment areas. Self-administered questionnaires and medical records were used to obtain such information as demographic factors, lifestyle, socioeconomic status, environmental exposure, medical history, and delivery information. In the period up to delivery, we collected bio-specimens, including blood, urine, hair, and umbilical cord blood. Fathers were also recruited, when accessible, and asked to fill in a questionnaire and to provide blood samples. RESULTS: The total number of pregnancies resulting in delivery was 100,778, of which 51,402 (51.0%) involved program participation by male partners. Discounting pregnancies by the same woman, the study included 95,248 unique mothers and 49,189 unique fathers. The 100,778 pregnancies involved a total of 101,779 fetuses and resulted in 100,148 live births. The coverage of children in 2013 (the number of live births registered in JECS divided by the number of all live births within the study areas) was approximately 45%. Nevertheless, the data on the characteristics of the mothers and children we studied showed marked similarity to those obtained from Japan's 2013 Vital Statistics Survey. CONCLUSIONS: Between 2011 and 2014, we established one of the largest birth cohorts in the world.


Subject(s)
Child Health , Environmental Exposure , Fathers/statistics & numerical data , Mothers/statistics & numerical data , Adult , Cohort Studies , Environmental Exposure/adverse effects , Female , Humans , Infant, Newborn , Japan , Male , Pregnancy , Socioeconomic Factors , Surveys and Questionnaires , Young Adult
6.
J Epidemiol ; 25(6): 452-8, 2015.
Article in English | MEDLINE | ID: mdl-25912098

ABSTRACT

BACKGROUND: The Japan Environment and Children's Study (JECS) is an ongoing nationwide birth cohort study launched in January 2011. In this progress report, we present data collected in the first year to summarize selected maternal and infant characteristics. METHODS: In the 15 Regional Centers located throughout Japan, the expectant mothers were recruited in early pregnancy at obstetric facilities and/or at local government offices issuing pregnancy journals. Self-administered questionnaires were distributed to the women during their first trimester and then again during the second or third trimester to obtain information on demographic factors, physical and mental health, lifestyle, occupation, environmental exposure, dwelling conditions, and socioeconomic status. Information was obtained from medical records in the first trimester and after delivery on medical history, including gravidity and related complications, parity, maternal anthropometry, and infant physical examinations. RESULTS: We collected data on a total of 9819 expectant mothers (mean age = 31.0 years) who gave birth during 2011. There were 9635 live births. The selected infant characteristics (singleton births, gestational age at birth, sex, birth weight) in the JECS population were similar to those in national survey data on the Japanese general population. CONCLUSIONS: Our final birth data will eventually be used to evaluate the national representativeness of the JECS population. We hope the JECS will provide valuable information on the impact of the environment in which our children live on their health and development.


Subject(s)
Congenital Abnormalities/epidemiology , Environmental Health , Environmental Pollutants/toxicity , Infant Welfare , Adult , Cohort Studies , Congenital Abnormalities/etiology , Environmental Exposure/adverse effects , Female , Humans , Infant, Newborn , Japan/epidemiology , Male , Maternal Exposure/adverse effects , Pregnancy , Young Adult
7.
Neurotoxicology ; 33(5): 1375-80, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22981892

ABSTRACT

Thalidomide is increasingly used in anticancer and anti-inflammation therapies. However, it is known for its teratogenicity and ability to induce peripheral neuropathy, although the mechanisms underlying its neurological effect in humans are unclear. In this study, we investigated the effect of thalidomide on the metabolism and neuronal differentiation of human neural progenitor cells. We found that levels of tyrosine, phenylalanine, methionine and glutathione, which are involved in dopamine and methionine metabolism, were decreased following thalidomide treatment. Morphological analysis revealed that treatment with 100 nM thalidomide, which is much lower than clinical doses, significantly decreased the number of dopaminergic (tyrosine hydroxylase-positive) neurons, compared with control cells. Our results suggest that these adverse neurological effects of thalidomide should be taken into consideration prior to its use for the treatment of neurodegenerative and other diseases.


