Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 313
Filtrar
1.
J Hazard Mater ; 444(Pt A): 130410, 2023 02 15.
Artículo en Inglés | MEDLINE | ID: mdl-36413896

RESUMEN

Uranium contamination is a widespread problem caused by natural and anthropogenic activities. Although microorganisms thrive in uranium-contaminated environments, little is known about the actual molecular mechanisms mediating uranium resistance. Here, we investigated the resistance mechanisms driving the adaptation of Cupriavidus metallidurans NA4 to toxic uranium concentrations. We selected a spontaneous mutant able to grow in the presence of 1 mM uranyl nitrate compared to 250 µM for the parental strain. The increased uranium resistance was acquired via the formation of periplasmic uranium-phosphate precipitates facilitated by the increased expression of a genus-specific small periplasmic protein, PrsQ2, regulated as non-cognate target of the CzcS2-CzcR2 two-component system. This study shows that bacteria can adapt to toxic uranium concentrations and explicates the complete genetic circuit behind the adaptation.


Asunto(s)
Cupriavidus , Uranio , Uranio/toxicidad , Cupriavidus/genética , Nitrato de Uranilo , Aclimatación
2.
Toxicol In Vitro ; 73: 105149, 2021 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-33753177

RESUMEN

In the situation of radiation triage, accidental exposure to uranium, or uranium contamination in food or water; haematopoietic decline or bone marrow sickness is observed in the aftermath followed by other systemic effects. Most studies done previously have been on cytogenetic analysis in blood lymphocytes of uranium miners wherein causal relationship was difficult to be established. This study provides new insights into the minimum risk level of uranium to human lymphocytes, DNA damage induced and alterations in the cell cycle progression through 96-h acute toxicity study. Cytotoxicity studies by MTT assay and flow cytometry showed that uranyl nitrate concentration of 1280 µM lead to 50% cell death, 640 µM caused 25% death, 250 µM caused 10% cell death and 5 µM was the NOAEL. Uranium caused DNA damages in a dose dependent manner as evident from comet and CBMN assays. A marked increase in G2/M phase cells was observed in the test culture groups. Halting of cell cycle at G2/M checkpoint also signified the extent of double strand breaks and genetic instability with increasing uranium dose in this study. Better cell cycle responses and lower genetic damage index observed in lower dosage of exposure, suggests adaptability and repair responses in human lymphocytes. Together these results advance our understanding of uranium effects on mammalian cells.


Asunto(s)
Linfocitos/efectos de los fármacos , Contaminantes Radiactivos/toxicidad , Nitrato de Uranilo/toxicidad , Ciclo Celular/efectos de los fármacos , Células Cultivadas , Ensayo Cometa , Daño del ADN , Inestabilidad Genómica/efectos de los fármacos , Humanos , Pruebas de Micronúcleos , Pruebas de Toxicidad Aguda , Uranio
3.
J Trace Elem Med Biol ; 64: 126708, 2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-33360916

RESUMEN

BACKGROUND: Despite their differences in physicochemical properties, both uranium (U) and fluoride (F) are nephrotoxicants at high doses but their adverse effects at low doses are still the subject of debate. METHODS: This study aims to improve the knowledge of the biological mechanisms involved through an adaptive response model of C57BL/6 J mice chronically exposed to low priming doses of U (0, 10, 20 and 40 mg/L) or F (0, 15, 30 and 50 mg/L) and then challenged with acute exposure of 5 mg/kg U or 7.5 mg/kg NaF. RESULTS: We showed that an adaptive response occurred with priming exposures to 20 mg/L U and 50 mg/L F, with decreased levels of the biomarkers KIM-1 and CLU compared to those in animals that received the challenge dose only (positive control). The adaptive mechanisms involved a decrease in caspase 3/7 activities in animals exposed to 20 mg/L U and a decrease in in situ VCAM expression in mice exposed to 50 mg/L F. However, autophagy and the UPR were induced independently of priming exposure to U or F and could not be identified as adaptive mechanisms to U or F. CONCLUSION: Taken together, these results allow us to identify renal adaptive responses to U and F at doses of 20 and 50 mg/L, probably through decrease apoptosis and inflammatory cell recruitment.


