Abstract
The three imidazole antimycotics clotrimazole, miconazole, and ketoconazole all inhibit the demethylation of lanosterol to ergosterol, resulting in inhibition of growth of Saccharomyces cerevisiae; this is a fungistatic action. At higher concentrations clotrimazole and miconazole are fungicidal, whereas ketoconazole is not. The fungicidal action reflects direct membrane damage by the imidazoles. Evidence for this is that ketoconazole is markedly less active than the other imidazoles in its ability to allow methylene blue entry into cells and to disrupt liposome model membranes. The possible clinical significance of these findings is discussed.
MeSH Terms
Aerobiosis
Anaerobiosis
Antifungal Agents/pharmacology
Clotrimazole/pharmacology
Ergosterol/biosynthesis
Imidazoles/pharmacology
Ketoconazole
Lanosterol/biosynthesis
Miconazole/pharmacology
Piperazines/pharmacology
Saccharomyces cerevisiae/drug effects,growth & development,metabolism
Chemicals
Antifungal Agents
Imidazoles
Piperazines
Lanosterol
Miconazole
Clotrimazole
Ketoconazole
Ergosterol
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Sud I J
Feingold D S
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16 references, click to expand
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