Faculty Bibliography

Endosulfan is a currently used organochlorine pesticide in China, with annual usage of 2300 t between 1994 and 2004. Concentrations of endosulfan (including α- and β-isomers and their metabolite endosulfan sulfate) were reported for surface soil collected in 2005 at 141 sites (6 background, 95 rural, and 40 urban) across China. The concentrations of total endosulfan (sum of α-endosulfan, β-endosulfan, and endosulfan sulfate) at all sites ranged from BDL (below detection limit) to 19000 pg/g dry weight (dw), with geometric mean (GM) 120 pg/g dw. Rural soils had the highest total endosulfan concentrations, with GM 160 pg/g dw, followed by urban soils (GM = 83 pg/g dw) and background soils (GM = 38 pg/g dw). The observed soil concentrations of α-endosulfan (GM = 6.5 pg/g dw) were much lower than those of β-endosulfan (GM = 49 pg/g dw) and endosulfan sulfate (GM = 47 pg/g dw). The fractional abundance of α-endosulfan F(α-endo) [α-endosulfan/(α-endosulfan + β-endosulfan)] for all soils ranged from 0.00040 to 0.91, with GM 0.10, much lower than those in technical products (ranged from 0.67 to 0.7), which most likely reflects that α-endosulfan is more volatile and degrades faster than β-endosulfan in soil. Consequently, half-life of β-endosulfan in soil is expected longer than α-endosulfan. Significant correlation between endosulfan sulfate and its parent isomers suggested that the presence of endosulfan sulfate originated from its parent isomers. Based on multiple linear regression model, inventories of endosulfan sulfate in Chinese agricultural soil in 2004 with a 1/4° longitude × 1/6° latitude resolution are established. Comparison between field measurements and modeling results showed significant correlations between the modeled and measured endosulfan concentrations, and 89%, 83%, and 70% of monitoring data fell between the lowest and the highest modeled concentrations for α- and β-endosulfan and endosulfan sulfate, respectively. The good agreement lends credibility to modeled soil concentrations of endosulfan. To our knowledge, this is the first soil concentration inventory for endosulfan sulfate, which paves the way for further study on its environmental behavior.

The herbicide 2,6-dichlorobenzonitril (DCBN) is a potent and tissue-specific toxicant to the olfactory mucosa (OM). The toxicity of DCBN is mediated by cytochrome P450 (P450)-catalyzed bioactivation; however, it is not known whether target-tissue metabolic activation is essential for toxicity. CYP2A5, expressed abundantly in both liver and OM, was previously found to be one of the P450 enzymes active in DCBN bioactivation in vitro. The aims of this study were to determine the role of CYP2A5 in DCBN toxicity in vivo, by comparing the extents of DCBN toxicity between Cyp2a5-null and wild-type (WT) mice, and to determine whether hepatic microsomal P450 enzymes (including CYP2A5) are essential for the DCBN toxicity, by comparing the extents of DCBN toxicity between liver-Cpr-null (LCN) mice, which have little P450 activity in hepatocytes, and WT mice. We show that the loss of CYP2A5 expression did not alter systemic clearance of DCBN (at 25 mg/kg); but it did inhibit DCBN-induced non-protein thiol depletion and cytotoxicity in the OM. Thus, CYP2A5 plays an essential role in mediating DCBN toxicity in the OM. In contrast to the results seen in the Cyp2a5-null mice, the rates of systemic DCBN clearance were substantially reduced, while the extents of DCBN-induced nasal toxicity were increased, rather than decreased, in the LCN mice, compared to WT mice. Therefore, hepatic P450 enzymes, although essential for DCBN clearance, are not necessary for DCBN-induced OM toxicity. Our findings form the basis for a mechanism-based approach to assessing the potential risks of DCBN nasal toxicity in humans.