Asunto(s)
Riñón/efectos de los fármacos , Fluoruro de Sodio/farmacología , Nitrato de Uranilo/farmacología , Administración Oral , Animales , Relación Dosis-Respuesta a Droga , Riñón/metabolismo , Masculino , Ratones , Ratones Endogámicos C57BL , Fluoruro de Sodio/administración & dosificación , Nitrato de Uranilo/administración & dosificación
4.
Chemosphere ; 254: 126855, 2020 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-32361538

RESUMEN

Under suboxic and anoxic environments, magnetite is one corrosion product of iron being used in nuclear waste canisters. Previous studies have reported a complete reduction of U(VI) on the surfaces of biogenic and natural magnetite crystals, while incomplete reductions to U(V)/U(IV)-containing species have been observed on chemosynthetic magnetite. To date, the reasons behind such disparities remain poorly studied. This study shows that uranyl nitrate or uranyl acetate is mainly reduced to UO2+x oxides (e.g., U4O9, U3O8, etc.) by chemosynthetic magnetite under acidic conditions. When extra zero valent-iron was added, the reaction rate was significantly increased, and an improved but still incomplete U(VI) reduction was observed. Nitrate and ferric ions are ubiquitous in natural environment. Results demonstrate that the nitrate ion associated with uranyl and the ferric ion contained in magnetite or generated from U(VI) reduction have a non-negligible oxidative effect on the final products, which could mainly account for the incomplete reduction of U(VI) by chemosynthetic magnetite in the absence or presence of extra zero valent-iron observed in this study. Furthermore, the surface loading of uranium in U-Fe systems can, in part, unravel the discrepancies in various observations. An enhanced understanding of the U-Fe reaction mechanism can facilitate predictions of the extent of uranium mobility with respect to nuclear waste disposal and radioactive decontamination.


Asunto(s)
Óxido Ferrosoférrico/química , Uranio/química , Contaminantes Radiactivos del Agua/química , Hierro/química , Nitratos , Compuestos Organometálicos , Oxidación-Reducción , Residuos Radiactivos , Nitrato de Uranilo , Contaminantes Radiactivos del Agua/análisis
5.
Health Phys ; 119(3): 322-326, 2020 09.
Artículo en Inglés | MEDLINE | ID: mdl-32301861

RESUMEN

This medical case report describes the first reported instance of occupational skin contamination with a uranyl nitrate solution containing highly enriched uranium. The report provides an overview of the unique medical treatment and management considerations in such a case. Internal dose assessment is covered in detail. The discussion covers key points regarding uranium characteristics, chemical and radiological damage to body tissues from HEU exposure, and resources available for assistance with a case of radiological contamination. This information adds to the limited medical literature on this topic and provides a valuable reference for medical personnel when dealing with this uncommon problem.


Asunto(s)
Exposición Profesional/efectos adversos , Exposición a la Radiación/efectos adversos , Piel/efectos de la radiación , Uranio/efectos adversos , Nitrato de Uranilo/efectos adversos , Descontaminación/métodos , Humanos , Masculino , Persona de Mediana Edad , Dosis de Radiación , Radioquímica
6.
J Hazard Mater ; 384: 121316, 2020 02 15.
Artículo en Inglés | MEDLINE | ID: mdl-31607578

RESUMEN

In this study, Staphylococcus aureus biofilms, which are considered a foe for being pathogenic, were tested for their uranium bioremediation capacity to find out if they can turn out to be a friend. Acid phosphatase activity, which is speculated to aid in bio-precipitation of U(VI) from uranyl nitrate solution, was assayed in biofilms of seven different S. aureus strains. The presence of acid phosphatase enzyme was detected in the biofilms of all S. aureus strains (in the range of 3.1 ± 0.21 to 26.90 ± 2.32 µi.u./g), and found to be higher when compared to that of their planktonic phenotypes. Among all, S. aureus V329 biofilm showed highest biofilm formation ability along with maximum phosphatase activity (26.9 ± 2.32 µi.u./g of biomass). Addition of phosphate enhanced the U(VI) remediation when treated with uranyl nitrate solution. S. aureus V329 biofilm showed significant U tolerance with only a 3-log reduction when exposed to 10 ppm U(VI) for 1 h. When treated in batch mode, V329 biofilm successfully remediated up to 47% of the 10 ppm U(VI). This new approach using the acid phosphatase from the S. aureus V329 biofilm presents an alternative method for the remediation of uranium contamination.


