Form D M, Auerbach R
Proc Soc Exp Biol Med. 1983 Feb;172(2):214-8. doi: 10.3181/00379727-172-41548.
The angiogenic capability of PGE2 was tested by implanting pellets of an ethylene vinyl acetate slow release polymer containing PGE2 on the chorioallantoic membrane of 8-day-old chicken embryos. Elvax pellets releasing approximately 0.2, 2.0, or 20 ng/day PGE2 were found to induce neovascular responses. In contrast, pellets releasing 2.0 or 20 ng/day of either PGA2, PGF2, or TXB2 did not appear to be angiogenic when compared with PGE2. These release rates of PGE2 are similar to those reported for a variety of tumors, activated macrophages, inflammatory exudates, and rheumatoid synovia, suggesting that PGE2 may be a key factor in various neovascular reactions.
通过将含有前列腺素E2(PGE2)的乙烯-醋酸乙烯酯缓释聚合物微丸植入8日龄鸡胚的绒毛尿囊膜,来测试PGE2的血管生成能力。发现每天释放约0.2、2.0或20 ng PGE2的Elvax微丸可诱导新生血管反应。相比之下,与PGE2相比,每天释放2.0或20 ng前列腺素A2(PGA2)、前列腺素F2(PGF2)或血栓素B2(TXB2)的微丸似乎没有血管生成作用。这些PGE2的释放速率与多种肿瘤、活化巨噬细胞、炎性渗出物和类风湿性滑膜炎所报道的相似,这表明PGE2可能是各种新生血管反应中的关键因素。