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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of anesthesia 7 (1993), S. 189-192 
    ISSN: 1438-8359
    Keywords: Propofol ; Intravenous anesthetic ; Histamine ; Whole blood ; in vitro
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We examined the property of emulsion form of propofol (ICI 35 868) to release histamine in whole blood in vitro. Heparinized whole blood from 10 healthy volunteers were incubated with medium and propofol at the final concentration of 0, 1, 10 and 100 µg·ml−1. The concentration of histamine in supernatant fluid after incubation was measured by radioimmunoassay. Histamine release was expressed as the percentage of the concentration of histamine released into supernatant fluid relative to the total cellular histamine content, which was yielded by destroying cell components in the whole blood. Histamine release in the presence of propofol at the concentrations of 1, 10 and 100 µg·ml−1 were almost the same as histamine release in the absence of propofol. We conclude that emulsion form of propofol has no property to release histamine in whole blood in vitro. (Mitsuhata H, Shimizu R: Evaluation of histamine-releasing property of propofol in whole blood in vitro. J Anesth 7: 189–192, 1993)
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of anesthesia 7 (1993), S. 206-209 
    ISSN: 1438-8359
    Keywords: Propofol ; Dog ; Histamine ; Intravenous anaesthetic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We examined a property of emulsion formation of propofol (ICI 35868) to release histamine into circulating plasma in dogs. Plasma histamine was measured with radioimmunoassay before (baseline), and 1, 5 and 10 min after the administration of 15 mg·kg−1 propofol. There were no significant differences between the plasma histamine levels at 1, 5 and 10 min after the administration of propofol and the baseline level. We conclude that the emulsion formation of propofol of 15 mg·kg−1 does not release histamine during induction of anesthesia in dogs. (Mitsuhata H, Shimizu R: Plasma histamine levels during induction of anesthesia with propofol in dogs. J Anesth 7: 206–209, 1993)
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of clinical immunology 15 (1995), S. 277-283 
    ISSN: 1573-2592
    Keywords: Anaphylaxis ; circulatory depression ; bronchospasm ; in vivo ; rabbit ; dog ; nitric oxide ; nitric oxide synthase inhibitor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Nitric oxide, synthesized from the guanidino group ofl-arginine by nitric oxide synthase, has an important role in pathophysiological changes associated with anaphylaxis. Nitric oxide production due to activation of constitutive nitric oxide synthase is detected using a nitric oxide-selective electrode in anaphylactic rabbitsin vivo. A nitric oxide synthase inhibitor attenuates hypotension and hemoconcentration and decreases venous return but does not improve cardiac depression. Nitric oxide functionally antagonizes the effects of vasoconstrictors released by anaphylaxisin vitro. In animals pretreated with a nitric oxide synthase inhibitor, the cardiac output falls significantly, although venous return is increased. Pulmonary resistance is significantly increased with a nitric oxide synthase inhibitor, andl-arginine attenuates the bronchospasm. These findings suggest that production of nitric oxide may reduce the pathophysiologic changes, except for vasodilatation, associated with anaphylaxis.
    Type of Medium: Electronic Resource
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