Asunto(s)
Fosfatasa Ácida/química , Biopelículas , Restauración y Remediación Ambiental/métodos , Staphylococcus aureus/enzimología , Uranio , Biodegradación Ambiental , Plancton/química , Nitrato de Uranilo/química
7.
Radiat Environ Biophys ; 58(3): 385-391, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-30972493

RESUMEN

The aim of this study was to determine the uranium distribution and histopathological changes in broiler organs (kidney, liver, and brain) and muscle after 7 days of contamination with high doses of uranyl nitrate hexahydrate (UN), and the protective efficiency of three different mineral adsorbents (organobentonite, organozeolite, and sepiolite). During the 7 days, the UN administration was 50 mg per day, and administration of adsorbents was 2 g per day immediately after UN. In control group where broilers received only UN, histopathological changes such as necrosis of intestinal villi, oedema, vacuolisation and abruption of epithelial cells in renal tubules, oedema and vacuolisation of the cytoplasm of hepatocytes, and dystrophic changes in the neurons of the medulla oblongata were observed. In contrast, when the adsorbents organobentonite, organozeolite, and sepiolite were administered, no histopathological changes were observed in liver and brain. The investigated adsorbents showed the highest protective effects in liver (80-92%), compared to the kidney (77-86%), brain (37-64%), and meat (31-63%).


Asunto(s)
Pollos , Minerales/química , Dosis de Radiación , Protectores contra Radiación , Nitrato de Uranilo/análisis , Animales , Peso Corporal , Ingestión de Alimentos , Hígado , Silicatos de Magnesio , Uranio/análisis , Uranio/toxicidad , Nitrato de Uranilo/toxicidad
8.
Artículo en Inglés | MEDLINE | ID: mdl-30934888

RESUMEN

Because of their nephrotoxicity and presence in the environment, uranium (U) and fluoride (F) represent risks to the global population. There is a general lack of knowledge regarding the mechanisms of U and F nephrotoxicity and the underlying molecular pathways. The present study aims to compare the threshold of the appearance of renal impairment and to study apoptosis and inflammation as mechanisms of nephrotoxicity. C57BL/6J male mice were intraperitoneally treated with a single dose of U (0, 2, 4 and 5 mg/kg) or F (0, 2, 5, 7.5 and 10 mg/kg) and euthanized 72 h after. Renal phenotypic characteristics and biological mechanisms were evaluated by urine biochemistry, gene/protein expression, enzyme activity, and (immuno)histological analyses. U and F exposures induced nephrotoxicity in a dose-dependent manner, and the highest concentrations induced severe histopathological alterations as well as increased gene expression and urinary excretion of nephrotoxicity biomarkers. KIM-1 gene expression was induced starting at 2 mg/kg U and 7.5 mg/kg F, and this increase in expression was confirmed through in situ detection of this biomarker of nephrotoxicity. Both treatments induced inflammation as evidenced by cell adhesion molecule expression and in situ levels, whereas caspase 3/7-dependent apoptosis was increased only after U treatment. Overall, a single dose of F or U induced histopathologic evidence of nephrotoxicity renal impairment and inflammation in mice with thresholds under 7.5 mg/kg and 4 mg/kg, respectively.


Asunto(s)
Riñón/efectos de los fármacos , Fluoruro de Sodio/toxicidad , Nitrato de Uranilo/toxicidad , Animales , Apoptosis/efectos de los fármacos , Biomarcadores/metabolismo , Caspasa 3/metabolismo , Caspasa 7/metabolismo , Receptor Celular 1 del Virus de la Hepatitis A/genética , Inflamación/inducido químicamente , Inflamación/metabolismo , Inflamación/patología , Riñón/metabolismo , Riñón/patología , Masculino , Ratones Endogámicos C57BL
9.
Biol Trace Elem Res ; 189(2): 405-411, 2019 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-30302617

RESUMEN

Uranium is a heavy metal of considerable environmental and occupational concern. It is well-known that the kidney is the major target organ of uranium exposure. Elucidating the mechanistic basis of uranium interactions is essential for monitoring the health risk. In the present study, we investigated the cellular mechanisms involved in uranyl nitrate-induced nephrotoxicity. Male Swiss albino mice were administrated with a single intraperitoneal dose of 2 and 4 mg/kg of uranyl nitrate at different time points 1, 3, 5, 7, 14, and 28 days. Uranyl nitrate intoxication-induced apoptosis in the kidney tissue was observed by TUNEL assay. To assess the proliferation, immunohistochemistry was performed using Ki67 proliferative marker followed by western blotting to confirm the involvement of key signaling molecules. The number of TUNEL positive nuclei peaked at third day after uranyl nitrate insult. The increased expression of proliferation marker Ki67 suggests the enhanced DNA repair process prominently at seventh day. Uranyl nitrate administration also resulted in activation of extracellular signal-regulated kinases (ERK), Akt, and c-Jun N-terminal kinases (JNK) expression. All these changes were found to be time-dependent. The result of the current study suggests that uranyl nitrate induces acute renal injury by activation of apoptosis through JNK pathway, while the early activation of signaling molecules Akt and ERK promotes the tubular cell proliferation and cell survival.


