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D Behne

Publications and source records attributed to D Behne.

54 records · Page 3Linked to original sources

Effects of a low selenium status on the distribution and retention of selenium in the rat.

In the tissues of rats fed a selenium-deficient diet the changes in the selenium content and the retention of the element after administration of a small amount of selenium to the depleted animals were determined. In the liver and in the erythrocytes, which are the main glutathione peroxidase pools, the decrease in the selenium content was great and the retention in the depleted rats only slightly increased in comparison with the control animals fed sufficient amounts of the element. In the testes and in the adrenals the decreases in the selenium content were the smallest, and here retention was about 15 times greater than in the control animals. Also in other tissues, such as the thymus, spleen, bone and kidney, retention was considerably increased in the depleted rats. The results indicate that regulation mechanisms exist, which in nutritional selenium deficiency cause reduced excretion of the element and priority of supply to certain tissues. This, in turn, leads to a redistribution of selenium in the organism and, as the glutathione peroxidase decreases to a greater extent than the selenium, also to a redistribution of the element among its different binding forms. As the selenium content is most probably kept up in particular in sites in which the element is most needed, the findings suggest important functions of selenium in these tissues.

Adrenal Glands↗

Distribution of selenium and glutathione peroxidase in the rat.

The selenium content was determined in the adrenals, brain, erythrocytes, femur, hair, heart, kidneys, lungs, muscle, pancreas, plasma, spleen, testes, and thymus of rats, which had been fed a commercial rat diet containing 0.3 mg Se/kg diet. In the plasma, the erythrocytes, and the soluble fraction of the tissues (with the exception of femur and hair) the activity of the glutathione peroxidase (GSH-Px) was measured, using both hydrogen peroxide and t-butyl hydroperoxide as substrates. From the masses of the tissues and the values for the selenium content and the GSH-Px activity, the distribution of the element and the enzyme in the body was calculated. For selenium the main pools were the muscle and the liver, and for the GSH-Px, the liver and the erythrocytes. By comparing the selenium content and the GSH-Px activity the percentage of the tissue selenium, which was bound to the enzyme in the soluble tissue fraction, was estimated. This percentage differed considerably from tissue to tissue, the highest value being found in the erythrocytes and the smallest in the testes. According to this estimation the majority of the selenium in the rat is not contained in the GSH-Px but in other compounds.

Animals↗

Selenium in the testis of the rat: studies on its regulation and its importance for the organism.

In male rats, fed for 10 weeks on a Torula yeast-based, low selenium and low vitamin E diet, the selenium level and the glutathione peroxidase activity in the blood and in several tissues decreased by 50 to 98% compared with animals that received the same basal diet supplemented with 0.25 mg Se/kg sodium selenite. In the testes, however, the selenium content did not differ from that of the control animals. Despite the low selenium levels in the extragonadal tissues and their increased requirement of this element due to the low vitamin E status, the selenium from an intravenously injected dose of sodium selenite was retained above all in the testes. After the removal of the pituitary gland, because of the decrease in the testicular mass and in the selenium content in the remaining testicular tissue, the amount of selenium in the testes was greatly reduced. After administration of pregnant mare's serum gonadotropin (PMS), due to the regeneration of the tissue and the simultaneous restoration of the selenium content, a relatively large amount of this element was shifted to the testes even though the selenium status in the other tissues was low. The results of these studies show that the selenium level in the male gonads is maintained by regulation mechanisms and that the supply of sufficient amounts of selenium to the testes has priority over the supply to other tissues.

Animals↗

The suitability of the iliac crest biopsy in the element analysis of bone and marrow.

Bone samples from the iliac crest were taken from 20 subjects and the content of some trace elements (iron, zinc, selenium, cobalt, strontium, aluminium, scandium, rubidium and fluorine) and of the matrix elements calcium, phosphorus and sodium was determined. The samples were taken in accordance with Burkhardt's method, which is often used in hospital for bone biopsies. The sources of errors occurring during the analysis of trace elements using this clinical procedure and the contamination of the samples by blood and the surrounding tissue are discussed. In-vivo activation analysis is also discussed as an alternative method of element analysis of the skeleton.

Aged↗

Selenium content and glutathione peroxidase activity in the plasma and erythrocytes of non-pregnant and pregnant women.

Decreases in the glutathione peroxidase activity and in the selenium content were found in the plasma of pregnant women as compared with a control group. In the erythrocytes, both parameters remained unchanged. In both groups a fraction of about 0.90 of the glutathione peroxidase in the blood, was contained in the erythrocytes, whereas the selenium was nearly evenly distributed between plasma and red blood cells. A positive correlation existed between the total amount of selenium in the erythrocytes and that in the plasma.

