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1.
Rev Environ Contam Toxicol ; 245: 65-127, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29119384

RESUMEN

Tributyltin (TBT) has been recognized as an endocrine disrupting chemical (EDC) for several decades. However, only in the last decade, was its primary endocrine mechanism of action (MeOA) elucidated-interactions with the nuclear retinoid-X receptor (RXR), peroxisome proliferator-activated receptor γ (PPARγ), and their heterodimers. This molecular initiating event (MIE) alters a range of reproductive, developmental, and metabolic pathways at the organism level. It is noteworthy that a variety of MeOAs have been proposed over the years for the observed endocrine-type effects of TBT; however, convincing data for the MIE was provided only recently and now several researchers have confirmed and refined the information on this MeOA. One of the most important lessons learned from years of research on TBT concerns apparent species sensitivity. Several aspects such as the rates of uptake and elimination, chemical potency, and metabolic capacity are all important for identifying the most sensitive species for a given chemical, including EDCs. For TBT, much of this was discovered by trial and error, hence important relationships and important sensitive taxa were not identified until several decades after its introduction to the environment. As recognized for many years, TBT-induced responses are known to occur at very low concentrations for molluscs, a fact that has more recently also been observed in fish species. This review explores the MeOA and effects of TBT in different species (aquatic molluscs and other invertebrates, fish, amphibians, birds, and mammals) according to the OECD Conceptual Framework for Endocrine Disruptor Testing and Assessment (CFEDTA). The information gathered on biological effects that are relevant for populations of aquatic animals was used to construct Species Sensitivity Distributions (SSDs) based on No Observed Effect Concentrations (NOECs) and Lowest Observed Effect Concentrations (LOECs). Fish appear at the lower end of these distributions, showing that they are as sensitive as molluscs, and for some species, even more sensitive. Concentrations in the range of 1 ng/L for water exposure (10 ng/g for whole-body burden) have been shown to elicit endocrine-type responses, whereas mortality occurs at water concentrations ten times higher. Current screening and assessment methodologies as compiled in the OECD CFEDTA are able to identify TBT as a potent endocrine disruptor with a high environmental risk for the original use pattern. If those approaches had been available when TBT was introduced to the market, it is likely that its use would have been regulated sooner, thus avoiding the detrimental effects on marine gastropod populations and communities as documented over several decades.


Asunto(s)
Ecología/tendencias , Disruptores Endocrinos/toxicidad , Exposición a Riesgos Ambientales/análisis , Compuestos de Trialquiltina/toxicidad , Animales , Disruptores Endocrinos/análisis , Disruptores Endocrinos/metabolismo , Exposición a Riesgos Ambientales/efectos adversos , Guías como Asunto , Humanos , Agencias Internacionales , Medición de Riesgo , Pruebas de Toxicidad , Compuestos de Trialquiltina/análisis , Compuestos de Trialquiltina/metabolismo
2.
BMC Microbiol ; 14: 102, 2014 Apr 23.
Artículo en Inglés | MEDLINE | ID: mdl-24755232

RESUMEN

BACKGROUND: A variety of conditions (culture media, inocula, incubation temperatures) are employed in antifouling tests with marine bacteria. Shewanella algae was selected as model organism to evaluate the effect of these parameters on: bacterial growth, biofilm formation, the activity of model antifoulants, and the development and nanomechanical properties of the biofilms.The main objectives were: 1) To highlight and quantify the effect of these conditions on relevant parameters for antifouling studies: biofilm morphology, thickness, roughness, surface coverage, elasticity and adhesion forces. 2) To establish and characterise in detail a biofilm model with a relevant marine strain. RESULTS: Both the medium and the temperature significantly influenced the total cell densities and biofilm biomasses in 24-hour cultures. Likewise, the IC50 of three antifouling standards (TBTO, tralopyril and zinc pyrithione) was significantly affected by the medium and the initial cell density. Four media (Marine Broth, MB; 2% NaCl Mueller-Hinton Broth, MH2; Luria Marine Broth, LMB; and Supplemented Artificial Seawater, SASW) were selected to explore their effect on the morphological and nanomechanical properties of 24-h biofilms. Two biofilm growth patterns were observed: a clear trend to vertical development, with varying thickness and surface coverage in MB, LMB and SASW, and a horizontal, relatively thin film in MH2. The Atomic Force Microscopy analysis showed the lowest Young modulii for MB (0.16 ± 0.10 MPa), followed by SASW (0.19 ± 0.09 MPa), LMB (0.22 ± 0.13 MPa) and MH2 (0.34 ± 0.16 MPa). Adhesion forces followed an inverted trend, being higher in MB (1.33 ± 0.38 nN) and lower in MH2 (0.73 ± 0.29 nN). CONCLUSIONS: All the parameters significantly affected the ability of S. algae to grow and form biofilms, as well as the activity of antifouling molecules. A detailed study has been carried out in order to establish a biofilm model for further assays. The morphology and nanomechanics of S. algae biofilms were markedly influenced by the nutritional environments in which they were developed. As strategies for biofilm formation inhibition and biofilm detachment are of particular interest in antifouling research, the present findings also highlight the need for a careful selection of the assay conditions.


