Environmental Toxins Linked to Neurodegeneration and Autism Activate the Brain’s Immune System

Microglia are the primary immune cells of the central nervous system and become activated in response to noxious stimuli, leading to a cycle of inflammation and cell death that has been implicated in the development of Parkinson’s disease and autism. This study examines the effects of environmental toxins, at levels commonly found in humans, on microglial cell survival and activation. The toxins used in this study include polybrominated diphenyl ether (PBDE) flame retardants, the food additive propionic acid (PPA), and the organochlorine pesticide dieldrin. These chemicals have been linked to neuronal damage, although their effects on microglial cells have not been fully studied. Our results indicate that microglial cell survival could be decreased by as much as 50% due to exposure to these toxins, without the production of certain cytokines produced by lipopolysaccharide (LPS)-induced activation. These effects are significant as further understanding of the role of microglia in neuronal damage could provide a pharmacologic target for future drug development as well as elucidate the pathology of neurodegenerative diseases

Characterization of the anodic growth and dissolution of oxide films on valve metals

Chemical dissolution processes coupled to anodic oxide growth taking place by a “high-field” conduction mechanism, are considered. The equation for the steady-state current density obtained during potentiodynamic polarization measurements is derived and the effect of the oxide dissolution rate on the overall potentiodynamic behaviour by applying repetitive scans with either fixed or increasing anodic switching potentials is discussed. The procedure for obtaining the current dissolution as well as the parameters that characterize the high-field growth is discussed. Keywords: Oxides growth, Valve metals, Oxides dissolution, High-field growth, Simulatio

Environmental Toxins Linked to Neurodegeneration and Autism Activate the Brain’s Immune System

Microglia are the primary immune cells of the central nervous system and become activated in response to noxious stimuli, leading to a cycle of inflammation and cell death that has been implicated in the development of Parkinson’s disease and autism. This study examines the effects of environmental toxins, at levels commonly found in humans, on microglial cell survival and activation. The toxins used in this study include polybrominated diphenyl ether (PBDE) flame retardants, the food additive propionic acid (PPA), and the organochlorine pesticide dieldrin. These chemicals have been linked to neuronal damage, although their effects on microglial cells have not been fully studied. Our results indicate that microglial cell survival could be decreased by as much as 50% due to exposure to these toxins, without the production of certain cytokines produced by lipopolysaccharide (LPS)-induced activation. These effects are significant as further understanding of the role of microglia in neuronal damage could provide a pharmacologic target for future drug development as well as elucidate the pathology of neurodegenerative diseases

Nanostructuring of anodic copper oxides in fluoride-containing ethylene glycol media

We demonstrate that the anodization of copper in alkaline water/ethylene glycol media containing fluoride ions generates nanostructured copper oxide films. By modifying the anodization conditions (fluoride and OH– concentrations, applied voltage and anodization time), nanofibrillar Cu2O as well as highly rough nanofibrillar network or nanoporous mixed Cu2O/CuO films are obtained. Raman and X-ray Photoemission Spectroscopy (XPS) results indicate that in fluoride presence, Cu(I) oxide is obtained when anodization takes place applying low voltages at a relatively low OH– concentration. In comparison, the subsequent oxidation to obtain Cu(II) species (CuO and Cu(OH)2) is promoted by increasing the OH– contents. According to the present results, an oxidation reaction scheme is proposed in order to gain a deeper understanding in the preparation of controlled nanostructured copper oxide films.Fil: Oyarzún Jerez, Diego Patricio. Universidad Andrés Bello; ChileFil: Lopez Teijelo, Manuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Ramos Cervantes, Wilkendry. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Linarez Pérez, Omar Ezequiel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Sánchez, Julio. Universidad de Santiago de Chile; ChileFil: Pizarro, Guadalupe del C.. Universidad Tecnológica Metropolitana; ChileFil: Acosta, Gabriela. Universidad de Chile; ChileFil: Flores, Marcos Ariel. Universidad de Chile; ChileFil: Arratia Perez, Ramiro. Universidad Andrés Bello; Chil