Department of Pharmacy, Jiangxi Provincial People's Hospital (the First Affiliated Hospital of Nanchang Medical College), Nanchang, PR China.
School of Pharmacy, Nanochang University, Nanchang, PR China.
J Med Microbiol. 2024 Feb;73(2). doi: 10.1099/jmm.0.001805.
is a major causative agent of superficial dermatomycoses such as onychomycosis and tinea pedis. Huangqin decoction (HQD), as a classical traditional Chinese medicine formula, was found to inhibit the growth of common clinical dermatophytes such as in our previous drug susceptibility experiments. The antifungal activity and potential mechanism of HQD against have not yet been investigated. The aim of this study was to investigate the antifungal activity and explore the potential mechanism of action of HQD against . The present study was performed to evaluate the antifungal activity of HQD against by determination of minimal inhibitory concentrations (MICs), minimal fungicidal concentrations (MFCs), mycelial growth, biomass, spore germination and structural damage, and explore its preliminary anti-dermatophyte mechanisms by sorbitol and ergosterol assay, HPLC-based ergosterol test, enzyme-linked immunosorbent assay and mitochondrial enzyme activity test. HQD was able to inhibit the growth of significantly, with an MIC of 3.125 mg ml and an MFC of 12.5 mg ml. It also significantly inhibited the hyphal growth, conidia germination and biomass growth of in a dose-dependent manner, and induced structural damage in different degrees for cells. HQD showed no effect on cell wall integrity, but was able to damage the cell membrane of by interfering with ergosterol biosynthesis, involving the reduction of squalene epoxidase (SE) and sterol 14α-demethylase P450 (CYP51) activities, and also affect the malate dehydrogenase (MDH), succinate dehydrogenase (SDH) and ATPase activities of mitochondria. These results revealed that HQD had significant anti-dermatophyte activity, which was associated with destroying the cell membrane and affecting the enzyme activities of mitochondria.
是引起甲真菌病和足癣等浅部皮肤真菌病的主要病原体。黄芩汤(HQD)作为一种经典的中药方剂,在我们之前的药敏实验中被发现能抑制常见临床皮肤真菌的生长,如。HQD 对 的抗真菌活性及其潜在作用机制尚未得到研究。本研究旨在研究 HQD 对 的抗真菌活性及其潜在作用机制。本研究旨在评估 HQD 对 的抗真菌活性,通过测定最小抑菌浓度(MICs)、最小杀菌浓度(MFCs)、菌丝生长、生物量、孢子萌发和结构损伤来评估 HQD 对 的抗真菌活性,并通过山梨醇和麦角固醇测定、基于 HPLC 的麦角固醇测定、酶联免疫吸附测定和线粒体酶活性测定来探讨其初步的抗真菌机制。HQD 能显著抑制 的生长,MIC 为 3.125mg/ml,MFC 为 12.5mg/ml。它还能显著抑制菌丝生长、孢子萌发和生物量生长,呈剂量依赖性,并对 细胞造成不同程度的结构损伤。HQD 对细胞壁完整性没有影响,但能通过干扰麦角固醇生物合成来破坏 的细胞膜,涉及到鲨烯环氧化酶(SE)和甾醇 14α-去甲基酶 P450(CYP51)活性的降低,还会影响线粒体的苹果酸脱氢酶(MDH)、琥珀酸脱氢酶(SDH)和 ATP 酶活性。这些结果表明,HQD 具有显著的抗真菌活性,与破坏细胞膜和影响线粒体酶活性有关。