Investigating the mechanism of action of Danhong injection and its components against myocardial ischemia–reperfusion injury

Peng-Zhen Lei, Charity Ngina Mwangi, Yuanlin Cao, Jingrui Chen, Yuting Huang, Yuefei Wang, Yan Zhu, Guanwei Fan, Miaomiao Jiang
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引用次数: 2

Abstract

Objective: The surgical treatment of myocardial infarction often causes myocardial ischemia–reperfusion injury (MI/RI). Danhong injection (DHI) has curative effects on coronary heart disease and angina pectoris. However, its therapeutic effects on MI/RI still require further validation. This study aims to investigate the components involved and mechanism of action of DHI against MI/RI. Methods: Primary metabolites (PM) and secondary metabolites (SM) were isolated from DHI. We established a rat model of MI/RI by administering PM, SM, and DHI. Cardiac morphology and functional parameters were evaluated using cardiac ultrasound. The metabolic effects of PM, SM, and DHI in the serum and myocardial tissue on MI/RI were investigated using 1hydrogen-nuclear magnetic resonance. Results: Our study showed that DHI, PM, and SM could improve cardiac function by correcting the dilated cardiac structure, alleviating inflammation by downregulating complement C2 expression, reducing reactive oxygen species (ROS) production by upregulating cyclooxygenase expression, and restoring normal energy supply by inhibiting fatty acid metabolism and stimulating glycometabolism. In addition, DHI and SM could attenuate the calcium overload and trigger an inflammatory response and oxidative stress by downregulating Ca2+/calmodulin-dependent protein kinase II expression. Conclusions: This study suggests that DHI and its components exerts resistance against MI/RI by ameliorating cardiac dysfunction, energy metabolism, and oxidative stress.
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探讨丹红注射液及其成分对心肌缺血再灌注损伤的作用机制
目的:心肌梗死手术治疗常引起心肌缺血再灌注损伤(MI/RI)。丹红注射液对冠心病、心绞痛有一定的治疗作用。然而,其治疗MI/RI的效果仍需进一步验证。本研究旨在探讨DHI对MI/RI的作用机制。方法:从DHI中分离初级代谢物(PM)和次级代谢物(SM)。我们通过给药PM、SM和DHI建立大鼠MI/RI模型。采用心脏超声检查心脏形态及功能参数。采用氢核磁共振技术研究血清和心肌组织中PM、SM和DHI对心肌梗死/心肌梗死的代谢影响。结果:我们的研究表明,DHI、PM和SM可以通过纠正扩张的心脏结构改善心功能,通过下调补体C2表达减轻炎症,通过上调环加氧酶表达减少活性氧(ROS)的产生,通过抑制脂肪酸代谢和刺激糖代谢恢复正常的能量供应。此外,DHI和SM可以通过下调Ca2+/钙调素依赖性蛋白激酶II的表达来减轻钙超载,引发炎症反应和氧化应激。结论:本研究提示DHI及其组分通过改善心功能障碍、能量代谢和氧化应激对心肌梗死/心肌梗死有抵抗作用。
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