沙枣提取物体内抗血管生成作用的研究

Mohammad Sako, M. Zihlif, F. Afifi
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摘要

血管生成是由已有的血管形成新的血管。它发生在生理和病理条件下。我们旨在评估沙枣水提取物的体内抗血管生成作用,以确定提取物对A549肺癌癌症细胞系的任何抗增殖作用,并研究其对A549细胞系中VEGF-A和FGF2表达的影响。实施台盼蓝排斥试验以确定提取物的任何可能的抗增殖作用。然后,使用相同的细胞系在小鼠身上进行基质胶塞测定,以测试提取物的抗血管生成作用。最后,用浓度为25、12.5和6.25µg/ml的提取物处理A549细胞,通过RT-qPCR研究VEGF-A和FGF2表达的变化。狭叶提取物对A549细胞没有表现出显著的抗增殖作用。浓度为12.5和6.25µg/ml的提取物对新血管生长的抑制作用分别为75.63%和45.26%。提取物不影响VEGF-A和FGF2在A549细胞中的表达。我们的研究结果表明,狭叶的水提取物具有强大的抗血管生成活性,同时既没有表现出显著的抗增殖作用,也没有影响A459细胞系中VEGF-A或FGF2的表达,这表明要么是唯一的直接抗血管生成作用,要么是与其他基因的旁分泌抑制同时具有直接和间接作用。
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Investigating the Anti-Angiogenic Effects of Elaeagnus angustifolia L. Extract in Vivo
Angiogenesis is the formation of new blood vessels from pre-existing ones. It occurs in both physiological and pathological conditions. We aimed to evaluate the antiangiogenic effect of Elaeagnus angustifolia L. water extract in vivo to determine any anti-proliferative effect of the extract on the A549 lung cancer cell line, and to investigate its effect on VEGF-A and FGF2 expression in the A549 cell line. Trypan blue exclusion test was implemented to establish any possible anti-proliferative effect of the extract. Then, Matrigel plug assay was performed on mice using the same cell line to test the antiangiogenic effect of the extract. Finally, A549 cells were treated with the extract at concentrations of 25, 12.5, and 6.25 µg/ml to investigate the changes in VEGF-A and FGF2 expression by RT-qPCR. E. angustifolia extract did not exhibit a significant anti-proliferative effect against A549 cells. The extract at concentrations of 12.5 and 6.25 µg/ml demonstrated an inhibitory effect against the growth of new blood vessels by 75.63 and 45.26%, respectively. The extract did not affect the expression of VEGF-A and FGF2 in A549 cells. Our findings show that water extract of E. angustifolia possesses potent antiangiogenic activity, while neither exhibiting significant anti-proliferative effect nor affecting VEGF-A or FGF2 expression in the A459 cell line, suggesting either sole direct antiangiogenic effect, or both direct and indirect effects with paracrine suppression of other genes.
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