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  • 1
    ISSN: 1432-0428
    Keywords: Spiny mice (Acomys cahirinus) ; isolated islets ; glucose ; theophylline ; arginine ; cytochalasin B ; vincristine ; insulin releasein vitro ; sensitivity to glucose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Immunoreactive insulin (IRI) release from collagenase isolated pancreatic islets of spiny mice (Acomys cahirinus) was examined in 15 min and 2 h incubations at glucose concentrations between 2.8 and 56 mM. The resultant glucose-insulin dose-response curves forAcomys islets were compared to those for similarly incubated rat islets. After 15 min incubations, IRI release fromAcomys islets was significantly lower than that from rat islets at all stimulating glucose concentrations. After 2 h incubations, however, maximal responses were similar forAcomys and rat islets, whereas thesensitivity ofAcomys islets to glucose was significantly less. Cyclic AMP 10 mM, theophylline 5 mM, arginine 10 mM, and cytochalasin B 10 Μg/ml, all enhanced IRI release in the presence of glucose 16.7 mM to a relatively greater extent fromAcomys than from rat islets. Vincristine 10−5M reduced IRI release from bothAcomys and rat islets, and this to a similar extent. The results suggest that defective IRI release fromAcomys islets may be the expression of decreased B-cell sensitivity to glucose, even though IRI release fromAcomys islets may improve in time with continued exposure to elevated glucose concentrations. The ability of B-cells ofAcomys to recognize other agents that enhance the action of glucose appeared unaltered.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0428
    Keywords: Ketone body turnover ; ketogenesis ; acetone ; lipolysis ; insulin ; diabetes ; glucagon ; somatostatin ; non-esterified fatty acids ; glycerol ; glucose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary To assess the role of glucagon and insulin in the acute regulation of ketone body kinetics in man, somatostatin was administered with various combinations of these hormones by replacement infusions in groups of six to seven normal subjects. Somatostatin-induced insulin and glucagon deficiency produced a threefold increase in total ketone body concentrations within 2 h. This increase was the combined result of enhanced production (71%), and decreased metabolic clearance (32%), as determined by14C-acetoacetate infusions. An associated elevation of non-esterified fatty acids (66%) and glycerol levels occurred. Glucagon replacement (2 ng · kg-1 · min-1) during insulin deficiency failed to enhance ketogenesis or lipolysis but lowered theβ-hydroxybutyrate/acetoacetate concentration ratios. Hyperglycaemia, observed during glucagon administration and insulin deficiency, did not diminish ketone body production or lipolysis. In contrast, insulin replacement (150 μU · kg-1 · min-1) diminished lipolysis, lowered ketone production, and elevated the metabolic clearance rate of ketone bodies. Glucagon infusions (2 and 4 ng · kg-1 · min-1) during somatostatin and insulin replacement did not accelerate ketone body production or raise non-esterified fatty acid levels, but produced a dose-dependent elevation of blood glucose levels. The results suggest that glucagon is not an important ketogenic hormone under the conditions studied.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1420-9071
    Keywords: Cortisol ; epinephrine ; leucine kinetics ; leucine oxidation ; branched chain amino acids ; protein turnover ; stress hormones ; free fatty acids ; glucose ; somatostatin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary To assess the interaction of the two major stress hormones epinephrine and cortisol in the regulation of leucine kinetics in man, epinephrine (50 ng/kg/min) was infused either alone or in combination with cortisol (2 μg/kg/min) into two groups of 6 postabsorptive normal male subjects during 180 min. Plasma leucine concentrations decreased by 28% (p〈0.05) from baseline during epinephrine treatment (plasma levels 515 pg/ml); this was due to a decrease of leucine appearance (determined by 1-13C-leucine infusions) by 23% (p〈0.025); leucine oxidation decreased by 29% (p〈0.05). However, when plasma cortisol concentrations were elevated to supraphysiological levels (16.3 μmol/l) during epinephrine administration, the decreases of leucine plasma concentrations, appearance and oxidation were abolished. Plasma glucose and FFA concentrations were similarly elevated during both kinds of treatment. Since leucine appearance represents a measurement of total body protein breakdown and leucine disappearance into non-oxidative pathways reflects protein synthesis, the data indicate that plasma epinephrine concentrations during severe stress exert a protein anabolic effect in man which may counteract catabolic properties of elevated plasma cortisol.
    Type of Medium: Electronic Resource
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