Asunto(s)
Lesión Renal Aguda/metabolismo , Quinasas MAP Reguladas por Señal Extracelular/metabolismo , Proteínas Quinasas JNK Activadas por Mitógenos/metabolismo , Fosfatidilinositol 3-Quinasas/metabolismo , Proteínas Proto-Oncogénicas c-akt/metabolismo , Lesión Renal Aguda/inducido químicamente , Animales , Apoptosis/efectos de los fármacos , Western Blotting , Inmunohistoquímica , Etiquetado Corte-Fin in Situ , Masculino , Ratones , Nitrato de Uranilo/toxicidad
10.
Dalton Trans ; 47(26): 8764-8770, 2018 Jul 03.
Artículo en Inglés | MEDLINE | ID: mdl-29916520

RESUMEN

Deferiprone (3-hydroxy-1,2-dimethyl-4(1H)-pyridone, DFP), which is a drug clinically used for removing heavy metals in vivo, was explored for its removal efficiency towards uranium. The reaction of uranyl nitrate hexahydrate with DFP at room temperature yielded the compound [(UO2)(H2O)(C7NO2H8)2]·4H2O (1), which crystallizes from a mixed solution of methanol and water (pH = 7.0). X-ray diffraction shows that the stable complexation of uranyl occurs from the coordination of two bidentate DFP ligands perpendicular to the O[double bond, length as m-dash]U[double bond, length as m-dash]O unit with a fifth coordinating oxygen atom coming from one water molecule, resulting in a pentagonal bipyramidal geometry. The formation constants of uranyl and DFP complexes were measured and the species distribution diagram illustrates that UO2L2 (94.6%) is the dominant uranyl-DFP complex in 0.1 M KCl solution at physiological pH = 7.4. The results from both crystallographic and potentiometric studies imply that the metal : ligand ratio is 1 : 2. The effectiveness of using DFP to remove uranium was examined at the cellular level, and the results suggest that it can significantly reduce the cellular uptake and increase the cellular release of U(vi) in renal proximal tubular epithelial cells (NRK-52E).


Asunto(s)
Complejos de Coordinación/química , Complejos de Coordinación/farmacología , Endocitosis/efectos de los fármacos , Piridonas/química , Termodinámica , Nitrato de Uranilo/química , Animales , Línea Celular , Complejos de Coordinación/síntesis química , Deferiprona , Humanos , Concentración de Iones de Hidrógeno , Ligandos , Metanol/química , Modelos Moleculares , Cloruro de Potasio/química , Ratas , Agua/química
11.
Chemosphere ; 201: 603-611, 2018 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-29544215

RESUMEN

Bicarbonate, ubiquitous in natural and waste waters is an important factor regulating the rate and efficiency of pollutant separation and transformation. For example, it can form complexes with U(VI) in the aqueous phase and at the solid-water interface. In this work, we investigated the effect of bicarbonate on the aging of nanoscale zero-valent (nZVI) in the context of U(VI) reduction and removal from wastewater. For fresh nZVI, over 99% aqueous uranium was separated in less than 10 min, of which 83% was reduced from U(VI) to U(IV). When nZVI was aged in water, its activity for U(VI) sequestration and reduction was significantly reduced. Batch experiments showed that for nZVI aged in the presence of 10 mM bicarbonate, only 20.3% uranium was reduced to U(IV) after 6 h reactions. Characterizations of the iron nanoparticles with spherical aberration corrected scanning transmission electron microscopy (Cs-STEM) suggest that in fresh nZVI, uranium was concentrated at the nanoparticle center; whereas in nZVI aged in bicarbonate, uranium was largely deposited on the outer surface of the nanoparticles. Furthermore, aged nZVI without bicarbonate contained more lepidocrocite (γ-FeOOH) while aged nZVI in the presence of bicarbonate had more magnetite/maghemite (Fe3O4/γ-Fe2O3). This could be attributed to the formation of carbonate green rust and pH buffer effect of . Primary mechanisms for U(VI) removal with nZVI include reduction, sorption and/or precipitation. Results demonstrate that bicarbonate alter the aging products of nZVI, and reduces the separation efficiency and reduction capability for uranium removal.


