Department of Chinese Medicine, Chang Gung Memorial Hospital-Kaohsiung Medical Center, Chang Gung University College of Medicine, Taiwan.
Evid Based Complement Alternat Med. 2011;2011:215035. doi: 10.1093/ecam/nep207. Epub 2011 Jan 11.
This study aimed to assess the potential anti-angiogenic mechanism of Phyllanthus urinaria (P. urinaria) and characterize the major compound in P. urinaria that exerts anti-angiogenic effect. The water extract of P. urinaria and Ellagic Acid were used to evaluate the anti-angiogenic effect in chorioallantoic membrane (CAM) in chicken embryo and human vascular endothelial cells (HUVECs). The matrix metalloproteinase-2 (MMP-2) activity was determined by gelatin zymography. The mRNA expressions of MMP-2, MMP-14 and tissue inhibitor of metalloproteinase-2 (TIMP-2) were analyzed by reverse transcription polymerase chain reaction (RT-PCR). Level of MMP-2 proteins in conditioned medium or cytosol was determined by western blot analysis. We confirmed that P. urinaria's in vivo anti-angiogenic effect was associated with a reduction in MMP-2 activity. Ellagic acid, one of the major polyphenolic components as identified in P. urinaria by high performance liquid chromatography mass spectrometry (HPLC/MS), exhibited the same anti-angiogenic effect in vivo. Both P. urinaria and Ellagic Acid inhibited MMP-2 activity in HUVECs with unchanged mRNA level. The mRNA expression levels of MMP-14 and TIMP-2 were not altered either. Results from comparing the change of MMP-2 protein levels in conditioned medium and cytosol of HUVECs after the P. urinaria or Ellagic Acid treatment revealed an inhibitory effect on the secretion of MMP-2 protein. This study concluded that Ellagic Acid is the active compound in P. urinaria to exhibit anti-angiogenic activity and to inhibit the secretion of MMP-2 protein from HUVECs.
本研究旨在评估叶下珠(Phyllanthus urinaria,P. urinaria)的潜在抗血管生成机制,并鉴定出发挥抗血管生成作用的 P. urinaria 中的主要化合物。采用叶下珠水提取物和鞣花酸(Ellagic Acid)评估其在鸡胚绒毛尿囊膜(CAM)和人血管内皮细胞(HUVECs)中的抗血管生成作用。通过明胶酶谱法测定基质金属蛋白酶-2(MMP-2)的活性。采用逆转录聚合酶链反应(RT-PCR)分析 MMP-2、MMP-14 和金属蛋白酶组织抑制剂-2(TIMP-2)的 mRNA 表达。通过 Western blot 分析测定条件培养基或胞浆中 MMP-2 蛋白的水平。我们证实,叶下珠的体内抗血管生成作用与 MMP-2 活性的降低有关。鞣花酸是通过高效液相色谱-质谱联用技术(HPLC/MS)在叶下珠中鉴定出的主要多酚类成分之一,在体内也表现出相同的抗血管生成作用。叶下珠和鞣花酸均能抑制 HUVECs 中 MMP-2 的活性,而 mRNA 水平不变。MMP-14 和 TIMP-2 的 mRNA 表达水平也没有改变。比较叶下珠或鞣花酸处理后 HUVECs 条件培养基和胞浆中 MMP-2 蛋白水平的变化,发现其对 MMP-2 蛋白分泌有抑制作用。本研究得出结论,鞣花酸是叶下珠发挥抗血管生成活性和抑制 HUVECs 中 MMP-2 蛋白分泌的活性化合物。