In vitro and in vivo anti-angiogenic activity of girinimbine isolated from Murraya koenigii

被引:19
|
作者
Iman, Venoos [1 ]
Karimian, Hamed [1 ]
Mohan, Syam [2 ]
Hobani, Yahya Hasan [2 ]
Noordin, Mohamed Ibrahim [1 ]
Mustafa, Mohd Rais [3 ]
Noor, Suzita Mohd [4 ]
机构
[1] Univ Malaya, Fac Med, Dept Pharm, Kuala Lumpur 50603, Malaysia
[2] Univ Jazan, Med Res Ctr, Jazan, Saudi Arabia
[3] Univ Malaya, Fac Med, Dept Pharmacol, Ctr Nat Prod & Drug Discovery CENAR, Kuala Lumpur 50603, Malaysia
[4] Univ Malaya, Fac Med, Dept Biomed Sci, Kuala Lumpur 50603, Malaysia
来源
关键词
angiogenesis; inhibitor; carbazole alkaloid; zebrafish; CARBAZOLE ALKALOIDS; BIOLOGICAL-ACTIVITY; TUMOR-GROWTH; ZEBRAFISH; INHIBITOR; INDUCTION; APOPTOSIS; CANCER; MECHANISMS; PATHWAYS;
D O I
10.2147/DDDT.S71557
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Girinimbine is a carbazole alkaloid isolated from the stem bark and root of Murraya koenigii. Here we report that girinimbine is an inhibitor of angiogenic activity both in vitro and in vivo. MTT results showed that girinimbine inhibited proliferation of human umbilical vein endothelial cells, while results from endothelial cell invasion, migration, tube formation, and wound healing assays demonstrated significant time-and dose-dependent inhibition by girinimbine. A proteome profiler array done on girinimbine-treated human umbilical vein endothelial cells showed that girinimbine had mediated regulation of pro-angiogenic and anti-angiogenic proteins. The anti-angiogenic potential of girinimbine was also evidenced in vivo in the zebrafish embryo model wherein girinimbine inhibited neo vessel formation in zebrafish embryos following 24 hours of exposure. Together, these results showed that girinimbine could effectively suppress angiogenesis, suggestive of its therapeutic potential as a novel angiogenesis inhibitor.
引用
收藏
页码:1281 / 1292
页数:12
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