Asunto(s)
Bicarbonatos/química , Hierro/química , Nanopartículas/química , Nitrato de Uranilo/análisis , Contaminantes Radiactivos del Agua/análisis , Compuestos Férricos/química , Óxido Ferrosoférrico/química , Microscopía Electrónica de Transmisión de Rastreo , Oxidación-Reducción , Propiedades de Superficie
12.
Luminescence ; 33(3): 611-615, 2018 May.
Artículo en Inglés | MEDLINE | ID: mdl-29356360

RESUMEN

Uranyl tris nitrato i.e. [UO2 (NO3 )3 ]- was formed by adding tetramethylammonium nitrate to uranyl nitrate in acetonitrile medium. The luminescence features of this complex in acetonitrile are very sensitive to water content, which could lead to the use of it as a luminescent probe for water present in acetonitrile. The luminescence intensity ratio of 507 to 467 nm peak of uranyl tris nitrato showed a linear response in the range 0-5% (v/v) water content in acetonitrile. The present method was applied for three synthetic samples of acetonitrile for water detection and the results obtained were compared using Karl Fischer titration. There was a good agreement in the values obtained by both the methods.


Asunto(s)
Acetonitrilos/química , Colorantes Fluorescentes/química , Mediciones Luminiscentes/métodos , Compuestos de Uranio/química , Nitrato de Uranilo/química , Agua/análisis , Calibración , Hidrólisis , Luminiscencia , Reproducibilidad de los Resultados
13.
Toxicol Appl Pharmacol ; 331: 135-141, 2017 09 15.
Artículo en Inglés | MEDLINE | ID: mdl-28602947

RESUMEN

Depleted uranium (DU) is a radioactive heavy metal used primarily in military applications. Published data from our laboratory have demonstrated that DU exposure in vitro to immortalized human osteoblast cells (HOS) is both neoplastically transforming and genotoxic. In vivo studies have also demonstrated that DU is leukemogenic and genotoxic. DU possesses both a radiological (alpha particle) and chemical (metal) component but is generally considered a chemical biohazard. Studies have shown that alpha particle radiation does play a role in DU's toxic effects. Evidence has accumulated that non-irradiated cells in the vicinity of irradiated cells can have a response to ionization events. The purpose of this study was to determine if these "bystander effects" play a role in DU's toxic and neoplastic effects using HOS cells. We investigated the bystander responses between DU-exposed cells and non-exposed cells by co-culturing the two equal populations. Decreased cell survival and increased neoplastic transformation were observed in the non-DU exposed cells following 4 or 24h co-culture. In contrast Ni (II)- or Cr(VI)- exposed cells were unable to alter those biological effects in non-Ni(II) or non-Cr(VI) exposed co-cultured cells. Transfer experiments using medium from the DU-exposed and non-exposed co-cultured cells was able to cause adverse biological responses in cells; these results demonstrated that a factor (s) is secreted into the co-culture medium which is involved in this DU-associated bystander effect. This novel effect of DU exposure could have implications for radiation risk and for health risk assessment associated with DU exposure.


Asunto(s)
Efecto Espectador/efectos de los fármacos , Efecto Espectador/efectos de la radiación , Osteoblastos/efectos de los fármacos , Osteoblastos/efectos de la radiación , Exposición a la Radiación/efectos adversos , Uranio/toxicidad , Efecto Espectador/fisiología , Supervivencia Celular/efectos de los fármacos , Supervivencia Celular/fisiología , Transformación Celular Neoplásica/efectos de los fármacos , Transformación Celular Neoplásica/metabolismo , Transformación Celular Neoplásica/efectos de la radiación , Técnicas de Cocultivo/métodos , Humanos , Osteoblastos/fisiología , Nitrato de Uranilo/toxicidad
14.
Toxicol Lett ; 257: 44-59, 2016 Aug 22.
Artículo en Inglés | MEDLINE | ID: mdl-27267564

