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  • Articles: DFG German National Licenses  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 264 (1969), S. 266-267 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    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 267 (1970), S. 265-277 
    ISSN: 1432-1912
    Keywords: Enzyme Induction ; Microsomal Hydroxylases ; Cytochrome P-450 ; Progesterone Metabolism ; Enzyminduktion ; Mikrosomale Hydroxylasen ; Cytochrom P-450 ; Progesteron-Stoffwechsel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The transformation of progesterone into four more polar metabolites was investigated using liver microsomes from untreated as well as phenobarbitaltreated rabbits. The formation of the four metabolites was dependent on oxygen and NADPH. The reactions were inhibited by CO and this inhibition by CO was partially reversible by light. The four reactions had the same pH-optimum at 7.4. The metabolite pattern was not changed by reducing the oxygen pressure, by inhibiting the reactions with CO, by diminishing the CO effect by light, by variation of the pH value, by separating microsomes into smooth and rough membranes, or by increasing the specific enzyme activities by a factor of 1.5, as a result of treating the microsomes by freezing, thawing, and consecutive centrifugation or filtration on agarose gel. Phenobarbital-treatment of the animals increased the formation of the four metabolites to different degrees, i.e. 3, 1.4, 15, and 6 fold, respectively. Since this procedure was the only one which changed the metabolite pattern, this effect is easier to explain by effects of the phenobarbital-treatment on the rate-limiting steps of the four reactions than by the assumption of four different enzymes catalyzing the metabolism of progesterone.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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