12 research outputs found

    The dosimetry of ionizing radiation

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    The Dosimetry of Ionizing Radiatio

    The dosimetry of ionizing radiation

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    The Dosimetry of Ionizing Radiation, Volume II, attempts to fill the need for updated reference material on the field of radiation dosimetry. This book presents some broad topics in dosimetry and a variety of radiation dosimetry instrumentation and its application. The book opens with a chapter that extends and applies the concepts of microdosimetry to biological systems. This is followed by separate chapters on the state- of-the-art equipment and techniques used to determine neutron spectra; studies to determine recombination effects in ionization chambers exposed to high-intensity pulsed r

    Characterization of an Acyl-Coa Thioesterase that Functions as a Major Regulator of Peroxisomal Lipid Metabolism

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    Peroxisomes function in b-oxidation of very long- and long-chain fatty acids, dicarboxylic fatty acids, bile acid intermediates, prostaglandins, leukotrienes, thromboxanes, pristanic acid and xenobiotic carboxylic acids. These lipids are mainly chain-shortened for excretion as the carboxylic acids or transported to mitochondria for further metabolism. Several of these carboxylic acids are slowly oxidized and may therefore sequester coenzyme A (CoASH). To prevent CoASH sequestration and to facilitate excretion of chain-shortened carboxylic acids, acyl-CoA thioesterases, which catalyze the hydrolysis of acyl-CoAs to the free acid and CoASH, may play important roles. We have here cloned and characterized a peroxisomal acyl-CoA thioesterase from mouse, named PTE-2, which was first isolated as a HIV-1 Nef binding protein in human (Liu et al. J. Biol. Chem. (1997) 272, 13779-13785, Watanabe et al. Biochem. Biophys. Res. Comm. (1997) 238, 234-239). PTE-2 is ubiquitously expressed and induced at mRNA level by treatment with the peroxisome proliferator WY-14,643 and fasting. Induction seen by these treatments was dependent on the peroxisome proliferator-activated receptor alpha (PPARa). Recombinant PTE-2 showed a broad chain-length specificity with acyl-CoAs from short- and medium-, to long-chain acyl- CoAs, and other substrates including trihydroxycoprostanoyl-CoA, hydroxymethylglutaryl-CoA and branched chain acyl-CoAs, all of which are present in peroxisomes. Highest activities were found with the CoA esters of primary bile acids choloyl-CoA and chenodeoxycholoyl-CoA as substrates. PTE-2 activity is inhibited by free CoASH, suggesting that intraperoxisomal free CoASH levels regulate the activity of this enzyme. The acyl-CoA specificity of recombinant PTE-2 closely resembles that of purified mouse liver peroxisomes, suggesting that PTE-2 is the major acyl-CoA thioesterase in peroxisomes. Addition of recombinant PTE-2 to incubations containing isolated mouse liver peroxisomes strongly inhibited bile 3 acid-CoA: amino acid N-acyltransferase activity, suggesting that this thioesterase can interfere with CoASH-dependent pathways. We propose that PTE-2 functions as a key regulator of peroxisomal lipid metabolism

    New insights into bile acid amidation

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    The European technical report on aquatic effect-based monitoring tools under the water framework directive

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    The Water Framework Directive (WFD), 2000/60/EC, requires an integrated approach to the monitoring and assessment of the quality of surface water bodies. The chemical status assessment is based on compliance with legally binding Environmental Quality Standards (EQSs) for selected chemical pollutants (priority substances) of EU-wide concern. In the context of the mandate for the period 2010 to 2012 of the subgroup Chemical Monitoring and Emerging Pollutants (CMEP) under the Common Implementation Strategy (CIS) for the WFD, a specific task was established for the elaboration of a technical report on aquatic effect-based monitoring tools. The activity was chaired by Sweden and co-chaired by Italy and progressively involved several Member States and stakeholders in an EU-wide drafting group. The main aim of this technical report was to identify potential effect-based tools (e.g. biomarkers and bioassays) that could be used in the context of the different monitoring programmes (surveillance, operational and investigative) linking chemical and ecological status assessment. The present paper summarizes the major technical contents and findings of the report
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