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  • 1
    ISSN: 0009-8981
    Keywords: Ion-pairing ; Liver enzyme ; Methyl conjugation ; Nicotinamide N-methyltransferase ; Pyridinium ion
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Free Radical Biology and Medicine 9 (1990), S. 99 
    ISSN: 0891-5849
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1420-908X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Histamine N-methyltransferase (HNMT) catalyzes the Nτ-methylation of histamine and structurally-related compounds. Levels of HNMT activity in the human red blood cell are regulated by inheritance. The inbred mouse is an ideal laboratory animal in which to study the genetics of inherited traits. Therefore, HNMT activity was measured in renal homogenates of A/J mice to establish optimal assay conditions and to determine the properties of mouse kidney HNMT as a first step toward testing the hypothesis that large strain-related variations in HNMT activity might exist among inbred strains of mice. ApparentK m values for histamine and S-adenosyl-l-methionine, the two cosubstrates for the reaction, were 26 and 1.7 μM, respectively. IC50 values for the inhibition of mouse kidney HNMT by amodiaquine and S-adenosyl-l-homocysteine were 1.67 and 11.8 μM, respectively. HNMT activity levels were then measured under optimal assay conditions in renal preparations from male animals of eleven inbred mouse strains chosen because of the availability of recombinant inbred (RI) animals derived from the parental strains. Average values for renal HNMT activity varied among strains by less than two-fold and ranged only from 26.2±0.51 (mean±SEM) units/mg protein in AKR/J mice to 39.1±2.58 units/mg protein in C57BL/6J animals. Renal HNMT activities in females of the three strains in which both sexes were studied were 11–13% higher than were those in renal tissue from males of the same strain. In summary, the properties of HNMT in the mouse kidney are similar to those of HNMT in other species, but strain variation in levels of enzyme activity among the 11 inbred mouse strains studied was insufficient for these animals to be used in biochemical genetic experiments.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 54 (1998), S. 773-777 
    ISSN: 1432-1041
    Keywords: Key words Ethanol ; Dietary fat absorption ; Orlistat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Abstract Objectives: The primary objective was to investigate the possible interference of ethanol on the orlistat effect on inhibition of dietary fat absorption and the possible interference of orlistat on the pharmacokinetics of ethanol. Secondary objectives were to assess the tolerability during concomitant dosing of orlistat and ethanol and to determine the ethanol effect on plasma levels of orlistat. Methods: This was a double-blind, placebo-controlled, parallel, randomized study performed in 30 (three parallel groups of ten subjects each) healthy normal weight male subjects between the ages of 20 and 30 years. A 5-day run-in period to accustom subjects to a standardized diet of 2500 kcal/day (30% fat) and to establish baseline fecal fat excretion was followed by a 6-day treatment period. Subjects were randomly assigned to one of three treatment groups (A = orlistat 120 mg t.i.d. and ethanol placebo, B = orlistat 120 mg t.i.d. and 40 g ethanol qd on days −1 and 6, and 40 g bid on days 1–5, and C = orlistat placebo tid and 40 g ethanol qd on days −1 and 6, and 40 g b.i.d. on days 1–5). Serial blood samples were collected for determination of ethanol serum concentrations at specified times over 5 h after each dose of ethanol on days −1 and 6, and for determination of orlistat plasma concentrations on days 1, 3, 5, and 6. Feces were collected quantitatively on days −5 through 8 for analysis of fecal fat. Results: The means of baseline-corrected fecal fat excretion values were comparable: 23.7 g for group A (orlistat) and 22.7 g for group B (orlistat and ethanol). No significant difference was found regarding ethanol pharmacokinetic parameters between treatments with orlistat and placebo. No apparent differences existed between the number of plasma samples with measurable orlistat concentrations in groups A and B. Conclusion: Concomitant ingestion of social amounts of ethanol did not alter the inhibitory effect of orlistat on dietary fat absorption during short-term treatment (6 days) with orlistat. Short-term treatment with orlistat had no significant influence on ethanol pharmacokinetics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 32 (1987), S. 207-210 
