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  • 1
    ISSN: 1432-0827
    Keywords: Calcium ; Intestine ; Growth ; Cortisol ; Hydroxyproline ; Parathyroid hormone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary This paper reports the effects of cortisol on intestinal management of calcium and on related changes on bone metabolism. Five groups of 12 rats each fed a standard diet (0.8% Ca) received 2, 6, 16, 32, and 128 mg/kg/day of cortisol hemisuccinate, subcutaneously. After 16 days, intestinal absorption and excretion of Ca were measured with the aid of45Ca. True Ca absorption increased as a function of dose up to 16 mg/kg/day and remained high with the larger doses. Endogenous fecal Ca excretion increased exponentially as a function of the dose from 16 mg/kg/day onwards. Therefore, a dual effect was observed: (a) an increase in true Ca absorption at low cortisol doses (which increased net Ca absorption); and (b) an increase in endogenous fecal Ca excretion at high doses (which reduced net Ca absorption). In no case was a depression of true Ca absorption observed. Growth rate and food conversion efficiency were depressed only with a cortisol dose of 128 mg/kg/day. The urinary excretion of hydroxyproline, pyrophosphate, and aminopolysaccharides decreased with low doses and increased above normal levels with the highest dose. When animals treated with 128 mg/kg/day of cortisol were fed Ca-enriched diets, net Ca absorption improved. Simultaneously, growth rate and food conversion efficiency approached normal values. In these experiments, net absorption of Ca was found to be inversely related to urinary excretion of hydroxyproline. The urinary rate of excretion of hydroxyproline is suggested as an indicator of the effect of a Ca supplement on cortisol affected connective tissue turnover.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 6 (1970), S. 133-142 
    ISSN: 1432-0827
    Keywords: Testosterone ; Dehydroepiandrosterone ; Glucosephosphate-dehydrogenase ; Glucose ; Bone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Description / Table of Contents: Résumé Les effets des androgènes (déhydroépiandrostérone et testostérone) sur le métabolisme des hydrates de carbone ont été étudiés en utilisant deux modèles expérimentaux. Le premier fait appel à la culturein vitro d'os embryonnaires d'oiseaux. Dans le deuxième modèle, on utilise des os non embryonnaires de mammifères, en cours d'ossification enchondralein vivo. Dans les deux cas, on note une augmentation de l'activité de la glucose-6-phosphate déhydrogénase et une oxydation différente de la glucose-1-14C et glucose-6-14C. Ces faits indiquent un changement dans le métabolisme du glucose allant vers la voie oxydative directe. En plus, le traitement provoque une hyperplasie de la couche hypertrophique dans l'épiphyse osseuse chez les souris prépubères.
    Abstract: Zusammenfassung Es wurden die Wirkungen von Androgenen (Dehydroepiandrosteron und Testosteron) auf den Kohlenhydratumsatz von Knochen mittels 2 experimenteller Modelle untersucht: einerseits anin vitro gezüchteten Bindegewebsknochen von Hühnerembryonen und andererseitsin vivo an nichtembryonalen Säugetierknochen mit endochondraler Ossifikation. In beiden Modellen läßt die Aktivitätszunahme der Glucose-6-phosphat-dehydrogenase und die unterschiedliche Oxydation von Glucose-1-14C und Glucose-6-14C eine Verschiebung des Glucosemetabolismus gegen den direkten oxydativen Abbau vermuten. Weiterhin erzeugt eine Behandlung mit diesen Hormonen eine Hyperplasie der hypertrophen Zellschicht an der Epiphysenplatte von vorpubertären Mäusen.
    Notes: Abstract An investigation on the effects of androgens (dehydroepiandrosterone and testosterone) on the carbohydrate metabolism of bone was carried out with two experimental models: avian embryonic membranous bone cultivatedin vitro, and mammal non-embryonic bone of endochondral ossificationin vivo. In both models, the increase in glucose-6-phosphate dehydrogenase activity and the differential oxidation of glucose-1-14C and glucose-6-14C suggest a shift in glucose metabolism toward the direct oxidative pathway. In addition, treatment with these hormones produces hyperplasia of the hypertrophic cell layer at the epiphyseal plate of prepubertal mice.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 2 (1968), S. 133-144 
    ISSN: 1432-0827
    Keywords: Dehydroepiandrosterone ; Testosterone ; Embryo ; Tissue culture ; Frontal bone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Description / Table of Contents: Résumé Les os frontaux d'embryons de poulet, de 12 jours de développement, cultivés sur coagulum de plasma avec sulfate de déhydroépiandrostérone (DS) en concentration 1 mM, montrent hyperplasie du périoste et synthèse augmentée du matrice osseuse. Ces phénomenes ne son pas vus quand on emploie les os frontaux de 11 jours de développement. La testostérone produit les mêmes effets que le DS. Le deux steroïdes semblent agir directement sur l'os selon on peut le déduire des conditions expérimentales. L'activité de la phosphatase alcaline des frontaux d'embryons de poulet de 12 jours de développement est augmentée de manière significative quand les rudiments son cultivés dans un milieu qui contient DS ou testostérone. Dans ces deux cas: a) on peut révéler l'activation de l'enzyme par des expériences de cinétique enzymatique et b) les vélocités maximes apparantes ont une grande correlation avec le logarithme des doses employées. Quand les deux steroïdes son essayés en conditions semblables, les deux produisent la même augmentation de l'activité phosphatasique.
