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心肌缺血再灌注损伤的防治新靶点寻找及其研究进展

侯凯, 谭昊宇, 刘静, 李运曼

侯凯, 谭昊宇, 刘静, 李运曼. 心肌缺血再灌注损伤的防治新靶点寻找及其研究进展[J]. 中国药科大学学报, 2022, 53(2): 164-170. DOI: 10.11665/j.issn.1000-5048.20220205
引用本文: 侯凯, 谭昊宇, 刘静, 李运曼. 心肌缺血再灌注损伤的防治新靶点寻找及其研究进展[J]. 中国药科大学学报, 2022, 53(2): 164-170. DOI: 10.11665/j.issn.1000-5048.20220205
HOU Kai, TAN Haoyu, LIU Jing, LI Yunman. Advance of novel target strategies participating in myocardial ischemia reperfusion injury[J]. Journal of China Pharmaceutical University, 2022, 53(2): 164-170. DOI: 10.11665/j.issn.1000-5048.20220205
Citation: HOU Kai, TAN Haoyu, LIU Jing, LI Yunman. Advance of novel target strategies participating in myocardial ischemia reperfusion injury[J]. Journal of China Pharmaceutical University, 2022, 53(2): 164-170. DOI: 10.11665/j.issn.1000-5048.20220205

心肌缺血再灌注损伤的防治新靶点寻找及其研究进展

基金项目: 中国药科大学“双一流”建设科技创新团队项目资助(No.CPU2018GY23)

Advance of novel target strategies participating in myocardial ischemia reperfusion injury

Funds: This project was supported by China Pharmaceutical University "Double First-Class" Construction Technology Innovation Team Project (No.CPU2018GY23)
  • 摘要: 急性心肌梗死(AMI)及心力衰竭并发症的发病率和病死率在全世界居高不下。经证实心肌梗死后冠状动脉的早期再灌注是典型而有效的治疗方法,但侧支和冠脉缺血再灌注损伤(MIRI)及相关心脏保护机制尚不清楚。AMI的发生机制是多因素的,它通过多种机制导致心肌细胞死亡,并影响其他类型的细胞,包括血小板、成纤维细胞、内皮细胞和平滑肌细胞以及免疫细胞。大多数心脏保护策略通过常见的终末效应物发挥作用,但在合并症患者中的效果可能并不理想。因此,研究触发和治疗MIRI病理生理学相关的多靶点防治策略有重要意义。特别关注心脏保护策略现状,以此简单阐述参与防治心肌缺血再灌注损伤的多靶点治疗组合以及在研新靶点,以期为MIRI的机制研究与新药研发提供思路。
    Abstract: Worldwide morbidity and mortality of acute myocardial infarction (AMI) and related heart failure are still high.While effective early reperfusion of the criminal coronary artery after a confirmed AMI is the typical and effective treatment at present, collateral myocardial ischemia reperfusion injury (MIRI) and pertinent cardio-protection are still challenging to address and have inadequately understood mechanisms.One important reason might be that AMI is multifactorial, causing cardiomyocyte death via multiple mechanisms, as well as affecting other cell types, including platelets, fibroblasts, endothelial and smooth muscle cells, and immune cells.Many cardioprotective strategies act through common end-effectors and may be suboptimal in patients with comorbidities.Therefore, unveiling the related multitarget strategies participating in triggering and resisting the pathobiology of MIRI is a promising and valuable frontier.The review specifically focuses on the recent MIRI advances that are supported by multitarget strategies and new targets under development in order to bring the rational combination of multitarget therapies up to date, as well as to identify findings that may facilitate the new drug of novel targets.
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出版历程
  • 收稿日期:  2021-10-27
  • 修回日期:  2022-02-27
  • 刊出日期:  2022-04-24

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