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At least 19 recordsLinked to original sources
PubMed1980

Transfer coefficients of radionuclides secreted in milk of dairy cows.

This study simulated experimentally the transfer of radionuclides to milk of dairy cows on a worst-case situation using various radionuclides known to emanate from nuclear power stations and which have been detected on particulates. Two lactating Holstein cows were administered orally one gelatin capsule containing 10 radionuclides in water-soluble form per day for 14 consecutive days. Milk samples were collected and aliquots analyzed in a germanium lithium-drifted detector coupled to a 2048-multichannel gamma-ray analyzer to measure small amounts of complex mixtures of radionuclides. The transfer coefficients of the radionuclides were calculated when their secretion in milk reached or approached a plateau of concentration. The radionuclides and their transfer coefficients to milk were: chromium51 less than .01%; manganese54 .033 +/- .005%; cobalt60 .01 +/- .002%; iron59 .0048 +/- .002%; zinc65 .31 +/- .07%; selenium75 .29 +/- .1%; antimony125 .011 +/- .003%; iodine131 .88 +/- .05%; and cesium137 .79 +/- .08%.

Animals↗
PubMed1989

A 14-kilodalton selenium-binding protein in mouse liver is fatty acid-binding protein.

In a previous study, we purified three selenium-binding proteins (molecular masses 56, 14, and 12 kDa) from mouse liver using column chromatography and sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The aim of the present study was to determine the amino acid sequence of the 14-kDa protein thereby establishing any relationship with known proteins. Although the amino terminus of the 14-kDa protein was blocked, separate in situ digestions of the protein with endoproteinases Glu-c and Lys-c gave overlapping peptides that provided a continuous sequence of 93 amino acids. This sequence exhibited a 92.5% sequence homology with rat liver fatty acid-binding protein. In situ enzymatic digestion and partial sequencing of a 12-kDa selenium-binding protein revealed identical homology to the 14-kDa protein. The 14-kDa protein bound specifically to an oleate-affinity column from which the protein and 75Se coeluted. Delipidation or sodium dodecyl sulfate treatment failed to remove 75Se from the protein, indicating that the selenium moiety was tightly bound to the protein. These observations confirm that the mouse liver selenium-binding 14-kDa protein is a fatty acid-binding protein. The nature of the selenium linkage to the protein still needs to be explored.

Amino Acid Sequence↗
PubMed1977

Choice of monitoring isotope in double label radioimmunoassays with nonimmunological separation techniques.

We discuss the suitability of some radioactive isotopes as volume markers in radioimmunoassays, from a radiochemical point of view. For three eligible isotopes (22Na, 60Co, and 75Se) we studied the concentration of the marker in the precipitate formed in the separation phase of radioimmunoassays. For all those kinds of separations tested (charcoal, ammonium sulfate, polyethylene glycol, and ethanol), binding or coprecipitation was virtually absent or negligible with 22Na but 75Se was strongly concentrated in the precipitate. Concentration of 60Co occurred only with charcoal and ethanol precipitation. Because heavy metals tend to bind to serum proteins, we conclude that of all radioactive isotopes commercially available only 22Na should be used in radioimmunoassays with nonimmunological separation methods.

Charcoal↗
PubMed1996

Isolation of 75Se binding protein from hepatic tissues of chick embryos.

Distribution study using 75Se shows that maximum accumulation was in liver tissues after 24h of 75Se administration. Induction of selenium binding protein (Se-P) in hepatic tissues of chick embryo was observed. Chick embryo hepatic Se-P was isolated after 24h of 75Se treatment using Sephadex G-75 column chromatography. Fractions of induced protein shows the presence of maximum concentration of 75Se. This induced protein was found to have an approximate molecular weight of 56 KD on molecular sieve. It also showed an absorbance maxima at 254 nm, which indicates the presence of high concentrations of sulphydryl groups.

Animals↗
PubMed1994

Application of short-lived radionuclides in neutron activation analysis of biological and environmental samples.

The application of short-lived nuclides, especially in connection with the 6LiD-converter, in biological and environmental samples is demonstrated on I and Br determination in human urine, on I in pet food, and on the analysis of all the halogens in volcanic gases in a single activation. Trace element determination in lichens indicates polluted and unpolluted areas. The use of the .74-s 38mCl enables the rapid screening of great number of samples.

Animal Feed↗
PubMed1992

Use of radiochemical methods as tools for speciation purposes in environmental and biological sciences.

