RESUMEN
Uranium is a naturally occurring heavy metal. Its extensive use in the nuclear cycle and for military applications has focused attention on its potential health effects. Acute exposures to uranium are toxic to the kidneys where they mainly cause damage to proximal tubular epithelium. The purpose of this study was to investigate the biological consequences of acute in vitro uranyl exposure and the influence of uranyl speciation on its cytotoxicity. NRK-52E cells, representative of rat kidney proximal epithelium, were exposed to uranyl-carbonate and -citrate complexes, which are the major complexes transiting through renal tubules after acute in vivo contamination. Before NRK-52E cell exposure, these complexes were diluted in classical or modified cell culture media, which can possibly modify uranyl speciation. In these conditions, uranium cytotoxicity appears after 16 h of exposure. The CI50 cytotoxicity index, the uranium concentration leading to 50% dead cells after 24 h of exposure, is 500 microM (+/-100 microM) and strongly depends on uranyl counterion and cell culture medium composition. Computer modeling of uranyl speciation is reported, enabling one to draw a parallel between uranyl speciation and its cytotoxicity.
Asunto(s)
Túbulos Renales Proximales/efectos de los fármacos , Compuestos Organometálicos/toxicidad , Animales , Carbonatos/química , Carbonatos/toxicidad , Recuento de Células , Línea Celular , Supervivencia Celular/efectos de los fármacos , Citratos/química , Citratos/toxicidad , Medios de Cultivo/química , Perros , Relación Dosis-Respuesta a Droga , Células Epiteliales/efectos de los fármacos , Células Epiteliales/patología , Humanos , Túbulos Renales Proximales/patología , Modelos Biológicos , Compuestos Organometálicos/química , Compuestos Organometálicos/clasificación , Ratas , Compuestos de Uranio/química , Compuestos de Uranio/clasificación , Compuestos de Uranio/toxicidadRESUMEN
A new active biomonitoring tool, keeping alive mosses for 2 months, had demonstrated the buffering action of the water presence on the biological activity of three moss species (chlorophyll fluorescence induction method on Pleurozium schreberi, Scleropodium purum, Eurhynchium praelongum). The two more resistant mosses were exposed on four different sites with parallel exposure of monthly bulk collectors during three successive periods of 2 months. The coarse and sedimentable particles of bulk collectors were separated into different size classes (> 1 mm; 1000-200 microm; 200-40 microm; 40-20 microm). Dry depositions and mosses were analysed by Inductively Coupled Plasma Mass Spectrometry (ICP-MS) for a stock (microg g(-1)- fluxes (microg m(-2) t(-1)) conversion. The "moss plate" allowed relative site (Ba, Cs, Sb, Sr, U) and species (Pb, Sb, Ti, V) comparisons. Two months were enough for a significant enrichment (Ba, Cd, Pb, Sb, Ti, U, V). Good explicative models were elaborated for Ba, Pb, Sb and Ti (r2 > 70%) including categorical (sites, moss species) and quantitative variables (fluxes of particles size classes). Entire and intact shoots of Scleropodium purum were analysed by detected synchrotron radiation induced X-ray fluorescence (SXRF). The in vivo distribution of the multi-elemental short term enrichment along the moss stem was mainly localized in the plant older parts (Pb, Ti, Cl, Se).
Asunto(s)
Contaminantes Atmosféricos/análisis , Bryopsida/fisiología , Monitoreo del Ambiente/métodos , Oligoelementos/análisis , Bryopsida/química , Bryopsida/crecimiento & desarrollo , Clorofila/análisis , Exposición a Riesgos Ambientales , Fluorescencia , Modelos Teóricos , Tamaño de la PartículaRESUMEN
As a part of an air-pollution biomonitoring survey, a procedure using inductively coupled plasma-mass spectrometry (ICP-MS) and microwave digestion was developed to achieve a high sample throughput and guarantee the accuracy of the results. This article presents an analytical method to measure 22 trace elements. As, Ba, Cd, Ce, Co, Cr, Cs, Cu, Fe, Hg, La, Mo, Ni, Pb, Rb, Sb, Sr, Th, Tl, U, V, W were analyzed in 563 mosses collected in France. The digestion was performed in polytetrafluoroethylene (PTFE) vessel using the mixture HNO3-H2O2-HF. The data were reprocessed taking into account the drift curve calculated for each element. The detection limits (DL) calculation was based on the standard deviations of the reagent blanks concentrations. The DL varied from one batch to another, because of the heterogeneity of the mosses' elemental contents. The DL ranged between 0.001 microg/g (Cs, Tl) and 70 microg/g (Fe) and were mainly around 0.01 microg/g (As, Cd, Ce, Co, Hg, La, Mo, Sb, Sr, U, V, W). The detection limits obtained were in agreement with the concentrations observed in the samples, except for Hg and Ni. The reproducibility between duplicates and the analytical precision were near 10%. The procedure was tested with the mosses' reference materials.