    Abstract: Zusammenfassung Wenn Stirnknochen von 12 Tage alten Hühnerembryonen in vitro auf koaguliertem Plasma mit Zusatz von 1 mM Dehydroepiandrosteronsulfat gezüchtet werden, so zeigen sie eine Hyperplasie des Periostes und eine erhöhte Synthese des Osteoidgewebes. Diese Erscheinung trifft nicht zu, ween 11 tägige Stirnknochen in gleicher Weise gezüchtet werden. Mit Testosteron werden gleiche Effekte wie mit Dehydroepiandrosteronsulfat erzielt. Aus den gewählten Versuchsverhältnissen kann abgeleitet werden, daß beide Steroide direkt auf den Knochen zu wirken scheinen. Die Aktivität der alkalischen Phosphatase im Stirnknochen des 12 Tage alten Hühnerembryos ist signifikant erhöht, wenn die Knochenansätze in einem Dehydroepiandrosteron oder Testosteron enthaltenden Medium gezüchtet werden. In beiden Fällen ergeben enzymkinetische Untersuchungen einerseits eine Aktivierung des Enzyms, andererseits eine gute Korrelation der erhaltenen scheinbaren Maximalgeschwindigkeiten mit dem Logarithmus der verwendeten Dosen. Bei gleichzeitiger Prüfung bewirkten beide Steroide gleichzeitig eine ähnliche Aktivitätszunahme der alkalischen Phosphatase.
    Notes: Abstract Chick embryo frontal bones at 12 days of development, cultivated in vitro on plasma clots with dehydroepiandrosterone sulfate in a concentration 1mM, exhibit periosteal hyperplasia and increased synthesis of osteoid tissue. These phenomena are not observed when 11-day frontals are cultivated in similar conditions. Testosterone produces the same effects as dehydroepiandrosterone sulfate. Both steroids seem to act directly on bone as can be inferred from the experimental conditions employed. The alkaline phosphatase activity of chick embryo frontal bones at 12 days of development is significantly increased when the rudiments are cultivated in a medium containing dehydro-epiandrosterone or testosterone. In both cases a) enzyme kinetics experiments revealed that there is activation of the enzyme and b) the apparent maximum velocities obtained are hihgly correlated with the logarithm of the doses employed. When assayed simultaneously, both steroids were found equally active in promoting the increase in alkaliue phosphatase activity.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0827
    Keywords: Respiratory alkalosis ; Ionized calcium ; 1,25 Dihydroxycholecalciferol ; Parathyroid hormone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The daily administration of supraphysiological doses of 1,25 dihydroxycholecalciferol (0.1–2.5 µg/d/100 g body weight) to rats, produced respiratory alkalosis. With the doses of 0.1–0.2 µg/d/100 g and feeding a diet with 0.7% of calcium, calcemias did not exceed 2.75 mM, and significantly reduced plasma ionized calcium levels were measured. The latter phenomenon was found associated with increased urinary excretion of cAMP, soft tissue calcium content, and polyuria with hypostenuria, all known effects of parathyroid hormone. These effects were absent in thyroparathyroidectomized rats treated in the same fashion. Present results suggest that the stimulus of low levels of plasma ionized calcium overcomes the probably inhibitory effect of the steroid on parathyroid hormone secretion.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-5233
    Keywords: Key words Phosphaturia ; Glomerular filtration ; Tubular reabsorption ; Parathyroid hormone ; Thyroparathyroidectomy ; Fractional excretion of phosphate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This report deals with the relationships between glucose (G) and insulin on the tubular transport of phosphate (P) in chronically diabetic rats with high plasma levels of parathyroid hormone (PTH). Alloxan-induced diabetes leads to phosphorus depletion of the soft tissues. This phenomenon appears associated with weight loss and negative P balances caused by the increased urinary P excretion. Administration of 2 IU of insulin/100 g body weight (bw) to diabetic rats normalized their P balance and body weight. The effect of parathyroid function on the P metabolism of diabetic rats was investigated with balance experiments. Diabetic rats, intact or thyroparathyroidectomized (TPTX), have a greater urinary excretion of P than their controls. However, in control rats, the ratio intact:TPTX for urinary P is 1.0:0.76, showing the antiphosphaturic effect of parathyroid ablation. For diabetic animals, on the other hand, the ratio is 1.0:1.44. The simultaneous deficit of insulin and PTH thus quadruples the urinary P loss, instead of compensating for each other. The contribution of insulin deficit and hyperglycemia to the defect in tubular reabsorption (TRP) was investigated with clearance experiments (done on anesthetized, perfused rats). Five experimental groups were used: Controls (C), diabetics (D), controls+glucose (C+G), diabetics+insulin (D+I) and diabetics+insulin+glucose (D+I+G). All experimental groups showed a linear relationship between the TRP of P and G. The regression equation for C is significantly different (F=40.1, P〈0.001) from that of D animals. The slope value measure the number of µmoles of P per µmol of G reabsorbed. For C and D rats, the ratio P:G approximates 1:4 and 1:20, respectively. The increase in P:G ratios represents the competition between both substrates for tubular resorption. Glycemias up to 11 mM (C and D+I) exist concurrent with the P:G ratio 1:4. Glycemias above 25 mM (D, C+G and D+I+G) produce a P:G ratio of 1:20. Fractional excretion of P (FEP) increased significantly in untreated, chronically diabetic rats (0.47± 0.12 vs controls=0.05±0.01, P〈0.001). After a single intramuscular injection of insulin, the FEP decreased as a function of insulin levels. To normalize the FEP of diabetic rats in short-term experiments, insulin had to be administered in doses that produce plasma insulin levels 25 times greater than normal. The general information afforded by the present experiments shows that in untreated, chronically diabetic rats, insulin deficit plays an indirect role. The absence of PTH enhances the effect of hyperglycemia. The latter and the concurrent tubular overload of glucose are the cause of hyperphosphaturia in these animals.
    Type of Medium: Electronic Resource
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