Manousek Jan, Kala Petr, Lokaj Petr, Ondrus Tomas, Helanova Katerina, Miklikova Marie, Brazdil Vojtech, Tomandlova Marie, Parenica Jiri, Pavkova Goldbergova Monika, Hlasensky Jiri
Department of Internal Medicine and Cardiology, University Hospital Brno, Brno, Czechia.
Department of Internal Medicine and Cardiology, Faculty of Medicine, Masaryk University, Brno, Czechia.
Front Cardiovasc Med. 2021 Oct 19;8:732708. doi: 10.3389/fcvm.2021.732708. eCollection 2021.
Indirect evidences in reviews and case reports on Takotsubo syndrome (TTS) support the fact that the existence of oxidative stress (OS) might be its common feature in the pre-acute stage. The sources of OS are exogenous (environmental factors including pharmacological and toxic influences) and endogenous, the combination of both may be present, and they are being discussed in detail. OS is associated with several pathological conditions representing TTS comorbidities and triggers. The dominant source of OS electrones are mitochondria. Our analysis of drug therapy related to acute TTS shows many interactions, e.g., cytostatics and glucocorticoids with mitochondrial cytochrome P450 and other enzymes important for OS. One of the most frequently discussed mechanisms in TTS is the effect of catecholamines on myocardium. Yet, their metabolic influence is neglected. OS is associated with the oxidation of catecholamines leading to the synthesis of their oxidized forms - aminochromes. Under pathological conditions, this pathway may dominate. There are evidences of interference between OS, catecholamine/aminochrome effects, their metabolism and antioxidant protection. The OS offensive may cause fast depletion of antioxidant protection including the homocystein-methionine system, whose activity decreases with age. The alteration of effector subcellular structures (mitochondria, sarco/endoplasmic reticulum) and subsequent changes in cellular energetics and calcium turnover may also occur and lead to the disruption of cellular function, including neurons and cardiomyocytes. On the organ level (nervous system and heart), neurocardiogenic stunning may occur. The effects of OS correspond to the effect of high doses of catecholamines in the experiment. Intensive OS might represent " for this acute clinical condition. TTS might be significantly more complex pathology than currently perceived so far.
关于应激性心肌病(TTS)的综述和病例报告中的间接证据支持以下事实:氧化应激(OS)的存在可能是其急性前期的共同特征。OS的来源是外源性的(包括药理和毒性影响在内的环境因素)和内源性的,两者可能同时存在,并且正在对此进行详细讨论。OS与代表TTS合并症和触发因素的几种病理状况相关。OS电子的主要来源是线粒体。我们对与急性TTS相关的药物治疗的分析显示出许多相互作用,例如,细胞毒性药物和糖皮质激素与线粒体细胞色素P450以及其他对OS重要的酶之间的相互作用。TTS中最常讨论的机制之一是儿茶酚胺对心肌的作用。然而,它们的代谢影响却被忽视了。OS与儿茶酚胺的氧化有关,导致其氧化形式——氨基色素的合成。在病理条件下,这条途径可能占主导地位。有证据表明OS、儿茶酚胺/氨基色素效应、它们的代谢和抗氧化保护之间存在干扰。OS的攻击可能导致抗氧化保护的快速消耗,包括同型半胱氨酸-蛋氨酸系统,其活性会随着年龄的增长而降低。效应亚细胞结构(线粒体、肌浆网/内质网)的改变以及随后细胞能量代谢和钙周转的变化也可能发生,并导致细胞功能的破坏,包括神经元和心肌细胞。在器官水平(神经系统和心脏),可能会发生神经心源性晕厥。OS的作用与实验中高剂量儿茶酚胺的作用相对应。强烈的OS可能代表“这种急性临床状况”。TTS可能是一种比目前所认识到的要复杂得多的病理状况。