Cocchi Veronica, Gasperini Sofia, Lenzi Monia
Department of Pharmacy and Biotechnology, Alma Mater Studiorum University of Bologna, 40127 Bologna, Italy.
Toxics. 2022 Mar 16;10(3):142. doi: 10.3390/toxics10030142.
A genotoxicological study was carried out on a substance-based medical device (SMD) containing anthraquinones in order to evaluate its potential mutagenic effect. The "In Vitro Mammalian Cell Micronucleus Test" was performed on human TK6 cells by flow cytometry. Cultures were treated with concentrations of SMD tested in the range of 0-2 mg/mL for short treatment time (3 h) both in the absence and presence of an exogenous metabolic activation system, followed by a recovery period in fresh medium (23 h) and for extended treatment time (26 h) without an exogenous metabolic activation system. At the end of both treatment times, cytotoxicity, cytostasis, apoptosis and micronuclei (MNi) frequency were analysed in treated cultures and then compared with those measured in concurrent negative control cultures. The SMD did not induce a statistically significant increase MNi frequency under any of experimental conditions tested. The negative outcome shows that the SMD is non-mutagenic in terms of its ability to induce chromosomal aberrations both in the absence and presence of an exogenous metabolic activation system. The study ended by analyzing intracellular ROS levels to exclude the pro-oxidant ability, typically linked to DNA damage. On the contrary, our results demonstrated the ability the SMD to counteract oxidative stress.
对一种含有蒽醌的基于物质的医疗器械(SMD)进行了遗传毒理学研究,以评估其潜在的诱变作用。通过流式细胞术对人TK6细胞进行了“体外哺乳动物细胞微核试验”。在不存在和存在外源性代谢活化系统的情况下,用0-2mg/mL范围内测试的SMD浓度处理培养物短时间(3小时),然后在新鲜培养基中恢复一段时间(23小时),并在不存在外源性代谢活化系统的情况下延长处理时间(26小时)。在两个处理时间结束时,分析处理后培养物中的细胞毒性、细胞生长抑制、凋亡和微核(MNi)频率,然后与同期阴性对照培养物中测量的结果进行比较。在任何测试的实验条件下,SMD均未诱导MNi频率出现统计学上的显著增加。阴性结果表明,在不存在和存在外源性代谢活化系统的情况下,SMD在诱导染色体畸变方面无诱变作用。该研究通过分析细胞内ROS水平来结束,以排除通常与DNA损伤相关的促氧化能力。相反,我们的结果证明了SMD具有对抗氧化应激的能力。