Data on the concentrations and accumulation profiles of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (DL-PCBs) in cetaceans are scarce. In this study, concentrations and accumulation profiles of PCDD/Fs and DL-PCBs were measured in the blubber of finless porpoises (Neophocaena phocaenoides) collected from Korean coastal waters. Total dioxin-like toxic equivalent (TEQ) concentrations (6.5-31 pg/g lipid weight) in finless porpoises were lower than those reported for cetaceans and pinnipeds from other countries. Significant gender-specific differences were found in the concentrations and accumulation profiles of PCDD/Fs and DL-PCBs and this difference was associated with maternal and lactation transfer of contaminants from mature females to their fetus. All of the PCDD/F homologue groups were detected in all of the samples and the proportions of PCDFs were higher than those of PCDDs. The dominant congeners found in finless porpoise blubber were 2,3,4,7,8-PeCDF, 1,2,3,4,7,8-HxCDF and OCDD for PCDD/Fs and PCB 118 for DL-PCBs. The accumulation profiles of PCDD/Fs in finless porpoise in our study were different from those found for cetaceans from other countries. Total TEQ levels in finless porpoises in Korea were below the suggested threshold values for adverse health effects in marine mammals.

Bioconcentration of perfluorinated compounds (PFCs) was studied in a biphasic (uptake and elimination) study with blackrock fish, Sebastes schlegeli. The blackrock fish was acclimated to varying salinities over a two-week period before the present study. Among the four selected PFCs: perfluorooctane sulfonate (PFOS), perfluoro-octanoic acid (PFOA), perfluorodecanoic acid (PFDA), and perfluoroundecanoic acid (PFUnDA), PFUnDA accumulated significantly in serum, followed by PFDA, PFOS, and PFOA, in that order, while the accumulation profile in liver was PFOS > PFUnDA > PFDA > PFOA. Total PFC levels in plasma were approximately four times greater than those found in liver. The uptake and elimination rate constants (K(u) and K(e)) of PFCs decreased as salinity decreased, suggesting delayed diffusion of PFCs between water and fish, possibly associated with the osmolality gradient. A significant correlation was found between bioconcentration factors (BCF) of PFCs and salinity, except for PFOA, possibly resulting from the effects of salinity on biological responses and chemical activity of PFCs. Even though salinity did not affect the kinetics of PFC accumulation in serum and liver, the results provide useful information on the toxicokinetics of PFCs for saltwater fish.

Since the 1970s, an increasing number of regulations have expanded the use of brominated and chlorinated flame retardants. Many of these chemicals are now recognized as global contaminants and are associated with adverse health effects in animals and humans, including endocrine and thyroid disruption, immunotoxicity, reproductive toxicity, cancer, and adverse effects on fetal and child development and neurologic function. Some flame retardants such as polybrominated diphenyl ethers (PBDEs) have been banned or voluntarily phased out by manufacturers because of their environmental persistence and toxicity, only to be replaced by other organohalogens of unknown toxicity. Despite restrictions on further production in some countries, consumer products previously treated with banned retardants are still in use and continue to release toxic chemicals into the environment, and the worldwide use of organohalogen retardants continues to increase. This paper examines major uses and known toxic effects of commonly-used organohalogen flame retardants, replacements for those that have been phased out, their combustion by-products, and their effectiveness at reducing fire hazard. Policy and other solutions to maintain fire safety while reducing toxicity are suggested. The major conclusions are: (1) Flammability regulations can cause greater adverse environmental and health impacts than fire safety benefits. (2) The current options for end-of-life disposal of products treated with organohalogens retardants are problematic. (3) Life-cycle analyses evaluating benefits and risks should consider the health and environmental effects of the chemicals, as well as their fire safety impacts. (4) Most fire deaths and most fire injuries result from inhaling carbon monoxide, irritant gases, and soot. The incorporation of organohalogens can increase the yield of these toxic by-products during combustion. (5) Fire-safe cigarettes, fire-safe candles, child-resistant lighters, sprinklers, and smoke detectors can prevent fires without the potential adverse effects of flame retardant chemicals. (6) Alternatives to organohalogen flame retardant chemicals include using less flammable materials, design changes, and safer chemicals. To date, before evaluating their health and environmental impacts, many flame retardant chemicals have been produced and used, resulting in high levels of human exposure. As a growing literature continues to find adverse impacts from such chemicals, a more systematic approach to their regulation is needed. Before implementing new flammability standards, decision-makers should evaluate the potential fire safety benefit versus the health and environmental impacts of the chemicals, materials, or technologies likely to be used to meet the standard. Reducing the use of toxic or untested flame retardant chemicals in consumer products can protect human and animal health and the global environment without compromising fire safety.

