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  • Cholinesterase reactivation  (1)
  • Rabbit atria  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 323 (1983), S. 45-48 
    ISSN: 1432-1912
    Schlagwort(e): Prejunctional receptors ; Dopamine receptors ; Rabbit atria
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary In isolated rabbit atria, dopamine (10−6 M to 3×10−6 M), in the presence of cocaine and atropine, inhibits the chronotropic responses to electrical stimulation of the sympathetic nerves without influencing the responses to isoprenaline. The inhibitory effect of dopamine is antagonized by cisflupenthixol in a concentration (2.5×10−6 M) that does not antagonize the inhibitory effect of clonidine. Phentolamine, in a concentration (10−5 M) that antagonizes clonidine, does not influence the inhibitory effect of dopamine. Apomorphine (10−6 M) also produces an inhibition of the nerve stimulation-induced chronotropic responses that can be prevented by cis-flupenthixol. These data suggest that prejunctional dopamine receptors are present in rabbit atria.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1432-0738
    Schlagwort(e): Pralidoxime methylsulphate ; Organophosphorus agent ; Plasma concentration ; Cholinesterase reactivation ; Poisoning ; Man
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract We measured in nine patients, poisoned by organophosphorus agents (ethyl parathion, ethyl and methyl parathion, dimethoate, or brompphos), erythrocyte and serum cholinesterase activities, and plasma concentrations of the organophosphorus agent. These patients were treated with pralidoxime methylsulphate (ContrathionR), administered as a bolus injection of 4.42 mg.kg−1 followed by a continuous infusion of 2.14 mg.kg−1/h, a dose regimen calculated to obtain the presumed “therapeutic” plasma level of 4 mg.l−1, or by a multiple of this infusion rate. Oxime plasma concentrations were also measured. The organophosphorus agent was still detectable in some patients after several days or weeks. In the patients with ethyl and methyl parathion poisoning, enzyme reactivation could be obtained in some at oxime concentrations as low as 2.88 mg.l−1; in others, however, oxime concentrations as high as 14.6 mg.l−1 remained without effect. The therapeutic effect of the oxime seemed to depend on the plasma concentrations of ethyl and methyl parathion, enzyme reactivation being absent as long as these concentrations remained above 30 μg.l−1. The bromophos poisoning was rather mild, cholinesterases were moderately inhibited and increased under oxime therapy. The omethoate inhibited enzyme could not be reactivated.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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