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  • Enzyme Induction  (2)
  • Systemic lupus erythematosus  (2)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 267 (1970), S. 265-277 
    ISSN: 1432-1912
    Schlagwort(e): Enzyme Induction ; Microsomal Hydroxylases ; Cytochrome P-450 ; Progesterone Metabolism ; Enzyminduktion ; Mikrosomale Hydroxylasen ; Cytochrom P-450 ; Progesteron-Stoffwechsel
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: 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.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 267 (1970), S. 307-326 
    ISSN: 1432-1912
    Schlagwort(e): Enzyme Induction ; Microsomal Enzymes ; Michaelis Constants ; Spectral Dissociation Constants ; Affinity for Oxygen and Carbon Monoxide ; Schlüsselwörter ; Enzyminduktion ; Mikrosomale Enzyme ; Michaelis-Konstanten ; Spektrale Dissoziationskonstanten ; Sauerstoff- und Kohlenmonoxid-AffinitÄt
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Phenobarbital treatment of rabbits was found to cause significant changes in some of the apparent Michaelis (K M) constants for p- and N-hydroxylation of aniline [reactions 1 and 2, resp.] and de-ethylation, p- and N-hydroxylation of N-ethylaniline [reactions 3,4, and 5, resp.], and in the spectral dissociation constants (K s) for aniline, N-ethylaniline and ethylisocyanide in isolated hepatic microsomes. The “critical” oxygen concentrations were increased in all reactions investigated. The distribution constants (K G) for CO, determined according to Warburg, decreased in the reactions 2, 3, and 4, and increased in reaction 1. Reaction 5 was not inhibited by CO in microsomes from untreated rabbits and was stimulated by CO after phenobarbital treatment of the animals. Depending on the reaction, theK M-values for aniline and N-ethylaniline were increased, decreased, or remained unchanged by the phenobarbital treatment of the animals. The most striking changes inK M-values were observed with the reactions 2 and 5 in which cytochrome P-450 is either not involved or is not a limiting factor. TheK s-value for ethylisocyanide measured after addition of dithionite to microsomes was increased. The correspondingK s-value measured without dithionite under aerobic conditions remained unchanged. TheK s value for aniline was decreased by the phenobarbital treatment of the animals. Using microsomes from untreated animals theK s value for N-ethylaniline could not be determined exactly. The order of magnitude of this value, however, was greater than that of the corresponding value from phenobarbital-treated animals. The observed alterations in affinity imply that induction by phenobarbital may be associated withqualitative as well as quantitative changes in the hepatic microsomal enzymes or membranes. The qualitative changes could be important for the accessibility of the reacting groups and/or substrate guiding.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    ISSN: 1437-160X
    Schlagwort(e): Immunoglobulin allotypes ; Systemic lupus erythematosus ; Genetics ; Gm ; Km ; HLA-antigens ; Autoantibodies ; Clinical symptoms
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Immunoglobulin heavy chain (G1m, G2m, G3m, A2m) and kappa light chain (Km) allotype and phenotype frequencies of 323 central European Caucasian patients with systemic lupus erythematosus (SLE) were examined and correlated with various genetic, serologic and clinical markers of SLE. No significant associations were found between immunoglobulin allotypes or phenotypes and all 20 parameters tested (nephritis, vasculitis, arthralgias, photosensitivity, discoid lesions, central nervous system disease, Raynaud's phenomenon, sex, anti-Ro, anti-La, anti-nRNP, HLA-DR1-DR7, HLA phenotypes B8-DR3, B7-DR2). It could therefore be assumed that Gm, A2m and Km allotypes were not associated with HLA-antigens and had no influence on the serologic and clinical expression of SLE.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    ISSN: 1437-160X
    Schlagwort(e): Systemic lupus erythematosus ; Recombinant U1-nRNP proteins ; Genetics
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract To investigate a possible involvement of HLA-class II alleles in the genetic predisposition for the formation of anti-U1-nRNP antibody in systemic lupus erythematosus (SLE), genomic DNA of 178 patients was typed for the DRB1, DQA1 and DQB1 alleles using a polymerase chain reaction (PCR) and non-radioactive-oligonucleotide typing. Antibodies against recombinant U1-nRNP proteins (U1-A- U1-C-and 70K-protein) were determined by ELISA. Anti-U1-C antibody was found in 26 (14.7%), anti-U1-A in 34 (19.2%) and anti-70K in 17 (9.6%) patients. A joint occurrence was observed for these antibodies against the recombinant U1-nRNP proteins: anti-U1-C and anti-U1-A antibodies occurred together more frequently than alone and than together with anti-U1-70K antibodies. The frequency of DRB1 * 04 was slightly increased in the patients with anti-U1-C as compared to the patients without anti-U1-C (P〈0.05, Pcorr=n.s., RR=2.4). The DQA1 * 0301 allele, which is in linkage disequilibrium with DRB1 * 04, is found more frequently in anti-U1-C-positive than in antibody-negative patients. The DQB1 * 0303 allele, detected in 12 of 176 SLE patients, was absent in the patients with any of the antibodies against the U1-nRNP proteins. All these deviations may be due to chance alone. We concluded that the presence of antibodies against recombinant U1-nRNP proteins was not significantly associated with any HLA DRB1, DQA1 and DQB1 allele in our group of SLE patients.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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