RESUMEN

The civilian and military use of uranium results in an increased risk of human exposure. The toxicity of uranium results from both its chemical and radiological properties that vary with isotopic composition. Validated biomarkers of health effects associated with exposure to uranium are neither sensitive nor specific to uranium radiotoxicity and/or radiological effect. This study aimed at investigating if serum proteins could be useful as biomarkers of both uranium exposure and radiological effect. Male Sprague-Dawley rats were chronically exposed through drinking water to low levels (40mg/L, corresponding to 1mg of uranium per animal per day) of either 4% (235)U-enriched uranium (EU) or 12% EU during 6 weeks. A proteomics approach based on two-dimensional electrophoresis (2D-DIGE) and mass spectrometry (MS) was used to establish protein expression profiles that could be relevant for discriminating between groups, and to identify some differentially expressed proteins following uranium ingestion. It demonstrated that the expressions of 174 protein spots over 1045 quantified spots were altered after uranium exposure (p<0.05). Using both inferential and non-supervised multivariate statistics, we show sets of spots features that lead to a clear discrimination between controls and EU exposed groups on the one hand (21 spots), and between 4% EU and 12% EU on the other hand (7 spots), showing that investigation of the serum proteome may possibly be of relevance to address both uranium contamination and radiological effect. Finally, using bioinformatics tools, pathway analyses of differentially expressed MS-identified proteins find that acute phase, inflammatory and immune responses as well as oxidative stress are likely involved in the response to contamination, suggesting a physiological perturbation, but that does not necessarily lead to a toxic effect.


Asunto(s)
Proteínas Sanguíneas/metabolismo , Proteoma , Traumatismos por Radiación/sangre , Uranio/toxicidad , Nitrato de Uranilo/toxicidad , Contaminantes Radiactivos del Agua/toxicidad , Proteínas de Fase Aguda/metabolismo , Animales , Biomarcadores/sangre , Análisis Discriminante , Ingestión de Líquidos , Mediadores de Inflamación/sangre , Masculino , Análisis Multivariante , Estrés Oxidativo/efectos de la radiación , Análisis de Componente Principal , Mapas de Interacción de Proteínas , Proteómica/métodos , Traumatismos por Radiación/diagnóstico , Ratas Sprague-Dawley , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción , Electroforesis Bidimensional Diferencial en Gel
15.
Toxicol Lett ; 254: 37-44, 2016 Jul 08.
Artículo en Inglés | MEDLINE | ID: mdl-27153795

RESUMEN

Consequences of uranium contamination have been extensively studied in brain as cognitive function impairments were observed in rodents. Locomotor disturbances have also been described in contaminated animals. Epidemiological studies have revealed increased risk of motor neuron diseases in veterans potentially exposed to uranium during their military duties. To our knowledge, biological response of spinal cord to uranium contamination has not been studied even though it has a crucial role in locomotion. Four groups of rats were contaminated with increasing concentrations of uranium in their drinking water compared to a control group to study cellular mechanisms involved in locomotor disorders. Nissl staining of spinal cord sections revealed the presence of chromatolytic neurons in the ventral horn. This observation was correlated with a decreased number of motor neurons in the highly contaminated group and a decrease of SMN1 protein expression (Survival of Motor Neuron 1). While contamination impairs motor neuron integrity, an increasing number of microglial cells indicates the trigger of a neuroinflammation process. Potential overexpression of a microglial recruitment chemokine, MCP-1 (Monocyte Chimioattractant Protein 1), by motor neurons themselves could mediate this process. Studies on spinal cord appear to be relevant for risk assessment of population exposed via contaminated food and water.


Asunto(s)
Intoxicación por Metales Pesados , Microglía/efectos de los fármacos , Neuronas Motoras/efectos de los fármacos , Síndromes de Neurotoxicidad/etiología , Intoxicación/etiología , Médula Espinal/efectos de los fármacos , Proteína 1 para la Supervivencia de la Neurona Motora/metabolismo , Nitrato de Uranilo/toxicidad , Animales , Quimiocina CCL2/metabolismo , Quimiotaxis/efectos de los fármacos , Regulación hacia Abajo , Mediadores de Inflamación/metabolismo , Masculino , Metales Pesados/metabolismo , Microglía/metabolismo , Microglía/patología , Neuronas Motoras/metabolismo , Neuronas Motoras/patología , Síndromes de Neurotoxicidad/genética , Síndromes de Neurotoxicidad/metabolismo , Síndromes de Neurotoxicidad/patología , Intoxicación/genética , Intoxicación/metabolismo , Intoxicación/patología , Ratas Sprague-Dawley , Médula Espinal/metabolismo , Proteína 1 para la Supervivencia de la Neurona Motora/genética , Nitrato de Uranilo/metabolismo
16.
Environ Sci Technol ; 50(8): 4459-67, 2016 Apr 19.
Artículo en Inglés | MEDLINE | ID: mdl-26998856

