Punarnavine, an alkaloid from Boerhaavia diffusa exhibits anti-angiogenic activity via downregulation of VEGF in vitro and in vivo

被引:25
作者
Saraswati, Sarita [1 ]
Alhaider, Abdulqader A. [2 ]
Agrawal, S. S. [3 ]
机构
[1] King Saud Univ, Camel Biomed Res Unit, Coll Pharm & Med, Riyadh, Saudi Arabia
[2] King Saud Univ, Coll Med, Dept Physiol, Riyadh 11461, Saudi Arabia
[3] Amity Univ, Noida, UP, India
关键词
VEGF; MMP-2; MMP-9; Ehrlich ascites carcinoma; Angiogenesis; ENDOTHELIAL GROWTH-FACTOR; INHIBITS INFLAMMATORY ANGIOGENESIS; EHRLICH ASCITES TUMOR; HEPATOPROTECTIVE ACTIVITY; BIOLOGICAL FUNCTIONS; SIGNALING PATHWAY; ETHANOLIC EXTRACT; BOSWELLIC ACID; MELANOMA-CELLS; CANCER;
D O I
10.1016/j.cbi.2013.09.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Punarnavine, a quinolizidine alkaloid isolated from Boerhaavia diffusa is known to possess analgesic, anti-inflammatory, hepato-protective, immunomodulatory and anti-proliferative properties. However, its roles in tumor angiogenesis and the involved molecular mechanism are still unknown. Therefore, we examined its anti-angiogenic effects and mechanisms in vitro and in vivo. We examined the effect of punarnavine on VEGF-A expression by RT-PCR, Western blotting and ELISA. In vivo antiangiogenic activity was determined using sponge implant angiogenesis assay and antitumor activity was evaluated against Ehrlich ascites carcinoma tumor. Punamavine significantly inhibited endothelial cell migration and invasion and capillary structure formation of HUVECs. Punamavine significantly at 50 mu M inhibited MMP-2 and MMP-9 expression in HUVECs in vitro. Punarnavine inhibited neovascularization in sponge implant assay. Punarnavine (15 mg/kg bw/d) treatment showed dose-dependent decrease in the ascitic fluid volume by 60.94% and tumor volume by 86.40% in Ehrlich ascites model. Reduction in peritoneal angiogenesis with punarnavine treatment suggests the anti-angiogenic activity of punarnavine. The present study sheds light on the potent anti-angiogenic of the punarnavine and can be extended further to develop therapeutic protocols for treatment of cancer. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:204 / 213
页数:10
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