Cellular Basis for the Antifungal Activity of Amiodarone

胺碘酮抗真菌活性的细胞基础

• 批准号: 7879726
• 负责人: RAJINI RAO
• 金额: $ 3.28万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-07-14 至 2011-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7879726
• 关键词: Amiodarone; Amphotericin B; Anabolism; Animal Model; Anti-Arrhythmia Agents; Antifungal Agents; Antioxidants; Apoptosis; Apoptotic; Appearance; Aspergillus; Aspergillus fumigatus; Atrial Fibrillation; Biochemical; Biochemical Genetics; Biological; Biological Assay; Calcineurin; Calcium; Candida; Candida albicans; Caspase; Caspase Inhibitor; Caspofungin; Cell Death; Cell membrane; Cells; Chelating Agents; Chemicals; Collection; Combined Modality Therapy; Cryptococcus; Cryptococcus neoformans; DNA Microarray Chip; Data; Databases; Defect; Development; Disseminated candidiasis; Dose; Drug Delivery Systems; Drug Design; Drug resistance; Drug toxicity; Drug usage; Ergosterol; Event; Exhibits; Fluconazole; Fungal Drug Resistance; Generations; Genes; Goals; Growth; Homeostasis; Hypersensitivity; In Vitro; Industrial fungicide; Intervention; Ion Channel; Itraconazole; Knock-out; Lead; Libraries; Link; Mediating; Miconazole; Microarray Analysis; Mitochondria; Modeling; Molecular; Molecular Profiling; Mus; Mutation; Mycoses; Pathway interactions; Pharmaceutical Preparations; Proteins; Reactive Oxygen Species; Research Personnel; Resistance; Reverse Transcriptase Polymerase Chain Reaction; Saccharomyces; Saccharomyces cerevisiae; Saccharomycetales; Serine; Signal Pathway; Signaling Pathway Gene; Testing; Time; Toxic effect; Vacuole; Ventricular Arrhythmia; Work; Yeasts; analog; base; cytochrome c; dronedarone; drug discovery; fungus; genome-wide; in vivo; inhibitor/antagonist; knockout gene; mitochondrial membrane; mutant; novel; pathogen; programs; public health relevance; research study; response; synergism; trafficking; weapons

The goal of this proposal is to elucidate the pathway of programmed cell death by a novel antifungal agent and explore its use as an antimycotic adjunct. Amiodarone is an effective antiarrhythmic drug that was recently discovered to have potent and broad range fungicidal activity. We have shown that amiodarone toxicity in the yeast Saccharomyces cerevisiae is mediated by disruption of calcium homeostasis, followed by the appearance of apoptosis markers and cell death. In Aim 1, we propose to use a combination of biochemical and cell biological approaches to determine the identity and temporal order of events leading from the initial burst of cytosolic calcium to cell death. We will seek to validate key findings in the pathogenic yeast Candida albicans as proof-of-principle for the universality of the fungicidal mechanism of amiodarone. In Aim 2, we will use a variety of genome-wide approaches to identify the genes and signaling pathways that contribute to amiodarone-induced cell death. Genes identified by these studies will be organized into biomodules and placed in cellular pathways by integrating experimental data from high-throughput biochemical assays with information from online databases to give a global view of drug toxicity. We have shown that low doses of amiodarone exhibit potent synergism with existing antifungals against pathogenic fungal species of Candida, Cryptococcus and Aspergillus. Drug synergy from these in vitro studies will form the basis for combination therapy that will be explored in a murine model of systemic Candidiasis (Aim3). Taken together these studies will develop the calcium-mediated cell death pathway as a major new drug discovery target opportunity. Amiodarone will serve as a model test compound for targeting this pathway and for validating the potential of a new class of antifungal potentiating agents. The public health relevance of this project arises from the emergence of new fungal pathogens and drug resistant fungi, and the urgent need for alternative strategies in the management of fungal infections.

本提案的目的是阐明一种新型抗真菌药物引起的细胞程序性死亡的途径 并探索其作为抗真菌辅助剂的用途。胺碘酮是一种有效的抗心律失常药物， 最近发现具有有效和广泛的杀真菌活性。我们已经证明胺碘酮 在酿酒酵母中的毒性是通过破坏钙稳态介导的， 凋亡标记物和细胞死亡的出现。在目标1中，我们建议使用以下组合： 生物化学和细胞生物学方法，以确定事件的身份和时间顺序， 从胞质钙离子的初始爆发到细胞死亡。我们将寻求验证致病性的关键发现， 酵母菌白色念珠菌作为胺碘酮杀真菌机制普遍性的原理证明。 在目标2中，我们将使用各种全基因组方法来识别基因和信号通路， 有助于胺碘酮诱导的细胞死亡。这些研究所确定的基因将被组织成 生物模块，并通过整合来自高通量的实验数据， 利用在线数据库中的信息进行生物化学测定，以提供药物毒性的全局视图。我们有 表明低剂量胺碘酮与现有抗真菌药对病原体 念珠菌属、隐球菌属和曲霉属的真菌种类。这些体外研究的药物协同作用将形成 联合治疗的基础将在系统性疟原虫病的鼠模型中探索（Aim3）。 综合这些研究将开发钙介导的细胞死亡途径作为一个主要的新药 发现目标的机会胺碘酮将作为靶向该途径的模型试验化合物， 用于验证一类新的抗真菌增效剂的潜力。 该项目的公共卫生相关性源于新的真菌病原体和药物的出现。 耐药真菌，并迫切需要在真菌感染的管理替代策略。