Subject(s)
Cell Differentiation/drug effects , Dopaminergic Neurons , Embryonic Stem Cells/drug effects , Immunosuppressive Agents/pharmacology , Thalidomide/pharmacology , Amino Acids/metabolism , Capillary Electrochromatography , Cell Line , Dopaminergic Neurons/cytology , Dopaminergic Neurons/drug effects , Dopaminergic Neurons/metabolism , Dose-Response Relationship, Drug , Glutathione/metabolism , Humans , Microtubule-Associated Proteins/metabolism , Principal Component Analysis , Tandem Mass Spectrometry , Tyrosine 3-Monooxygenase/metabolism
8.
J Hum Genet ; 57(7): 434-41, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22648180

ABSTRACT

We hypothesized that single-nucleotide polymorphisms (SNPs) of genes involved in environmental endocrine disruptors (EEDs) metabolism might influence the risk of male genital malformations. In this study, we explored for association between 384 SNPs in 15 genes (AHR, AHRR, ARNT, ARNT2, NR1I2, RXRA, RXRB, RXRG, CYP1A1, CYP1A2, CYP1B1, CYP2B6, CYP3A4, CYP17A1 and CYP19A1) and risk of cryptorchidism (CO) and hypospadias (HS) in 334 Japanese (JPN) males (141 controls, 95 CO and 98 HS) and 187 Italian (ITA) males (129 controls and 58 CO). In the JPN study group, five SNPs from ARNT2 (rs2278705 and rs5000770), CYP1A2 (rs2069521), CYP17A1 (rs4919686) and NR1I2 (rs2472680) were significantly associated at both allelic and genotypic levels with risk of at least one genital malformation phenotype. In the ITA study group, two SNPs in AHR (rs3757824) and ARNT2 (rs1020397) were significantly associated with risk of CO. Interaction analysis of the positive SNPs using multifactor dimensionality reduction demonstrated that synergistic interaction between rs2472680, rs4919686 and rs5000770 had 62.81% prediction accuracy for CO (P=0.011) and that between rs2069521 and rs2278705 had 69.98% prediction accuracy for HS (P=0.001) in JPN population. In a combined analysis of JPN and ITA population, the most significant multi-locus association was observed between rs5000770 and rs3757824, which had 65.70% prediction accuracy for CO (P=0.055). Our findings indicate that genetic polymorphisms in genes involved in EED metabolism are associated with risk of CO and HS.


Subject(s)
Cryptorchidism/genetics , Endocrine Disruptors/metabolism , Gene-Environment Interaction , Hypospadias/genetics , Adolescent , Aryl Hydrocarbon Receptor Nuclear Translocator/genetics , Aryl Hydrocarbon Receptor Nuclear Translocator/metabolism , Asian People/genetics , Basic Helix-Loop-Helix Transcription Factors/genetics , Basic Helix-Loop-Helix Transcription Factors/metabolism , Case-Control Studies , Child , Child, Preschool , Cryptorchidism/epidemiology , Cytochrome P-450 CYP1A2/genetics , Cytochrome P-450 CYP1A2/metabolism , Estrogen Receptor alpha/genetics , Estrogen Receptor alpha/metabolism , Gene Frequency , Genetics, Population , Humans , Hypospadias/epidemiology , Infant , Italy , Japan , Male , Polymorphism, Single Nucleotide , Risk Factors , Steroid 17-alpha-Hydroxylase/genetics , Steroid 17-alpha-Hydroxylase/metabolism , White People/genetics
9.
PLoS One ; 7(5): e36711, 2012.
Article in English | MEDLINE | ID: mdl-22574217