RESUMEN

The adsorption mechanism of U(VI) and Eu(III) on carbonaceous nanofibers (CNFs) was investigated using batch, IR, XPS, XANES, and EXAFS techniques. The pH-dependent adsorption indicated that the adsorption of U(VI) on the CNFs was significantly higher than the adsorption of Eu(III) at pH < 7.0. The maximum adsorption capacity of the CNFs calculated from the Langmuir model at pH 4.5 and 298 K for U(VI) and Eu(III) were 125 and 91 mg/g, respectively. The CNFs displayed good recyclability and recoverability by regeneration experiments. Based on XPS and XANES analyses, the enrichment of U(VI) and Eu(III) was attributed to the abundant adsorption sites (e.g., -OH and -COOH groups) of the CNFs. IR analysis further demonstrated that -COOH groups were more responsible for U(VI) adsorption. In addition, the remarkable reducing agents of the R-CH2OH groups were responsible for the highly efficient adsorption of U(VI) on the CNFs. The adsorption mechanism of U(VI) on the CNFs at pH 4.5 was shifted from inner- to outer-sphere surface complexation with increasing initial concentration, whereas the surface (co)precipitate (i.e., schoepite) was observed at pH 7.0 by EXAFS spectra. The findings presented herein play an important role in the removal of radionuclides on inexpensive and available carbon-based nanoparticles in environmental cleanup applications.


Asunto(s)
Europio/análisis , Nanofibras/química , Nanofibras/ultraestructura , Nitrato de Uranilo/análisis , Contaminantes Radiactivos del Agua/análisis , Adsorción , Europio/química , Microscopía Electrónica de Rastreo , Microscopía Electrónica de Transmisión , Propiedades de Superficie , Nitrato de Uranilo/química , Contaminantes Radiactivos del Agua/química , Espectroscopía de Absorción de Rayos X
17.
Ren Fail ; 38(5): 770-5, 2016 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-26984368

RESUMEN

Uranium is a radioactive heavy metal ubiquitous in the natural environment. In its chemical form, it is known to induce nephrotoxicity both in human and in animals. Its toxicity is dose and time dependent, also varies with form of uranium. In the present study, we assessed the nephrotoxicity induced by a single dose of uranyl nitrate (UN) in mice at different time intervals and recovery from its toxicity. Two doses of 2 and 4 mg/kg body weight of uranyl nitrate was injected intraperitoneally and animals were sacrificed after 1, 3, 5, 14, and 28 d of administration. Histopathological and biochemical alterations of post-UN dosing in comparison to control were evaluated. Tubular damage to about 75% was observed after 3 d (4 mg/kg) and the biochemical parameters such as serum creatinine, urea, and blood urea nitrogen levels were also significantly increased. Progression of tubular damage was not found after 5 d. Dose-dependent recovery of uranyl nitrate-treated animals was observed after 14 and 28 d of dosing. The concentration of uranium retained in kidney correlates with biochemical and histopathological analysis.


Asunto(s)
Túbulos Renales , Nitrato de Uranilo/toxicidad , Lesión Renal Aguda/diagnóstico , Lesión Renal Aguda/etiología , Lesión Renal Aguda/patología , Animales , Creatinina/sangre , Modelos Animales de Enfermedad , Progresión de la Enfermedad , Relación Dosis-Respuesta en la Radiación , Pruebas de Función Renal/métodos , Túbulos Renales/patología , Túbulos Renales/efectos de la radiación , Ratones , Recuperación de la Función , Factores de Tiempo , Urea/sangre
18.
Inorg Chem ; 54(23): 11557-62, 2015 Dec 07.
Artículo en Inglés | MEDLINE | ID: mdl-26583259

RESUMEN

Cyclic peptides with two phosphoserines and two glutamic acids were developed to mimic high-affinity binding sites for uranyl found in proteins such as osteopontin, which is believed to be a privileged target of this ion in vivo. These peptides adopt a ß-sheet structure that allows the coordination of the latter amino acid side chains in the equatorial plane of the dioxo uranyl cation. Complementary spectroscopic and analytical methods revealed that these cyclic peptides are efficient uranyl chelating peptides with a large contribution from the phosphorylated residues. The conditional affinity constants were measured by following fluorescence tryptophan quenching and are larger than 10(10) at physiological pH. These compounds are therefore promising models for understanding uranyl chelation by proteins, which is relevant to this actinide ion toxicity.


