Laboratório de Toxicologia, Departamento de Ciências Biológicas, Universidade do Porto, Rua Aníbal Cunha, Porto, Portugal.
Curr Med Chem. 2011;18(15):2272-314. doi: 10.2174/092986711795656081.
Pathologic heart conditions, particularly heart failure (HF) and ischemia-reperfusion (I/R) injury, are characterized by sustained elevation of plasma and interstitial catecholamine levels, as well as by the generation of reactive oxygen species (ROS) and reactive nitrogen species (RNS). Despite the continuous and extensive research on catecholamines since the early years of the XX(th) century, the mechanisms underlying catecholamine-induced cardiotoxicity are still not fully elucidated. The role of catecholamines in HF, stress cardiomyopathy, I/R injury, ageing, stress, and pheochromocytoma will be thoroughly discussed. Furthermore and although the noxious effects resulting from catecholamine excess have traditionally been linked to adrenoceptors, in fact, several evidences indicate that oxidative stress and the oxidation of catecholamines can have important roles in catecholamine-induced cardiotoxicity. Accordingly, the reactive intermediates formed during catecholamine oxidation have been associated with cardiac toxicity, both in in vitro and in vivo studies. An insight into the influence of ROS, RNS, and catecholamine oxidation products on several heart diseases and their clinical course will be provided. In addition, the source and type of oxidant species formed in some heart pathologies will be referred. In this review a special focus will be given to the research of cardiac pathologies where catecholamines and oxidative stress are involved. An integrated vision of these matters is required and will be provided along this review, namely how the concomitant surge of catecholamines and ROS occurs and how they can be interconnected. The concomitant presence of these factors can elicit peculiar and not fully characterized responses on the heart. We will approach the existing data with new perspectives as they can help explaining several controversial results regarding cardiovascular diseases and the redox ability of catecholamines.
病理性心脏状况,特别是心力衰竭(HF)和缺血再灌注(I / R)损伤,其特征是血浆和间质儿茶酚胺水平持续升高,以及活性氧(ROS)和活性氮(RNS)的产生。尽管自 20 世纪初以来对儿茶酚胺进行了持续广泛的研究,但儿茶酚胺诱导的心脏毒性的机制仍未完全阐明。儿茶酚胺在心力衰竭、应激性心肌病、I / R 损伤、衰老、应激和嗜铬细胞瘤中的作用将被彻底讨论。此外,尽管由于儿茶酚胺过多而产生的有害影响传统上与肾上腺素能受体有关,但实际上,有几项证据表明,氧化应激和儿茶酚胺的氧化可以在儿茶酚胺诱导的心脏毒性中起重要作用。因此,儿茶酚胺氧化过程中形成的反应中间体与体外和体内研究中的心脏毒性有关。将深入了解 ROS、RNS 和儿茶酚胺氧化产物对几种心脏病及其临床过程的影响。此外,还将提到一些心脏病理学中形成的氧化剂种类和来源。在这篇综述中,将特别关注涉及儿茶酚胺和氧化应激的心脏病理学研究。需要对这些问题进行综合考虑,并将在这篇综述中提供,即儿茶酚胺和 ROS 如何同时出现以及它们如何相互关联。这些因素的同时存在可能会引起心脏的特殊且不完全特征的反应。我们将用新的观点来探讨现有的数据,因为它们可以帮助解释关于心血管疾病和儿茶酚胺的氧化还原能力的一些有争议的结果。