Asunto(s)
Biopelículas/crecimiento & desarrollo , Desinfectantes/metabolismo , Shewanella/fisiología , Biopelículas/efectos de los fármacos , Biopelículas/efectos de la radiación , Medios de Cultivo/química , Compuestos Organometálicos/metabolismo , Piridinas/metabolismo , Pirroles/metabolismo , Shewanella/efectos de los fármacos , Shewanella/crecimiento & desarrollo , Shewanella/efectos de la radiación , Temperatura , Compuestos de Trialquiltina/metabolismo
3.
Appl Microbiol Biotechnol ; 90(1): 353-60, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21132289

RESUMEN

Natural attenuation can reduce contamination of tributyltin (TBT), but persistence of the xenobiotic can cause long-term issues in the environment. Biostimulation is used to accelerate biodegradation. This study investigated the ability of individual organic nutrients and growth factors to enhance TBT biodegradation by sediment microorganisms (SED) and Enterobacter cloacae strain TISTR1971 (B3). The supplements that produced high biomass yield were selected for degradation enhancement. For TBT degradation at initial concentration of 0.1 mg/l, negative or limited degradation was observed in some selected supplements indicating that increasing the biomass did not necessarily promote degradation. Consequently, the addition of nutrients was expected to increase both dioxygenase activity and the degrader population. At different concentrations of supplements, a mixture of succinate/glycerol showed the highest removal for SED which reduced TBT by 77%, 75%, and 68% for 0.1×, 1×, and 10× supplement concentration, respectively. For B3, the addition of succinate showed degradation of 49% (0.1×), 75% (1×), and 77% (10×). Most nutrients and amino acids had an inhibitory effect at 1× or 10× levels. Excess amount of the nutrients added can inhibit the initial degradation of TBT. Therefore, TBT biostimulation requires supplements that increase the capability of TBT degraders at an appropriate amount.


Asunto(s)
Enterobacter cloacae/crecimiento & desarrollo , Enterobacter cloacae/metabolismo , Sedimentos Geológicos/microbiología , Compuestos de Trialquiltina/metabolismo , Aminoácidos/metabolismo , Biodegradación Ambiental , Medios de Cultivo/metabolismo , Enterobacter cloacae/aislamiento & purificación , Ácido Succínico/metabolismo , Vitaminas/metabolismo
4.
Chemosphere ; 63(3): 449-57, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16289217

RESUMEN

Concentrations and body burdens of 14 trace elements (Hg, Cr, Mn, Co, Cu, Zn, Sr, Ag, Cd, V, Se, Pb, Mo, and Fe) and butyltins (BTs) (tributyltin TBT, dibutyltin DBT, and monobutyltin MBT) were determined in various tissues of a mature male Dall's porpoise (Phocoenoides dalli) collected off the Sanriku coast of Japan. Selective accumulation in this porpoise was observed for Hg, Mn, Cu, Ag, Mo, Fe, and total BTs (TBT, DBT, and MBT) in the liver, Cd in the kidney, Zn, Sr, V, Pb, and Co in the bone, and Se in the skin. In contrast, Cr concentrations in all tissues were similar. This distribution pattern in this mature porpoise was in general agreement with the accumulation characteristics of trace elements and butyltins reported for other marine mammals. The whole body of the porpoise contained approximately 62 g Fe, 8.8 g Zn, 4.0 g Sr, 0.6g Se, 0.41 g Cu, 0.19 g Hg, 0.17 g Cd, 0.16 g Mn, 0.05 g Cr, 0.009 g Ag, 0.008 g Mo, 0.005 g Pb, 0.004 g Co, and 0.7 mg of BTs (0.4 mg TBT, 0.2 mg DBT, and 0.1 mg MBT). Metabolism of TBT to its breakdown products of this porpoise seems to be limited, since TBT still accounted for about half of the total burden of BTs. As in the cases of Hg, Mn, Cu, Se, and Fe, the muscle was the most important reservoir (43%) for the whole body burden of total BTs, 80% of which was TBT, and thus muscle played a crucial role in the higher body composition of TBT in this Dall's porpoise.


