在Candida spp中由利引起的基因表达的抗真菌和分子分析
Leilson Carvalho de Oliveira1, Lara Elloyse de Almeida Moreira1, Vitória Pessoa Farias Cabral2
1School of Pharmacy, Laboratory of Bioprospection in Antimicrobial Molecules (LABIMAN), Federal University of Ceará, Fortaleza, CE, Brazil; Center for Drug Research and Development (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil.
Microbial pathogenesis
|January 31, 2026
概括
抗精神病药物哈洛佩里多尔对包括耐药菌株在内的Candida物种表现出抗真菌活性. 它通过诱导亡和氧化应激来起作用,为 кандидоз提供了潜在的药物重定向策略.
科学领域:
- 菌群学 菌群学 菌群学是指菌群学
- 药理学 药理学是指药理学的学科.
- 生物化学 生物化学
背景情况:
- 由于抗真菌耐药性日益增加,疹病面临着越来越大的挑战.
- 药物再利用为新疗法开发提供了一个可行的策略.
- 利 (HAL) 显示出潜在的抗微生物特性.
研究的目的:
- 评估哈洛佩里多尔对敏感和耐药的Candida菌株的抗真菌活性.
- 评估哈洛佩里多尔与常规抗真菌药物的协同作用.
- 阐明利的抗真菌作用背后的机制.
主要方法:
- 汁微稀释和棋盘测试确定了最小抑制度 (MIC) 和协同作用.
- 流细胞计和光显微镜评估了细胞效应.
- 机械学研究研究了亡,氧化应激和线粒体功能.
主要成果:
- 利的MIC值在26.67至256微克/毫升之间.
- 观察到与阿醇 (富可纳,伊特拉可纳) 和安福特乙的协同效应.
- 利诱导了亡,氧化应激,破坏了平衡,并在Candida物种中损坏了DNA.
结论:
- 哈洛佩里多尔对Candida spp.具有显著的抗真菌潜力.
- 该药物与现有的抗真菌剂有效协同作用.
- 由氧化应激和线粒体功能障碍引发的亡是哈洛佩里多尔抗真菌作用的主要机制.
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