ABSTRACT

BACKGROUND/PURPOSE: The effect of low-dose bisphenol A (BPA) exposure on human reproductive health is still controversial. To better understand the molecular basis of the effect of BPA on human reproductive health, a genome-wide screen was performed using human foreskin fibroblast cells (hFFCs) derived from child hypospadias (HS) patients to identify novel targets of low-dose BPA exposure. METHODOLOGY/PRINCIPAL FINDINGS: Gene expression profiles of hFFCs were measured after exposure to 10 nM BPA, 0.01 nM 17ß-estradiol (E2) or 1 nM 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) for 24 h. Differentially expressed genes were identified using an unpaired Student's t test with P value cut off at 0.05 and fold change of more than 1.2. These genes were selected for network generation and pathway analysis using Ingenuity Pathways Analysis, Pathway Express and KegArray. Seventy-one genes (42 downregulated and 29 upregulated) were identified as significantly differentially expressed in response to BPA, among which 43 genes were found to be affected exclusively by BPA compared with E2 and TCDD. Of particular interest, real-time PCR analysis revealed that the expression of matrix metallopeptidase 11 (MMP11), a well-known effector of development and normal physiology, was found to be inhibited by BPA (0.47-fold and 0.37-fold at 10 nM and 100 nM, respectively). Furthermore, study of hFFCs derived from HS and cryptorchidism (CO) patients (n = 23 and 11, respectively) indicated that MMP11 expression was significantly lower in the HS group than in the CO group (0.25-fold, P = 0.0027). CONCLUSIONS/SIGNIFICANCE: This present study suggests that an involvement of BPA in the etiology of HS might be associated with the downregulation of MMP11. Further study to elucidate the function of the novel target genes identified in this study during genital tubercle development might increase our knowledge of the effects of low-dose BPA exposure on human reproductive health.


Subject(s)
Environmental Pollutants/pharmacology , Fibroblasts/drug effects , Fibroblasts/metabolism , Foreskin/pathology , Hypospadias/pathology , Phenols/pharmacology , Benzhydryl Compounds , Child, Preschool , Dose-Response Relationship, Drug , Estradiol/pharmacology , Fibroblasts/pathology , Genomics , Humans , Male , Matrix Metalloproteinase 11/genetics , Polychlorinated Dibenzodioxins/pharmacology , Receptors, Aryl Hydrocarbon/metabolism , Receptors, Estrogen/metabolism , Reproducibility of Results , Reproduction/drug effects , Signal Transduction/drug effects , Transcriptome/drug effects
10.
Risk Anal ; 32(9): 1595-604, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22384860

ABSTRACT

Lack of data on daily inhalation rate and activity of children has been an issue in health risk assessment of air pollutants. This study aimed to obtain the daily inhalation rate and intensity and frequency of physical activity in relation to the environment in Japanese preschool children. Children aged four-six years (n= 138) in the suburbs of Tokyo participated in this study, which involved three days' continuous monitoring of physical activity using a tri-axial accelerometer and parent's completion of a time/location diary during daily life. The estimated three-day mean daily inhalation rate (body temperature, pressure, saturated with water vapor) was 9.9 ± 1.6 m(3) /day (0.52 ± 0.09 m(3) /kg/day). The current daily inhalation rate value of 0.580 m(3) /kg/day proposed for use in health risk assessment in Japan is confirmed to be valid to calculate central value of inhaled dose of air pollutants in five- to six-year-old children. However, the 95th percentile daily inhalation rate of 0.83 m(3) /kg/day based on measurement for five-year-old children is recommended to be used to provide an upper bound estimate of exposure that ensure the protection of all five- to six-year-old children from the health risk of air pollutants. Children spent the majority of their time in sedentary and light level of physical activity (LPA) when indoors, while 85% of their time when outdoors was spent in LPA and moderate-to-vigorous physical activity. The results suggest the need to consider variability of minute respiratory ventilation rate according to the environment for more refined short-term health risk assessment.


