Division of Clinical Pharmacology, Department of Medicine, Vanderbilt University Medical Center, 2200 Pierce Ave, PRB 554, Nashville, TN, 37232, USA.
Pflugers Arch. 2023 Jul;475(7):857-866. doi: 10.1007/s00424-023-02806-y. Epub 2023 Mar 30.
In the past century, the lifespan of the human population has dramatically increased to the 80 s, but it is hindered by a limited health span to the 60 s due to an epidemic increase in the cardiovascular disease which is a main cause of morbidity and mortality. We cannot underestimate the progress in understanding the major cardiovascular risk factors which include cigarette smoking, dietary, and sedentary lifestyle risks. Despite their clinical significance, these modifiable risk factors are still the major contributors to cardiovascular disease. It is, therefore, important to understand the specific molecular mechanisms behind their pathological effects to develop new therapies to improve the treatment of cardiovascular disease. In recent years, our group and others have made a progress in understanding how these risk factors can promote endothelial dysfunction, smooth muscle dysregulation, vascular inflammation, hypertension, lung, and heart diseases. These factors, despite differences in their nature, lead to stereotypical alterations in vascular metabolism and function. Interestingly, cigarette smoking has a tremendous impact on a very distant site from the initial epithelial exposure, namely circulation and vascular cells mediated by a variety of stable cigarette smoke components which promote vascular oxidative stress and alter vascular metabolism and function. Similarly, dietary and sedentary lifestyle risks facilitate vascular cell metabolic reprogramming promoting vascular oxidative stress and dysfunction. Mitochondria are critical in cellular metabolism, and in this work, we discuss a new concept that mitochondria are a common pathobiological target for these risk factors, and mitochondria-targeted treatments may have a therapeutic effect in the patients with cardiovascular disease.
在过去的一个世纪中,人类的寿命已经大大延长到了 80 多岁,但由于心血管疾病的流行发病率急剧上升,导致健康寿命限制在 60 多岁。我们不能低估在理解主要心血管风险因素方面所取得的进展,这些因素包括吸烟、饮食和久坐不动的生活方式风险。尽管这些可改变的风险因素具有临床意义,但它们仍然是心血管疾病的主要诱因。因此,了解其病理作用背后的特定分子机制对于开发改善心血管疾病治疗的新疗法非常重要。近年来,我们小组和其他小组在理解这些风险因素如何促进内皮功能障碍、平滑肌失调、血管炎症、高血压、肺部和心脏病方面取得了进展。尽管这些因素性质不同,但它们导致血管代谢和功能的典型改变。有趣的是,吸烟对远离最初上皮暴露的部位(即循环和血管细胞)产生了巨大影响,这是由各种稳定的香烟烟雾成分介导的,这些成分促进血管氧化应激并改变血管代谢和功能。同样,饮食和久坐不动的生活方式风险促进了血管细胞代谢重编程,促进了血管氧化应激和功能障碍。线粒体在细胞代谢中至关重要,在这项工作中,我们提出了一个新概念,即线粒体是这些风险因素的共同病理生物学靶标,针对线粒体的治疗可能对心血管疾病患者具有治疗效果。