Xiang Mi, Zhao Xin, Lu Yingdong, Zhang Yang, Ding Fan, Lv Lifei, Wang Yuling, Shen Zihuan, Li Li, Cui Xiangning
Department of Cardiovascular, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Department of Pathology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Front Cardiovasc Med. 2023 Jan 10;9:1038523. doi: 10.3389/fcvm.2022.1038523. eCollection 2022.
Modified Linggui Zhugan Decoction (MLZD) is a Traditional Chinese Medicine prescription developed from Linggui Zhugan Decoction (LZD) that has been used for the clinical treatment of ischemic cardiovascular diseases. However, the cardioprotective mechanism of MLZD against post-myocardial infarction (MI) ventricular remodeling remains unclear.
We explored the effects of MLZD on ventricular remodeling and their underlying mechanisms, respectively, in SD rats with MI models and in H9c2 cardiomyocytes with oxygen-glucose deprivation (OGD) models. The cardiac structure and function of rats were measured by echocardiography, HE staining, and Masson staining. Apoptosis, inflammation, mitochondrial structure and function, and sirtuin 3 (SIRT3) expression were additionally examined.
MLZD treatment significantly ameliorated cardiac structure and function, and thus reversed ventricular remodeling, compared with the control. Further research showed that MLZD ameliorated mitochondrial structural disruption, protected against mitochondrial dynamics disorder, restored impaired mitochondrial function, inhibited inflammation, and thus inhibited apoptosis. Moreover, the decreased expression level of SIRT3 was enhanced after MLZD treatment. The protective effects of MLZD on SIRT3 and mitochondria, nevertheless, were blocked by 3-TYP, a selective inhibitor of SIRT3.
These findings together revealed that MLZD could improve the ventricular remodeling of MI rats by ameliorating mitochondrial damage and its associated apoptosis, which might exert protective effects by targeting SIRT3.
加味苓桂术甘汤(MLZD)是由苓桂术甘汤(LZD)衍化而来的中药方剂,已用于缺血性心血管疾病的临床治疗。然而,MLZD对心肌梗死后(MI)心室重构的心脏保护机制仍不清楚。
我们分别在MI模型的SD大鼠和氧糖剥夺(OGD)模型的H9c2心肌细胞中探讨了MLZD对心室重构的影响及其潜在机制。通过超声心动图、HE染色和Masson染色测量大鼠的心脏结构和功能。另外检测细胞凋亡、炎症、线粒体结构和功能以及沉默调节蛋白3(SIRT3)的表达。
与对照组相比,MLZD治疗显著改善了心脏结构和功能,从而逆转了心室重构。进一步研究表明,MLZD改善了线粒体结构破坏,防止线粒体动力学紊乱,恢复受损的线粒体功能,抑制炎症,从而抑制细胞凋亡。此外,MLZD治疗后SIRT3表达水平降低的情况得到改善。然而,MLZD对SIRT3和线粒体的保护作用被SIRT3的选择性抑制剂3-TYP阻断。
这些发现共同表明,MLZD可以通过改善线粒体损伤及其相关的细胞凋亡来改善MI大鼠的心室重构,这可能通过靶向SIRT3发挥保护作用。