Subject(s)
Air Pollution , Inhalation Exposure , Child , Child, Preschool , Female , Humans , Japan , Male , Motor Activity
11.
PLoS One ; 7(12): e52756, 2012.
Article in English | MEDLINE | ID: mdl-23285176

ABSTRACT

BACKGROUND/PURPOSE: We hypothesized that polymorphic differences among individuals might cause variations in the effect that environmental endocrine disruptors (EEDs) have on male genital malformations (MGMs). In this study, individual variation in the genetic response to low-dose bisphenol A (BPA) was investigated in human foreskin fibroblast cells (hFFCs) derived from child cryptorchidism (CO) and hypospadias (HS) patients. METHODOLOGY/PRINCIPAL FINDINGS: hFFCs were collected from control children without MGMs (n=5) and child CO and HS patients (n=8 and 21, respectively). BPA exposure (10 nM) was found to inhibit matrix metalloproteinase-11 (MMP11) expression in the HS group (0.74-fold, P=0.0034) but not in the control group (0.93-fold, P=0.84) and CO group (0.94-fold, P=0.70). Significantly lower levels of MMP11 expression were observed in the HS group compared with the control group (0.80-fold, P=0.0088) and CO group (0.79-fold, P=0.039) in response to 10 nM BPA. The effect of single-nucleotide polymorphism rs5000770 (G>A), located within the aryl hydrocarbon receptor nuclear translocator 2 (ARNT2) locus, on individual sensitivity to low-dose BPA was investigated in the HS group. A significant difference in neurotensin receptor 1 (NTSR1) expression in response to 10 nM BPA was observed between AA and AG/GG groups (n=6 and 15, respectively. P=0.031). However, no significant difference in ARNT2 expression was observed (P=0.18). CONCLUSIONS/SIGNIFICANCE: This study advances our understanding of the specificity of low-dose BPA effects on human reproductive health. Our results suggest that genetic variability among individuals affects susceptibility to the effects of EEDs exposure as a potential cause of HS.


Subject(s)
Benzhydryl Compounds/adverse effects , Cryptorchidism/genetics , Endocrine Disruptors/adverse effects , Fibroblasts/drug effects , Fibroblasts/metabolism , Foreskin/cytology , Hypospadias/genetics , Phenols/adverse effects , Alternative Splicing , Aryl Hydrocarbon Receptor Nuclear Translocator/genetics , Basic Helix-Loop-Helix Transcription Factors/genetics , Benzhydryl Compounds/administration & dosage , Cells, Cultured , Cryptorchidism/etiology , Endocrine Disruptors/administration & dosage , Environmental Exposure/adverse effects , Gene Order , Genotype , Humans , Hypospadias/etiology , Male , Phenols/administration & dosage , RNA, Messenger/genetics , RNA, Messenger/metabolism
12.
FEBS Lett ; 585(20): 3310-5, 2011 Oct 20.
Article in English | MEDLINE | ID: mdl-21945317

ABSTRACT

Recent human studies found that the mRNA expression level of aryl-hydrocarbon receptor nuclear translocator 2 (ARNT2) was positively associated with the prognosis of breast cancer. In this study, we used small interfering RNA techniques to knockdown ARNT2 expression in MCF7 human breast cancer cells, and found that an almost 40% downregulation of ARNT2 mRNA expression increased the expression of sensitive to apoptosis gene (3.36-fold), and decreased the expression of von Hippel-Lindau (0.27-fold) and matrix metalloproteinase-1 (0.35-fold). The metabolite analysis revealed the contents of glucose, glycine, betaine, phosphocholine, pyruvate and lactate involved in the hypoxia-inducible factor (HIF)-1-dependent glycolytic pathway were significantly lower in cells treated with siARNT2. Our results suggested that ARNT2 might play an important role in the modulation of HIF-1-regulated signaling and metabolism.


Subject(s)
Aryl Hydrocarbon Receptor Nuclear Translocator/biosynthesis , Basic Helix-Loop-Helix Transcription Factors/biosynthesis , Breast Neoplasms/metabolism , Gene Expression Regulation, Neoplastic , Neoplasm Proteins/biosynthesis , RNA, Small Interfering/metabolism , Signal Transduction , Aryl Hydrocarbon Receptor Nuclear Translocator/genetics , Basic Helix-Loop-Helix Transcription Factors/genetics , Breast Neoplasms/genetics , Cell Line, Tumor , Female , Gene Knockdown Techniques , Humans , Hypoxia-Inducible Factor 1/genetics , Hypoxia-Inducible Factor 1/metabolism , Neoplasm Proteins/genetics , RNA, Small Interfering/genetics
13.
Toxicol Lett ; 206(2): 152-7, 2011 Oct 10.
Article in English | MEDLINE | ID: mdl-21771643

