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M Janghorbani

Publications and source records attributed to M Janghorbani.

81 records · Page 5Linked to original sources

Measurement of 68Zn and 70Zn in human blood in reference to the study of zinc metabolism.

A method based on radiochemical neutron activation analysis has been developed for measurement of the stable isotopes 68Zn and 70Zn in human plasma and red cells. The method has been applied to measure the extent of 70Zn enrichment in plasma samples from four healthy adult volunteers who had each consumed a single 3.2 mg dose of 70ZnCl2 in fasting state. It is shown that measurements of 70Zn/68Zn ratio in plasma and red cell sample sizes of 2 ml can be made with precisions of 10% or less depending on the degree of enrichment achieved. The limiting factor in the precision of these measurements appears to be related to the counting statistics of the 386 kev photopeak (71mZn) which improves with increased enrichment. Clinical feasibility trials on these subjects with regard to plasma and red cell 70Zn enrichment have been carried out over a 24-h postadministration period. The results are consistent with kinetic studies reported in literature with radiozinc, and show that this method can be used to study kinetics of plasma appearance of 70Zn after oral administration of the isotope under physiological intake conditions. The present results further indicate that under these experimental conditions, enrichment of red cells can be measured after 24 h or longer postadministration periods, but short-term measurements yield marginal results. This new method provides an alternative approach to the use of radiolabeled zinc for the study of human zinc metabolism and appearance of isotopic zinc in plasma after oral administration under physiological intake conditions. It can be applied to all human population groups as a noninvasive and safe method which does not require safety considerations arising from human use of radiotracers. However, its application is both more expensive and limited in terms of sample throughput as compared with the radiotracer technique.

Adult↗

Comparative measurement of zinc absorption in rats with stable isotope 70Zn and radioisotope 65Zn.

The use of stable isotopes in a study on zinc bioavailability was evaluated in rats by comparing the zinc absorption of a stable isotope 70Zn and a radioisotope 65Zn simultaneously. The rats of low zinc status were obtained by feeding 1.2% phytic acid from sodium phytate and 12 ppm zinc from zinc sulfate in a semipurified diet for 14 days. The rats were then randomly assigned into five groups of ten rats. The rats were intubated with a test diet mixture with a phytate:zinc molar ratio of 0, 6.25, 12.5, 25 or 50 along with one microCi of 65Zn and 0.02 mg of 70Zn in 2.5 ml of intubating solution. Four hours after the intubation, rats were allowed to consume the diets having the same phytate:zinc ratio as used for intubation ad libitum. Feces were collected every 24 hours for a total of 168 hours. The 65Zn and 70Zn content of diets and fecal samples were determined and the percent of zinc absorption was calculated. The results of this study indicated that the zinc absorption determined by these two isotopes were highly correlated with a correlation coefficient ratio of 0.914.

Absorption↗

Feasibility of intrinsic labeling of poultry meat with stable isotope of selenium (74Se) for use in human metabolic studies.

Sixteen day-old cockerel broiler-type chickens were placed on a simplified, corn-soybean meal broiler starter ration. Each chick was gavaged on 12 separate days over a growth period of 42 days with solutions of Na2SeO3 (control group) or Na74SeO3 (test group). The animals were killed on the 43rd day and the concentrations of the stable isotopes 74Se and 76Se were determined in meat, skin and liver samples using the method of radiochemical neutron activation analysis. We found that significant enrichment of 74Se occurred in the tissues of test animals as compared with the controls and that the degree of enrichment achieved was sufficient to allow use of these chickens in human feeding experiments designed to investigate bioavailability of dietary selenium employing the method of stable isotopes and fecal monitoring.

Animals↗

Accurate analysis of stable isotopes 68Zn, 70Zn, and 58Fe in human feces with neutron activation analysis.

Accurate isotopic analysis of human fecal samples is discussed in relation to mineral bioavailability studies of human subjects. It is shown that for bioavailability investigations of Zn and Fe, the method of neutron activation analysis is suitable for routine application to clinical experiments; and the human fecal samples resulting from diet suitably enriched in isotopes 70Zn and 58Fe can be routinely analyzed with relative precisions of about 1% for the isotopes 68Zn, 70Zn and 58Fe.

Feces↗

Use of stable isotopes to determine bioavailability of minerals in human diets using the method of fecal monitoring.

