Mechanisms of Diphenylamine Xenobiotic Reactivity and Toxicity

二苯胺异生物质反应性和毒性的机制

基本信息

  • 批准号:
    RGPIN-2020-06305
  • 负责人:
  • 金额:
    $ 2.33万
  • 依托单位:
  • 依托单位国家:
    加拿大
  • 项目类别:
    Discovery Grants Program - Individual
  • 财政年份:
    2022
  • 资助国家:
    加拿大
  • 起止时间:
    2022-01-01 至 2023-12-31
  • 项目状态:
    已结题

项目摘要

Background: Diphenylamine (DPA) occurs both naturally and synthetically, and DPA derivatives (DPAs) have widespread industrial use, including in the manufacturing of dyes, rubbers, pesticides, pharmaceuticals, and are found in munition sites. As a result of their widespread use, DPAs also occur in wastewater treatment plants in Canada, and in fish. Xenobiotics like DPAs are not typically reactive but may be oxidized to produce reactive metabolites. The latter are of toxicological concern since they can weaken cells and cause damage to their proteins and DNA. This proposal focuses on unexplored pathways of DPAs metabolism and the ensuing biological consequences. The ubiquitous use and environmental occurrence of DPA derivatives necessitate these studies. Rationale: Preliminary studies have shown that some DPAs can form two types of reactive metabolites: free radical metabolites and hydroxylated metabolites. These metabolites were formed from the heme protein, myeloperoxidase (MPO), which is found in specific blood cells. However, MPO does not usually produce hydroxylated metabolites, and the latter can be further oxidized to quinone- like reactive metabolites. As such, there are fundamental questions about how MPO produces two different types of reactive metabolites. Moreover, metabolism studies using industrial antioxidant DPAs, which are massively produced and imported, have not been reported. Therefore, the potential of DPAs toxicity has not been thoroughly evaluated, nor is it known how relatively harmful different DPAs metabolites are compared to their unmetabolized precursors. Hypotheses: 1) MPO can produce both free radical and hydroxylated metabolites of DPAs. 2) MPO enzymatic activity is a requirement for the toxicity of DPAs. Aims: 1) To characterize the reactive metabolites formed from DPAs by isolated MPO and MPO-positive vs MPO-negative cells. 2) To determine the cellular effects and responses from DPAs in MPO-positive vs MPO-negative cells. 3) To determine damage of specific macromolecule (protein, DNA) intracellular targets by DPAs, and to carry out proteomic and metabolomic studies. 4) To understand the basis of metabolism and toxicity using structure-activity relationships. Significance: This proposal will reveal significant advances in our understanding of how MPO produces different reactive metabolites of DPAs, and evaluate their cellular toxicity pathways. As thousands of tonnes of DPAs being used in certain industrial processes, it is vital to study the effects of DPAs to appreciate their potential hazards. These research findings can contribute to government policymakers regarding the use of DPAs. The application of diverse techniques that involve analytical techniques, mechanistic toxicology, omics technologies, and computational analyses are proposed, which will benefit the training of highly qualified personnel in Canada.
背景:二苯胺 (DPA) 存在于天然和合成中,DPA 衍生物 (DPA) 具有广泛的工业用途,包括用于染料、橡胶、杀虫剂、药品的制造,并且在弹药库中也有发现。由于其广泛使用,DPA 也存在于加拿大的废水处理厂和鱼类中。像 DPA 这样的异生物质通常不具有反应性,但可能会被氧化产生反应性代谢物。后者受到毒理学关注,因为它们会削弱细胞并对其蛋白质和 DNA 造成损害。该提案重点关注未探索的 DPA 代谢途径以及随之而来的生物学后果。 DPA 衍生物的普遍使用和环境存在使得这些研究成为必要。理由:初步研究表明,一些 DPA 可以形成两种类型的反应性代谢物:自由基代谢物和羟基化代谢物。这些代谢物由血红素蛋白髓过氧化物酶 (MPO) 形成,存在于特定的血细胞中。然而,MPO通常不会产生羟基化代谢物,后者可以进一步氧化为醌类反应性代谢物。因此,关于 MPO 如何产生两种不同类型的反应性代谢物存在一些基本问题。此外,使用大量生产和进口的工业抗氧化剂DPA进行代谢研究尚未见报道。因此,DPA 毒性的潜力尚未得到彻底评估,也不知道不同 DPA 代谢物与其未代谢前体相比的相对危害性如何。 假设:1) MPO 可以产生 DPA 的自由基和羟基化代谢物。 2) MPO酶活性是DPA毒性的必要条件。目的: 1) 表征分离的 MPO 和 MPO 阳性细胞与 MPO 阴性细胞从 DPA 形成的反应性代谢产物。 2) 确定 DPA 在 MPO 阳性细胞和 MPO 阴性细胞中的细胞效应和反应。 3)确定DPA对细胞内特定大分子(蛋白质、DNA)靶标的损伤,并开展蛋白质组学和代谢组学研究。 4)利用构效关系了解代谢和毒性的基础。 意义:该提案将揭示我们对 MPO 如何产生 DPA 的不同反应性代谢物并评估其细胞毒性途径的理解的重大进展。由于某些工业过程中使用了数千吨 DPA,因此研究 DPA 的影响以了解其潜在危害至关重要。这些研究结果可以为政府决策者提供有关 DPA 使用的信息。提出了涉及分析技术、机械毒理学、组学技术和计算分析等多种技术的应用,这将有利于加拿大高素质人才的培训。

