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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 378 (1978), S. 93-97 
    ISSN: 1432-2013
    Keywords: Calcium uptake ; Insulin release ; Islets of Langerhans ; Lanthanum ; Magnesium ; Pancreatic islets ; Potassium ; Sodium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Microdissected pancreatic islets of noninbredob/ob-mice were used to study ionic effects on the lanthanum-nondisplaceable45Ca2+ uptake by islet cells. Omission of Mg2+ from the incubation medium had no effect, but the45Ca2+ uptake was increased by omission of Na+ and decreased by omission of K+. Excess Mg2+ (1.2–15 mM) inhibited and excess K+ (4.7–25 mM) stimulated the45Ca2+ uptake in a concentration-dependent manner. Stimulation of45Ca2+ uptake in Na+-deficient islets was associated with an enhancement of the basal insulin release. Total abolishment of glucose-stimulated45Ca2+ uptake in K+-deficient islets did not preclude a significant secretory response to glucose. It is concluded that the lanthanum-nondisplaceable45Ca2+ uptake shows a partial correlation to insulin release.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 340 (1973), S. 51-58 
    ISSN: 1432-2013
    Keywords: 3-O-methyl-d-glucose ; Membrane Transport ; Pancreatic Islets ; Pancreatic β-Cells ; Insulin Release ; Glucose Receptor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The transport and oxidation of 3-O-methyl-d-(U-14C)glucose was studied in microdissected pancreatic islets of obese-hyperglycemic mice. There was no significant production of14CO2 during incubation for 2 h. A comparison with the uptake of sucrose and mannitol indicated that 3-O-methyl-d-glucose was uniformly distributed across the β-cell plasma membrane. Externald-glucose inhibited the entry of 3-O-methyl-d-glucose and caused a significant net loss of 3-O-methyl-d-glucose from islets equilibrated with this compound. The transport of 3-O-methyl-D-glucose was also markedly reduced in the presence of phlorizin or phloretin, whereasd-mannoheptulose ord-glucosamine exerted a slight inhibition. The results support our hypothesis that the transport ofd-glucose into the pancreatic β-cells is carriermediated, and indicate that 3-O-methyl-d-glucose is a non-metabolizable substrate for this carrier in the pancreatic islets. Since in contrast tod-glucose 3-O-methyl-d-glucose does not stimulte insulin release from the type of islets used, the secretagoric recognition system ford-glucose is probably not identical with the membrane transport system.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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