Effect of Angelica Sinensis extract on the angiogenesis of preovulatory follicles (F1–F3) in late-phase laying hens

• Published in: Poultry science 2023-02, Vol.102 (2), p.102415-102415, Article 102415
• Main Authors: Ping, Zhenlei, Chen, Xin, Fang, Lixue, Wu, Kai, Liu, Chang, Chen, Hao, Jiang, Xiaowen, Ma, Jun, Yu, Wenhui
• Format: Article
• Language: English
• Subjects: Angelica sinensis; Angelica Sinensis extract; angiogenesis; Animals; beta-sitosterol; blood; blood circulation; caffeic acid; cell adhesion; Chickens; endothelial cells; Female; ferulic acid; fluorescent antibody technique; follicle microvascular endothelial cell; gene ontology; genome; granulosa cell; Granulosa Cells; medicinal plants; Molecular Docking Simulation; Ovarian Follicle - metabolism; pharmacology; phosphorylation; PHYSIOLOGY AND REPRODUCTION; poultry science; preovulatory follicle; Reproducibility of Results; Theca Cells - metabolism; vascular endothelial growth factor A; Vascular Endothelial Growth Factor A - genetics; Vascular Endothelial Growth Factor A - metabolism; vascular endothelial growth factor receptor-2; Western blotting
• ISSN: 0032-5791; 1525-3171
• DOI: 10.1016/j.psj.2022.102415

In order to form follicles and ovulate normally, there must be abundant blood vessels. Angelica sinensis (Oliv.) Diels (AS), as a traditional Chinese medicinal herb, has the effects of tonifying the blood and activating the blood circulation. However, the effect of AS on angiogenesis in hen-follicles remains to be discovered. In this study, we identified vascular richness, granulosa layer thickness, expression of platelet endothelial cell adhesion molecule-1 (CD31) and the content of vascular endothelial growth factor A (VEGFA) in granulosa layers to elucidate the effect of AS extract on angiogenesis in preovulatory follicles (F1–F3) of late-phase laying hens (75 wk). Based on network pharmacology, we predicted beta-sitosterol, ferulic acid, and caffeic acid as the main active components of AS, and hypoxia-inducible factor-1α (HIF1α), vascular endothelial growth factor receptor 2 (VEGFR2) as hub targets of AS in angiogenesis. The intersection targets were enriched by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, and the hub targets were verified by immunofluorescence and western blot. Molecular docking of active components with hub targets was performed and verified in vitro. The results showed that AS extract promoted angiogenesis in preovulatory follicles and increased granulosa cell layer thickness, CD31 expression and content of VEGFA. Experiments in vitro and in vivo demonstrated that AS extract promoted the expression of HIF1α and VEGFA, up-regulated the phosphorylation levels of VEGFR2. These results further demonstrated the reliability of molecular docking and network pharmacology findings. In summary, AS extract can promote angiogenesis in the preovulatory follicles in late-phase laying hens. [Display omitted]