文摘
D. bilabiata inhibited angiogenesis both in vitro and in vivo. The extracellular MMP-2 activity was reduced by D.bilabiata both in vitro and in vivo dose-dependently. D. bilabiata inhibited MMP-2, and MMP-14 and enhanced TIMP-2 and RECK in mRNA level. D. bilabiata induced the dose-dependent decrease of MMP-2 and increase of TIMP-2 secretion. The gene expressions of VEGF-A, -B, -C, -D and VEGFR-1, -2, -3 were all inhibited by D. bilabiata.