ABSTRACT

Environmental chemicals with estrogenic activity, known as xenoestrogens, may cause impaired reproductive development and endocrine-related cancers in humans by disrupting endocrine functions. Aryl-hydrocarbon receptor nuclear translocator 2 (ARNT2) is believed to play important roles in a variety of physiological processes, including estrogen signaling pathways, that may be involved in the pathogenesis and therapeutic responses of endocrine-related cancers. However, much of the underlying mechanism remains unknown. In this study, we investigated whether ARNT2 expression is regulated by a range of representative xenoestrogens in human cancer cell lines. Bisphenol A (BPA), benzyl butyl phthalate (BBP), and 1,1,1-trichloro-2,2-bis(2-chlorophenyl-4-chlorophenyl)ethane (o,p'-DDT) were found to be estrogenic toward BG1Luc4E2 cells by an E-CALUX bioassay. ARNT2 expression was downregulated by BPA, BBP, and o,p'-DDT in a dose-dependent manner in estrogen receptor 1 (ESR1)-positive MCF-7 and BG1Luc4E2 cells, but not in estrogen receptor-negative LNCaP cells. The reduction in ARNT2 expression in cells treated with the xenoestrogens was fully recovered by the addition of a specific ESR1 antagonist, MPP. In conclusion, we have shown for the first time that ARNT2 expression is modulated by xenoestrogens by an ESR1-dependent mechanism in MCF-7 breast cancer cells.


Subject(s)
Aryl Hydrocarbon Receptor Nuclear Translocator/metabolism , Basic Helix-Loop-Helix Transcription Factors/metabolism , Breast Neoplasms/metabolism , Down-Regulation/drug effects , Endocrine Disruptors/pharmacology , Estrogen Receptor alpha/metabolism , Estrogens, Non-Steroidal/pharmacology , Xenobiotics/pharmacology , Aryl Hydrocarbon Receptor Nuclear Translocator/genetics , Basic Helix-Loop-Helix Transcription Factors/genetics , Benzhydryl Compounds , Cell Line, Tumor , DDT/pharmacology , Estrogen Receptor alpha/antagonists & inhibitors , Estrogen Receptor alpha/genetics , Female , Genes, Reporter/drug effects , Humans , Neoplasm Proteins/antagonists & inhibitors , Neoplasm Proteins/genetics , Neoplasm Proteins/metabolism , Osmolar Concentration , Ovarian Neoplasms/metabolism , Phenols/pharmacology , Phthalic Acids/pharmacology , Piperidines/pharmacology , Pyrazoles/pharmacology , RNA, Messenger/metabolism , Response Elements/drug effects
14.
Sci Total Environ ; 409(16): 3073-7, 2011 Jul 15.
Article in English | MEDLINE | ID: mdl-21665019

ABSTRACT

The activity of 5- to 6-year-old Japanese children (n=29) was monitored for 3 consecutive days, including one weekend day, using an ActivTracer tri-axial accelerometer. The daily inhalation rate and time spent in sedentary, light, or moderate to vigorous levels of physical activity (MVPA) were estimated from the accelerometer measurements based on previously developed regression equations. The 3-day mean daily inhalation rate (STPD) was estimated at 8.3±1.4 m(3) day(-1) in 10 subjects who completed 3 days of monitoring. The time spent in sedentary, light, or MVPA each day was 320, 415, and 81 min day(-1), respectively. Analysis of between-day reliability indicated that 3 days of monitoring with the ActivTracer tri-axial accelerometer provided an acceptable estimate of daily inhalation rate (intra-class correlation coefficient [ICC]=0.892), but low to moderate reliability for the time spent in different levels of activities (ICC=0.43 to 0.58). We observed a significant difference in the daily inhalation rate between weekdays and the weekend day, possibly due to differences in time spent in MVPA. This finding suggests that a weekend day should be included to obtain more reliable estimates of daily inhalation rate using an accelerometer.


