Elewski B E
Department of Dermatology, University Hospitals of Cleveland, Ohio 44106.
J Am Acad Dermatol. 1993 May;28(5 Pt 1):S28-S34. doi: 10.1016/s0190-9622(09)80305-8.
An understanding of the mechanisms of action and in vitro profiles of antifungal agents is pivotal to selecting effective treatments for dermatophytoses. The principal mechanisms of action of antifungal drugs include disruption of spindle and cytoplasmic microtubule function (e.g., griseofulvin), depletion of or binding to ergosterol (e.g., terbinafine, ketoconazole, and amphotericin B), and accumulation of squalene (terbinafine). It is likely that antifungal agents that deplete or bind to ergosterol have fungistatic activity only; agents that produce a concomitant accumulation of intracellular squalene have fungicidal activity. Although the mechanism of action markedly influences the clinical efficacy of an antifungal agents, in vitro and in vivo antimycotic profiles and bioavailability factors such as drug access to the stratum corneum also contribute to the effectiveness of antifungal agents.
了解抗真菌药物的作用机制和体外特性对于选择有效的皮肤癣菌病治疗方法至关重要。抗真菌药物的主要作用机制包括破坏纺锤体和细胞质微管功能(如灰黄霉素)、麦角固醇的耗竭或结合(如特比萘芬、酮康唑和两性霉素B)以及角鲨烯的积累(特比萘芬)。可能仅耗竭或结合麦角固醇的抗真菌药物仅具有抑菌活性;产生细胞内角鲨烯同时积累的药物具有杀菌活性。尽管作用机制显著影响抗真菌药物的临床疗效,但体外和体内抗真菌特性以及生物利用度因素(如药物进入角质层的情况)也对抗真菌药物的有效性有影响。