Department for Pharmacology of Cellular Signaling Systems and Experimental Therapeutics, Institute of Pharmacology and Toxicology, National Academy of Medical Science, Kyiv, Ukraine.
Cardiovasc Toxicol. 2024 Aug;24(8):776-788. doi: 10.1007/s12012-024-09878-x. Epub 2024 Jun 25.
Oxidative stress results from the production of reactive oxygen species (ROS) and reactive nitrogen species (RNS) in quantities exceeding the potential activity of the body's antioxidant system and is one of the risk factors for the development of vascular dysfunction in diabetes and exposure to ionizing radiation. Being the secondary products of normal aerobic metabolism in living organisms, ROS and RNS act as signaling molecules that play an important role in the regulation of vital organism functions. Meanwhile, in high concentrations, these compounds are toxic and disrupt various metabolic pathways. The various stress factors (hyperglycemia, gamma-irradiation, etc.) trigger free oxygen and nitrogen radicals accumulation in cells that are capable to damage almost all cellular components including ion channels and transporters such as Na/K-ATPase, BK, and TRP channels. Vascular dysfunctions are governed by interaction of ROS and RNS. For example, the reaction of ROS with NO produces peroxynitrite (ONOO), which not only oxidizes DNA, cellular proteins, and lipids, but also disrupts important signaling pathways that regulate the cation channel functions in the vascular endothelium. Further increasing in ROS levels and formation of ONOO leads to reduced NO bioavailability and causes endothelial dysfunction. Thus, imbalance of ROS and RNS and their affect on membrane ion channels plays an important role in the pathogenesis of vascular dysfunction associated with various disorders.
氧化应激是由于活性氧(ROS)和活性氮(RNS)的产生量超过了机体抗氧化系统的潜在活性,是糖尿病血管功能障碍和电离辐射暴露发展的危险因素之一。ROS 和 RNS 作为信号分子,是生物体内正常需氧代谢的次级产物,在调节重要的机体功能方面发挥着重要作用。同时,在高浓度下,这些化合物是有毒的,并破坏各种代谢途径。各种应激因素(高血糖、γ 射线照射等)会触发细胞内游离氧和氮自由基的积累,这些自由基能够损伤包括离子通道和转运体在内的几乎所有细胞成分,如 Na/K-ATP 酶、BK 和 TRP 通道。血管功能障碍受 ROS 和 RNS 的相互作用控制。例如,ROS 与 NO 的反应产生过氧亚硝酸盐(ONOO),它不仅氧化 DNA、细胞蛋白质和脂质,还破坏调节血管内皮阳离子通道功能的重要信号通路。ROS 水平的进一步升高和 ONOO 的形成导致 NO 生物利用度降低,引起内皮功能障碍。因此,ROS 和 RNS 的失衡及其对膜离子通道的影响在与各种疾病相关的血管功能障碍发病机制中起着重要作用。