Hašková Pavlína, Jansová Hana, Bureš Jan, Macháček Miloslav, Jirkovská Anna, Franz Katherine J, Kovaříková Petra, Šimůnek Tomáš
Charles University in Prague, Faculty of Pharmacy in Hradec Králové, Heyrovského 1203, 500 05 Hradec Králové, Czechia.
Duke University, Department of Chemistry, 124 Science Dr., Durham, NC, 22708, USA.
Toxicology. 2016 Sep 14;371:17-28. doi: 10.1016/j.tox.2016.10.004. Epub 2016 Oct 12.
Catecholamines may undergo iron-promoted oxidation resulting in formation of reactive intermediates (aminochromes) capable of redox cycling and reactive oxygen species (ROS) formation. Both of them induce oxidative stress resulting in cellular damage and death. Iron chelation has been recently shown as a suitable tool of cardioprotection with considerable potential to protect cardiac cells against catecholamine-induced cardiotoxicity. However, prolonged exposure of cells to classical chelators may interfere with physiological iron homeostasis. Prochelators represent a more advanced approach to decrease oxidative injury by forming a chelating agent only under the disease-specific conditions associated with oxidative stress. Novel prochelator (lacking any iron chelating properties) BHAPI [(E)-Ń-(1-(2-((4-(4,4,5,5-tetramethyl-1,2,3-dioxoborolan-2-yl)benzyl)oxy)phenyl)ethylidene) isonicotinohydrazide] is converted by ROS to active chelator HAPI with strong iron binding capacity that efficiently inhibits iron-catalyzed hydroxyl radical generation. Our results confirmed redox activity of oxidation products of catecholamines isoprenaline and epinephrine, that were able to activate BHAPI to HAPI that chelates iron ions inside H9c2 cardiomyoblasts. Both HAPI and BHAPI were able to efficiently protect the cells against intracellular ROS formation, depletion of reduced glutathione and toxicity induced by catecholamines and their oxidation products. Hence, both HAPI and BHAPI have shown considerable potential to protect cardiac cells by both inhibition of deleterious catecholamine oxidation to reactive intermediates and prevention of ROS-mediated cardiotoxicity.
儿茶酚胺可能会发生铁促进的氧化反应,从而形成具有氧化还原循环能力的反应性中间体(氨基色素)和活性氧(ROS)。它们都会诱导氧化应激,导致细胞损伤和死亡。最近研究表明,铁螯合是一种合适的心脏保护工具,具有保护心脏细胞免受儿茶酚胺诱导的心脏毒性的巨大潜力。然而,细胞长时间暴露于经典螯合剂可能会干扰生理铁稳态。前螯合剂是一种更先进的方法,通过仅在与氧化应激相关的疾病特定条件下形成螯合剂来减少氧化损伤。新型前螯合剂(缺乏任何铁螯合特性)BHAPI [(E)-N-(1-(2-((4-(4,4,5,5-四甲基-1,2,3-二氧硼杂环戊烷-2-基)苄基)氧基)苯基)亚乙基]异烟酰肼]被ROS转化为具有强铁结合能力的活性螯合剂HAPI,能有效抑制铁催化的羟基自由基生成。我们的结果证实了儿茶酚胺异丙肾上腺素和肾上腺素氧化产物的氧化还原活性,它们能够将BHAPI激活为HAPI,HAPI可螯合H9c2心肌母细胞内的铁离子。HAPI和BHAPI都能够有效保护细胞免受细胞内ROS形成、还原型谷胱甘肽耗竭以及儿茶酚胺及其氧化产物诱导的毒性影响。因此,HAPI和BHAPI通过抑制有害的儿茶酚胺氧化为反应性中间体以及预防ROS介导的心脏毒性,都显示出保护心脏细胞的巨大潜力。