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1,4-萘醌衍生物的抗真菌潜力、作用机制及毒性

Antifungal potential, mechanism of action, and toxicity of 1,4-naphthoquinone derivatives.

作者信息

de Almeida Juan Diego Ribeiro, Fonseca Raissa Sayumy Kataki, de Sousa Naira Sulany Oliveira, Cortez Ana Cláudia Alves, Lima Emerson Silva, de Souza Oliveira Juliana Gomes, de Souza Érica Simplício, Frickmann Hagen, de Souza João Vicente Braga

机构信息

1Postgraduate Program in Biotechnology and Natural Resources of the Amazon, Higher School of Health Sciences, Amazonas State University (UEA), Manaus, Amazonas, Brazil.

2Mycology Laboratory, National Institute for Amazonian Research (INPA), Manaus, Amazonas, Brazil.

出版信息

Eur J Microbiol Immunol (Bp). 2024 Aug 23;14(3):289-295. doi: 10.1556/1886.2024.00072. Print 2024 Sep 11.

Abstract

BACKGROUND

The rising prevalence of fungal infections and challenges such as adverse effects and resistance against existing antifungal agents have driven the exploration of new antifungal substances.

METHODS

We specifically investigated naphthoquinones, known for their broad biological activities and promising antifungal capabilities. It specifically examined the effects of a particular naphthoquinone on the cellular components of Candida albicans ATCC 60193. The study also assessed cytotoxicity in MRC-5 cells, Artemia salina, and the seeds of tomatoes and arugula.

RESULTS

Among four tested naphthoquinones, 2,3-DBNQ (2,3-dibromonaphthalene-1,4-dione) was identified as highly effective, showing potent antifungal activity at concentrations between 1.56 and 6.25 μg mL-1. However, its cytotoxicity in MRC-5 cells (IC50 = 15.44 µM), complete mortality in A. salina at 50 μg mL-1, and significant seed germination inhibition suggest limitations for its clinical use.

CONCLUSIONS

The findings indicate that primary antifungal mechanism of 2,3-DBNQ might involve disrupting fungal membrane permeability, which leads to increased nucleotide leakage. This insight underscores the need for further research to enhance the selectivity and safety of naphthoquinones for potential therapeutic applications.

摘要

背景

真菌感染患病率不断上升,以及现有抗真菌药物的副作用和耐药性等挑战,推动了对新型抗真菌物质的探索。

方法

我们专门研究了萘醌类化合物,它们以广泛的生物活性和有前景的抗真菌能力而闻名。具体研究了一种特定萘醌对白色念珠菌ATCC 60193细胞成分的影响。该研究还评估了其对MRC-5细胞、卤虫以及番茄和芝麻菜种子的细胞毒性。

结果

在四种测试的萘醌中,2,3-DBNQ(2,3-二溴萘-1,4-二酮)被确定为高效,在1.56至6.25μg mL-1的浓度下显示出强大的抗真菌活性。然而,其对MRC-5细胞的细胞毒性(IC50 = 15.44µM)、在50μg mL-1时对卤虫的完全致死率以及对种子萌发的显著抑制表明其临床应用存在局限性。

结论

研究结果表明,2,3-DBNQ的主要抗真菌机制可能涉及破坏真菌膜通透性,从而导致核苷酸泄漏增加。这一见解强调了进一步研究以提高萘醌类化合物在潜在治疗应用中的选择性和安全性的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dbf/11393642/05798c541b0e/eujmi-14-289-g001.jpg

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