Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Key Laboratory of Chinese Internal Medicine of Ministry of Education and Beijing, Dongzhimen Hospital, Beijing, China.
Oxid Med Cell Longev. 2021 Nov 19;2021:1481236. doi: 10.1155/2021/1481236. eCollection 2021.
Endothelial dysfunction, induced by oxidative stress, is an essential factor affecting cardiovascular disease. Uncoupling of endothelial nitric oxide synthase (eNOS) leads to a decrease in nitric oxide (NO) production, an increase in reactive oxygen species (ROS) production, NO consumption, and NO synthesis. As a main active ingredient of astragalus, astragaloside IV can reduce the apoptosis of endothelial cells during oxidative stress. This review is aimed at exploring the mechanism of astragaloside IV in improving oxidative stress-mediated endothelial dysfunction relevant to cardiovascular diseases. The findings showed that the astragaloside IV can prevent or reverse the uncoupling of eNOS, increase eNOS and NO, and enhance several activating enzymes to activate the antioxidant system. In-depth validation and quantitative experiments still need to be implemented.
内皮功能障碍是由氧化应激引起的,是影响心血管疾病的一个重要因素。内皮型一氧化氮合酶 (eNOS) 的解偶联导致一氧化氮 (NO) 生成减少,活性氧 (ROS) 生成增加,NO 消耗和 NO 合成增加。黄芪是一种主要的活性成分,黄芪甲苷可以减少氧化应激诱导的内皮细胞凋亡。本综述旨在探讨黄芪甲苷改善与心血管疾病相关的氧化应激介导的内皮功能障碍的机制。研究结果表明,黄芪甲苷可以预防或逆转 eNOS 的解偶联,增加 eNOS 和 NO,并增强几种激活酶来激活抗氧化系统。仍需要进行深入的验证和定量实验。