项目成果

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Siraki, Arno其他文献

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{{ truncateString('Siraki, Arno', 18)}}的其他基金

Mechanisms of Diphenylamine Xenobiotic Reactivity and Toxicity
二苯胺异生物质反应性和毒性的机制
  • 批准号:
    RGPIN-2020-06305
  • 财政年份:
    2021
  • 资助金额:
    $ 2.33万
  • 项目类别:
    Discovery Grants Program - Individual
Mechanisms of Diphenylamine Xenobiotic Reactivity and Toxicity
二苯胺异生物质反应性和毒性的机制
  • 批准号:
    RGPIN-2020-06305
  • 财政年份:
    2020
  • 资助金额:
    $ 2.33万
  • 项目类别:
    Discovery Grants Program - Individual
The role of electron transfer reactions in the cytotoxicity mechanism of xenobiotics
电子转移反应在异生素细胞毒性机制中的作用
  • 批准号:
    RGPIN-2014-04878
  • 财政年份:
    2018
  • 资助金额:
    $ 2.33万
  • 项目类别:
    Discovery Grants Program - Individual
The role of electron transfer reactions in the cytotoxicity mechanism of xenobiotics
电子转移反应在异生素细胞毒性机制中的作用
  • 批准号:
    RGPIN-2014-04878
  • 财政年份:
    2017
  • 资助金额:
    $ 2.33万
  • 项目类别:
    Discovery Grants Program - Individual
The role of electron transfer reactions in the cytotoxicity mechanism of xenobiotics
电子转移反应在异生素细胞毒性机制中的作用
  • 批准号:
    RGPIN-2014-04878
  • 财政年份:
    2016
  • 资助金额:
    $ 2.33万
  • 项目类别:
    Discovery Grants Program - Individual
The role of electron transfer reactions in the cytotoxicity mechanism of xenobiotics
电子转移反应在异生素细胞毒性机制中的作用
  • 批准号:
    RGPIN-2014-04878
  • 财政年份:
    2015
  • 资助金额:
    $ 2.33万
  • 项目类别:
    Discovery Grants Program - Individual
The role of electron transfer reactions in the cytotoxicity mechanism of xenobiotics
电子转移反应在异生素细胞毒性机制中的作用
  • 批准号:
    RGPIN-2014-04878
  • 财政年份:
    2014
  • 资助金额:
    $ 2.33万
  • 项目类别:
    Discovery Grants Program - Individual
PGSB
PGSB
  • 批准号:
    255605-2002
  • 财政年份:
    2003
  • 资助金额:
    $ 2.33万
  • 项目类别:
    Postgraduate Scholarships
PGSB
PGSB
  • 批准号:
    255605-2002
  • 财政年份:
    2002
  • 资助金额:
    $ 2.33万
  • 项目类别:
    Postgraduate Scholarships

相似海外基金

Mechanisms of Diphenylamine Xenobiotic Reactivity and Toxicity
二苯胺异生物质反应性和毒性的机制
  • 批准号:
    RGPIN-2020-06305
  • 财政年份:
    2021
  • 资助金额:
    $ 2.33万
  • 项目类别:
    Discovery Grants Program - Individual
Mechanisms of Diphenylamine Xenobiotic Reactivity and Toxicity
二苯胺异生物质反应性和毒性的机制
  • 批准号:
    RGPIN-2020-06305
  • 财政年份:
    2020
  • 资助金额:
    $ 2.33万
  • 项目类别:
    Discovery Grants Program - Individual
Nucleic Acid-Like Diphenylamine Chromogen
核酸样二苯胺显色剂
  • 批准号:
    6216890
  • 财政年份:
    1962
  • 资助金额:
    $ 2.33万
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