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薰衣草精油:一种有前途的抗真菌和抗生物膜剂,可对抗口腔白色念珠菌。

Lavandula dentata L. essential oil: a promising antifungal and antibiofilm agent against oral Candida albicans.

机构信息

Universidade Federal da Paraíba - UFPB, Centro de Ciências da Saúde - CCS, Programa de Pós-graduação em Produtos Naturais e Sintéticos Bioativos - PgPNSB, João Pessoa, PB, Brasil.

Universidade Federal de Campina Grande - UFCG, Centro de Saúde e Tecnologia Rural - CSTR, Patos, PB, Brasil.

出版信息

Braz J Biol. 2024 Aug 5;84:e283646. doi: 10.1590/1519-6984.283646. eCollection 2024.

DOI:10.1590/1519-6984.283646
PMID:39109727
Abstract

Candida albicans is the main fungal species involved in oral candidiasis, and its increasing resistance to pharmacological treatment encourages the search for improved antifungal agents. Lavandula dentata L. essential oil (LD-EO) has been recognized for its antimicrobial activity, but little is known about its role against oral C. albicans. This study evaluated the antifungal and antibiofilm activities, mechanisms of action, and toxicity of LD-EO from Brazil against oral strains of C. albicans. Antifungal activity was assessed based on Minimum Inhibitory Concentration (MIC), Minimum Fungicidal Concentration (MFC), association study with miconazole (Checkerboard method), and sorbitol and ergosterol assays. Inhibition of biofilm formation and disruption of preformed biofilm were considered when studying the effects of the product. Additionally, the toxicity of LD-EO was evaluated by a hemolysis assay on human erythrocytes. Phytochemical analysis by gas chromatography-mass spectrometry identified eucalyptol (33.1%), camphor (18.3%), and fenchone (15.6%) as major constituents. The test substance showed mainly fungicidal activity (MIC100 = 8 μg/mL; MFC = 16 μg/mL), including against two miconazole-resistant isolates of C. albicans. The effects of LD-EO were synergistic with those of miconazole and appeared not to involve damage to the fungal cell wall or plasma membrane. Its effectiveness in inhibiting biofilm formation was higher than the effect of disrupting preformed biofilm. Finally, the product exhibited low hemolytic activity at MIC. Based on the favorable and novel results described here, LD-EO could constitute a promising therapeutic alternative for oral candidiasis, including miconazole-resistant cases.

摘要

白色念珠菌是引起口腔念珠菌病的主要真菌物种,其对药物治疗的耐药性增加促使人们寻找更好的抗真菌药物。薰衣草精油(LD-EO)已被证明具有抗菌活性,但对其抑制口腔白色念珠菌的作用知之甚少。本研究评估了巴西产 LD-EO 对口腔白色念珠菌的抗真菌和抗生物膜活性、作用机制和毒性。抗真菌活性基于最低抑菌浓度(MIC)、最低杀菌浓度(MFC)、与咪康唑的联合研究(棋盘法)以及山梨糖醇和麦角固醇测定来评估。在研究产品的作用时,还考虑了抑制生物膜形成和破坏已形成生物膜的效果。此外,通过人红细胞溶血试验评估 LD-EO 的毒性。气相色谱-质谱联用的植物化学分析鉴定出桉树脑(33.1%)、樟脑(18.3%)和葑酮(15.6%)为主要成分。测试物质主要表现出杀菌活性(MIC100 = 8 μg/mL;MFC = 16 μg/mL),包括对两种耐咪康唑的白色念珠菌分离株。LD-EO 的作用与咪康唑协同,似乎不涉及真菌细胞壁或质膜的损伤。其抑制生物膜形成的效果高于破坏已形成生物膜的效果。最后,该产品在 MIC 时显示出较低的溶血活性。基于这里描述的有利和新颖的结果,LD-EO 可能成为口腔念珠菌病(包括耐咪康唑的病例)的一种有前途的治疗替代方案。

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