载丁香酚壳聚糖纳米生物聚合物对烟曲霉CYP51A和CYP51B表达的影响

Q4 Medicine
Abozar Nasiri-Jahrodi, M. Shams-Ghahfarokhi, Mehdi Razzaghi Abyaneh
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引用次数: 0

摘要

背景:烟曲霉是侵袭性曲霉病的病原体,也是免疫抑制个体死亡的主要原因。本研究旨在研究载丁香酚壳聚糖纳米颗粒对烟曲霉三唑耐药基因CYP51a和CYP51b表达的影响。采用美国临床与实验室标准协会M38-E3法测定了载丁香酚纳米壳聚糖、壳聚糖、丁香酚和伊曲康唑在浓度分别为4.6 ~ 2400、11.7 ~ 12000、2 ~ 2048和1 ~ 256 μ g/mL时的最小抑菌浓度。采用实时聚合酶链反应检测暴露于0.5、1和2倍MIC浓度的NPs和伊曲康唑的烟曲霉中CYP51A和CYP51B的表达。结果:负载丁香酚的壳聚糖纳米颗粒成功还原了丁香酚,伊曲康唑的含量分别为6000、256和4 μg/mL。real-time PCR结果还显示,载丁香酚壳聚糖纳米颗粒增加了CYP51A和CYP51B的表达,并呈剂量依赖性。在150、300和600 μg/mL浓度下,真菌CYP51A和CYP51B mRNA水平的表达量分别显著增加1.26、1.93、3.1倍和1.2、2.1、2.4倍(p < 0.05)。然而,与伊曲康唑相比,制备的纳米颗粒对这些基因表达的影响似乎较低。研究结果表明,丁香酚壳聚糖纳米颗粒处理可提高CYP51的抗真菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Eugenol-Loaded Chitosan Biopolymer Nanoparticles on CYP51A and CYP51B Expression in Aspergillus fumigatus
Backgrounds: Aspergillus fumigatus is a pathogen responsible for invasive aspergillosis and the main leading cause of death in immunosuppressed individuals. The present study aimed to evaluate the impact of eugenol-loaded chitosan nanoparticles on the expression of CYP51a and CYP51b , two well-known genes responsible for triazole drug resistance in A. fumigatus . The minimum inhibitory concentration (MIC) of eugenol-loaded chitosan nanoparticles, chitosan, eugenol, and itraconazole was determined based on the Clinical and Laboratory Standards Institute M38-E3 method at concentrations of 4.6-2400, 11.7-12000, 2-2048, and 1-256 μ g/mL, respectively. The expression of CYP51A and CYP51B was evaluated in A. fumigatus exposed to 0.5, 1, and 2× of MIC concentration of NPs and itraconazole using the real-time polymerase chain reaction. Findings: The obtained results showed that eugenol-loaded chitosan nanoparticles sucessfully reduced eugenol, and itraconazole was measured to be 6000, 256, and 4 μg/mL, respectively. The results of real-time PCR also revealed that eugenol-loaded chitosan nanoparticles increased the expression of both CYP51A and CYP51B in a dose-dependent manner. The expression of fungal CYP51A and CYP51B at mRNA level was significantly increased 1.26, 1.93, and 3.1-fold as well as 1.2, 2.1, and 2.4-fold at concentrations of 150, 300, and 600 μg/mL , respectively ( p <.05). However, it seems that the prepared nanoparticles had a lower impact on the expression of these genes compared to itraconazole. findings the treatment of with eugenol-chitosan nanoparticles increase the of the CYP51 suggesting the antifungal property of these nanoparticles.
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来源期刊
CiteScore
0.50
自引率
0.00%
发文量
20
审稿时长
6 weeks
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