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人参皂苷 Rb1 对心肌缺血/再灌注损伤的作用:临床前证据和可能的机制。

Ginsenoside Rb1 for Myocardial Ischemia/Reperfusion Injury: Preclinical Evidence and Possible Mechanisms.

机构信息

Department of Cardiology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.

出版信息

Oxid Med Cell Longev. 2017;2017:6313625. doi: 10.1155/2017/6313625. Epub 2017 Dec 21.

Abstract

Ginseng is an important herbal drug that has been used worldwide for many years. Ginsenoside Rb1 (G-Rb1), the major pharmacological extract from ginseng, possesses a variety of biological activities in the cardiovascular systems. Here, we conducted a preclinical systematic review to investigate the efficacy of G-Rb1 for animal models of myocardial ischemia/reperfusion injury and its possible mechanisms. Ten studies involving 211 animals were identified by searching 6 databases from inception to May 2017. The methodological quality was assessed by using the CAMARADES 10-item checklist. All the data were analyzed using RevMan 5.3 software. As a result, the score of study quality ranged from 3 to 7 points. Meta-analyses showed that G-Rb1 can significantly decrease the myocardial infarct size and cardiac enzymes (including lactate dehydrogenase, creatine kinase, and creatine kinase-MB) when compared with control group ( < 0.01). Significant decrease in cardiac troponin T and improvement in the degree of ST-segment depression were reported in one study ( < 0.05). Additionally, the possible mechanisms of G-Rb1 for myocardial infarction are antioxidant, anti-inflammatory, antiapoptosis, promoting angiogenesis and improving the circulation. Thus, G-Rb1 is a potential cardioprotective candidate for further clinical trials of myocardial infarction.

摘要

人参是一种重要的草药,在全球范围内已经使用了多年。人参皂苷 Rb1(G-Rb1)是从人参中提取的主要药理成分,在心血管系统中具有多种生物学活性。在这里,我们进行了一项临床前系统评价,以研究 G-Rb1 对心肌缺血/再灌注损伤动物模型的疗效及其可能的机制。通过从 2017 年 5 月开始搜索 6 个数据库,共确定了 10 项涉及 211 只动物的研究。使用 CAMARADES 10 项清单评估方法学质量。所有数据均使用 RevMan 5.3 软件进行分析。结果,研究质量评分范围为 3 至 7 分。荟萃分析表明,与对照组相比,G-Rb1 可显著降低心肌梗死面积和心肌酶(包括乳酸脱氢酶、肌酸激酶和肌酸激酶-MB)(<0.01)。一项研究报告称,G-Rb1 可显著降低心肌肌钙蛋白 T 水平并改善 ST 段压低程度(<0.05)。此外,G-Rb1 对心肌梗死的可能作用机制包括抗氧化、抗炎、抗细胞凋亡、促进血管生成和改善循环。因此,G-Rb1 是一种有潜力的心肌梗死候选药物,值得进一步进行临床试验。

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