Department of Zoology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Department of Zoology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Mutat Res Genet Toxicol Environ Mutagen. 2022 Jun;878:503481. doi: 10.1016/j.mrgentox.2022.503481. Epub 2022 Mar 9.
Potassium bromate (KBrO) is an oxidising agent that is extensively used as a food additive, it is also a product of cosmetic and pharmaceutical relevance. The objective of this study was to evaluate the oxidative stress, genotoxicity, and apoptosis induced by KBrO in an experimental animal model. To study the toxic effects and oxidative stress, different doses of KBrO below LD (The half maximal lethal dose, 50, 100 and 150 mg/kg body weight) were given intraperitoneally to the mice for multiple time periods (24, 48, and 72 h). The results showed that KBrO significantly induces oxidative damage by increasing the levels of reactive oxygen species (ROS) and lipid peroxidase and depleted the levels of catalase (CAT), superoxide dismutase (SOD) and glutathione (GSH) enzymes in the serum and liver. Moreover, a significant increase of chromosomal aberrations in bone marrow cells and an elevated incidence of micronuclei in the peripheral blood of mice were observed. KBrO induces 3 ´ -OH end double-strand DNA breaks, which was evident in liver sections of the treated mice, and increases the percentage of apoptotic cells, as observed in TUNEL assays and flow cytometry analysis. The present findings indicate that KBrO induces oxidative stress, genotoxicity, and cytotoxicity in a dose- and time-dependent manner in mice.
溴酸钾(KBrO)是一种广泛用作食品添加剂的氧化剂,也是化妆品和制药相关产品的产物。本研究的目的是评估 KBrO 在实验动物模型中诱导的氧化应激、遗传毒性和细胞凋亡。为了研究毒性作用和氧化应激,用不同剂量的 KBrO(低于半数致死剂量 50、100 和 150mg/kg 体重)对小鼠进行腹腔内注射,持续不同时间(24、48 和 72 小时)。结果表明,KBrO 通过增加活性氧(ROS)和脂质过氧化物的水平,耗竭血清和肝脏中过氧化氢酶(CAT)、超氧化物歧化酶(SOD)和谷胱甘肽(GSH)酶的水平,显著诱导氧化损伤。此外,还观察到骨髓细胞中染色体畸变明显增加,小鼠外周血中微核的发生率升高。KBrO 诱导 3´-OH 末端双链 DNA 断裂,这在经处理的小鼠肝组织切片中是明显的,并且通过 TUNEL 测定和流式细胞术分析观察到细胞凋亡的百分比增加。本研究结果表明,KBrO 以剂量和时间依赖的方式诱导小鼠发生氧化应激、遗传毒性和细胞毒性。