Subject(s)
Air Pollutants/analysis , Air Pollution/statistics & numerical data , Environmental Monitoring/instrumentation , Inhalation Exposure/statistics & numerical data , Child , Child, Preschool , Female , Humans , Inhalation , Inhalation Exposure/analysis , Japan , Male , Pilot Projects
15.
J Air Waste Manag Assoc ; 61(1): 46-54, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21305887

ABSTRACT

Inhalation rate is an essential factor for determining the inhaled dose of air pollutants. Here, accelerometers were used to develop regression equations for predicting the minute ventilation rate (V(E)) to estimate the daily inhalation rate in young children. Body acceleration and heart rate were measured in 29 Japanese preschool children (6 yr of age) during nine different levels of activities (lying down, sitting, standing, playing with plastic bricks, walking, building with blocks, climbing stairs, ball tossing, and running) using the Actical omnidirectional accelerometer, the ActivTracer triaxial accelerometer, and a heart rate monitor. Measurements were calibrated against the V(E) measured by the Douglas bag method. ActivTracer accelerometer measurements gave a strong correlation with V(E) (Pearson's r = 0.913), which was marginally stronger than that for the Actical counts (r = 0.886) and comparable to the correlation between heart rate and logarithmic V(E) (r = 0.909). According to the linear regression equation, the V(E) for lying down, sitting, standing, playing with plastic bricks, walking, and running was overestimated by 14-60% by the Actical and by 14-37% by the ActivTracer. By comparison, for building with blocks, climbing stairs, and ball tossing, the V(E) was underestimated by 19-23% by the Actical and by 13-18% by the ActivTracer. When these three activities were excluded, a stronger correlation was found between the V(E) and ActivTracer measurements (r = 0.949); this correlation was 0.761 for the three excluded activities. Discriminant analysis showed that the ratio between vertical and horizontal acceleration obtained by the ActivTracer could discriminate walking from building with blocks, climbing stairs, and ball tossing with a sensitivity of 75%. The error in estimating V(E) was considerably improved for the ActivTracer measurements by the use of two regression equations developed for each type of activity.


Subject(s)
Monitoring, Ambulatory , Respiratory Rate , Child , Female , Humans , Male , Regression Analysis , Respiratory Function Tests
16.
Proc Natl Acad Sci U S A ; 107(37): 16331-5, 2010 Sep 14.
Article in English | MEDLINE | ID: mdl-20805476

ABSTRACT

Dioxins have been reported to exert various adverse effects, including cell-cycle dysregulation in vitro and impairment of spatial learning and memory after in utero exposure in rodents. Furthermore, children born to mothers who are exposed to dioxin analogs polychlorinated dibenzofurans or polychlorinated biphenyls have developmental impairments in cognitive functions. Here, we show that in utero exposure to dioxins in mice alters differentiation patterns of neural progenitors and leads to decreased numbers of non-GABAergic neurons and thinner deep neocortical layers. This reduction in number of non-GABAergic neurons is assumed to be caused by accumulation of cyclin-dependent kinase inhibitor p27(Kip1) in nuclei of neural progenitors. Lending support to this presumption, mice lacking p27(Kip1) are not susceptible to in utero dioxin exposure. These results show that environmental pollutants may affect neocortical histogenesis through alterations of functions of specific gene(s)/protein(s) (in our case, dioxins), exerting adverse effects by altering functions of p27(Kip1).