Chemical speciation for a few elements can be facilitated to a great extent by incorporating a suitable radioisotope into the system and measuring the radiation of the isolated species. This radiospiking can be applied to in vitro and in vivo labelled experiments. Radionuclides are, however, also present as an anthropogenic contaminant from various nuclear fission activities. The radiotracer should be added under such conditions that it behaves in exactly the same way as the isotopes it represents. It should possess an adequate radioactive half-life, and preferably be a gamma-emitter because of the ease of detection. Radiotracer labelling is now widely used to study speciation problems of many essential and toxic elements in body fluids and tissues. It can be used to trace the different locations where the element is metabolized and stored, and subsequently to detect the element in the isolated biocomponents. The determination of the location of a radiotracer in a cell by autoradiography proved to be impractical because of the lack of resolution. Radiochemistry is similarly very useful for investigating particular aspects of the speciation of heavy metals as they occur in the ecosystem, and to follow the fate and effects of fission nuclides in the environment as they are carried around by the water and air masses. However, in certain circumstances the behaviour of fission products appears to be different from that of their stable analogues. For the actinides they simply do not exist. Radiochemical methods are a major tool for identifying and quantifying the nuclides in the different species.

Animals↗
PubMed1974

Thrombopoietin.

Explore the source record for details and available documents.

Animals↗
PubMed1995

[Nuclear medicine methods for the diagnosis of adrenal tumors].

Adrenal scintigraphy using 131I-6-beta-iodomethyl-19-norcholesterol or 6-methyl-75Se-methyl-19-norcholesterol is a function-dependent imaging method which, in association with high-resolution spatial imaging techniques, plays an essential role in the study of adrenocortical hyperfunction. It can distinguish between bilateral cortical hyperplasia and monolateral adenoma or carcinoma and can lateralise the adenoma. In patients with Cushing syndrome, in addition to allowing a distinction to be made between ACTH-dependent forms and independent forms, adrenocortical scintigraphy is particularly appropriate to identify non-common forms of adenomatous hyperplasia. Adrenocortical scintigraphy, performed during dexamethasone administration, is an accurate mean of differentiating bilateral adrenal hyperplasia from monolateral forms (adenoma or carcinoma) in patients with Conn's syndrome. Owing to the gradual spread of high-resolution spatial imaging techniques, the problem of the diagnostic classification of so-called "incidentalomas" (clinically silent masses discovered by chance) is a subject of considerable interest. Adreno-cortical scintigraphy appears to be able to provide an important contribution to identifying the functional behaviour of these tumours. Since the early 80s meta-iodobenzyl-guanidine (MIBG), marked with 131I or 123I, with a structure similar to norepinephrine and characterized by selective tropism for sympathetic and chromaffin tissue, has been used for the scintigraphic study of adrenal medulla. MIBG scintigraphy has been found to be particularly appropriate for the study of intra- and extra-adrenal, single and multiple, benign and malignant pheochromocytomas. This method has a high overall sensitivity and specificity. Lastly, MIBG scintigraphy is useful in the study of neuroblastoma.

3-Iodobenzylguanidine↗
PubMed1993

Single and dual labelling of cytotoxic target cells. Comparison of three radioactive tracers, [35S]methionine, [75Se]selenomethionine, and chromium-51.

[75Se]selenomethionine (75SeM) has been shown to provide several advantages over Na(2)51CrO4 (51Cr) labelling of metabolizing target cells: high labelling efficiency and low spontaneous release of 75SeM-labelled target cells permit improved monitoring of cytotoxicity due to extended effector/target ratios in short- and long-term assays. Unfortunately, 75SeM will soon be difficult to obtain. Therefore we studied the suitability of [35S]methionine (35SM) as a substitute for 75SeM. Furthermore, we explored the potential of dual labelling of suspension target cells applying combinations of 35SM and 51Cr or 75SeM and 51Cr. 35SM is a suitable substitute for 75SeM retaining most of the advantages of 75SeM labelling. Although considerably higher labelling of cells is possible we obtained the most efficient labelling with 100-400 kBq/ml of 35SM or 75SeM resulting in a relatively high uptake (3-15 cpm/cell) and very low spontaneous release (1-2%/h) up to 24 h. This permits short- and long-term cytotoxic assays and the use of low numbers of target cells (1 x 10(3)) providing increased cytotoxic sensitivity with reduced amounts of effector cells. Suitable dual labelling of target cells with 35SM plus 51Cr or 75SeM plus 51Cr documented convincingly identical release kinetics for 35SM and 75SeM but partially discordant ones for 51Cr. Depending on the target cell used dual labelling permits discrimination and monitoring of different cytotoxic or release mechanisms in cellular cytotoxicity.

Chromium Radioisotopes↗