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  • 1
    ISSN: 1439-0973
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Beschreibung / Inhaltsverzeichnis: Zusammenfassung Es wird über diein vitro- undin vivo- Wirksamkeit einer Kombination von Roxithromycin und Co-trimoxazol gegenBorrelia burgdorferi berichtet.In vitro zeigte sich, daß Roxithromycin über eine ausgezeichnete Wirksamkeit gegenüberB. burgdorferi verfügt, Co-trimoxazol war jedoch unwirksam. Die Kombination beider Chemotherapeutika führt zu einem geringen synergistischen Effekt u.z., um eine Verdünnungsstufe bei einer Co-trimoxazol-Konzentration von 256/8mg/1. Bei einer 0.015 mg/l Roxithromycin-Konzentration in Kombination mit 256/4 mg/l zeigte sich in Vergleich zu positiven Kontrollen ein eindeutig reduziertes Wachstum der Mikroorganismen. Die Motilität war sogar eindeutig reduziert, wenn beide Substanzen nur sehr niedrige Konzentrationen aufwiesen. Bei einer offenen prospektiven Pilot-Studie, bei 17 Patienten mit einer gesicherten Borreliose in Stadium II/III, die mit einer Kombination von Roxithromycin (300 mg b.i.d.) 5 Wochen behandelt wurden, waren danach 13 ausgeheilt, vier hatten weiterhin Symptome nach 6 bis 12 Monaten. Das Ergebnis entspricht der einer i.v. Penizillin-oder Ceftriaxon-Behandlung.
    Notizen: Summary Spirochaetal infections have been successfully treated with penicillin; more recently, erythromycin has been used in cases with known penicillin allergy. The discovery of the spirochaeteBorrelia burgdorferi and the elaboration of a new generation of macrolides with properties that differ from older macrolides have led to new ways of treating spirochaetal disease with these compounds. This paper presents data on thein vitro andin vivo efficacy of a combination of roxithromycin and co-trimoxazole againstB. burgdorferi. In vitro (checkerboard technique;B. burgdorferi strain B31; modified BSK II medium) it was found that while roxithromycin showed excellent efficacy againstB. burgdoferi (MIC 0.031 mg/l), co-trimoxazole had no effect. However, the combination of both chemotherapeutics led to a minor synergistic effect, decreasing the MIC for roxithromycin by one dilution step at concentrations of co-trimoxazole from 256 to 8 mg/l. In addition, a clearly reduced growth of microorganisms was seen at concentrations of roxithromycin as low as 0.015 mg/l in combination with 256 to 4 mg/l co-trimoxazole, when compared to the positive controls. Most interestingly, however, the motility ofB. burgdorferi was markedly reduced even when the two drugs were combined at very low concentrations. In anin vivo, non-randomised, open, prospective pilot study it was found that of 17 patients, with confirmed late Lyme borreliosis (stage II/III), treated with combined roxithromycin (300 mg b.i.d.) and co-trimoxazole for 5 weeks, 13 (76%) recovered completely by the end of treatment, and four continued to have symptoms on follow-up at 6 and 12 months. This success rate is similar to that seen with i.v. penicillin and ceftriaxone. It appears that the reduced motility ofB. burgdorferi makes the pathogen mor accessibile to the immune system.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1573-7241
    Schlagwort(e): Ischemia ; coronary K-channel ; glycolysis ; heart
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Several authors have alluded to the possible involvement of EDRF (NO) in ischemia-induced coronary artery dilation. Alternatively, it has been suggested that opening of ATP-dependent K channels could play a key role in this context. We studied the effects of sulfonylureas and NG-nitro-L-arginine (LNNA), a specific inhibitor of endothelial NO (EDRF) synthesis, on ischemia-induced coronary vasodilation in isolated Langendorff-perfused guinea pig hearts arrested with 15 mM KCl in normal Tyrode, and isolated pig coronary arteries precontracted with 43 mM KCl. In Isolated Langerdorff-perfused guinea pig heart, when hypoxia was simulated by switching 100% O2 in the perfusate to 100% N2, coronary perfusion pressure (CPP) fell from 90 cm H2O by 45 ± 5 cm H2O. In the presence of LNNA, a specific inhibitor of NO synthetase in endothelial cells, CPP dropped by 44 ± 6 cm H2O (n = 6; ± SEM, no statistically significant). On biochemical simulation of ischemia (addition of iodoacetate [IAA]), CPP dropped 40 ± 6 cm H2O, and in experiments performed under the same conditions but in the presence of LNNA, CPP dropped by 38 ± 5 cm H2O (n = 6; ± SEM; not statistically significant). When ischemia was simulated metabolically by equimolar replacement of 10 mM glucose with 2-deoxyglucose (DOG), an inhibitor of glycolysis CPP decreased by 24 ± 1 cm H2O (n = 6; ± SEM) after 15 minutes. This fall in CPP was almost prevented by 20 μM glibenclamide, whereas in the presence of 20 μM LNNA the DOG-induced decrease in CPP was not significantly inhibited, and CPP decreased by 22 ± 2.6 cm H2O (n = 6; ± SEM). In isolated pig coronary artery rings, maximal tension, achieved by depolarizing the smooth muscle cells by 43 mM KCl, decreased by 37 ± 7% upon simulated hypoxia by replacing 100% O2 with 100% N2 in the perfusate (n = 6; ± SEM) in arteries with intact endothelium. In arteries without endothelium, maximal tension also dropped by 35 ± 6% (not statistically significant). In the same experiments the decrease in tension could be largerly inhibited in the presence of 50 μM glibenclamide. Our results clearly show that in isolated perfused guinea pig hearts, as well as in isolated pig coronary arteries, EDRF does not play a decisive role in the coronary dilatory response to hypoxia and ischemia.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    ISSN: 1573-7241
    Schlagwort(e): sulfonylureas ; heart ; ischemia ; diabetes
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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