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  • Digitale Medien  (2)
  • β-Adrenoceptor antagonists  (2)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 320 (1982), S. 63-66 
    ISSN: 1432-1912
    Schlagwort(e): β-Adrenoceptor antagonists ; Intrinsic sympathomimetic activity ; Glucose tolerance test ; Insulin ; Glucose
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The effect of β-adrenoceptor antagonists on the intravenous glucose tolerance test was investigated in conscious dogs. dl-Celiprolol (cardioselective with ISA=intrinsic sympathomimetic activity) 200 and 1000 μg/kg i.v., dl-metoprolol (cardio-selective without ISA) 200 and 1000 μg/kg i.v., dl-pindolol (non-selective with ISA) 5 and 25 μg i.v. and l-bupranolol (non-selective without ISA) 10 and 50 μg/kg i.v. were used in the study. The influence of β-adrenoceptor antagonists on the plasma glucose and immunoreactive insulin following the intravenous glucose tolerance test were evaluated by calculating the respective areas under the plasma curve. The present investigtion clearly demonstrates the marked difference between the various β-adrenoceptor antagonists on heart rate and, especially on metabolic parameters. dl-Metoprolol, a β-adrenoceptor antagonist with cardioselectivity and without ISA can be assumed not to alter plasma insulin level and glucose assimilation. l-Bupranolol, a non-selective β-adrenoceptor antagonist without ISA reduces plasma insulin level and probably enhances peripheral glucose uptake, resulting in an “unchanged” glucose tolerance. dl-Celiprolol or dl-pindolol, β-adrenoceptor antagonists with ISA, but cardioselective or non-selective enhance both, basal insulin level and insulin level after glucose stimulation but must be assumed to decrease peripheral glucose uptake since here too glucose tolerance was unchanged.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1432-1912
    Schlagwort(e): β-Adrenoceptor antagonists ; (+)- and (−)-Configuration ; Membrane stabilizing activity ; Glucose tolerance test ; Insulin ; Glucose ; Insulin-glucagon ration
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The relevance of the steric configuration to the effects of two non-selective β-adrenoceptor antagonists without intrinsic sympathomimetic activity (+)- and (−)-bupranolol (10 and 50 μg/kg i.v.) and (+)- and (−)-propranolol (100 and 500 μg/kg i.v.) on the i.v. glucose tolerance test (IVGTT) were investigated in conscious, normoglycemic dogs. The effects of the β-adrenoceptor antagonists on plasma glucose, and insulin levels and insulin-glucagon ratio following IVGTT were evaluated by calculating the respective areas under the curve (AUC). The AUC values for plasma glucose were significantly increased by the (−)-configuration of both β-adrenoceptor antagonists. In the (+)-configuration only propranolol (500 μg/kg i.v.) increased the AUC value for plasma glucose significantly. The AUC values for plasma insulin and also for the plasma insulinglucagon ratio were significantly decreased by (−)-propranolol (500 μg/kg i.v.) and by (−)-bupranolol (10 and 50 μg/kg i.v.). Thus the impairment of glucose tolerance, due to suppression of the plasma insulin level, depends mainly on the β-adrenoceptor antagonistic activity of the (−)-configuration.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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