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Toxicol Sci ; 156(1): 54-71, 2017 03 01.
Artículo en Inglés | MEDLINE | ID: mdl-28013213

RESUMEN

High systemic levels of oestrogens are cholestatic and primary biliary cholangitis (PBC)-which is characterized by hepatic ductular inflammation-is thought to be triggered by exposure to xenobiotics such as those around landfill sites. Xenoestrogens may be a component of this chemical trigger. We therefore hypothesized that xenoestrogens are present at higher levels in the proximity of landfill sites. To test this hypothesis, soil samples were collected, extracts prepared and biological oestrogenic activity examined using cell-based reporter gene assays. Extracts from several sample sites around a landfill site contained a chemical(s) which activated the human ERα in a dose-dependent manner. Extracts from 3 separate control sampling sites were absent of any detectable activity. The mouse ERα and 2 variant mouse ERß cDNAs were cloned and extracts from sample sites around a landfill site also activated these receptors. One variant murine ERß was constitutively active when expressed in cholangiocytes, was readily inactivated by ICI182780 and activated in a dose-responsive, ICI182780-inhibitable manner by oestrogen. However, when this receptor was activated by extracts from landfill site soils, ICI182780 failed to antagonize activation. ERß was readily detectable in murine cholangiocytes and exposing mice acutely to a pooled ER activating soil extracts also gave rise to a mild cholestatic injury. These data indicate that the environment around landfill sites may contain higher levels of xenoestrogens; that these chemicals have "super-activating" characteristics with a variant ERß and therefore these chemicals could be a component of a xenobiotic insult that triggers PBC.


Asunto(s)
Empalme Alternativo , Conductos Biliares/efectos de los fármacos , Colestasis/inducido químicamente , Receptor beta de Estrógeno/agonistas , Estrógenos/toxicidad , Contaminantes del Suelo/toxicidad , Animales , Conductos Biliares/citología , Conductos Biliares/metabolismo , Conductos Biliares/patología , Línea Celular , Línea Celular Tumoral , Células Cultivadas , Colestasis/metabolismo , Colestasis/patología , Colestasis/prevención & control , Antagonistas del Receptor de Estrógeno/farmacología , Receptor alfa de Estrógeno/agonistas , Receptor alfa de Estrógeno/antagonistas & inhibidores , Receptor alfa de Estrógeno/genética , Receptor alfa de Estrógeno/metabolismo , Receptor beta de Estrógeno/antagonistas & inhibidores , Receptor beta de Estrógeno/genética , Receptor beta de Estrógeno/metabolismo , Estrógenos/química , Estrógenos/aislamiento & purificación , Femenino , Genes Reporteros/efectos de los fármacos , Humanos , Cinética , Masculino , Ratones , Ratones Desnudos , Proteínas Recombinantes/química , Proteínas Recombinantes/metabolismo , Contaminantes del Suelo/antagonistas & inhibidores , Contaminantes del Suelo/aislamiento & purificación , Reino Unido , Instalaciones de Eliminación de Residuos
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