Subject(s)
Cerebral Cortex/drug effects , Cerebral Cortex/metabolism , Cyclin-Dependent Kinase Inhibitor p27/metabolism , Maternal Exposure , Polychlorinated Dibenzodioxins/toxicity , Uterus/drug effects , Active Transport, Cell Nucleus/drug effects , Animals , Cell Cycle/drug effects , Cell Nucleus/drug effects , Cell Nucleus/metabolism , Cerebral Cortex/abnormalities , Cerebral Cortex/cytology , Cyclin-Dependent Kinase Inhibitor p27/deficiency , Female , Mice , Mice, Inbred C57BL , Mice, Knockout
17.
J Toxicol Sci ; 35(1): 115-23, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20118632

ABSTRACT

Profiles of Chemical Effects on Cells (pCEC) is a toxicogenomics database with a system of classifying chemicals that have effects on human health. This database stores and handles gene expression profiling information and categories of toxicity data. Chemicals are classified according to the specific tissues and cells they affect, the gene expression changes they induce, their toxicity and biological functions in this database system. The pCEC system also analyzes relationships between chemicals and the genes they affect in specific tissues and cells. The reason why we developed pCEC is to support decision-making within the context of environmental regulation. Especially, exposure to environmental chemicals during fetal and newborn development may result in a predisposition to various disorders such as cancer, learning disabilities and allergies later in life. The identification and prediction of hazardous chemicals using limited information are important issues in human health risk management. Therefore, various toxicity information including lethal dose 50 (LD50), toxicity pathways and pathological data were loaded into pCEC. pCEC is also a facility for query, analysis and prediction of unknown toxicochemical reaction pathways and biomarkers which are based on toxicoinformatical data mining approaches. This database is available online at http://project.nies.go.jp/eCA/cgi-bin/index.cgi. The current version of the database has information on the hepatotoxicity, reproductive toxicity and embryotoxicity of chemicals.


Subject(s)
Databases as Topic , Environmental Pollutants/toxicity , Risk Assessment/methods , Toxicogenetics , Animals , Computational Biology , Databases, Factual , Environmental Pollutants/classification , Gene Expression Profiling , Humans , Lethal Dose 50 , Predictive Value of Tests , Protein Array Analysis
18.
Biol Reprod ; 82(3): 636-43, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20007409

ABSTRACT

TCDD (2,3,7,8-tetrachlorodebenzo-p-dioxin) requires the presence of the aryl hydrocarbon receptor (Ahr) gene for its toxic effects, such as reproductive disorders in male offspring of maternally exposed rats and mice. To study the involvement of the Ahr gene in producing the toxic phenotype with respect to testicular development, we administered a relatively high dose of TCDD to mice with three different maternally derived Ahr genotypic traits, and then compared several Ahr-dependent alterations among male reproductive systems on Postnatal Day 14. Reduction in anogenital distance and expression of prostatic epithelial genes in the urogenital complex (UGC) were detected in Ahr(+/+) and Ahr(+/-) mice exposed to TCDD, whereas no difference was observed in Ahr(-/-) mice. In situ hybridization revealed the absence of probasin mRNA expression in the prostate epithelium, despite the obvious development of prostatic lobes in TCDD-exposed mice. In contrast to obvious prostatic dysfunction and induction of cytochrome P450 (CYP) family genes in the UGC by TCDD, no alterations in testicular functions were observed in germ cell/Sertoli cell/interstitial cell marker gene expression or CYP family induction. No histopathological changes were observed among the three genotypes and between control and TCDD-exposed mice. Therefore, mouse external genitalia and prostatic development are much more sensitive to TCDD treatment than testis. Further, the Ahr gene, analyzed in this study, does not significantly contribute to testicular function during perinatal and immature stages, and the developing mouse testis appears to be quite resistant to TCDD exposure.


Subject(s)
Polychlorinated Dibenzodioxins/toxicity , Receptors, Aryl Hydrocarbon/physiology , Testis/embryology , Testis/growth & development , Urogenital System/embryology , Urogenital System/growth & development , Animals , Animals, Newborn , Female , Fetal Development/drug effects , Fetal Development/genetics , Gene Expression Regulation, Developmental/drug effects , Genetic Predisposition to Disease , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Pregnancy , Rats , Receptors, Aryl Hydrocarbon/genetics , Receptors, Aryl Hydrocarbon/metabolism , Reproduction/drug effects , Reproduction/genetics , Testis/drug effects , Testis/metabolism , Urogenital System/drug effects , Urogenital System/metabolism
19.
Toxicol Appl Pharmacol ; 231(3): 374-83, 2008 Sep 15.
Article in English | MEDLINE | ID: mdl-18606429

