Autism is characterized by social deficits, repetitive behaviors, and cognitive inflexibility. The risk factors appear to include genetic and environmental conditions, such as prenatal infections and maternal dietary factors. Previous investigations by our group have demonstrated that prenatal exposure to lipopolysaccharide (LPS), which mimics infection by gram-negative bacteria, induces autistic-like behaviors. To understand the causes of autistic-like behaviors, we evaluated maternal serum metal concentrations, which are involved in intrauterine development and infection/inflammation. We identified reduced maternal levels of zinc, magnesium, selenium and manganese after LPS exposure. Because LPS induced maternal hypozincemia, we treated dams with zinc in an attempt to prevent or ease the impairments in the offspring. We evaluated the social and cognitive autistic-like behaviors and brain tissues of the offspring to identify the central mechanism that triggers the development of autism. Prenatal LPS exposure impaired play behaviors and T-maze spontaneous alternations, i.e., it induced autistic-like behaviors. Prenatal LPS also decreased tyrosine hydroxylase levels and increased the levels of mammalian target of rapamycin (mTOR) in the striatum. Thus, striatal dopaminergic impairments may be related to autism. Moreover, excessive signaling through the mTOR pathway has been considered a biomarker of autism, corroborating our rat model of autism. Prenatal zinc treatment prevented these autistic-like behaviors and striatal dopaminergic and mTOR disturbances in the offspring induced by LPS exposure. The present findings revealed a possible relation between maternal hypozincemia during gestation and the onset of autism. Furthermore, prenatal zinc administration appears to have a beneficial effect on the prevention of autism.
In occupational assessments where workers are exposed to metal dust, the liquid condensate of exhaled breath (EBC) may provide unique indication of pulmonary exposure. The main goal of this study was to demonstrate the quality of EBC to biological monitoring of human exposure. A pilot study was performed in a group of metal dust-exposed workers and a group of nonexposed individuals working in offices. Only metal dust-exposed workers were followed along the working week to determine the best time of collection. Metal analyses were performed with inductively coupled plasma mass spectrometry (ICP-MS). Analytical methodology was tested using an EBC sample pool for several occupationally exposed metals: potassium, chromium, manganese, copper, zinc, strontium, cadmium, antimony, and lead. Metal contents in EBC of exposed workers were higher than controls at the beginning of the shift and remained augmented throughout the working week. The results obtained support the establishment of EBC as an indicator of pulmonary exposure to metals.
The level and change in concentration of trace elements in the fluids of a body may be the result and an evidence of alterations in life functions. In the search for trace element alterations in the human body it is necessary to know referenced values for as many elements as possible. In this work, Proton Induced X-ray Emission (PIXE) was used to study elemental concentrations in human blood serum of 30 healthy donors. The serum samples were obtained by centrifugation and were micro-pipetted on 10µm thick Nuclepore film for PIXE analysis. The elemental concentrations were calculated relative to an internal yttrium standard added during sample preparation. A total of 9 elements were measured (P, S, Cl, K, Ca, Fe, Cu, Zn and Br) in good agreement with literature data. The accuracy of the method was verified analysing reference serum samples from the NIPH-Québec (ICP04S-06 and ICP02S-05). A preliminary statistical analysis indicated a log-normal distribution only for Fe and Cu, while concentration data for the other elements followed the normal distributions. This result indicates the need for stronger statistical data set since the distribution of the elemental concentrations may be a criterion to access their role in biological functions.
The Group 2 (vitamin D3+Ethylene Glycol 0.5%) was the best model to induce nephrocalcinosis in rats after 28 days.
Melanoma is a serious skin cancer that, if found and treated in its early stages can be cured before it gets invasive and develops metastasis. The incidence of this disease has steadily increased in white populations throughout the world in the last decades. Although the basis for this rise is incompletely understood, it is known that solar exposure and genetic factors are important precursors of melanoma. Nowadays, some studies are correlating some trace elements in blood and tissues with the disease. In this work, trace element concentrations in blood serum of patients with melanoma where measured by PIXE (Particle Induced X-ray Emission) to verify if there is a link between the concentrations of elements in the blood serum and melanoma. If the hypothesis is proven, elements in the blood serum could also be used as markers for melanoma. The samples were collected in the São Paulo Hospital and analyzed by PIXE after an internal standard addition. Concentrations of Chlorine (Cl), Potassium (K), Calcium (Ca), Copper (Cu), Zinc (Zn) and Bromine (Br) were measured in serum of 30 patients with melanoma and 116 control individuals. The elemental concentrations were calculated relative to an internal Gallium standard. The accuracy of the method was verified analyzing an IAEA A-13 Blood (International Atomic Energy Agency) and a QMEQAS08S-06 serum (National Institute of Public Health). The results of this work showed no significant difference between melanoma and control group (independent t-test and U-test, p = 0.05).
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