Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, 119991, Russia.
Biochemistry (Mosc). 2022 Nov;87(11):1367-1386. doi: 10.1134/S0006297922110153.
The proposed in our studies mechanism of dinitrosyl iron complex (DNIC) formation through the main step of disproportionation of two NO molecules in complex with Fe2+ ion leads to emergence of the resonance structure of dinitrosyl-iron fragment of DNIC, [Fe2+(NO)(NO)]. The latter allowed suggesting capacity of these complexes to function as donor of both neutral NO molecules as well as nitrosonium cations (NO), which has been demonstrated in experiments. Analysis of biological activity of DNICs with thiol-containing ligands presented in this review demonstrates that NO molecules and nitrosonium cations released from the complexes exert respectively positive (regulatory) and negative (cytotoxic) effects on living organisms. It has been suggested to use dithiocarbamate derivatives to enhance selective release of nitrosonium cations from DNIC in living organisms followed by simultaneous incorporation of the released NO molecules into the biologically non-active mononitrosyl iron complexes with dithiocarbamate derivatives.
我们研究提出的二亚硝酰铁复合物(DNIC)形成机制是通过 Fe2+ 离子与两个 NO 分子配合物的歧化的主要步骤进行的,导致 DNIC 的二硝酰-铁片段的共振结构的出现,[Fe2+(NO)(NO)]。后者使这些复合物能够作为中性 NO 分子以及硝酰阳离子(NO+)的供体发挥作用,这在实验中得到了证明。本综述中介绍的含巯基配体的 DNIC 的生物活性分析表明,从复合物中释放的 NO 分子和硝酰阳离子分别对生物体发挥积极(调节)和消极(细胞毒性)的作用。有人建议使用二硫代氨基甲酸盐衍生物来增强硝酰阳离子从 DNIC 在生物体中的选择性释放,随后将释放的 NO 分子同时掺入具有二硫代氨基甲酸盐衍生物的生物非活性单硝酰铁复合物中。