The Center for Cardiology, Department of Cardiology 1, Laboratory of Molecular Cardiology, University Medical Center, Langenbeckstr. 1, 55131, Mainz, Germany; The Partner Site Rhine-Main, German Center for Cardiovascular Research (DZHK), Langenbeckstr. 1, 55131, Mainz, Germany.
The Jagiellonian University, Jagiellonian Centre for Experimental Therapeutics (JCET), Bobrzynskiego 14, 30-348, Krakow, Poland; Jagiellonian University Medical College, Grzegorzecka 16, 31-531, Krakow, Poland.
Free Radic Biol Med. 2020 Sep;157:15-37. doi: 10.1016/j.freeradbiomed.2020.02.026. Epub 2020 Mar 1.
According to the latest Global Burden of Disease Study data, non-communicable diseases in general and cardiovascular disease (CVD) in particular are the leading cause of premature death and reduced quality of life. Demographic shifts, unhealthy lifestyles and a higher burden of adverse environmental factors provide an explanation for these findings. The expected growing prevalence of CVD requires enhanced research efforts for identification and characterisation of novel therapeutic targets and strategies. Cardiovascular risk factors including classical (e.g. hypertension, diabetes, hypercholesterolaemia) and non-classical (e.g. environmental stress) factors induce the development of endothelial dysfunction, which is closely associated with oxidant stress and vascular inflammation and results in CVD, particularly in older adults. Most classically successful therapies for CVD display vasoprotective, antioxidant and anti-inflammatory effects, but were originally designed with other therapeutic aims. So far, only a few 'redox drugs' are in clinical use and many antioxidant strategies have not met expectations. With the present review, we summarise the actual knowledge on CVD pathomechanisms, with special emphasis on endothelial dysfunction, adverse redox signalling and oxidative stress, highlighting the preclinical and clinical evidence. In addition, we provide a brief overview of established CVD therapies and their relation to endothelial dysfunction and oxidative stress. Finally, we discuss novel strategies for redox-based CVD therapies trying to explain why, despite a clear link between endothelial dysfunction and adverse redox signalling and oxidative stress, redox- and oxidative stress-based therapies have not yet provided a breakthrough in the treatment of endothelial dysfunction and CVD.
根据最新的全球疾病负担研究数据,非传染性疾病,尤其是心血管疾病,是导致过早死亡和生活质量下降的主要原因。人口结构变化、不健康的生活方式以及更多不利环境因素的负担,解释了这些发现。预计心血管疾病的患病率将会上升,这需要加强研究,以确定和描述新的治疗靶点和策略。心血管危险因素包括经典(如高血压、糖尿病、高胆固醇血症)和非经典(如环境应激)因素,这些因素会导致内皮功能障碍的发展,内皮功能障碍与氧化应激和血管炎症密切相关,导致心血管疾病,特别是在老年人中。大多数经典的心血管疾病治疗方法具有血管保护、抗氧化和抗炎作用,但最初是为了其他治疗目的而设计的。迄今为止,只有少数“氧化还原药物”在临床上使用,许多抗氧化策略并未达到预期效果。本综述总结了心血管疾病发病机制的现有知识,特别强调了内皮功能障碍、不良氧化还原信号和氧化应激,突出了临床前和临床证据。此外,我们还简要概述了已确立的心血管疾病治疗方法及其与内皮功能障碍和氧化应激的关系。最后,我们讨论了基于氧化还原的心血管疾病治疗的新策略,试图解释为什么尽管内皮功能障碍与不良氧化还原信号和氧化应激之间存在明确联系,但基于氧化还原和氧化应激的治疗方法尚未在治疗内皮功能障碍和心血管疾病方面取得突破。