UCIBIO-Applied Molecular Biosciences Unit, REQUIMTE, Laboratory of Toxicology, Department of Biological Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge Viterbo Ferreira nº 228, 4050-313 Porto, Portugal.
Associate Laboratory i4HB-Institute for Health and Bioeconomy, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.
Int J Mol Sci. 2024 May 10;25(10):5209. doi: 10.3390/ijms25105209.
Mycoses are one of the major causes of morbidity/mortality among immunocompromised individuals. Considering the importance of these infections, the World Health Organization (WHO) defined a priority list of fungi for health in 2022 that include as belonging to the critical priority group and () to the medium priority group. The existence of few available antifungal drugs, their high toxicity, the acquired fungal resistance, and the appearance of new species with a broader spectrum of resistance, points out the need for searching for new antifungals, preferably with new and multiple mechanisms of action. The cyclam salt H[H(PhCH)Cyclam]Cl was previously tested against several fungi and revealed an interesting activity, with minimal inhibitory concentration (MIC) values of 8 µg/mL for and of 128 µg/mL for . The main objective of the present work was to deeply understand the mechanisms involved in its antifungal activity. The effects of the cyclam salt on yeast metabolic viability (resazurin reduction assay), yeast mitochondrial function (JC-1 probe), production of reactive oxygen species (DCFH-DA probe) and on intracellular ATP levels (luciferin/luciferase assay) were evaluated. H[H(PhCH)Cyclam]Cl induced a significant decrease in the metabolic activity of both and , an increase in Reactive Oxygen Species (ROS) production, and an impaired mitochondrial function. The latter was observed by the depolarization of the mitochondrial membrane and decrease in ATP intracellular levels, mechanisms that seems to be involved in the antifungal activity of H[H(PhCH)Cyclam]Cl. The interference of the cyclam salt with human cells revealed a CC value against HEK-293 embryonic kidney cells of 1.1 μg/mL and a HC value against human red blood cells of 0.8 μg/mL.
真菌感染是免疫功能低下个体发病和死亡的主要原因之一。考虑到这些感染的重要性,世界卫生组织(WHO)在 2022 年定义了一份真菌优先清单,用于健康领域,其中[()]被归为高度优先组,[()]被归为中度优先组。现有的抗真菌药物数量有限,毒性高,真菌耐药性的出现,以及具有更广泛耐药谱的新物种的出现,都表明需要寻找新的抗真菌药物,最好具有新的、多重作用机制。环脒盐 H[H(PhCH)Cyclam]Cl 此前已被用于测试多种真菌,结果显示出有趣的活性,对[()]的最小抑菌浓度(MIC)值为 8 µg/mL,对[()]的 MIC 值为 128 µg/mL。本研究的主要目的是深入了解其抗真菌活性的作用机制。评估了环脒盐对酵母代谢活力(resazurin 还原测定法)、酵母线粒体功能(JC-1 探针)、活性氧(ROS)产生(DCFH-DA 探针)和细胞内 ATP 水平(荧光素/荧光素酶测定法)的影响。H[H(PhCH)Cyclam]Cl 显著降低了[()]和[()]的代谢活性,增加了活性氧(ROS)的产生,并损害了线粒体功能。线粒体膜去极化和细胞内 ATP 水平下降表明后者与 H[H(PhCH)Cyclam]Cl 的抗真菌活性有关。该环脒盐对人细胞的干扰显示对 HEK-293 胚胎肾细胞的 CC 值为 1.1 µg/mL,对人红细胞的 HC 值为 0.8 µg/mL。