Tongmai Yangxin pill alleviates myocardial ischemia/reperfusion injury by regulating mitochondrial fusion and fission through the estrogen receptor alpha/peroxisome proliferator-activated receptor gamma coactivator-1 alpha signaling pathway

IF 5.4 2区 医学 Q1 CHEMISTRY, MEDICINAL Journal of ethnopharmacology Pub Date : 2025-04-09 Epub Date: 2025-03-15 DOI:10.1016/j.jep.2025.119639
Lu Yu , Xu Wang , Qina Lei , Yutong Liu , Zhu Li , Xiangdong Dai , Zhihui Song , Yuanyuan He , Shan Gao , Chunquan Yu , Lin Li
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Abstract

Ethnopharmacological relevance

The Tongmai Yangxin Pill (TMYX) is derived from the Zhigancao decoction recorded in Treatise on Cold Damage Disorders (Shang Han Lun) by Zhang Zhongjing during the Han dynasty. The prescription of TMYX reflects a therapeutic rationale and efficacy unique to traditional Chinese medicine. TMYX is clinically effective in alleviating myocardial ischemia-reperfusion injury (MI/RI). However, the precise active ingredients and underlying mechanisms remain unclear.

Aim of the study

The primary objective of this study was to investigate the potential of TMYX in addressing MI/RI by activating the estrogen receptor ERα. We hypothesized that this action upregulates PGC-1α activity, subsequently promoting a balanced regulation of mitochondrial fusion and fission.

Materials and methods

UPLC-Q-TOF-MS/MS was used to identify the active components of TMYX. Subsequently, a network pharmacology approach was used to uncover the therapeutic targets and underlying pharmacological mechanisms through which TMYX mitigates MI/RI. Lastly, the anticipated outcomes were confirmed through in vivo and in vitro experimental validations.

Results

Using UPLC-Q-TOF-MS/MS, we successfully identified 53 distinct compounds in TMYX. Network pharmacology analysis revealed 20 key TMYX targets associated with MI/RI. Enrichment studies using GO and KEGG analyses revealed that these targets were mainly associated with mitochondrial processes and estrogen signaling pathways. Both in vivo and in vitro studies confirmed that TMYX markedly improved mitochondrial function through the ERα/PGC-1α signaling cascade, leading to a reduction in the size of myocardial infarctions and the incidence of apoptosis. Notably, combining TMYX with siERα abolished the protective effect of TMYX on the mitochondria.

Conclusion

TMYX therapy can improve cardiac function in MI/RI. This effect is likely mediated by the ERα/PGC-1α signaling pathway. However, given the complex multi-component composition of traditional Chinese medicine formulas, additional studies are necessary to confirm the findings of this research.

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通脉养心丸通过雌激素受体α /过氧化物酶体增殖体激活受体γ共激活因子-1 α信号通路调节线粒体融合和裂变,减轻心肌缺血/再灌注损伤
通脉养心丸(TMYX)源于汉代张仲景《商汉论》中记载的知草汤。TMYX的处方反映了中医独特的治疗原理和疗效。TMYX在缓解心肌缺血再灌注损伤(MI/RI)方面具有临床疗效。然而,确切的有效成分和潜在的机制尚不清楚。本研究的主要目的是探讨TMYX通过激活雌激素受体ERα来解决MI/RI的潜力。我们假设这种作用上调PGC-1α活性,随后促进线粒体融合和裂变的平衡调节。材料与方法采用suplc - q - tof -MS/MS对TMYX的有效成分进行鉴定。随后,网络药理学方法被用来揭示TMYX减轻MI/RI的治疗靶点和潜在的药理学机制。最后,通过体内和体外实验验证了预期结果。结果通过UPLC-Q-TOF-MS/MS鉴定出53个不同的化合物。网络药理学分析发现了20个与MI/RI相关的关键TMYX靶点。利用GO和KEGG分析的富集研究显示,这些靶点主要与线粒体过程和雌激素信号通路相关。体内和体外研究均证实,TMYX可通过ERα/PGC-1α信号级联显著改善线粒体功能,减少心肌梗死面积和细胞凋亡发生率。值得注意的是,TMYX与siERα联合可消除TMYX对线粒体的保护作用。结论tmyx治疗可改善MI/RI患者的心功能。这种作用可能是由ERα/PGC-1α信号通路介导的。然而,鉴于中药配方的复杂多组分组成,需要进一步的研究来证实本研究的结果。
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2,3,5-triphenyltetrazolium chloride (TTC)
来源期刊
Journal of ethnopharmacology
Journal of ethnopharmacology 医学-全科医学与补充医学
CiteScore
10.30
自引率
5.60%
发文量
967
审稿时长
77 days
期刊介绍: The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.
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