ISSN:1528-7394    

DOI:10.1080/009841000156501

出版商:Informa UK Ltd    

年代:2000

数据来源: Taylor

摘要:

Inorganic mercury is mainly eliminated by urinary and fecal excretion, but it is also eliminated by exhalation and sweat. There are only a few reports on exhalation of mercury in humans. In volunteers with short-term mercury exposure, an increased exhalation of mercury was found after alcohol intake. The aim of this study was to determine mercury in end-exhaled air and the influence of ethanol on mercury exhalation in subjects with longterm mercury exposure from diet, amalgam fillings, or the work environment. Fourteen subjects, with different grades of mercury exposure, were given 0.2 g ethanol/kg body weight. Measurements of mercury in end-exhaled air were performed before and after alcohol intake. Mercury in end-exhaled air could be detected in all subjects. In 10 individuals without amalgam fillings the mercury concentration was 3 to 12 pg/L. A marked increase, in general about fivefold, in mercury concentrations in end-exhaled air was seen in all subjects 30 min after intake of alcohol, regardless of the level of mercury exposure. Higher ethanol doses resulted in higher mercury levels in end-exhaled air and longer time periods before a return to background levels. An increase was seen even after an ethanol dose of only 0.1 g ethanol/kg body weight (about 0.08 L wine). The decrease in exhaled mercury at higher alcohol doses followed approximately zero-order kinetics and probably reflects the elimination of ethanol in tissues. In conclusion, low levels of mercury can be detected in end-exhaled air also in individuals without amalgam fillings. About a fivefold increase was seen 30 min after alcohol intake, and the relative increase seemed to be independent of the body burden of mercury. Exhalation of mercury represents only a small percentage of the total elimination of mercury.

ISSN:1528-7394    

DOI:10.1080/009841000156510

出版商:Informa UK Ltd    

年代:2000

数据来源: Taylor

摘要:

The effects of motorcycle exhaust particulate (MEP) on human cytochrome P-450 (P-450)-dependent monooxygenases were determined using human hepatoma cell line HepG2 and lung carcinoma cell line NCI-H322 treated with organic extracts of MEP from a two-stroke engine. Gas chromatography and mass spectrometry analysis of MEP extract revealed the presence of carcinogens benzo[a]pyrene, benz[a]anthracene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[g,h,i]perylene, chrysene, and indeno[1,2,3-c,d]pyrene in the chemical mixture. Treatment with MEP extract produced concentration- and time-dependent increases of monooxygenase activity in HepG2 cells. Treatment of the cells with 100 µg/ml MEP extract for 24 h markedly increased benzo[a]pyrene hydroxylation, 7-ethoxycoumarin, and 7-ethoxyresorufin O-deethylation activities in microsomes. Immunoblot analysis of microsomal proteins using mouse monoclonal antibody 1-12-3 against P-450 1A1 revealed that MEP extract induced a P-450-immunorelated protein in the hepatoma cells. RNA blot analysis of cellular total RNA using a human P-450 1A1 3?-end cDNA probe showed that MEP extract increased the level of a hybridizable P-450 mRNA. These P-450 1A1 inductive effects of MEP extract were similar to those from treatment with 10 µM benzo[a]pyrene or 3-methylcholanthrene (3-MC) in HepG2 cells. Treatment of lung carcinoma NCI-H322 cells with 100 µg/ml MEP extract, 10 µM benzo[a]pyrene, or 3-MC resulted in induction of monooxygenase activity, protein, and mRNA of P-450 1A1, similar to the induction observed with the hepatoma cells. The present study demonstrates that MEP extract has the ability to induce human hepatic and pulmonary P-450 1A1 in the liver- and lung-derived cell lines, and the induction involves a pretranslational mechanism. Induction of the human hepatic and pulmonary P-450 1A1 in vitro may provide important information in the assessment of MEP metabolism and toxicity in humans.

ISSN:1528-7394    

DOI:10.1080/009841000156529

出版商:Informa UK Ltd    

年代:2000

数据来源: Taylor

摘要:

To determine whether there is any biological basis for complaints that fabric softener emissions can cause acute adverse effects in certain individuals, screening tests were performed in which groups of mice were exposed to the emissions of 5 commercial fabric softener products (antistatic pads used in laundry dryers) for 90 min. Pneumotachographs and a computerized version of ASTM test method E-981 were used to measure acute changes in several respiratory cycle parameters, especially the pause after inspiration, the pause after expiration, and the midexpiratory airflow velocity. From these changes, sensory irritation (SI), pulmonary irritation (PI), and airflow limitation (AFL) of differing intensities were measured with each of the five brands tested. At the peak effect, SI ranged from 21 to 58% of the breaths, PI ranged from 4 to 23% of the breaths, and AFL ranged from 6 to 32% of the breaths. After three exposures, histopathology revealed mild inflammation of interalveolar septae of the lungs. Gas chromatography/ mass spectroscopy (GC/MS) analysis of the emissions of one pad identified several known irritants (isopropylbenzene, styrene, trimethylbenzene, phenol, and thymol). Laundry that had been dryed with one the fabric softener pads emitted sufficient chemicals to elicit SI in 49% of breaths at the peak effect. Placing one fabric softener pad in a small room overnight resulted in an atmosphere that caused marked SI (61% of breaths). These results demonstrate that some commercial fabric softeners emit mixtures of chemicals that can cause SI, PI, and reduce midexpiratory airflow velocity in normal mice. The results provide a toxicological basis to explain some of the human complaints of adverse reactions to fabric softener emissions.

ISSN:1528-7394    

DOI:10.1080/009841000156538

出版商:Informa UK Ltd    

年代:2000

数据来源: Taylor

摘要:

Constructed wetlands are becoming increasingly popular as low-cost, high-efficiency means of treating agricultural and municipal wastewaters. Monitoring programs for constructed wetlands usually measure physical and chemical characteristics of wetland treatment, including hydraulic residence time and removal of nutrients (N, P), suspended solids, and biochemical oxygen demand (BOD). However, toxicity abatement is seldom measured as evidence of wetland treatment efficiency. In this study, toxicity tests combined with chemical measurements were employed to measure the efficiency of a constructed wetland in treating swine wastes during fall and winter sampling periods. Although the wetland system operated at three wastewater loading rates, only the high-loading-rate cells were tested because of their year-round flows. Wastewater samples were collected prior to, during, and following wetland treatment to track treatment progress as effluents passed through the wetland cells. Toxicity tests withCeriodaphnia dubiashowed significant toxicity abatement of wastewater as it progressed through the constructed wetland system; however, residual toxicity was still observed in the final wetland effluent. No seasonal differences were observed in toxicity abatement between fall and winter wastewater samples, although nitrate and BOD were removed more efficiently during the fall. Results suggest that, while the constructed wetland system is effective in reducing toxicity in swine wastewater, further pre- or posttreatment or additional dilution is necessary before treated effluents are discharged into surface water.

ISSN:1528-7394    

DOI:10.1080/009841000156547

出版商:Informa UK Ltd    

年代:2000

数据来源: Taylor