Selenium in food and the human body: a review

Selenium levels in soil generally reflect its presence in food and the Se levels in human populations. Se food content is influenced by geographical location, seasonal changes, protein content and food processing. Periodic monitoring of Se levels in soil and food is necessary. Diet is the major Se source and approximately 80% of dietary Se is absorbed depending on the type of food consumed. Se bioavailability varies according to the Se source and nutritional status of the subject, being significantly higher for organic forms of Se. Se supplements can be beneficial for subjects living in regions with very low environmental levels of Se. Several strategies have been followed: (1) employment of Se-enriched fertilizers; (2) supplementation of farm animals with Se; (3) consumption of multimicronutrient supplements with Se. Nevertheless, detailed investigations of possible interactions between Se supplements and other food components and their influence on Se bioavailability are needed. Suppliers also need to provide more information on the specific type of Se used in supplements. In addition, research is lacking on the mechanisms through which Se is involved in hepatocyte damage during hepatopathies. Although Se potential as an antioxidant for the prevention of cardiovascular diseases (CVD) is promising, additional long-term intervention trials are necessary. As a result, indiscriminate Se supplements cannot be reliably recommended for the prevention of CVD in human beings. Some interesting findings reported an association of Se intake with a reduced prevalence and risk for prostate and colon cancer. However, random trials for other cancer types are inconclusive. As a final conclusion, the general population should be warned against the employment of Se supplements for prevention of hepatopathies, cardiovascular or cancer diseases, because benefits of Se supplementation are still uncertain, and their indiscriminate use could generate an increased risk of Se toxicity.     

Chemical contaminants, health indicators, and reproductive biomarker responses in fish from rivers in the Southeastern United States

Largemouth bass (Micropterus salmoides) and common carp (Cyprinus carpio) were collected from 13 sites located in the Mobile (MRB), Apalachicola-Flint-Chattahoochee (ARB), Savannah (SRB), and Pee Dee (PRB) River Basins to document spatial trends in accumulative chemical contaminants, health indicators, and reproductive biomarkers. Organochlorine residues, 2,3,7,8-tetrachlorodibenzo-p-dioxin-like activity (TCDD-EQ), and elemental contaminants were measured in composite samples of whole fish, grouped by species and gender, from each site. Mercury (Hg) and polychlorinated biphenyls (PCBs) were the primary contaminants of concern. Concentrations of Hg in bass samples from all basins exceeded toxicity thresholds for piscivorous mammals (>0.1 microg/g ww), juvenile and adult fish (>0.2 microg/g ww), and piscivorous birds (>0.3 microg/g ww). Total PCB concentrations in samples from the MRB, ARB, and PRB were >480 ng/g ww and may be a risk to piscivorous wildlife. Selenium concentrations also exceeded toxicity thresholds (>0.75 microg/g ww) in MRB and ARB fish. Concentrations of other formerly used (total chlordanes, dieldrin, endrin, aldrin, mirex, and hexachlorobenzene) and currently used (pentachlorobenzene, pentachloroanisole, dacthal, endosulfan, gamma-hexachlorocyclohexane, and methoxychlor) organochlorine residues were generally low or did not exceed toxicity thresholds for fish and piscivorous wildlife. TCDD-EQs exceeded wildlife dietary guidelines (>5 pg/g ww) in MRB and PRB fish. Hepatic ethoxyresorufin O-deethylase (EROD) activity was generally greatest in MRB bass and carp. Altered fish health indicators and reproductive biomarker were noted in individual fish, but mean responses were similar among basins. The field necropsy and histopathological examination determined that MRB fish were generally in poorer health than those from the other basins, primarily due to parasitic infestations. Tumors were found in few fish (n=5; 0.01%); ovarian tumors of smooth muscle origin were found in two ARB carp from the same site. Intersex gonads were identified in 47 male bass (42%) representing 12 sites and may indicate exposure to potential endocrine disrupting compounds. Comparatively high vitellogenin concentrations (>0.35 mg/mL) in male fish from the MRB, SRB, and PRB indicate exposure to estrogenic or anti-androgenic chemicals.     

1-Hydroxypyrene and 3-hydroxybenzo[a]pyrene as biomarkers of exposure to PAH in various environmental exposure situations

Objective

To evaluate the utility of urinary 3-hydroxybenzo[a]pyrene (3-OH-B[a]P) as a biomarker of exposure to polycyclic aromatic hydrocarbons (PAHs) in various environmental exposure scenarios alongside the more usually studied 1-hydroxypyrene (1-OH-Pyr).

