基于网络药理学和实验验证,当归藁本内酯可抑制血管平滑肌A7r5细胞的迁移

Chunmei LI , Zhe XIE , Siqing HE , Shumiao HE , Yongqi LI , Qun LU
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引用次数: 0

摘要

目的当归的主要成分——白芷内酯(Lig)对多种心血管疾病具有保护作用。我们之前的研究表明,Lig抑制血管平滑肌细胞的增殖。本研究旨在研究Lig对血管紧张素II (Angiotensin II, Ang II)诱导的血管平滑肌A7r5细胞迁移的影响,并基于网络药理学探讨其作用机制。方法本研究采用划伤愈合实验和跨井迁移实验评估Lig对Angⅱ诱导的血管平滑肌A7r5细胞的迁移活性,并采用网络药理学方法预测可能的靶分子。采用Western blot分析、明胶酶谱分析和小干扰RNA (siRNA)技术,探讨了Lig对Angⅱ诱导的A7r5细胞迁移的作用机制。结果网络药理学结果显示,Lig可抑制Angⅱ诱导的A7r5细胞的迁移,这可能与c-Myc和MMPs有关。我们的研究结果显示,Lig可以显著降低Ang ii诱导的A7r5细胞中c-Myc和MMP-2蛋白表达水平的升高,但不影响MMP-9蛋白表达水平。我们的数据进一步表明,c-Myc siRNA与Lig一样,可以明显抑制细胞迁移,同时降低MMP-2的表达。结论Lig的抗迁移作用可能与c-Myc/MMP-2通路有关,Lig在预防心血管疾病方面具有广阔的应用前景。
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Ligustilide from Radix Angelica Sinensis prevents the migration of vascular smooth muscle A7r5 cells based on network pharmacology and experimental verification

Objective

Ligustilide (Lig), a major component of Radix Angelica Sinensis, exhibits a protective effect on many cardiovascular diseases. Our previous study showed that Lig inhibited the proliferation of vascular smooth muscle cells. In this study, we aimed to investigate the effect of Lig on the migration of vascular smooth muscle A7r5 cells induced by Angiotensin II (Ang II) and explore the mechanism underlying based on network pharmacology.

Methods

In this study, scratch-wound healing assay and transwell migration assay were used to assess the migration activity of Lig on Ang II-induced vascular smooth muscle A7r5 cells, and network pharmacology method was used to predict the possible target molecules. Western blot analysis, Gelatin zymography assay, and small interfering RNA (siRNA) were used to determine the underlying mechanism of Lig on the migration in Ang II-induced A7r5 cells.

Results

We found that Lig could prevented the migration induced by Ang II in A7r5 cells, which could be associated with c-Myc and MMPs from the results of network pharmacology. Our results revealed that Lig could significantly reduce the increase in the protein expression levels of c-Myc and MMP-2 in Ang II-induced A7r5 cells, but not affect the protein expression levels of MMP-9. Our data further showed that c-Myc siRNA, just as Lig, could obviously inhibit the cell migration accompanied by decreased MMP-2 expression.

Conclusion

These findings suggested the anti-migratory effect of Lig could be associated with the c-Myc/MMP-2 pathway, and Lig administration had a promising potential for preventing cardiovascular diseases.

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