Effect of antimycotic agents on the activity of aspartyl proteinases secreted by Candida albicans

التفاصيل البيبلوغرافية
العنوان: Effect of antimycotic agents on the activity of aspartyl proteinases secreted by Candida albicans
المؤلفون: Bernhard Hube, Gerald Hamm, Nikola Krnjaic, Hans C. Korting, Martin Schaller, M. Niewerth
المصدر: Journal of medical microbiology. 52(Pt 3)
سنة النشر: 2003
مصطلحات موضوعية: Microbiology (medical), Antifungal Agents, Microbiology, Amprenavir, chemistry.chemical_compound, Amphotericin B, Candida albicans, medicine, Cell Adhesion, Aspartic Acid Endopeptidases, Protease inhibitor (pharmacology), Furans, Saquinavir, Sulfonamides, biology, Dose-Response Relationship, Drug, General Medicine, HIV Protease Inhibitors, biology.organism_classification, Corpus albicans, chemistry, Terbinafine, Ketoconazole, Carbamates, Pepstatin, medicine.drug
الوصف: The inhibitory effect of human immunodeficiency virus (HIV) proteinase inhibitors amprenavir and saquinavir and antifungal agents terbinafine, ketoconazole, amphotericin B and ciclopiroxolamine on aspartyl proteinases (Saps) secreted by Candida albicans was tested in an in vitro spectophotometric assay. As expected, both HIV proteinase inhibitors showed a significant inhibitory effect on Sap activity, which was comparable to that of the classical aspartyl proteinase inhibitor pepstatin A (P < 0.001). Antifungal drugs such as ketoconazole, terbinafine and amphotericin B had no, or only minor, inhibitory effects on proteolytic activity. In contrast, a significant reduction in Sap activity could be demonstrated during treatment with the antifungal agent ciclopiroxolamine (P < 0.001). These results point to a multiple effect of this antimycotic agent and might explain the reduced adherence of C. albicans to human epithelial cells at subinhibitory doses.
تدمد: 0022-2615
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b8c595ecf10234a1d7d58c9cd345a4a
https://pubmed.ncbi.nlm.nih.gov/12621090
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....7b8c595ecf10234a1d7d58c9cd345a4a
قاعدة البيانات: OpenAIRE