National Reference Laboratory of Veterinary Drug Residues (HZAU)/MOA Key Laboratory of Food Safety Evaluation, Huazhong Agricultural University, Wuhan 430070, People's Republic of China.
Chem Biol Interact. 2010 May 14;185(3):227-34. doi: 10.1016/j.cbi.2010.02.030. Epub 2010 Feb 25.
Quinoxaline 1,4-dioxides (QdNOs) derivatives, the potent synthetic antibacterial group used in food-producing animals, are assumed to have pro-oxidant properties. However, how oxidative stress mediated their adrenal toxicity is far from clear. The aim of this study was to assess the ability of three QdNOs, i.e. olaquindox (OLA), mequindox (MEQ), and cyadox (CYA), to produce reactive oxygen species (ROS) and oxidative cell damage in porcine adrenocortical cells. Multiple approaches such as cell activity assay, biochemical detectation, flow cytometry and fluorescent were used to study the integrated role of ROS homeostasis, mitochondrial redox metabolism and cell apoptosis as well as chemical stability of these drugs. The results showed that OLA and MEQ treatment evoked a significant dose and time-dependent cell damage in adrenocortical cells, well CYA displayed much less toxicity. As for the intracellular ROS production, OLA irritated a persistent and utmost release of ROS while MEQ made a similar but weaker reaction. CYA, however, had a short and unstable release of intracellular ROS. On the other hand, quinoxalinine-2-carboxylie acid (QCA), one of the metabolites of OLA and MEQ, did not cause any significant production of ROS and showed relatively lower toxicity than its parents. Moreover, an imbalance in the redox metabolism and mitochondrial membrane damage has been implicated in adrenal toxicity of QdNOs. ROS scavengers partially reversed QdNOs-induced mitochondrial damage, indicating that mitochondria may be a major target and critical for ROS-mediated cell death. In a word, these results suggested that ROS is a key mediator of QdNOs-induced cell death via mitochondria-dependent pathway in adrenocortical cells. The results provide a mechanism approach in understanding the characterize of adrenal damage caused by QdNOs in vitro, which would in turn, help in designing the appropriate therapeutic strategies of these kind of feed additives.
喹喔啉 1,4-二氧化物(QdNOs)衍生物是一种用于食品生产动物的强效合成抗菌剂,被认为具有促氧化剂特性。然而,氧化应激如何介导其肾上腺毒性尚不清楚。本研究旨在评估三种 QdNOs,即奥拉喹多(OLA)、马喹多(MEQ)和赛多昔(CYA)在猪肾上腺皮质细胞中产生活性氧物种(ROS)和氧化细胞损伤的能力。本研究采用细胞活性测定、生化检测、流式细胞术和荧光等多种方法,研究了 ROS 动态平衡、线粒体氧化还原代谢和细胞凋亡以及这些药物的化学稳定性的综合作用。结果表明,OLA 和 MEQ 处理可引起肾上腺皮质细胞明显的剂量和时间依赖性细胞损伤,而 CYA 则显示出较弱的毒性。至于细胞内 ROS 的产生,OLA 可刺激持续且最强的 ROS 释放,而 MEQ 则产生类似但较弱的反应。然而,CYA 仅短暂且不稳定地释放细胞内 ROS。另一方面,喹喔啉-2-羧酸(QCA),是 OLA 和 MEQ 的代谢物之一,不会引起 ROS 的显著产生,并且比其母体毒性相对较低。此外,氧化还原代谢失衡和线粒体膜损伤与 QdNOs 的肾上腺毒性有关。ROS 清除剂部分逆转了 QdNOs 诱导的线粒体损伤,表明线粒体可能是 ROS 介导的细胞死亡的主要靶标和关键。总之,这些结果表明,ROS 是 QdNOs 通过线粒体依赖性途径诱导细胞死亡的关键介质。这些结果提供了一种机制方法来理解 QdNOs 在体外引起的肾上腺损伤的特征,这反过来又有助于设计这些饲料添加剂的适当治疗策略。