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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 279 (1973), S. 417-420 
    ISSN: 1432-1912
    Keywords: Cats ; Histamine ; Burimamide ; Gastric Acid Secretion ; Gastric Mucosal Blood Flow
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In anaesthetized cats burimamide inhibits gastric acid secretion, reduces gastric mucosal blood flow, rises blood pressure and increases cardiac frequency. The effects or burimamide on blood pressure, cardiac frequency and on gastric acid secretion are antagonized by reduction of adrenergic influences by adrenalectomy of adrenergic blocking agents. The results indicate that burimamide releases catecholamines which are at least in part responsible for the effects of burimamide.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 285 (1974), S. 337-353 
    ISSN: 1432-1912
    Keywords: Cats ; H2-Receptor-Antagonists ; Gastric Acid Secretion ; Gastric Mucosal Blood Flow ; Acid Base Balance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. In anaesthetized acute gastric fistula cats the effect was studied of the histamine-H2-receptor-antagonists burimamide and metiamide on histamine-stimulated gastric acid secretion, gastric mucosal blood flow, and acid base balance of the arterial blood and the gastric venous drainage. 2. Both burimamide and metiamide inhibit gastric secretion and gastric mucosal blood flow. The effects of metiamide are more pronounced than those of burimamide. On acid base balance both histamine-H2-receptor-antagonists have essentially the same effects which reflect the reduced loss of H+ from the stomach. 3. The inhibitory effects of burimamide on the stomach are at least in part antagonized by the histamine-H1-receptor-antagonist mepyramine (which presumably prevents burimamide from releasing catecholamines) and by the α-adrenergic blocking agent phenoxybenzamine, providing indirect evidence for the view that these effects of burimamide are mediated by catecholamines. 4. Phenoxybenzamine and mepyramine do not antagonize the gastric inhibitory effects of metiamide indicating that metiamide is void of catecholamine releasing properties. 5. Phenoxybenzamine and mepyramine influence acid base balance only when the inhibition of gastric acid secretion by burimamide was diminished. They prevented the histamine-mediated drop in arterial pO2, indicating that this histamine effect can be attributed to catecholamines, too.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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