Use of stable isotopes to determine bioavailability of minerals, by the method of fecal monitoring, in human diets is discussed. Analytical expressions are developed to permit prediction of the accuracy of the method as a function of several variables involved. The effects of extent of absorption, natural abundance of the selected isotope, and the enrichment ratio of administered diet on the accuracy of the estimate of absorption are examined. the method of neutron activation analysis as applied to the isotopic measurement of trace minerals including iron, zinc, copper, chromium, and nickel is briefly discussed. The method of fecal monitoring for zinc and iron is illustrated with data obtained in a healthy adult subject receiving a diet enriched with 70Zn and 58Fe.

Adult↗

Absorption of iron in young men studied by monitoring excretion of a stable iron isotope (58Fe) in feces.

Fecal excretion of a stable iron isotope (58Fe) in five young adult men consuming a diet enriched with the isotope added as an extrinsic tag was investigated as a possible tool for the study of iron absorption. Data are presented to illustrate rapidity and completeness of unabsorbed 58Fe excretion. Procedures are outlined to investigate the extent of 58Fe re-entry into the gastrointestinal tract of the absorbed 58Fe from the label with the cumulative fecal 58Fe method and its limitations are discussed. Two methods of estimating 58Fe absorption are discussed and compared.

Administration, Oral↗

Selenium content of enteral formulas.

Selenium content of several complete enteral formulas and modular enteral components was determined by neutron activation analysis. Formulas based on egg albumin provided the highest content of selenium. Most of the remaining formulas had selenium contents that would provide an amount less than the proposed safe and adequate range of intake. Selenium supplementation should be considered for these latter formulas.

Enteral Nutrition↗

Kinetics of a single administration of 74Se-selenite by oral and intravenous routes in adult humans.

The purpose of this study was to explore the fate of a single dose of labeled selenium as determined by its route of administration. Thus, the appearance of a stable isotope of selenium, administered as 74-Se-selenite, was measured in plasma, urine, and feces, with neutron activation analysis, following a 81.7 micrograms dose of 74Se-selenite given either intravenously or orally in two groups (n = 4) of healthy, young adult men, who were otherwise maintained on a diet providing a constant and adequate selenium intake. From these isotopic data, measurable parameters of urine excretion, total body retention and selenite-exchangeable metabolic pool (Se-EMP) were defined to provide a quantitative assessment of selenium metabolism in these subjects. The initial 24-hr urine excretion of the label was higher for the intravenously administered label (18.2 +/- 2.1% of dose) compared to the oral dose (11.7 +/- 2.6% absorbed dose). Thereafter, the excretion of isotope was the same for both groups. For equivalent entry of Se into the body, measured total body retention and Se-EMP were the same for both groups. These initial kinetic data suggest that the overall utilization of selenium from a single administration of selenite is comparable for the two routes of intake and that the host's selenium requirement can probably be met adequately via the intravenous administration of selenite.

Administration, Oral↗

Bioavailability of magnesium diglycinate vs magnesium oxide in patients with ileal resection.

BACKGROUND: Patients who have undergone ileal resection are at risk for developing magnesium depletion/deficiency because of poor absorption and decreased intake as well as increased endogenous losses. Magnesium repletion is difficult to accomplish because of the cathartic action of most oral magnesium supplements at therapeutic doses. The results of in vitro and in situ studies show that magnesium diglycinate (chelate) represents a highly available form of magnesium that is absorbed in part as an intact dipeptide in the proximal small intestine. METHODS: We conducted a double-blind, randomized crossover trial with 12 patients who had ileal resections in order to compare the bioavailability of a 100-mg dose of 26Mg-labeled chelate with MgO in this patient population. RESULTS: For the patient group as a whole, 26Mg absorption was low but was not different for the two supplements (23.5% vs 22.8% for magnesium chelate and MgO, respectively). However, 26Mg absorption was substantially greater from the chelate (23.5% vs 11.8%; p < .05) in the four patients who showed the greatest impairment of magnesium absorption with MgO and was better tolerated by all patients. Peak isotope enrichment also occurred significantly earlier after 26Mg chelate than after 26MgO ingestion (mean difference 3.2 +/- 1.3 hours; p < .05), and the area under the enrichment vs time curve was greater after chelate ingestion (p < .05). CONCLUSIONS: Data from this study support the suggestion that some portion of magnesium diglycinate is absorbed intact, probably via a dipeptide transport pathway. Magnesium diglycinate may be a good alternative to commonly used magnesium supplements in patients with intestinal resection.

Administration, Oral↗