Pro-angiogenic effects of Ilexsaponin A1 on human umbilical vein endothelial cells in vitro and zebrafish in vivo

被引:23
作者
Li, Jingjing [1 ]
Zhang, Jinming [2 ]
Zou, Liang [3 ]
Lee, Simon Ming-Yuen [4 ,5 ]
Yang, Cui [6 ,7 ]
Seto, Sai-Wang [8 ]
Leung, George Pak-Heng [1 ]
机构
[1] Univ Hong Kong, Dept Pharmacol & Pharm, Hong Kong, Hong Kong, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Coll Pharm, Chengdu, Sichuan, Peoples R China
[3] Chengdu Univ, Sch Med, Chengdu, Sichuan, Peoples R China
[4] Univ Macau, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[5] Univ Macau, Inst Chinese Med Sci, Macau, Peoples R China
[6] Yunnan Minzu Univ, State Ethn Affairs Commiss, Key Lab Chem Ethn Med Resources, Ethn Drug Screening & Pharmacol Ctr, Kunming 650500, Yunnan, Peoples R China
[7] Yunnan Minzu Univ, Minist Educ, Kunming 650500, Yunnan, Peoples R China
[8] Univ Western Sydney, Natl Inst Complementary Med, Campbelltown, NSW, Australia
关键词
Ilexsaponin A1; Ilex pubescens; Pro-angiogenesis; Zebrafish; Endothelial cells; FOCAL ADHESION KINASE; GROWTH-FACTOR VEGF; ILEX-PUBESCENS; TARGETING ANGIOGENESIS; PROMOTES ANGIOGENESIS; SIGNALING PATHWAY; TOXICITY; MODEL; ANDROGRAPHOLIDE; PROLIFERATION;
D O I
10.1016/j.phymed.2017.10.006
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Ilexsaponin A1 is the major bioactive ingredient of Ilex pubescens Hook. et Arn. This plant has been conventionally used in Traditional Chinese Medicine for the treatment of cardiovascular diseases including stroke, coronary arterial disease, and peripheral vascular diseases. Purpose: To investigate the pro-angiogenic effect of Ilexsaponin A1 and its mechanism of action. Study design: Human umbilical vein endothelial cells (HUVECs) and transgenic zebrafish Tg(fli1:EGFP) were employed as an in vitro and in vivo model respectively. Methods: Pro-angiogenic effects of Ilexsaponin A1 were examined by assessing endothelial cell proliferation, migration, invasion and tube formation. The mechanism of pro-angiogenic effects was investigated by measuring the expression level of various signalling proteins. Furthermore, vascular endothelial growth factor (VEGF) tyrosine kinase inhibitor II (VRI)-induced vascular insufficient transgenic zebrafish model was used to confirm the results of the HUVECs results in vivo. Results: Ilexsaponin A1 significantly promoted cell proliferation, migration, invasion and tube formation in HUVECs, and rescued blood vessel loss in VRI-induced vascular insufficient zebrafish. Ilexsaponin A1 upregulated p-Akt, p-mTOR, p-Src, p-FAK, p-MEK, and p-Erk1/2 in HUVECs. Conclusion: This study showed that Ilexsaponin A1 exhibits pro-angiogenic activity in HUVECs and VRI-induced vascular insufficient zebrafish, probably by activating Akt/mTOR, MAPK/ERK and Src-and FAK-dependent signalling pathways. The findings suggest that Ilexsaponin A1 and probably I. pubescens, a major source of Ilexsaponin A1, could be developed as a potential therapeutic agent for preventing or treating cardiovascular diseases and/or other diseases related to vascular insufficiency.
引用
收藏
页码:229 / 237
页数:9
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