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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 15 (1978), S. 475-479 
    ISSN: 1432-0428
    Keywords: Manganese ; magnesium ; calcium ; insulin release ; glucagon release ; isolated ; perfused pancreas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Since Mn++ apparently interferes with excitation-contraction coupling by both reducing inward movement of Ca++ across the cell membrane and by displacing Ca++ from an intracellular store, studies were performed in the isolated, perfused canine pancreas to elucidate the existence of a similar effect in stimulus-secretion coupling and to draw comparisons with the effect of Mg++, which antagonizes Ca++ at the cell membrane. The results show: 1. that Mn++ (0.05, 0.125, and 0.25 mmol/l) inhibits the release of insulin and glucagon in a dose-dependent fashion during the first 3–4 min of infusion followed by a dose-dependent increase in hormone release, the ‘escape phase’. 2. The inhibitory action of Mn++ (0.25 mmol/l) upon release of both hormones is progressively counteracted when perfusate calcium is increased from 0.7 to 1.3 to 5.0 mmol/l. 3. Mg++ (5 mmol/l) inhibits the release of both hormones with no sign of an ‘escape phase’. 4. Mn++ (0.5 mmol/l) during calcium depletion causes a gradual stimulation of the release of both hormones. The dual action of Mn++ upon hormone release from the endocrine pancreas suggests that Mn++ can cross the cell membrane and can interfere with stimulus-secretion coupling both at the membrane level, by competitively inhibiting the Ca++ influx, and at some intracellular level by releasing calcium from an intracellular store.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 13 (1977), S. 297-303 
    ISSN: 1432-0428
    Keywords: Isolated ; perfused pancreas ; glucagon release ; calcium ; glucose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Using the isolated, perfused canine pancreas the importance of calcium for the normal secretory function of the pancreatic alpha cell was investigated. It was found that 1. increases in perfusate Ca++ from 1.3 to 4.8 mM and from 1.3 to 8.2 mM during perfusion with glucose concentrations of 25 and 150 mg/100 ml stimulate the release of both glucagon and insulin in a dose-related and a glucose-dependent fashion. The hormone responses to increases in calcium were, with few exceptions, biphasic 2. a ‘Ca++ free’ medium inhibited release of both hormones, and increases in perfusate glucose from 25 to 150 mg/100 ml were unable to suppress glucagon or to stimulate insulin. Addition of calcium (8.2 mM) resulted in re-establishment of the normal regulatory role of glucose upon release of both hormones, now being in a hyperactivated state by the high Ca++ concentration; 3. sudden Ca++ depletion of the perfusate from 2 mM at a glucose concentration of 200 mg/100 ml inhibited immediately the release of both hormones to very low levels, which remained low until the addition of Ca++ (2 mM). Ca++ is therefore an essential requirement for the normal secretory process of pancreatic glucagon, possibly involving uptake and accumulation within the A cell, as established for the B cell. It is suggested that Ca++ exerts its effect on the microtubular microfilamentous system.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0428
    Keywords: Diabetes ; streptozotocin ; somatostatin release ; glucagon release ; isolated canine perfused pancreas ; glucoreceptor ; glucose ; arginine ; isoproterenol ; calcium ; radioimmunoassay
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Somatostatin release from the isolated pancreas of 3 normal and 6 streptozotocin diabetic dogs has been measured in response to various stimuli to determine whether abnormalities in somatostatin release are present in the diabetic pancreas. Simultaneous measurement of glucagon secretion was also made. In the pancreas from normal dogs increases in perfusate glucose from 25 to 200 mg/100 ml induced a 2–3 fold increase in somatostatin release and a two thirds decrease in glucagon secretion. In contrast, in the diabetic pancreas glucose caused no change in the secretion of the two hormones. In the diabetic pancreas addition of insulin to the perfusate (25,000 μU/ml) for periods from 10 to 75 minutes aimed at restoring normal extracellular insulin levels in the islets failed to restore either somatostatin or glucagon secretion to normal. In contradistinction to the lack of effect of glucose, the somatostatin and glucagon responses to arginine (5 mmol/l), isoproterenol (2 ng/ml) and calcium (5 mmol/l) were normal in the diabetic pancreas. The data suggests the presence of a selective glucoreceptor abnormality of the D as well as of B and A cells in the streptozotocin diabetic dog.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 16 (1979), S. 261-266 
    ISSN: 1432-0428
    Keywords: Perfused pancreas ; somatostatin ; insulin ; glucagon ; calcium ; acetylcholine ; glucose ; isoproterenol ; arginine ; radioimmunoassay ; dog pancreas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of calcium on somatostatin secretion was investigated in the isolated, perfused canine pancreas preparation and compared with those of acetylcholine, glucose, isoproterenol and arginine. Calcium (5 mmol/l) stimulated somatostatin release in a typical biphasic response pattern being about 5 times as potent as acetylcholine (1 μmol/l), arginine (5 mmol/l), and isoproterenol (2 ng/ml) while the release of insulin and glucagon in response to calcium and the other secretagogues were of the same magnitude. Somatostatin release increased progressively when perfusate calcium was increased step-wise from 0 through 1.25 and 2.5 to 5.0 mmol/l. Calcium stimulated the secretion of somatostatin in the absence of glucose. The stimulatory effect of calcium was, however, modulated by the glucose concentration being about twice as large at 200 mg/100 ml as at 25 mg/100 ml glucose in the perfusion medium.
    Type of Medium: Electronic Resource
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