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  • 1990-1994
  • 1970-1974  (2)
  • Circulation  (1)
  • Cyclophosphamide  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 277 (1973), S. 71-88 
    ISSN: 1432-1912
    Keywords: Cyclophosphamide ; Embryonic Development ; DNA-Dependent RNA Polymerases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary On day 13+0 h of gestation rats received 10 mg/kg cyclophosphamide i.p. 3, 9, and 24 h after administration of the drug the activities of the DNA-dependent RNA polymerase reactions were measured in the whole embryo and in parts of it (head, upper and lower extremities and trunk). The activities of these enzymes were correlated with the increase in the RNA content of these tissues. A relationship was established light and electron microscopically between the biochemical results and the specific alterations which occur in different structures of the embryonic tissue. The results of these investigations show that: 1. cyclophosphamide leads-in dependency on the time-to a decrease or increase in the Mn++- and/or Mg++-stimulated RNA polymerase reactions in isolated cell nuclei of individual parts of the embryo 2. alterations in the enzyme activities of individual parts of the embryo are not detected when the enzyme activity of the whole embryo is measured at the early day 13 of gestation 3. towards the end of gestation malformations can be demonstrated only in those parts of the embryo, where 24 h after the administration of cyclophosphamide the enzyme pattern shows a highly significant deviation from that of the controls and where cell necroses can be demonstrated light and electron microscopically. Moreover, in the nucleolus of the neuroepithelium segregation of its components takes place which correlates well with the decreased r-RNA polymerase activity. In this paper a disturbance of the transcription mechanisms is discussed as being the primary mode of action of cyclophosphamide in cell metabolism.
    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
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