Jay D, Cuéllar A, Jay E G, García C, Gleason R, Muñoz E
Departamento de Bioquimica, Instituto Nacional de Cardiologia Ignacio Chávez, México D.F.
Arch Biochem Biophys. 1992 Nov 1;298(2):740-6. doi: 10.1016/0003-9861(92)90474-b.
The purpose of this study was to determine if captopril, an angiotensin-converting enzyme inhibitor, could interact with iron ions and so modify a Fenton type reaction. Results indicate that different degrees of thiobarbituric acid-reactive substance from deoxyribose are obtained in an ascorbate-driven Fenton system depending on the order of addition of captopril and iron to the incubation medium. Similar results were obtained with the chelating reagents ethylenediaminetetraacetic acid and diethylenetriaminepentaacetic acid, indicating that the buffer solution plays a relevant role when a particular iron complex is formed with a chelating agent. These metal complexes produce oxidizing species in a Fenton type system whose nature is discussed.
本研究的目的是确定血管紧张素转换酶抑制剂卡托普利是否能与铁离子相互作用,从而改变芬顿型反应。结果表明,在抗坏血酸驱动的芬顿体系中,根据卡托普利和铁添加到孵育介质中的顺序不同,可从脱氧核糖中获得不同程度的硫代巴比妥酸反应性物质。用螯合剂乙二胺四乙酸和二乙烯三胺五乙酸也得到了类似的结果,表明当特定的铁络合物与螯合剂形成时,缓冲溶液起着重要作用。这些金属络合物在芬顿型体系中产生氧化物质,并对其性质进行了讨论。