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Possible mechanisms for induction of oxidative stress and suppression of systemic nitric oxide production caused by exposure to environmental chemicals

机译:暴露于环境化学品引起的氧化应激诱导和系统性一氧化氮生成抑制的可能机制

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摘要

The cytotoxic effects evoked by exposure to environmental chemicals having electrophilic properties are often attributable to covalent attachment to intracellular macromolecules through sulfhydryl groups or enzyme-mediated redox cycling, leading to the generation of reactive oxygen species (ROS). When huge amounts of ROS form they overwhelm antioxidant defenses resulting in the induction of oxidative stress. Nitric oxide (NO) which plays a crucial role in vascular tone, is formed by endothelial NO synthase (eNOS). Since a decrease in systemic NO production is implicated in the pathophysiological actions of vascular diseases, dysfunction of eNOS by environmental chemicals is associated with cardiopulmonary-related diseases and mortality. In this review, we introduce the mechanism-based toxicities (covalent attachment and redox cycling) of electrophiles. Therefore, this review will focus on the possible mechanisms for the induction of oxidative stress and impairment of NO production caused by environmental chemicals.
机译:暴露于具有亲电特性的环境化学品中引起的细胞毒性作用通常可归因于通过巯基或酶介导的氧化还原循环共价附着于细胞内大分子,从而导致活性氧(ROS)的产生。当形成大量的ROS时,它们会淹没抗氧化剂防御能力,从而导致氧化应激。一氧化氮(NO)是由内皮一氧化氮合酶(eNOS)形成的,在血管紧张度中起着至关重要的作用。由于系统性NO产生的减少与血管疾病的病理生理作用有关,因此环境化学药品引起的eNOS功能障碍与心肺相关疾病和死亡率有关。在这篇综述中,我们介绍了亲电试剂的基于机理的毒性(共价连接和氧化还原循环)。因此,本综述将重点关注由环境化学物质引起的氧化应激和NO生成受损的可能机制。

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