Szalay J, Goldberg R, Klug R
Acta Ophthalmol (Copenh). 1976 Dec;54(6):731-42. doi: 10.1111/j.1755-3768.1976.tb01792.x.
Light and electron microscopy is used to examine the effect of exogenous PGE1 on the permeability and reactivity of rat iridial blood vessels. Results show that topical PGE1 causes an increase in the permeability of iridial vessles to carbon particles (200 A diameter). The technique of carbon labelling is used to quantitate increases in permeability caused by varying concentrations of PGE1 (0.001-1.0 mg/ml). Regression analysis shows that there is a linear relationship (P less than 0.02) between carbon labelling and PGE1 concentration over the range of concentrations tested. In other experiments rats were treated with the systemic histamine liberator Compound 48/80, or with topical applications of histamine diphosphate in order to examine the effects of exogenous and endogenous histamine upon iridial blood vessel permeability. These procedures produce only minimal labelling of iridial vessels. It therefore seems likely that PGE1 has a direct effect on iridial vessels and does not act indirectly by bringing about the liberation of endogenous histamine.
利用光学显微镜和电子显微镜来检测外源性前列腺素E1(PGE1)对大鼠虹膜血管通透性和反应性的影响。结果显示,局部应用PGE1会导致虹膜血管对碳颗粒(直径200埃)的通透性增加。采用碳标记技术来定量不同浓度PGE1(0.001 - 1.0毫克/毫升)所引起的通透性增加。回归分析表明,在所测试的浓度范围内,碳标记与PGE1浓度之间存在线性关系(P < 0.02)。在其他实验中,给大鼠注射全身性组胺释放剂化合物48/80,或局部应用磷酸组胺,以检测外源性和内源性组胺对虹膜血管通透性的影响。这些操作仅使虹膜血管产生极少的标记。因此,PGE1似乎对虹膜血管有直接作用,而非通过促使内源性组胺释放来间接发挥作用。