University of Latvia Faculty of Medicine, Medical Biochemistry Department, Riga, Latvia.
National Academy of Sciences of Belarus, Institute of Genetics and Cytology, Minsk, Belarus.
Arh Hig Rada Toksikol. 2023 Apr 4;74(1):1-7. doi: 10.2478/aiht-2023-74-3707. Print 2023 Mar 1.
This review summarises current knowledge about the genotoxic and genoprotective effects of 1,4-dihydropyridines (DHP) with the main focus on the water-soluble 1,4-DHPs. Most of these water-soluble compounds manifest very low calcium channel blocking activity, which is considered "unusual" for 1,4-DHPs. Glutapyrone, diludine, and AV-153 decrease spontaneous mutagenesis and frequency of mutations induced by chemical mutagens. AV-153, glutapyrone, and carbatones protect DNA against the damage produced by hydrogen peroxide, radiation, and peroxynitrite. The ability of these molecules to bind to the DNA may not be the only mechanism of DNA protection, as other mechanisms such as radical scavenging or binding to other genotoxic compounds may take place and enhance DNA repair. These uncertainties and reports of high 1,4-DHP concentrations damaging the DNA call for further and preclinical research, pharmacokinetic in particular, as it can help pinpoint the exact mechanism(s) of the genotoxic and/or genoprotective action of 1,4-DHPs.
这篇综述总结了 1,4-二氢吡啶(DHP)的遗传毒性和遗传保护作用的现有知识,主要关注水溶性 1,4-DHPs。这些水溶性化合物大多数表现出非常低的钙通道阻断活性,这被认为是“不寻常”的 1,4-DHPs。Glutapyrone、diludine 和 AV-153 降低自发突变率和化学诱变剂诱导的突变频率。AV-153、glutapyrone 和 carbatones 可保护 DNA 免受过氧化氢、辐射和过氧亚硝酸盐产生的损伤。这些分子与 DNA 结合的能力可能不是 DNA 保护的唯一机制,因为可能会发生其他机制,如自由基清除或与其他遗传毒性化合物结合,并增强 DNA 修复。这些不确定性和高浓度 1,4-DHP 损害 DNA 的报告呼吁进一步进行临床前研究,特别是药代动力学研究,因为它可以帮助确定 1,4-DHPs 的遗传毒性和/或遗传保护作用的确切机制。