20 research outputs found

    Hepatic proteome changes in solea senegalensis exposed to contaminated estuarine sediments: a laboratory and in situ survey

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    Assessing toxicity of contaminated estuarine sediments poses a challenge to ecotoxicologists due to the complex geochemical nature of sediments and to the combination of multiple classes of toxicants. Juvenile Senegalese soles were exposed for 14 days in the laboratory and in situ (field) to sediments from three sites (a reference plus two contaminated) of a Portuguese estuary. Sediment characterization confirmed the combination of metals, polycyclic aromatic hydrocarbons and organochlorines in the two contaminated sediments. Changes in liver cytosolic protein regulation patterns were determined by a combination of two-dimensional electrophoresis with de novo sequencing by tandem mass spectrometry. From the forty-one cytosolic proteins found to be deregulated, nineteen were able to be identified, taking part in multiple cellular processes such as anti-oxidative defence, energy production, proteolysis and contaminant catabolism (especially oxidoreductase enzymes). Besides a clear distinction between animals exposed to the reference and contaminated sediments, differences were also observed between laboratory- and in situ-tested fish. Soles exposed in the laboratory to the contaminated sediments failed to induce, or even markedly down-regulated, many proteins, with the exception of a peroxiredoxin (an anti-oxidant enzyme) and a few others, when compared to reference fish. In situ exposure to the contaminated sediments revealed significant up-regulation of basal metabolism-related enzymes, comparatively to the reference condition. Down-regulation of basal metabolism enzymes, related to energy production and gene transcription, in fish exposed in the laboratory to the contaminated sediments, may be linked to sedimentbound contaminants and likely compromised the organisms’ ability to deploy adequate responses against insult.info:eu-repo/semantics/publishedVersio

    Physicochemical time series of karst springs as a tool to differentiate the source of spring water

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    Podenow Anticline is located in the Zagros Mountain Range, southern Iran. This anticline is exposed in an outcrop of Tertiary karstic limestone-dolomite Asmari Formation which is sandwiched between two impermeable marly formations. Part of the Podenow aquifer is discharged by 23 springs on the southern flank. Nineteen of these springs are concentrated in an area less than 0.5 km2. The major ions, electrical conductivity, temperature and pH of these springs were measured once every two to three weeks for a period of 17 months. Geological setting, geomorphology, topography, lithology of the karst aquifer and surrounding formations, ratio of SO4 to total anions, time series of specific conductance, hydrograph of springs, elevation of water level in piezometers and aquifer water balance were used to determine the probable catchment area of the springs. These parameters indicate that the sources of four springs are most probably the southern flanks and the sources of the other springs are both the southern and northern flanks. The time series of specific conductance of the fourteen Atashkadeh springs overlap which implies that all of these springs share a common conduit and the same catchment area. But the catchment area of one of the Atashkadeh springs is different from the other springs, even though it is surrounded by those other springs. A later tracer study confirmed the above discussion

    Thigh-length compression stockings and DVT after stroke

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    Controversy exists as to whether neoadjuvant chemotherapy improves survival in patients with invasive bladder cancer, despite randomised controlled trials of more than 3000 patients. We undertook a systematic review and meta-analysis to assess the effect of such treatment on survival in patients with this disease

    A multicentric study to evaluate the use of relative retention times in targeted proteomics

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    Despite the maturity reached by targeted proteomic strategies, reliable and standardized protocols are urgently needed to enhance reproducibility among different laboratories and analytical platforms, facilitating a more widespread use in biomedical research. To achieve this goal, the use of dimensionless relative retention times (iRT), defined on the basis of peptide standard retention times (RT), has lately emerged as a powerful tool. The robustness, reproducibility and utility of this strategy were examined for the first time in a multicentric setting, involving 28 laboratories that included 24 of the Spanish network of proteomics laboratories (ProteoRed-ISCIII). According to the results obtained in this study, dimensionless retention time values (iRTs) demonstrated to be a useful tool for transferring and sharing peptide retention times across different chromatographic set-ups both intra- and inter-laboratories. iRT values also showed very low variability over long time periods. Furthermore, parallel quantitative analyses showed a high reproducibility despite the variety of experimental strategies used, either MRM (multiple reaction monitoring) or pseudoMRM, and the diversity of analytical platforms employed. BIOLOGICAL SIGNIFICANCE: From the very beginning of proteomics as an analytical science there has been a growing interest in developing standardized methods and experimental procedures in order to ensure the highest quality and reproducibility of the results. In this regard, the recent (2012) introduction of the dimensionless retention time concept has been a significant advance. In our multicentric (28 laboratories) study we explore the usefulness of this concept in the context of a targeted proteomics experiment, demonstrating that dimensionless retention time values is a useful tool for transferring and sharing peptide retention times across different chromatographic set-ups.All laboratories from Spain are members of ProteoRed (Plataforma de Recursos Biomoleculares y Bioinformáticos) and are supported by grant PT13/0001 funded by Instituto de Salud Carlos III (ISCIII) and FEDER.S
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