Department of Natural Product Chemistry, College of Pharmacy, Jilin University, Changchun, China.
Rapid Commun Mass Spectrom. 2022 Feb 28;36(4):e9219. doi: 10.1002/rcm.9219.
Panax ginseng (PG) and American ginseng (AMG) are both medicinal plants of the Panax genus in the Acanthopanax family. Although PG and AMG have similar components of ginsenosides, there are many differences of their bioactivities. In this study, the biochemical mechanisms of different bioactivities of PG and AMG were explored by researching the differential metabolites in plasma after administration of each of PG and AMG.
In order to explore the material basis of differential bioactivities, two groups of mice were administrated orally with PG and AMG, and the method of metabolomics was used to identify the differential metabolites in plasma. Then network pharmacology was used based on the differential metabolites. Afterward, the metabolite-target-pathway network of PG and AMG was constructed; thus the pathways related to different bioactivities were analyzed.
Through principal component analysis and orthogonal projections to latent structures discriminant analysis, there were 10 differential metabolites identified in the PG group and 8 differential metabolites identified in the AMG group. Based on network pharmacology, the differential metabolites were classified and related to differential bioactivities of PG and AMG. In the PG group, there were 6 metabolites related to aphrodisiac effect and exciting the nervous system, and 5 metabolites associated with raised blood pressure. In the AMG group, 5 metabolites were classified as having the effect of inhibiting the nervous system, and 6 metabolites were related to antihypertensive effect.
This study explored the material basis of the differential biological activities between PG and AMG, which is significant for the research of PG and AMG use and to promote human health.
人参(PG)和西洋参(AMG)均为五加科人参属药用植物,虽然 PG 和 AMG 的化学成分中均含有多种三萜皂苷类成分,但在生物活性方面存在较大差异。本研究通过给予 PG 和 AMG 后比较其血浆中的差异代谢物,探讨 PG 和 AMG 不同生物活性的生化机制。
为了探索其产生差异生物活性的物质基础,采用代谢组学方法,分别给予 PG 和 AMG 灌胃,观察各组小鼠血浆中的差异代谢物,再基于差异代谢物进行网络药理学分析,构建 PG 和 AMG 的代谢物-靶标-通路网络,分析差异生物活性相关通路。
通过主成分分析和正交偏最小二乘判别分析,鉴定出 PG 组有 10 个差异代谢物,AMG 组有 8 个差异代谢物。基于网络药理学,对差异代谢物进行分类,发现 PG 组中与壮阳、兴奋神经系统相关的有 6 个代谢物,与升高血压相关的有 5 个代谢物;AMG 组中与抑制神经系统相关的有 5 个代谢物,与降压相关的有 6 个代谢物。
本研究探讨了 PG 和 AMG 生物活性差异的物质基础,为研究 PG 和 AMG 的应用以及促进人类健康提供了依据。