番麻提取物联合氟康唑对白色念珠菌的抑菌活性研究。

IF 2 Q3 PHARMACOLOGY & PHARMACY
Drug Target Insights Pub Date : 2025-01-13 eCollection Date: 2025-01-01 DOI:10.33393/dti.2025.3171
Abhay P Mishra, Masande Yalo, Jennifer Nambooze, Carolina H Pohl, Gabré Kemp, Lekgoana K Setsiba, Motlalepula G Matsabisa
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引用次数: 0

摘要

简介:白色念珠菌生物膜形成是抗真菌耐药性的重要因素,需要新的治疗策略。林璎。这是一种传统的草药,在对抗微生物感染方面显示出了希望。本研究的目的是评价木香叶甲醇提取物单独或加氟康唑对白色念珠菌的抑菌活性。方法:采用LC-MS分析甲醇提取物的化学成分,XTT法测定其代谢活性,扫描电镜(SEM)观察其形态特征。此外,我们还对苦楝甲醇叶提取物中Sap3受体(PDB: 2H6T)进行了分子对接筛选。结果:LC-MS分析检出17种可能的植物化学物质。甲醇提取物对生物膜形成的抑制呈剂量依赖性,在240 μg/ml浓度下最大抑制率约为60%,氟康唑的抑制率从15 μg/ml增加到240 μg/ml,从32%增加到76%。在15 μg/ml和240 μg/ml剂量下,村草与氟康唑联合用药可显著提高抑菌率,抑菌率从74%提高到78%。对照和处理过的白色念珠菌生物膜的扫描电镜显示,这种组合改变了形态和细胞完整性的丧失,证实了这些发现。植物化学物质对Sap3酶也具有很高的结合亲和力(分别为-9.7至8.0 kcal/mol),因此可能具有治疗白色念珠菌的潜力。结论:结果表明,在亚抑制浓度下,木香草甲醇提取物中的化合物可能与氟康唑协同抑制白色念珠菌生物膜的形成。这一发现为抗真菌治疗方案的制定和发展铺平了道路,这些治疗方案可能会限制利用该植物部分的氟康唑耐药性的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization and enhanced antibiofilm activity of Annona muricata extract in combination with fluconazole against Candida albicans.

Introduction: Candida albicans biofilm formation is a significant contributor to antifungal resistance, necessitating new treatment strategies. Annona muricata Lin., a traditional herbal remedy, has shown promise in combating microbial infections. The purpose of this study was to assess the antibiofilm activity of the methanol extract of A. muricata leaves alone or with the addition of fluconazole against C. albicans.

Methods: Phytochemicals from the methanol extract were analyzed by LC-MS, the XTT assay was used for metabolic activity, and morphological characteristics were examined using scanning electron microscopy (SEM). Molecular docking screening of identified compounds in A. muricata methanol leaves extract against a Sap3 receptor (PDB: 2H6T) was also performed.

Results: The LC-MS analysis detected 17 possible phytochemicals. The methanol extract showed a dose-dependent inhibition of biofilm formation, with maximum inhibition of ~60% observed at 240 μg/ml, and inhibition by fluconazole increased from 32% to 76% as the concentration increased from 15 to 240 μg/ml. The combination of A. muricata and fluconazole increased the inhibition significantly, from 74% to 78% at 15 μg/ml to 240 μg/mL, respectively. SEM of control and treated C. albicans biofilms showed an altered morphology and loss of cell integrity by the combination, corroborating the findings. Plant phytochemicals also possess high binding affinity (-9.7 to 8.0 kcal/mol, respectively) for the Sap3 enzyme and may therefore have therapeutic potential against C. albicans.

Conclusion: Consequently, the findings indicate that compounds in the A. muricata methanol extract may function in concert with fluconazole at sub-inhibitory concentrations to suppress C. albicans biofilm formation. This finding paves the way for the formulation and development of antifungal treatment regimens that may limit the development of fluconazole resistance employing this plant part.

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Drug Target Insights
Drug Target Insights PHARMACOLOGY & PHARMACY-
CiteScore
2.70
自引率
0.00%
发文量
5
审稿时长
8 weeks
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