Zhang Jingjing, Shi Xiaolu, Gao Jinhuan, Zhou Rui, Guo Feifei, Zhang Yi, Fan Fangfang, Zhai Qu, Sun Mingjie, Yang Hongjun
Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Beijing Key Laboratory of TCM Basic Research on Prevention and Treatment of Major Disease, Experimental Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Evid Based Complement Alternat Med. 2021 Jan 15;2021:2480465. doi: 10.1155/2021/2480465. eCollection 2021.
Myocardial infarction (MI) is one of the leading causes of death worldwide. However, there is no effective treatment for MI. In this study, trimetazidine (TMZ) and Danhong injection (DHI), representing western medicine and traditional Chinese medicine for MI, were used as tools to identify vital processes in alleviating MI injury. Administration of DHI and TMZ obviously decreased myocardial infarct size, improved ultrasonic heart function, and reduced creatine kinase (CK), lactate dehydrogenase (LDH), and glutamic oxaloacetic transaminase (AST) levels after MI. RNA-seq results indicated calcium ion handling and negative regulation of apoptotic process were vital processes and DHI and TMZ obviously reduced the expression of CaMK II and inhibited cleaved caspase-3 and Bax. Furthermore, DHI and TMZ increased p-S16-PLB, p-S16T17-PLB, CACNA1C, p-RyR2, and p-PKA expression but did not affect SERCA2a expression. In addition to the enhancement of cardiac myocyte shortening amplitude, maximum shortening velocity, and calcium transients, DHI and TMZ increased sarcoplasmic reticulum calcium content and enhanced SERCA2a calcium uptake capability by upregulating the phosphorylation of PLB but did not affect calcium exclusion by NCX. In conclusion, DHI and TMZ protect against MI through inhibiting apoptosis by downregulating CaMKII pathway and enhancing cardiac myocyte contractile functions possibly through the PKA signaling pathway.
心肌梗死(MI)是全球主要的死亡原因之一。然而,目前尚无针对MI的有效治疗方法。在本研究中,曲美他嗪(TMZ)和丹红注射液(DHI)分别作为治疗MI的西药和中药,被用于确定减轻MI损伤的关键过程。给予DHI和TMZ后,明显减小了心肌梗死面积,改善了超声心动功能,并降低了MI后肌酸激酶(CK)、乳酸脱氢酶(LDH)和谷草转氨酶(AST)水平。RNA测序结果表明,钙离子处理和凋亡过程的负调控是关键过程,DHI和TMZ明显降低了CaMK II的表达,并抑制了裂解的半胱天冬酶-3和Bax。此外,DHI和TMZ增加了p-S16-PLB、p-S16T17-PLB、CACNA1C、p-RyR2和p-PKA的表达,但不影响SERCA2a的表达。除了增强心肌细胞的缩短幅度、最大缩短速度和钙瞬变外,DHI和TMZ还通过上调PLB的磷酸化增加了肌浆网钙含量,并增强了SERCA2a的钙摄取能力,但不影响NCX的钙排出。总之,DHI和TMZ可能通过PKA信号通路下调CaMKII途径抑制细胞凋亡,并增强心肌细胞收缩功能,从而对MI起到保护作用。