Erythrocytes↗

Effects of pregnancy and lactation on the serum selenium content of rats.

The serum selenium content of rats was measured by means of neutron activation analysis. It was found to drop between the 12th day of pregnancy and term and to return to its original level within 2 days after delivery. Hysterectomy on the 10th day of gestation prevented this decrease. Nursing had no influence on the element level. The findings suggest that placental secretions might be involved in the control of the serum selenium content of rats during pregnancy.

Animals↗

[Enteral absorption of high calcium doses determined by means of stable isotopes (author's transl)].

The calcium absorption was determined in 8 healthy test persons (average age 25.6 years) after oral administration of 500 mg and 1000 mg of this element. A double isotope method with enriched stable calcium isotopes was used which can be applied without any restriction as, unlike in radiotracer techniques, any exposure to ionizing radiation is avoided. The calcium administered orally was labelled with 48Ca, the CaCl2 injected intravenously with 46Ca. The determination of both isotopes in serum and urine samples was carried out by means of neutron activation analysis. Independent of the calcium dose given, an absorption of 30% was found. From the 46Ca content in the serum samples a mean value of 6.4 +/- 1.0 g calcium or 98.8 +/- 15.4 mg Ca/kg body weight was calculated for the 24 hr-exchangeable calcium body pool.

Adult↗

Effects of sex hormones and of pregnancy on the selenium metabolism.

In order to obtain information about the hormonal regulation of the selenium metabolism, the element level in the blood serum of rats was determined by means of neutron activation analysis after administration of sex hormones and during pregnancy. While the decreases in the mean selenium concentrations found after the treatment with progesterone and progesterone + estrone were too low to enable us to establish response patterns, marked changes were observed in the serum of gravid rats. Here the selenium level dropped significantly (P less than 0.001) by 25% between the 10th and 15th day of gestation.

Animals↗

Study on sex-specific transferrin polymorphism and on the identification of transferrins by radioactive labelling.

Sex-specific differences with regard to the intensity of transferrin bands were observed in a noninbred adult mouse population after separation of the serum proteins by polyacrylamide gel electrophoresis. Amongst the female animals, an additional protein fraction was found just above the position of the transferrin bands. By means of a tracer method, using 59Fe-labelling, it could be shown that the additional fraction is not a part of the transferrin bands.

Age Factors↗

Studies on 16 kDa selenium-containing proteins enriched by means of preparative electrophoresis.

By in vivo labeling with [75Se]selenite and separation of the proteins in the tissue homogenates by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), several selenium-containing proteins or protein subunits were detected in rat tissues (liver, lung, spleen and prostate). Their distribution among the cell components was investigated after fractionation by means of differential centrifugation. The selenium-containing proteins in the 16 kDa range were found to be mainly membrane-bound. By two-dimensional electrophoresis they were resolved into three labeled spots, two with the same relative molecular mass and pI values of about 4.8 and 5.0 and the third with a slightly lower molecular mass and a pI of 4.8. For further investigation they were concentrated and separated from the other labeled compounds by SDS-PAGE using preparative flow-through electrophoresis.

Animals↗

Newly found selenium-containing proteins in the tissues of the rat.

The Se-containing proteins in 27 tissues of the rat were investigated by in vivo labeling with 75Se-selenite, separation of the tissue homogenate proteins by SDS-polyacrylamide gel electrophoresis, and determination of the labeled proteins by autoradiography. By using Se-depleted rats and a 75Se-tracer with a high specific activity, Se compounds present at only very low concentrations could be detected. Besides the 13 Se-containing proteins previously described, for which apparent molecular masses of 12, 15, 18, 20, 22, 25, 28, 34, 56, 60, 65, 70, and 75 kD have been found here, a further 15 75Se-labeled bands, with apparent molecular masses of 8, 10, 15.5, 16.5, 24, 32, 34.5, 38, 40, 41, 44, 45, 46.5, 53 and 116 kD could be distinguished. Two-dimensional separation of the kidney homogenate proteins showed that some of the Se-containing bands could be resolved into several labeled spots. Most of the newly found compounds were present in various tissues, but with some the enrichment in certain tissues suggested specific sites of action.

Animals↗

Combination of neutron activation analysis, tracer techniques, and biochemical methods in the investigation of selenium metabolism.

In several studies on rats, the metabolism of selenium was investigated. The quantitative determination of the element was carried out by instrumental neutron activation analysis. For in vivo tracer experiments, 75Se-labeled selenium compounds were used. In addition to these methods, procedures for the measurement of the selenoenzyme glutathione peroxidase, and for the investigation of other selenoproteins, were applied. In this way, information on the specific pools and sites of action of the element, on biologically important selenoproteins and the regulation of the selenium metabolism, was obtained.

Animals↗