Qu Shuiqing, Deng Shuoqiu, Yang Ting, Yang Yuanmin, Zhang Yu, Zheng Zhongyuan, Chen Lina, Li Yujie
Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China; Artemisinin Research Center, China Academy of Chinese Medical Sciences, Beijing, China.
Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China; Artemisinin Research Center, China Academy of Chinese Medical Sciences, Beijing, China.
Ecotoxicol Environ Saf. 2022 Apr 1;234:113379. doi: 10.1016/j.ecoenv.2022.113379. Epub 2022 Mar 9.
Exposure to diesel exhaust particles (DEP) increases the risk of ischemic heart disease, especially heart attacks and ischemic/thrombotic strokes. Shengmai Yin (SMY) is a traditional Chinese medicine used to treat coronary heart disease. The aim of this study was to determine the protective role of SMY and the mechanism by which SMY affects DEP-induced cardiovascular injury. This study is expected to provide the basis for the development of an adaptive signature of SMY in the prevention of atherosclerotic cardiovascular disease and premature death from global air pollution exposure. We developed animal models of myocardial ischemia and atherosclerosis (AS) in response to DEP exposure. After SMY treatment, serum lipids returned to normal. Aortic plaque area and MMP9 expression were significantly reduced and collagen fiber expression increased after SMY treatment compared to DEP exposure alone. Thus, the risk of plaque formation and vulnerability is reduced. In addition, SMY improved left ventricular structure, morphology, function, blood flow, infarct area, myocardial damage, and ROS accumulation to varying degrees in ApoE mice. These results indicate that the use of SMY is effective, to varying degrees, for the treatment of dyslipidemia, atherosclerosis, myocardial ischemia, and oxidative stress in ApoE mice. SMY has a potential protective effect in DEP-aggravated AS in people with myocardial ischemia.
接触柴油尾气颗粒(DEP)会增加患缺血性心脏病的风险,尤其是心脏病发作和缺血性/血栓性中风。生脉饮(SMY)是一种用于治疗冠心病的中药。本研究的目的是确定SMY的保护作用以及SMY影响DEP诱导的心血管损伤的机制。本研究有望为开发SMY在预防动脉粥样硬化性心血管疾病和因全球空气污染暴露导致的过早死亡方面的适应性特征提供依据。我们建立了DEP暴露所致心肌缺血和动脉粥样硬化(AS)的动物模型。SMY治疗后,血脂恢复正常。与单独DEP暴露相比,SMY治疗后主动脉斑块面积和MMP9表达显著降低,胶原纤维表达增加。因此,斑块形成和易损性的风险降低。此外,SMY在不同程度上改善了ApoE小鼠的左心室结构、形态、功能、血流、梗死面积、心肌损伤和ROS积累。这些结果表明,使用SMY对治疗ApoE小鼠的血脂异常、动脉粥样硬化、心肌缺血和氧化应激有不同程度的效果。SMY对心肌缺血患者中DEP加重的AS具有潜在的保护作用。