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首页> 外文期刊>American Journal of PharmTech Research >Anti-Angiogenic Activity of L-Type Voltage Gated Calcium Channel Blocker, Nifedipine: An In-Vitro and In-Vivo Study
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Anti-Angiogenic Activity of L-Type Voltage Gated Calcium Channel Blocker, Nifedipine: An In-Vitro and In-Vivo Study

机译:L型电压门控钙通道阻滞剂硝苯地平的抗血管生成活性:体内和体外研究

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ABSTRACT Angiogenesis is the development of new blood vessels. A wealthy number of ion channels are found on the endothelial cells. These ion channels play a vital action in cell proliferation and in related angiogenesis. We aimed to investigate the effects of Nifedipine (L-Type voltage gated calcium channel blocker). The anti-angiogenic activities of Nifedipine was investigated by measuring its effects on number of branches formed, angiogenic score, number of sprouts formed, weight of sponge implanted, Hemoglobin content and histopathological studies by in-vitro (aortic ring assay) and in-vivo (sponge implantation method) methods. The test and standard drug (Bevacizumab) groups were compared with the control group using One-way ANOVA, followed by post hoc test, the Dennett’s test to compare mean of all the groups with the control mean. The results revealed that Nifedipine treatment led to significant inhibition of proliferation and related angiogenesis in the dose dependent manner and were quite comparable with the standard antiangiogenic drug Bevacizumab. These scientific findings indicate the clinical benefits of Nifedipine in pathological situations involving excessive angiogenesis. Negative regulation of cell cycle progression at various checkpoints and cell migration may be the underlying molecular mechanisms for antiangiogenic action. Keywords: Angiogenesis, aortic ring assay, sponge implantation method.
机译:摘要血管生成是新血管的发展。在内皮细胞上发现了大量的离子通道。这些离子通道在细胞增殖和相关血管生成中起着至关重要的作用。我们旨在研究硝苯地平(L型电压门控钙通道阻滞剂)的作用。通过测量硝苯地平对分支的形成,血管生成分数,形成的芽数,植入的海绵的重量,血红蛋白含量以及通过体外(主动脉环测定)和体内的组织病理学研究的作用,来研究硝苯地平的抗血管生成活性。 (海绵植入法)方法。使用单向方差分析将测试组和标准药物(贝伐单抗)组与对照组进行比较,然后进行事后检验,Dennett检验,以比较所有组的平均值与对照组的平均值。结果表明,硝苯地平治疗以剂量依赖性方式导致增殖和相关血管生成的显着抑制,并且与标准抗血管生成药物贝伐单抗相当。这些科学发现表明硝苯地平在涉及过度血管生成的病理情况下的临床益处。在各个检查点和细胞迁移过程中细胞周期进程的负调控可能是抗血管生成作用的潜在分子机制。关键词:血管生成,主动脉环测定,海绵植入法。

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