Asunto(s)
Quelantes/química , Imitación Molecular , Péptidos Cíclicos/química , Fosfopéptidos/química , Nitrato de Uranilo/química , Secuencia de Aminoácidos , Sitios de Unión , Calcio/química , Quelantes/síntesis química , Dicroismo Circular , Ácido Glutámico/química , Iminoácidos , Osteopontina/química , Péptidos Cíclicos/síntesis química , Fosfopéptidos/síntesis química , Fosfoserina/química , Estructura Secundaria de Proteína , Espectrometría de Masa por Ionización de Electrospray , Triptófano/química
19.
Toxicol Appl Pharmacol ; 287(3): 306-15, 2015 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-26148447

RESUMEN

Depleted uranium (DU) has been widely used in both civilian and military activities, and the kidney is the main target organ of DU during acute high-dose exposures. In this study, the nephrotoxicity caused by DU in metallothionein-1/2-null mice (MT-/-) and corresponding wild-type (MT+/+) mice was investigated to determine any associations with MT. Each MT-/- or MT+/+ mouse was pretreated with a single dose of DU (10mg/kg, intraperitoneal injection) or an equivalent volume of saline. After 4days of DU administration, kidney changes were assessed. After DU exposure, serum creatinine and serum urea nitrogen in MT-/- mice significantly increased than in MT+/+ mice, with more severe kidney pathological damage. Moreover, catalase and superoxide dismutase (SOD) decreased, and generation of reactive oxygen species and malondialdehyde increased in MT-/- mice. The apoptosis rate in MT-/- mice significantly increased, with a significant increase in both Bax and caspase 3 and a decrease in Bcl-2. Furthermore, sodium-glucose cotransporter (SGLT) and sodium-phosphate cotransporter (NaPi-II) were significantly reduced after DU exposure, and the change of SGLT was more evident in MT-/- mice. Finally, exogenous MT was used to evaluate the correlation between kidney changes induced by DU and MT doses in MT-/- mice. The results showed that, the pathological damage and cell apoptosis decreased, and SOD and SGLT levels increased with increasing dose of MT. In conclusion, MT deficiency aggravated DU-induced nephrotoxicity, and the molecular mechanisms appeared to be related to the increased oxidative stress and apoptosis, and decreased SGLT expression.


Asunto(s)
Enfermedades Renales/metabolismo , Riñón/metabolismo , Metalotioneína/deficiencia , Nitrato de Uranilo , Animales , Antioxidantes/metabolismo , Apoptosis/efectos de los fármacos , Proteínas Reguladoras de la Apoptosis/metabolismo , Biomarcadores/sangre , Nitrógeno de la Urea Sanguínea , Creatinina/sangre , Modelos Animales de Enfermedad , Riñón/patología , Enfermedades Renales/inducido químicamente , Enfermedades Renales/genética , Enfermedades Renales/patología , Masculino , Metalotioneína/genética , Ratones Noqueados , Estrés Oxidativo/efectos de los fármacos , Especies Reactivas de Oxígeno/metabolismo , Proteínas de Transporte de Sodio-Glucosa/efectos de los fármacos , Proteínas de Transporte de Sodio-Glucosa/metabolismo , Factores de Tiempo
20.
Radiat Environ Biophys ; 54(2): 217-24, 2015 May.
Artículo en Inglés | MEDLINE | ID: mdl-25652083

RESUMEN

The use of phosphate mineral products in animal nutrition, as a major source of phosphor and calcium, can lead to uranium entering the food chain. The aim of the present study was to determine the protective effect of natural sepiolite and sepiolite treated with acid for broilers after oral intake of uranium. The broilers were contaminated for 7 days with 25 mg/uranyl nitrate per day. Two different adsorbents (natural sepiolite and sepiolite treated with acid) were given via gastric tube immediately after the oral administration of uranium. Natural sepiolite reduced uranium distribution by 57% in kidney, 80% in liver, 42% in brain, and 56% in muscle. A lower protective effect was observed after the administration of sepiolite treated with acid, resulting in significant damage of intestinal villi in the form of shortening, fragmentation, and necrosis, and histopathological lesions on kidney in the form of edema and abruption of epithelial cells in tubules. When broilers received only sepiolite treated with acid (no uranyl nitrate), shortening of intestinal villi occurred. Kidney injuries were evident when uranium concentrations in kidney were 0.88 and 1.25 µg/g dry weight. It is concluded that adding of natural sepiolite to the diets of broilers can reduce uranium distribution in organs by significant amount without adverse side effects.


Asunto(s)
Alimentación Animal/análisis , Pollos , Silicatos de Magnesio/química , Uranio/química , Adsorción , Animales , Concentración de Iones de Hidrógeno , Mucosa Intestinal/metabolismo , Factores de Tiempo , Uranio/aislamiento & purificación , Uranio/metabolismo , Uranio/toxicidad , Nitrato de Uranilo/química
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...