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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.

Phthalate esters, commonly used as plasticizers, show anti-androgenic activity and cause male reproductive malformation in experimental animals. However, the effects of prenatal exposure to phthalate esters in humans have not been extensively studied. The purpose of this study was to examine the relationship between prenatal exposure to phthalate esters and the anogenital distance (AGD) as a reproductive endpoint in human male newborns. Spot urine samples were collected from 111 Japanese pregnant women after obtaining their informed consent. Seven urinary phthalate ester metabolites were determined by high performance liquid chromatography-tandem mass spectrometry. Urinary isoflavones concentrations were measured as possible covariates because their oestrogenicities and high exposure levels among Japanese have the potential to affect male genital development. Birth outcomes and AGD, the distance from the centre of the anus to external genitalia, were measured for their male newborns. In a multiple regression model, the log-transformed mono-2-ethylhexyl phthalate concentration (specific gravity-corrected) was negatively significant, and maternal smoking status was positively significant, in explaining anogenital index (AGI) when potential covariates were controlled for. Urinary isoflavones did not significantly contribute to AGI in any models. Our results suggest that prenatal exposure to di(2-ethylhexyl) phthalate affects reproductive development in human males.

In order to rationalize the lightning protection design of distribution lines, lightning phenomena on TEPCO's distribution lines were continuously observed. The observations were carried out with still cameras and lightning surge monitoring sensors. The results elucidate the lightning performance of distribution lines. For example, direct lightning strokes are the major cause of the present distribution line faults. This fact suggests that it is important to investigate observation data on direct lightning strokes. The observation data were analyzed by means of a direct lightning analysis model. The calculated waveforms were compared with the measured waveforms on distribution lines. The probability distributions of the surge currents and voltages were calculated by the Monte Carlo method. These results provide new data on lightning performance. © 2009 Wiley Periodicals, Inc. Electron Comm Jpn, 91(10): 28– 37, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/ecj.10164

Summary This article describes a methodology for the quantitative assessment of the environmental fate of gallium and arsenic from the disposal of mobile phones containing gallium arsenide (GaAs) semiconductors, using data from Japan. The product lifetime of mobile phones is short, and the recycling systems for such phones are currently underdeveloped. As a result, many mobile phones are disposed of via incineration and landfilling. The disposal of GaAs semiconductors could lead to some releases of gallium and arsenic to air and water. The methodology presented here begins with an estimation of the cumulative number of disposed mobile phones, using a logistic curve. Then, thermodynamic simulation and laboratory experiments are carried out to assess how much gallium and arsenic may be released into the environment. Using this method, the cumulative number of mobile phones disposed of in Japan is calculated to be 610 million by 2010. Distribution among air emissions, the leachate, and the insoluble residue (in landfilled incinerator ash) was determined to be 4.20 × 10-2%, 1.58 × 10-1%, and 99.8% for gallium, and 2.00 × 10-1%, 19.5%, and 80.3% for arsenic, respectively. For phones that are disposed of directly in landfills, it is estimated that nearly 100% of the gallium and arsenic exists as the insoluble residue. We suggest that, in the conditions present in Japan, disposal of mobile phones directly into the landfill is preferable to the incineration with subsequent landfill of ash with respect to gallium and arsenic emissions into the environment. The proposed methodology may be adapted for the assessment of the environmental fate of problematic substances from the disposal of similar products.

HPLC-ICP-MS, employing a silica-based LC-SCX cation-exchange column, styrene-divinylbenzene copolymer-based PRP-X100 anion exchange column, an ODS reversed-phase and gel-permeation (polyvinyl alcohol-based resin) GS-220 columns, has been used for the separation, identification, and quantification of arsenic compounds, particularly arsenobetaine (AB), present in NIES candidate certified reference material (CRM) no. 18 human urine. AB is the predominant arsenic species, followed by dimethylarsinic acid, methylarsonic acid and arsenic acid. The peak of each arsenic compound has been validated by spiking of the authentic standard solution to the urine sample and by using the above chromatographic systems. The high concentration of chloride that co-elutes with the arsenic acid from the LC-SCX and with the AB from the GS-220 columns has interfered with the ion signals of arsenic acid and AB, by forming the molecular ions 40 Ar 35 Cl and 38 Ar 37 Cl + in the plasma. Thus, the concentration of AB has been carefully estimated on the GS-220 after extracting the chloride interference ( 37 Cl: 35 Cl = 1:3.1271) by measuring the 40 Ar 37 Cl + . The peak of AB overlapped with the peak of arsenous acid and hindered the estimation of AB on the ODS and PRP-X100 columns. But AB has been baseline separated from the other arsenic compounds and also from the chloride with 20 mM pyridine at pH 2.60 on the LC-SCX. So, the LC-SCX column has been proven and used for the determination of AB in NIES candidate CRM no. 18 human urine. The concentrations of AB, estimated by the standard addition method and found using the LC-SCX and GS-220 columns, are 70.5 ± 5.5 (n = 20) and 71.5 ± 4 μgl -1 (n = 9). The concentration of AB thus found has been applied as the baseline value for the collaborative study to certify the AB in the NIES candidate CRM no. 18 human urine.

The carbon and nitrogen stable isotopic composition of the scalp hair and diet of Gidra-speaking people in four villages in Papua New Guinea is presented. The isotopic composition of hair was measured, while that of the diet was estimated from food consumption survey data and the measured isotopic composition and protein and carbohydrate contents of food items. The average isotopic ratios of the hair samples and of the diet varied among the four study villages, which were selected because of their diverse ecological settings. Comparison was made between hair and calculated dietary isotopic compositions. Two of the four diet-hair enrichment values obtained for 13C (+1.8 and 2.2%‰) were similar to those previously reported (1.4–2.0%‰), but the other two values (3.7 and 4.8%) were greater than in earlier reports. 15N enrichment was systematically greater (by 1%‰) than reported values (∼4.3%‰) except for one village, where a much greater enrichment (6.9%‰) was found. The factors potentially relevant to these deviations are discussed. Possible errors in estimating the dietary isotopic composition and minor modifications of dietary habits revealed by food consumption surveys could explain most of the discrepancies. However, the great enrichment of 15N found in one of the villages remains unexplained. © 1996 Wiley-Liss, Inc.

Arsenobetaine was detected and quantified unambiguously in human plasma, serum and red blood cells by the combination of HPLC with ICP MS. Three different column conditions, i.e. two ionpair chromatographies for anionic (LC-1) and cationic (LC-2) compounds and gel-permeation chromatography (LC-3), were employed to confirm the assignment. Arsenobetaine was detected in every sample as a major component of the water-soluble arsenic compounds, with an increasing concentration in plasma < serum < blood cell fractions. It was the sole detectable arsenic compound in LC-1 and LC-2, while a broad peak corresponding to high-molecular-weight compounds was identified in addition to arsenobetaine in LC-3.