    ISSN: 1432-1041
    Keywords: indobufen ; red blood cells ; deformability ; obstructive vascular diseases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary We have studied the effect of indobufen, a cyclo-oxygenase blocking agent which has proved useful in patients with obstructive vascular disease, on red blood cell (RBC) filterability in vitro and in a pilot study ex vivo. The addition of indobufen in vitro to blood samples from 10 healthy volunteers did not significantly modify RBC deformability. We evaluated the ex vivo effect of indobufen (200 mg bd) in 14 patients with obstructive vascular disease. A significant improvement in RBC deformability was noted on the 5th, 14th, and 28th days of treatment, 2 h after the morning dose. Acetylsalicylic acid given to 6 similar patients had no effect suggesting that the positive haemorheological effect of indobufen is probably not linked to its cyclooxygenase blocking effect.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1573-7284
    Keywords: Viridans streptococci ; Bacteremia in cancer patients
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Viridans streptococci septicemia was documented in ten cancer patients, 7 of whom were neutropenic (〈 1000/mmc). Pneumonia was presumed to be the source of bacteremia in six patients. Viridans streptococci isolated from sputum culture in an immunocompromised host must be regarded as the potential etiological agent, then further characterized and checked for antibiotic sensitivity.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1439-0973
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung In einer prospektiven, randomisierten Studie wurde die Kombination Amikacin plus Piperacillin plus Trimethoprim/Sulfamethoxazol mit der Standard-Zweierkombination Amikacin-Piperacillin in der empirischen Behandlung von Fieberschüben bei granulozytopenischen Patienten verglichen. 161 Fieberepisoden wurden ausgewertet, davon waren 74 mit Amikacin plus Piperacillin und 87 mit Amikacin plus Piperacillin plus Trimethoprim/Sulfamethoxazol behandelt worden. Bei Patienten, die die Antibiotika-Dreierkombination erhalten hatten, war der Gesamt-Therapieerfolg wie auch das Ansprechen mikrobiologisch nachgewiesener Infektionen mit 84% bzw. 82% signifikant besser als bei Patienten, die nur Amikacin-Piperacillin erhalten hatten, mit Ansprechraten von 63% bzw. 60% (p 〈 0,05). Bei Auswertung der Ansprechraten nach Infektionslokalisation oder Erregern fanden sich hingegen keine signifikanten Unterschiede zwischen den beiden Gruppen. Die Zugabe von Trimethoprim/Sulfamethoxazol zu Amikacin-Piperacillin verstärkte offensichtlich die Toxizität der Antibiotikatherapie mit vermehrtem Auftreten von Übelkeit und Erbrechen, doch standen diese Nebenwirkungen eindeutig in Beziehung zur Infusionsgeschwindigkeit von Trimethoprim/Sulfamethoxazol. Die Ergebnisse dieser Studie sprechen für die Verwendung einer Kombination von drei Antibiotika anstelle einer Zweierkombination in der empirischen Therapie von Fieberschüben bei granulozytopenischen Patienten.
    Notes: Summary In a prospective randomized trial parenteral trimethoprim/sulphamethoxazole was added to amikacin plus piperacillin in order to compare triple-drug antibiotic combination with a standard regimen as empiric therapy of fever in patients with granulocytopenia. One hundred and sixty-one episodes were evaluated; 74 episodes with amikacin plus piperacillin and 87 episodes with amikacin plus piperacillin plus trimethoprim/sulphamethoxazole. The overall response to therapy (63% vs. 84%) as well as the response of microbiologically documented infections (60% vs. 82%) was significantly better in patients treated with the triple-drug combination (p 〈 0.05). However, no statistically significant differences in response to antibiotics at different infection sites or with regard to any single pathogen was found between the two groups. Trimethoprim/sulphamethoxazole seemed to be responsible for additional toxicity (nausea and vomiting) when added to amikacin plus piperacillin, but these side-effects were clearly related to the rate of infusion of trimethoprim/sulphamethoxazole. The findings of this study support the use of a three-drug versus a two-drug combination as empiric antibiotic regimen in febrile granulocytopenic patients.
    Type of Medium: Electronic Resource
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