Camel Biomedical Research Unit, College of Pharmacy and Medicine, King Saud University, Riyadh, Saudi Arabia.
Chem Biol Interact. 2013 Nov 25;206(2):204-13. doi: 10.1016/j.cbi.2013.09.007. Epub 2013 Sep 20.
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. Punarnavine significantly inhibited endothelial cell migration and invasion and capillary structure formation of HUVECs. Punarnavine significantly at 50 μM 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.
瓜馥木中的喹喏里西啶生物碱 Punarnavine 具有镇痛、抗炎、肝保护、免疫调节和抗增殖作用。然而,其在肿瘤血管生成中的作用及其涉及的分子机制尚不清楚。因此,我们在体外和体内研究了它的抗血管生成作用和机制。我们通过 RT-PCR、Western blot 和 ELISA 检查了 Punarnavine 对 VEGF-A 表达的影响。通过海绵植入血管生成试验测定体内抗血管生成活性,并评价其对艾氏腹水癌肿瘤的抗肿瘤活性。Punarnavine 显著抑制内皮细胞迁移和侵袭以及 HUVECs 的毛细血管结构形成。Punarnavine 显著抑制 MMP-2 和 MMP-9 在体外 HUVECs 中的表达。Punarnavine 抑制海绵植入物试验中的新血管生成。Punarnavine(15mg/kg bw/d)治疗可使艾氏腹水瘤模型中的腹水体积减少 60.94%,肿瘤体积减少 86.40%。Punarnavine 治疗可减少腹膜血管生成,提示 Punarnavine 具有抗血管生成活性。本研究揭示了 Punarnavine 的强大抗血管生成作用,并可进一步扩展以开发治疗癌症的治疗方案。