Asunto(s)
Marsopas/metabolismo , Contaminantes Químicos del Agua/análisis , Animales , Carga Corporal (Radioterapia) , Monitoreo del Ambiente , Japón , Hígado/química , Masculino , Metales Pesados/análisis , Metales Pesados/metabolismo , Compuestos Orgánicos de Estaño/análisis , Compuestos Orgánicos de Estaño/metabolismo , Selenio/análisis , Selenio/metabolismo , Compuestos de Trialquiltina/análisis , Compuestos de Trialquiltina/metabolismo , Contaminantes Químicos del Agua/metabolismo
5.
Mol Endocrinol ; 19(10): 2502-16, 2005 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-15941851

RESUMEN

Retinoid X receptor (RXR) is a nuclear receptor that plays important and multiple roles in mammalian development and homeostasis. We previously reported that, in human choriocarcinoma cells, tributyltin chloride and triphenyltin hydroxide, which are typical environmental contaminants and cause masculinization in female mollusks, are potent stimulators of human chorionic gonadotropin production and aromatase activity, which play key endocrine functions in maintaining pregnancy and fetal development. However, the molecular mechanism through which these compounds stimulate these endocrine functions remains unclear. Our current study shows that trialkyltin compounds, including tributyltin chloride and triphenyltin hydroxide, function as RXR agonists. Trialkyltins directly bind to the ligand-binding domain of RXR with high affinity and function as transcriptional activators. Unlike the natural RXR ligand, 9-cis-retinoic acid, the activity of trialkyltins is RXR specific and does not activate the retinoic acid receptor pathway. In addition, trialkyltins activate RXR to stimulate the expression of a luciferase reporter gene containing the human placental promoter I.1 sequence of aromatase, suggesting that trialkyltins stimulate human placental endocrine functions through RXR-dependent signaling pathways. Therefore, our results suggest that activation of RXR may be a novel mechanism by which trialkyltins alter human endocrine functions.


Asunto(s)
Placenta/efectos de los fármacos , Placenta/fisiopatología , Receptores X Retinoide/agonistas , Receptores X Retinoide/metabolismo , Compuestos de Trialquiltina/metabolismo , Compuestos de Trialquiltina/toxicidad , Animales , Aromatasa/genética , Aromatasa/metabolismo , Secuencia de Bases , Sitios de Unión , Línea Celular , Gonadotropina Coriónica/biosíntesis , ADN Complementario/genética , Contaminantes Ambientales/metabolismo , Contaminantes Ambientales/toxicidad , Femenino , Humanos , Técnicas In Vitro , Ligandos , Embarazo , Unión Proteica , Estructura Terciaria de Proteína , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Receptores X Retinoide/química , Transducción de Señal/efectos de los fármacos , Transfección
6.
FEMS Microbiol Lett ; 167(2): 321-6, 1998 Oct 15.
Artículo en Inglés | MEDLINE | ID: mdl-9809434

RESUMEN

The toxicity of inorganic metal species towards Saccharomyces cerevisiae has been shown to be markedly dependent on cellular fatty acid composition. In this investigation, the influence of fatty acid supplementation on the toxicity of the lipophilic organometal, tributyltin was investigated. Growth of S. cerevisiae was increasingly inhibited when the tributyltin concentration was increased from 0 to 10 microM. However, the inhibitory effect was partly alleviated by supplementation of the medium with 1 mM linoleate (18:2), a treatment that leads to large-scale incorporation of this polyunsaturated fatty acid (to > 60% of total fatty acids) in yeast membrane lipids. Cells that were previously enriched with 18:2 also showed reduced loss of vitality compared to cells grown in the absence of a fatty acid supplement, when exposed to tributyltin. For example, addition of tributyltin to a concentration of 0.1 microM was associated with an approximate 10% reduction in the H+ efflux activity of 18:2-enriched cells, but a 70% reduction in that of fatty acid-unsupplemented cells. Despite the increased tributyltin resistance of 18:2-enriched S. cerevisiae, the level of cell-associated tributyltin was found to be approximately two-fold higher in these organisms than in fatty acid-unsupplemented cells. These results demonstrate an increased resistance of 18:2-enriched membranes to the direct toxic action(s) of tributyltin. This is in contrast to the previously reported effect of 18:2 enrichment on sensitivity of S. cerevisiae to inorganic metal cations.


Asunto(s)
Ácido Linoleico/farmacología , Saccharomyces cerevisiae/efectos de los fármacos , Compuestos de Trialquiltina/farmacología , Medios de Cultivo , Relación Dosis-Respuesta a Droga , Membranas/química , Fuerza Protón-Motriz , Saccharomyces cerevisiae/química , Saccharomyces cerevisiae/crecimiento & desarrollo , Factores de Tiempo , Compuestos de Trialquiltina/metabolismo
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