Methods

Two groups of 15 and 10 non smoking, healthy men and women, were exposed for approximately 6 h to ambient air at two outdoor locations close to metallurgical industries, and at one indoor location in an urban setting. Atmospheric measurements of 16 “priority” PAHs were carried out during each exposure. Urinary 1-OH-Pyr and 3-OH-B[a]P were also analysed, samples being taken the morning before exposure, at the end of exposure, then 4 and 15 h after the end of exposure. Urinary 1-OH-Pyr and 3-OH-B[a]P were analysed using high performance liquid chromatograph with fluorescence detection. Limits of detection (LOD) were 0.092 nmol/L and 0.28 pmol/L for 1-OH-Pyr and 3-OH-B[a]P respectively.

Results

Average ambient air concentrations varied from 0.27 to 2.87 ng/m³ for pyrene, 0.04 to 1.20 ng/m³ for B[a]P, and from 70.0 to 910.6 ng/m³ for the sum of the 16 PAH (ΣPAHs). Concentrations of 1-OH-Pyr were not correlated with atmospheric concentrations of PAHs to which subjects were exposed, nor with the concentrations of 3-OH-B[a]P. Nearly 80% of measurements of 3-OH-B[a]P were lower than the LOD and no relationship between atmospheric concentrations and urinary metabolites was observable. However, the percentage of post-exposure values of 3-OH-B[a]P greater than the LOD increased significantly with the median of atmospheric concentrations of Pyr, B[a]P and ΣPAH at the different sites (test of linear trend, p < 0.02 in all cases).

Conclusion

Although we used very sensitive techniques for the measurements of urinary metabolites, especially for 3-OH-B[a]P, neither 1-OH-Pyr nor 3-OH-B[a]P were an unequivocal biomarker of exposure to atmospheric PAHs in environmental exposure scenarios relevant to the general population. It would be interesting to investigate other urinary monohydroxy PAH metabolites in this context.     

Impact of a highly contaminated river on a more important hydrologic system: changes in organic markers

The Fensch River is a tributary of the Moselle River. It is a highly contaminated river that drains an industrial area. The objective of this preliminary study is to determine its impact on the Moselle River by analysing the extractable organic matter (EOM) coming from the sediments at the molecular scale. EOM is described in term of aromatic hydrocarbons, aliphatic hydrocarbons and polar compounds. EOM coming from Fensch River sediments is mainly composed of anthropogenic molecules. Aromatic hydrocarbons are dominated by parent Polycyclic Aromatic Hydrocarbons (PAHs) underlining the pyrogenic origin of this fraction. Aliphatic hydrocarbons consist of diagenetic hopanes and a broad UCM that are characteristics of thermal mature organic matter. Upstream the confluence the EOM of the Moselle River is mainly from vegetal origin. It is composed of high molecular weight n-alkanes with an odd over even predominance, degredation products of phytol and stigmasterol. The occurrence of PAHs and diagenetic hopanes underlines that the Moselle River is already contaminated before the confluence. The Fensch River input drastically changes the EOM of the Moselle River. Amount of PAHs is doubled and the fingerprints of both aliphatic hydrocarbons and polar compounds highlight the combination of both natural and anthropogenic sources.     

Development of high sensitivity potentiometric NOx sensor and its application to breath analysis

Using a combination of similar potentiometric sensors connected in series, a strategy for measuring NO at ppb concentrations has been demonstrated. Sensors numbering from 2 to 20 were fabricated, with each sensor based on YSZ electrolyte with WO₃ sensing electrode and Pt-zeolite/Pt as the reference electrode. Use of a catalytic filter allows for the cancellation of interferences due to oxidizable gases, such as CO. The optimum operating temperature of the filter and sensor was determined to be 250 and 425 °C, respectively. For human breath samples, the interference from water was acute enough that only scrubbing through a dry ice/acetone bath led to adequate performance for detection of NO in the 5-80 ppb range with a 20-sensor array. A more practical strategy suitable for clinical analysis was demonstrated by using water saturated air as the background gas. A linear calibration curve in the range suitable for use in clinical analysis is demonstrated.