Mechanisms of adverse host responses to antibiotics
宿主对抗生素不良反应的机制
基本信息
- 批准号:7054675
- 负责人:
- 金额:$ 19.96万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2005
- 资助国家:美国
- 起止时间:2005-04-15 至 2008-03-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (PROVIDED BY APPLICANT): Recent events of bioterrorism and the rapid global spread of emerging infectious diseases has revealed a compelling need to develop effective and safe therapeutics that can be readily applied to large and genetically diverse populations, typical of the United States. In a comprehensive review of the 2001 anthrax bioterrorist attack, investigation of "adherence, barriers to adherence, and adverse events associated with long-term use of antimicrobial agents" was considered to be a high priority research area. The objective of this research is to elucidate molecular mechanisms underlying adverse host responses to antimicrobial agents used to treat NIAID Priority Pathogens. This proposal focuses on the fluoroquinolones, particularly ciprofloxacin, which was the primary antibiotic used for anthrax post-exposure prophylaxis, and is an option for treatment of other NIAID Priority Pathogens. Side effects of the fluoroquinolones leading to nonadherence most commonly involve the gastrointestinal (GI) tract. The novel hypothesis to be explored in this proposal is that many of these adverse side effects result from the formation of reactive fluoroquinolone metabolites in the liver and/or GI tract. Major metabolites of the fluoroquinolones in humans are acyl glucuronides, which have a high potential for covalent adduct formation with biomolecules. In preliminary studies, we show evidence for spontaneous degradation and acyl migration of ciprofloxacin and trovafloxacin glucuronides similar to that observed with glucuronides of the nonsteroidal anti-inflammatory drugs. Consistent with the exploratory nature of an R21 Research Project, the specific aims of this proposal are as follows. Firstly, we will use primary human hepatocytes and human intestinal cell lines to quantify the Cytotoxicity of 3 fluoroquinolones frequently associated with adverse GI side effects in people (trovafloxacin, grepafloxacin and sparfloxacin) compared with 3 fluoroquinolones less commonly associated with these side effects (ciprofloxacin, ofloxacin, and norfloxacin) . Secondly, we will determine whether inhibition of enzymes potentially responsible for reactive metabolite formation (UGT, CYP and acyl CoA ligase) minimizes the in vitro toxicity of these drugs. By the completion of these studies we will have developed an understanding of the biochemical pathways potentially responsible for clinically important adverse side effects of the fluoroquinolones. In future work we will verify these findings through in vivo studies and identify host genetic factors that may account for individual variability in side effect susceptibility. Our ultimate goal is to optimize the broader clinical application of these drugs through a pharmacogenetic approach in situations where long-term treatment of large and genetically diverse populations is necessitated.
描述(由申请人提供):最近的生物恐怖主义事件和新兴传染病的快速全球传播揭示了迫切需要开发有效和安全的治疗方法,这些方法可以很容易地应用于美国典型的大型和遗传多样性人群。在对2001年炭疽生物恐怖袭击的全面审查中,对“依从性、依从性障碍和与长期使用抗菌药物相关的不良事件”的调查被认为是一个高度优先的研究领域。本研究的目的是阐明用于治疗NIAID优先病原体的抗菌药物引起宿主不良反应的分子机制。该提案侧重于氟喹诺酮类药物,特别是环丙沙星,这是用于炭疽暴露后预防的主要抗生素,也是治疗其他NIAID优先病原体的一种选择。氟喹诺酮类药物的副作用导致的不依从性最常见的涉及胃肠道(GI)。在该提议中探索的新假设是,许多这些不良副作用是由肝脏和/或胃肠道中反应性氟喹诺酮代谢物的形成引起的。氟喹诺酮类药物在人体内的主要代谢产物是酰基葡萄糖醛酸苷,其与生物分子形成共价加合物的可能性很高。在初步研究中,我们发现环丙沙星和曲伐他汀葡萄糖醛酸苷的自发降解和酰基迁移的证据与非甾体抗炎药葡萄糖醛酸苷的观察结果相似。根据R21研究项目的探索性质,本提案的具体目标如下。首先,我们将使用原代人肝细胞和人肠细胞系来量化3种氟喹诺酮类药物(曲伐沙星、格帕沙星和司帕沙星)的细胞毒性,与3种氟喹诺酮类药物(环丙沙星、氧氟沙星和诺氟沙星)的细胞毒性进行比较。其次,我们将确定抑制可能导致反应性代谢物形成的酶(UGT、CYP和酰基CoA连接酶)是否可以最大限度地降低这些药物的体外毒性。通过完成这些研究,我们将了解可能导致氟喹诺酮类药物临床重要不良副作用的生化途径。在未来的工作中,我们将通过体内研究来验证这些发现,并确定可能导致副作用易感性个体差异的宿主遗传因素。我们的最终目标是通过药物遗传学方法优化这些药物在需要长期治疗大型和遗传多样性人群的情况下更广泛的临床应用。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Michael H Court其他文献
Assessment of cytochrome P450 induction in canine intestinal organoid models
犬肠道类器官模型中细胞色素 P450 诱导的评估
- DOI:
- 发表时间:
2024 - 期刊:
- 影响因子:0
- 作者:
Itsuma Nagao;Meg Nakazawa;Takashi Goyama;Michael H Court;Yoko M. Ambrosini - 通讯作者:
Yoko M. Ambrosini
Abstracts presented at the World Congress of Veterinary Anaesthesiology, September 12–16, 2006, Santos, Brazil
- DOI:
10.1111/j.1467-2995.2007.00371a.x - 发表时间:
2007-07-01 - 期刊:
- 影响因子:
- 作者:
B Duncan X Lascelles;Michael H Court;Elizabeth M Hardie;Sheilah A Robertson - 通讯作者:
Sheilah A Robertson
Michael H Court的其他文献
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{{ truncateString('Michael H Court', 18)}}的其他基金
MicroRNAs as effectors of variable human drug metabolism
MicroRNA 作为可变人类药物代谢的效应器
- 批准号:
8514016 - 财政年份:2012
- 资助金额:
$ 19.96万 - 项目类别:
MicroRNAs as effectors of variable human drug metabolism
MicroRNA 作为可变人类药物代谢的效应器
- 批准号:
8574401 - 财政年份:2012
- 资助金额:
$ 19.96万 - 项目类别:
MicroRNAs as effectors of variable human drug metabolism
MicroRNA 作为可变人类药物代谢的效应器
- 批准号:
8341339 - 财政年份:2012
- 资助金额:
$ 19.96万 - 项目类别:
MicroRNAs as effectors of variable human drug metabolism
MicroRNA 作为可变人类药物代谢的效应器
- 批准号:
8827811 - 财政年份:2012
- 资助金额:
$ 19.96万 - 项目类别:
MicroRNAs as effectors of variable human drug metabolism
MicroRNA 作为可变人类药物代谢的效应器
- 批准号:
8653584 - 财政年份:2012
- 资助金额:
$ 19.96万 - 项目类别:
Mechanisms of adverse host responses to antibiotics
宿主对抗生素不良反应的机制
- 批准号:
6925811 - 财政年份:2005
- 资助金额:
$ 19.96万 - 项目类别:
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