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探索黄芪甲苷在缺血性心脏病中的作用:对临床前心脏毒性模型的全面系统评价和荟萃分析。

Exploring Astragaloside IV in Ischemic Heart Disease: A Comprehensive Systematic Review and Meta-Analysis of Preclinical Cardiotoxicity Models.

作者信息

Greeny Alosh, Viswanatha Gollapalle Lakshminarayanashastry, Shenoy Rekha Raghuveer, Hanumanthappa Shylaja, Chellappan Dinesh Kumar, Sandhu Jagnoor Singh, Khanna Saumya, Krishnadas Nandakumar

机构信息

Department of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education (MAHE), Manipal, Karnataka, India.

Independent Researcher, Bangalore, Karnataka, India.

出版信息

J Biochem Mol Toxicol. 2025 Jul;39(7):e70365. doi: 10.1002/jbt.70365.

Abstract

This systematic review and meta-analysis were conducted to evaluate the therapeutic efficacy of Astragaloside IV (As-IV) in ischemic heart disease based on the preclinical evidence and to correlate the cardioprotective effect with various available mechanisms. This systematic review and meta-analysis were conducted based on the results of a thorough literature search in databases of published papers, such as PubMed, Embase, and Google Scholar. A total of 18 studies that met the inclusion/exclusion criteria were included. The meta-analysis has shown the significant therapeutic efficacy of As-IV on ischemic heart disease. As-IV has decreased the myocardial infarction size, the left ventricular weight indices, the left ventricular internal diameter in systole, and the left ventricular internal diameter in diastole. As-IV has decreased the level of the third type of collagen and the decreased activity of creatine kinase and lactate dehydrogenase. Also, As-IV has markedly decreased the rate of apoptosis and the expression of the proapoptotic markers such as caspase-3 and Bax. The left ventricular systolic pressure, as well as the arterial shortening edge and the ejection fraction, has increased. The levels of the antiapoptotic protein Bcl-2 increased. In addition, As-IV has a powerful anti-inflammatory influence by inhibiting the main markers of inflammation, such as TLR4, IL-1, TNF-α, and TGF-β. As-IV has also caused an effect on angiogenesis by increasing the VEGF level. The results have revealed the As-IV, as a decent universal medicine for ischemic heart disease because of its variety of actions and effectiveness.

摘要

本系统评价和荟萃分析旨在基于临床前证据评估黄芪甲苷(As-IV)对缺血性心脏病的治疗效果,并将其心脏保护作用与各种现有机制相关联。本系统评价和荟萃分析是基于对已发表论文数据库(如PubMed、Embase和谷歌学术)进行全面文献检索的结果开展的。共纳入18项符合纳入/排除标准的研究。荟萃分析表明As-IV对缺血性心脏病具有显著的治疗效果。As-IV减小了心肌梗死面积、左心室重量指数、左心室收缩内径和左心室舒张内径。As-IV降低了Ⅲ型胶原蛋白水平,降低了肌酸激酶和乳酸脱氢酶的活性。此外,As-IV显著降低了凋亡率以及促凋亡标志物如半胱天冬酶-3和Bax的表达。左心室收缩压以及动脉缩短率和射血分数均有所增加。抗凋亡蛋白Bcl-2水平升高。此外,As-IV通过抑制炎症的主要标志物如TLR4、IL-1、TNF-α和TGF-β发挥强大的抗炎作用。As-IV还通过提高VEGF水平对血管生成产生影响。结果表明,As-IV因其多种作用和有效性,是一种治疗缺血性心脏病的有效通用药物。

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