A study was conducted to evaluate exposure to polybrominated diphenyl ethers (PBDEs) among 144 men and women 55 to 74 years residing along the Hudson River. The results indicated a median serum PBDE concentration of 23.9 ng/g lipid wt. This value is similar to those of other New York State studies of populations that are younger and proportionately more likely to be male, suggesting that pathways do not differ by age or sex. Individual congeners were highly correlated, but they were not associated with concentrations of polychlorinated biphenyls (PCBs). Persons with a body mass index (BMI) > 30 had a geometric mean ΣPBDE concentration of 46.7 versus 25.2 ng/g lipid wt for persons with a BMI ≤ 30 (p = .006). Fresh water fish consumption was not associated with serum PBDE concentrations in this population.

The widespread distribution of perfluorinated chemicals (PFCs) in different environmental matrices has prompted concern about the sources, fate, and transport of these classes of chemicals. PFCs are present in the atmosphere, but only a few studies have investigated their occurrence in precipitation. In this study, concentrations of 20 PFCs, including C3-C5 short-chain PFCs, were quantified using HPLC-MS/MS in precipitation samples from Japan (n = 31), the United States (n = 12), China (n = 5), India (n = 2), and France (n = 2). Among the PFCs measured, perfluoropropanoic acid (PFPrA) was detected in all of the precipitation samples. Average total PFC concentrations ranged from 1.40 to 18.1 ng/L for the seven cities studied. The greatest total PFC concentrations were detected in Tsukuba, Japan, whereas the lowest concentrations were detected in Patna, India. PFPrA, perfluorooctanoic acid (PFOA), and perfluorononanoic acid (PFNA) were found to be the dominant PFCs in Japanese and U.S. precipitation samples. No observable seasonal trend was found in precipitation samples from two locations in Japan. Annual fluxes of PFCs were estimated for Japan and the U.S. and the evidence for precipitation as an effective scavenger of PFCs in the atmosphere is reported.

Perchlorate, ClO(4)(-), interferes with iodide (I(-)) uptake by the sodium-iodide symporter (NIS) and thereby affects thyroid hormone production in the body. Studies have reported human exposures to perchlorate based on measurements in urine, but little is known about the levels in blood. In this study, we determined concentrations of perchlorate, iodide, and other anions (e.g., chlorate [ClO(3)(-)], bromate [BrO(3)(-)], bromide [Br(-)]) in 131 whole blood samples collected from Chinese donors aged 0.4 to 90 yr, in Nanchang, China. Perchlorate, iodide, and bromide were detected in all of the samples analyzed, whereas chlorate was found in only 27% of the samples and bromate was found in only 2%. The mean (range) concentrations of perchlorate, iodide, and bromide were 2.68 (0.51-10.5), 42.6 (1.58-812), and 2120 (1050-4850) ng/mL, respectively. Perchlorate levels in blood from Nanchang adults were 10-fold greater than levels that have been previously reported for U.S. adults. The iodide/perchlorate molar ratio ranged from 3.05 to 15.3 for all age groups, and the ratio increased with age (r = 0.732, p < 0.01). Perchlorate and bromide concentrations decreased significantly with age, whereas iodide concentrations increased with age. No significant gender-related differences in blood perchlorate, iodide, or bromide levels were found. A significant negative correlation was found between the concentrations of perchlorate and iodide in blood. Exposure doses of perchlorate were estimated for infants, toddlers, children, adolescents, and adults based on the measured concentrations in blood, using a simple pharmacokinetic model. The mean exposure doses of perchlorate for our age groups ranged from 1.12 (adults) to 2.22 μg/kg bw/day (infants), values higher than the United States Environmental Protection Agency's (USEPA) reference dose (RfD: 0.7 μg/kg bw/day). This is the first study on perchlorate and iodide levels in whole blood from infants, toddlers, children, adolescents, and adults from a city in China with known high perchlorate levels.