ABSTRACT

Congenital hydronephrosis is a serious disease occurring among infants and children. Besides the intrinsic genetic factors, in utero exposure to a xenobiotic, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), has been suggested to induce hydronephrosis in rodents owing to anatomical obstruction in the ureter. Here, we report that hydronephrosis induced in mouse pups exposed lactationally to TCDD is not associated with anatomical obstruction, but with abnormal alterations in the subepithelial mesenchyma of the ureter. In the kidneys of these pups, the expressions of a battery of inflammatory cytokines including monocyte chemoattractant protein (MCP)-1, tumor necrosis factor alpha (TNFalpha) and interleukin (IL)-1beta were up-regulated as early as postnatal day (PND) 7. The amounts of cyclooxygenase (COX)-2 mRNA and protein as well as prostaglandin E2 (PGE(2)) were conspicuously up-regulated in an arylhydrocarbon-receptor-dependent manner in the TCDD-induced hydronephrotic kidney, with a subsequent down-regulation of the gene expressions of Na+ and K+ transporters, NKCC2 and ROMK. Daily administration of a COX-2 selective inhibitor to newborns until PND 7 completely abrogated the TCDD-induced PGE(2) synthesis and gene expressions of inflammatory cytokines and electrolyte transporters, and eventually prevented the onset of hydronephrosis. These findings suggest an essential role of COX-2 in mediating the TCDD action of inducing hydronephrosis through the functional impairment rather than the anatomical blockade of the ureter.


Subject(s)
Cyclooxygenase 2/metabolism , Hydronephrosis/enzymology , Lactation/metabolism , Maternal Exposure/adverse effects , Polychlorinated Dibenzodioxins/toxicity , Animals , Animals, Suckling/metabolism , Cyclooxygenase 2/physiology , Dioxins/toxicity , Enzyme Activation/drug effects , Enzyme Activation/physiology , Female , Hydronephrosis/chemically induced , Hydronephrosis/pathology , Lactation/drug effects , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Pregnancy
20.
Toxicol In Vitro ; 22(4): 1050-61, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18289828

ABSTRACT

The retinoic acid receptors (RARs) play key roles in various biological processes in response to endogenous retinoic acids. However, excessive embryonic exposure to specific ligands for each subtype of the RAR was reported to induce specific developmental abnormalities. We measured the RAR agonistic activity of 543 chemicals using an assay system adopting yeast cells transfected with the human RAR gamma and a coactivator. Eighty-five of the 543 chemicals, including 16 organochlorine pesticides, 14 styrene dimers, 9 monoalkylphenols and 6 parabens, exhibited RAR gamma agonistic effects in this assay. In particular, monoalkylphenols having a 6-9 carbon alkyl group para to the phenolic hydroxyl group possessed high affinity for the RAR gamma, and their activities were 1.363-0.446% of that of all-trans RA. para-Alkylphenols chlorinated at the ortho position also were about as active or more active than their unchlorinated analogs. In addition, all tested styrene dimers showed positive effects, and the activity of 1-phenyltetralin, the strongest in this category, was 1.169% that of all-trans RA. A number of chemicals having binding affinity for the RAR gamma were revealed in this study (both newly identified and confirmed), further comprehensive studies of in vitro and in vivo effects via the RARs are required for the reliable risk assessment of chemicals. In vitro receptor binding studies represent an important step in hazard identification and suggest a potential mechanism of action, which can be an important step in risk assessment and in particular for screening studies to identify potential toxicity and inform mechanistic studies.


Subject(s)
Receptors, Retinoic Acid/agonists , Transcriptional Activation/drug effects , Xenobiotics/pharmacology , Humans , Risk Assessment/methods , Saccharomyces cerevisiae/metabolism , Two-Hybrid System Techniques , Xenobiotics/chemistry , Retinoic Acid Receptor gamma
SELECTION OF CITATIONS
SEARCH DETAIL
...