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  • Articles: DFG German National Licenses  (2)
  • 1990-1994
  • 1970-1974  (2)
  • Actinomycin D  (1)
  • Cats  (1)
Source
  • Articles: DFG German National Licenses  (2)
Material
Years
  • 1990-1994
  • 1970-1974  (2)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 275 (1972), S. 31-44 
    ISSN: 1432-1912
    Keywords: Embryonic Development ; Actinomycin D ; DNA-dependent RNA Polymerases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In order to elucidate the phase specificity of the embryo-lethal and teratogenic action of actinomycin D (day 5–10 of gestation) rats received 3H-actinomycin D at different times of gestation. The distribution of the radioactivity in the fetus and the placenta was measured. Moreover, the effects of actinomycin D on the RNA polymerase reactions in isolated nuclei of the decidual and fetal tissue were studied. The biochemical results were correlated electron microscopically with specific alterations occurring in different structures of the total implantation sites. These studies show that the time-dependent embryo-lethal and teratogenic effects of actinomycin D result from a lesion of the embryo and the decidua. The effects of the decidua occur at an earlier time and are more pronounced as compared to those of the embryo. Since the decidua is significant for the nutrition of the embryo till closure of the yolk-sac and beginning of the yolk-sac circulation (day 10 of gestation), the direct effects of actinomycin D on the embryo are intensified by the lesion of the decidua. After day 10 of gestation till the beginning of the placental function 3H-actinomycin D passes over to the embryo. But the concentration-even after a dose of 1 mg/kg-does not suffice to inhibit in vivo RNA polymerase reactions in isolated nuclei.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 270 (1971), S. 79-86 
    ISSN: 1432-1912
    Keywords: Circulation ; dp/dt max ; Cats ; β-Adrenergic Blocking Drugs ; Isoproterenol Antagonism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In closed-chest cats, anaesthetized with pentobarbital, a comparative study was carried out of the cardiovascular actions of fourβ-receptor blocking agents [propanolol, practolol,d(-) INPEA and LB 46] as well as of their antagonism to the effects of isoproterenol. Theβ-receptor blocking agents were injected intravenously in increasing doses until the positive inotropic action of isoproterenol was abolished. Changes in maximum rate of rise of ventricular pressure (dp/dt max) were taken as a measure of the inotropic action. Heart rate, enddiastolic ventricular pressure, ventricular pressure, arterial pressure and ECG were recorded. The following results were obtained: 1. Propranolol and practolol decreaseddp/dt max to a greater extent than did INPEA, whereas LB 46 in small doses was without effect and at larger doses caused an increase indp/dt max. 2. Propranolol caused a more pronounced decrease in heart rate than did practol or INPEA. Small doses of LB 46 decreased the heart rate, but this decrease was not further enhanced by increasing the dose. 3. Propranolol, practolol and INPEA decreased systolic and diastolic pressure more markedly than did LB 46. 4. The hypotensive action of isoproterenol was antagonized by propranolol, LB 46 or INPEA to a greater extent than its inotropic action; practolol however, had no influence upon the hypotensive action of isoproterenol. 5. The enddiastolic ventricular pressure was not affected by theβ-adrenergic blocking agents, but was significantly enhanced by a subsequent injection of noradrenaline.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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