Intake of a diet rich in phytoestrogens has been associated with a decreased risk for hormone-dependent cancers in humans. Biomonitoring of phytoestrogens in human urine has been used to assess the intake of phytoestrogens. Although studies have reported phytoestrogen levels in urine specimens from the United States and Japan, little is known of human intake of phytoestrogens in other Asian countries. In this study we determined the concentrations of seven phytoestrogens, namely, enterolactone, enterodiol, daidzein, equol, O-desmethylangolensin (O-DMA), genistein, and coumestrol, in 199 human urine samples from three Asian countries, Vietnam (Hanoi and Ho Chi Minh), Cambodia (Phnom Penh), and India (Chennai and Kolkata), using a simple, sensitive, and reliable liquid chromatography (LC)-tandem mass spectrometry (MS/MS) method. The residue levels of phytoestrogens in urine samples from the three Asian countries were compared with the concentrations in 26 urine samples from Japan (Ehime) and 16 urine samples from the United States (Albany), analyzed in this study. Among the phytoestrogens analyzed, isoflavones such as daidzein and genistein were predominant in urine samples from Vietnam; samples from Cambodia and India contained higher concentrations of enterolactone than isoflavones. Urinary concentrations of isoflavones in samples from Hanoi, Vietnam, were notably higher than the concentrations in samples from Cambodia, India, and the United States and similar to the concentrations in samples from Japan. The lowest concentrations of daidzein and the highest concentrations of enterolactone were found in urine samples from India. Concentrations of equol and O-DMA, which are microbial transformation products of daidzein (produced by gut microflora), were notably high in urine samples from Hanoi, Vietnam. The ratios of the concentration of equol or O-DMA to that of daidzein were significantly higher in samples from Hanoi than from Japan, indicating high biotransformation efficiency of daidzein by the population in Hanoi. High concentrations of equol, in addition to isoflavones, in urine have been linked to reduced breast cancer risk in previous studies, and, thus, the Vietnamese population may have potential protective effect against breast cancer. This study suggests that the dietary intake and profiles of phytoestrogens vary considerably, even among Asian countries.

Effect of potassium salt of perfluorooctane sulfonic acid (PFOS) on the osmoregulation of marine teleost (blackrock fish), Sebastes schlegeli, was investigated under varying salinities, by monitoring serum osmolality, Na(+), K(+), Cl(-), Ca(2+) and Mg(2+) concentrations in serum, serum glucose, and gill Na(+)-K(+) ATPase (NKA) activity. The fish was acclimatized to four salinity levels (10, 17.5, 25, and 34 psu) for 2 weeks before a 6-d exposure to 100 or 1000 microg L(-1) of PFOS. Six fish from each exposure group were sampled at 24, 48, and 144 h after exposures, and serum, liver and gills were collected for analysis. NKA activity decreased by 34% and 31% relative to control at salinity levels of 25 and 34 psu, respectively, following exposure to 1000 microg L(-1) PFOS. PFOS did not affect serum osmolality, Na(+), Cl(-), Ca(2+) and Mg(2+) concentrations; however, serum K(+) concentration increased during initial exposure period and then decreased after 144 h. Serum glucose levels decreased with increasing PFOS concentrations, implying high energy demand in response to exposure. Overall, PFOS exposure impaired NKA activity, altered potassium ion concentrations in serum, and reduced serum glucose levels while no other effects on serum concentrations of ionic salts were observed.